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Molecular genetics of infertility: loss-of-function mutations in humans and corresponding knockout/mutated mice

https://doi.org/10.1093/humupd/dmaa034
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/embj.201387329openalex-snapshot
STAG3‐mediated stabilization of REC8 cohesin complexes promotes chromosome synapsis during meiosis
inferredcites →https://doi.org/10.1002/gene.10200openalex-snapshot
Targeted disruption of the heat shock transcription factor (hsf)‐2 gene results in increased embryonic lethality, neuronal defects, and reduced spermatogenesis
inferredcites →https://doi.org/10.1002/humu.21264openalex-snapshot
Mutations in SOHLH1 gene associate with nonobstructive Azoospermia
inferredcites →https://doi.org/10.1002/humu.21543openalex-snapshot
Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort
inferredcites →https://doi.org/10.1002/humu.22046openalex-snapshot
The androgen receptor gene mutations database: 2012 update
inferredcites →https://doi.org/10.1002/humu.23423openalex-snapshot
STX2is a causative gene for nonobstructive azoospermia
inferredcites →https://doi.org/10.1002/humu.23916openalex-snapshot
Mutation update for the NR5A1 gene involved in DSD and infertility
inferredcites →https://doi.org/10.1002/mrd.22197openalex-snapshot
A novel m.6307A>G mutation in the mitochondrialCOXIgene in asthenozoospermic infertile men
inferredcites →https://doi.org/10.1002/mrd.22768openalex-snapshot
A novel functional variant in Wilms’ Tumor 1 (WT1) is associated with idiopathic non‐obstructive azoospermia
inferredcites →https://doi.org/10.1002/path.4843openalex-snapshot
Motile and non‐motile cilia in human pathology: from function to phenotypes
inferredcites →https://doi.org/10.1002/wdev.42openalex-snapshot
The molecular and cellular basis of gonadal sex reversal in mice and humans
inferredcites →https://doi.org/10.1006/abbi.2000.1880openalex-snapshot
Mammalian Sperm Acrosome: Formation, Contents, and Function
inferredcites →https://doi.org/10.1006/dbio.1998.9087openalex-snapshot
Characterization of Oocyte and Follicle Development in Growth Differentiation Factor-9-Deficient Mice
inferredcites →https://doi.org/10.1006/dbio.2001.0535openalex-snapshot
The Mouse Meiotic Mutation mei1 Disrupts Chromosome Synapsis with Sexually Dimorphic Consequences for Meiotic Progression
inferredcites →https://doi.org/10.1007/s00018-019-03192-4openalex-snapshot
Vps13b is required for acrosome biogenesis through functions in Golgi dynamic and membrane trafficking
inferredcites →https://doi.org/10.1007/s00109-002-0376-9openalex-snapshot
Novel mutations affecting SRY DNA-binding activity: the HMG box N65H associated with 46,XY pure gonadal dysgenesis and the familial non-HMG box R30I associated with variable phenotypes
inferredcites →https://doi.org/10.1007/s00418-012-1031-3openalex-snapshot
Galnt3 deficiency disrupts acrosome formation and leads to oligoasthenoteratozoospermia
inferredcites →https://doi.org/10.1007/s00439-012-1234-7openalex-snapshot
A dominant-negative mutation of HSF2 associated with idiopathic azoospermia
inferredcites →https://doi.org/10.1007/s00439-017-1822-7openalex-snapshot
Dosage effects of ZP2 and ZP3 heterozygous mutations cause human infertility
inferredcites →https://doi.org/10.1007/s00439-019-01990-1openalex-snapshot
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation
inferredcites →https://doi.org/10.1007/s00439-020-02110-0openalex-snapshot
Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD
inferredcites →https://doi.org/10.1007/s00441-017-2592-1openalex-snapshot
Dynamic of contribution of UBPy-sorted cargo to acrosome biogenesis: effects of its derailment in a mouse model of globozoospermia, the infertile Vps54 (L967Q) mutant
inferredcites →https://doi.org/10.1007/s10815-014-0187-2openalex-snapshot
Identification of a novel m.9588G > A missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men
inferredcites →https://doi.org/10.1007/s10815-015-0443-0openalex-snapshot
The Nsun7 (A11337)-deletion mutation, causes reduction of its protein rate and associated with sperm motility defect in infertile men
inferredcites →https://doi.org/10.1007/s10815-015-0445-yopenalex-snapshot
Deleterious mutation in SYCE1 is associated with non-obstructive azoospermia
inferredcites →https://doi.org/10.1007/s10815-016-0715-3openalex-snapshot
A new mutation identified in SPATA16 in two globozoospermic patients
inferredcites →https://doi.org/10.1007/s10815-018-1188-3openalex-snapshot
A novel mutation in the TUBB8 gene is associated with complete cleavage failure in fertilized eggs
inferredcites →https://doi.org/10.1007/s10815-018-1374-3openalex-snapshot
Whole-exome sequencing identified a novel mutation of AURKC in a Chinese family with macrozoospermia
inferredcites →https://doi.org/10.1007/s10815-019-01404-1openalex-snapshot
Novel mutation in the ZP1 gene and clinical implications
inferredcites →https://doi.org/10.1007/s10815-019-01553-3openalex-snapshot
Novel compound heterozygous mutations in WEE2 causes female infertility and fertilization failure
inferredcites →https://doi.org/10.1007/s11427-016-0274-9openalex-snapshot
Association analysis between HFM1 variations and idiopathic azoospermia or severe oligozoospermia in Chinese Men
inferredcites →https://doi.org/10.1016/0092-8674(95)90275-9openalex-snapshot
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
inferredcites →https://doi.org/10.1016/j.ajhg.2008.04.018openalex-snapshot
Transcription Factor FIGLA is Mutated in Patients with Premature Ovarian Failure
inferredcites →https://doi.org/10.1016/j.ajhg.2010.08.018openalex-snapshot
WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome
inferredcites →https://doi.org/10.1016/j.ajhg.2011.01.018openalex-snapshot
DPY19L2 Deletion as a Major Cause of Globozoospermia
inferredcites →https://doi.org/10.1016/j.ajhg.2011.02.007openalex-snapshot
A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation
inferredcites →https://doi.org/10.1016/j.ajhg.2011.09.006openalex-snapshot
XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription
inferredcites →https://doi.org/10.1016/j.ajhg.2012.10.003openalex-snapshot
Loss-of-Function Mutations in LRRC6 , a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms, Cause Primary Ciliary Dyskinesia
inferredcites →https://doi.org/10.1016/j.ajhg.2012.11.002openalex-snapshot
Splice-Site Mutations in the Axonemal Outer Dynein Arm Docking Complex Gene CCDC114 Cause Primary Ciliary Dyskinesia
inferredcites →https://doi.org/10.1016/j.ajhg.2013.04.008openalex-snapshot
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
inferredcites →https://doi.org/10.1016/j.ajhg.2013.07.013openalex-snapshot
Loss-of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects
inferredcites →https://doi.org/10.1016/j.ajhg.2013.08.015openalex-snapshot
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
inferredcites →https://doi.org/10.1016/j.ajhg.2013.11.017openalex-snapshot
Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella
inferredcites →https://doi.org/10.1016/j.ajhg.2014.11.002openalex-snapshot
MCM9 Mutations Are Associated with Ovarian Failure, Short Stature, and Chromosomal Instability
inferredcites →https://doi.org/10.1016/j.ajhg.2016.06.012openalex-snapshot
Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens
inferredcites →https://doi.org/10.1016/j.ajhg.2016.06.022openalex-snapshot
Mutations in DNAJB13 , Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility
inferredcites →https://doi.org/10.1016/j.ajhg.2016.06.024openalex-snapshot
Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest
inferredcites →https://doi.org/10.1016/j.ajhg.2016.08.004openalex-snapshot
Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome
inferredcites →https://doi.org/10.1016/j.ajhg.2016.11.002openalex-snapshot
Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome
inferredcites →https://doi.org/10.1016/j.ajhg.2016.11.019openalex-snapshot
Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects
inferredcites →https://doi.org/10.1016/j.ajhg.2017.04.012openalex-snapshot
Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella
inferredcites →https://doi.org/10.1016/j.ajhg.2017.08.001openalex-snapshot
A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility
inferredcites →https://doi.org/10.1016/j.ajhg.2017.08.009openalex-snapshot
Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2
inferredcites →https://doi.org/10.1016/j.ajhg.2017.08.018openalex-snapshot
Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest
inferredcites →https://doi.org/10.1016/j.ajhg.2018.02.015openalex-snapshot
Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility
inferredcites →https://doi.org/10.1016/j.ajhg.2018.03.007openalex-snapshot
Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse
inferredcites →https://doi.org/10.1016/j.ajhg.2018.03.024openalex-snapshot
C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia
inferredcites →https://doi.org/10.1016/j.ajhg.2018.03.025openalex-snapshot
Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms
inferredcites →https://doi.org/10.1016/j.ajhg.2018.06.010openalex-snapshot
Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome
inferredcites →https://doi.org/10.1016/j.ajhg.2018.07.013openalex-snapshot
Loss of Calmodulin- and Radial-Spoke-Associated Complex Protein CFAP251 Leads to Immotile Spermatozoa Lacking Mitochondria and Infertility in Men
inferredcites →https://doi.org/10.1016/j.ajhg.2018.07.014openalex-snapshot
A Homozygous Ancestral SVA-Insertion-Mediated Deletion in WDR66 Induces Multiple Morphological Abnormalities of the Sperm Flagellum and Male Infertility
inferredcites →https://doi.org/10.1016/j.ajhg.2018.12.013openalex-snapshot
Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice
inferredcites →https://doi.org/10.1016/j.ajhg.2019.02.020openalex-snapshot
Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice
inferredcites →https://doi.org/10.1016/j.ajhg.2019.04.015openalex-snapshot
Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia
inferredcites →https://doi.org/10.1016/j.ajhg.2019.10.007openalex-snapshot
Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility
inferredcites →https://doi.org/10.1016/j.ajhg.2019.10.010openalex-snapshot
Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice
inferredcites →https://doi.org/10.1016/j.ajhg.2019.12.003openalex-snapshot
Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic Hypogonadism
inferredcites →https://doi.org/10.1016/j.ajhg.2020.05.001openalex-snapshot
Bi-allelic Missense Pathogenic Variants in TRIP13 Cause Female Infertility Characterized by Oocyte Maturation Arrest
inferredcites →https://doi.org/10.1016/j.ajhg.2020.05.010openalex-snapshot
Homozygous Mutations in BTG4 Cause Zygotic Cleavage Failure and Female Infertility
inferredcites →https://doi.org/10.1016/j.bbrc.2014.06.020openalex-snapshot
Two novel mutations in COII and tRNAHis mitochondrial genes in asthenozoospermic infertiles men
inferredcites →https://doi.org/10.1016/j.cell.2017.04.034openalex-snapshot
Ubiquitination-Deficient Mutations in Human Piwi Cause Male Infertility by Impairing Histone-to-Protamine Exchange during Spermiogenesis
inferredcites →https://doi.org/10.1016/j.cub.2005.07.056openalex-snapshot
Wee1B Is an Oocyte-Specific Kinase Involved in the Control of Meiotic Arrest in the Mouse
inferredcites →https://doi.org/10.1016/j.cub.2009.02.047openalex-snapshot
Tdrd6 Is Required for Spermiogenesis, Chromatoid Body Architecture, and Regulation of miRNA Expression
inferredcites →https://doi.org/10.1016/j.devcel.2009.10.012openalex-snapshot
The TDRD9-MIWI2 Complex Is Essential for piRNA-Mediated Retrotransposon Silencing in the Mouse Male Germline
inferredcites →https://doi.org/10.1016/j.ebiom.2019.03.075openalex-snapshot
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks
inferredcites →https://doi.org/10.1016/j.fertnstert.2007.11.062openalex-snapshot
Analysis of the SRY gene in two sex-reversed XY sisters identifies two new novel point mutations in the high mobility group box domain
inferredcites →https://doi.org/10.1016/j.fertnstert.2009.04.009openalex-snapshot
Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility
inferredcites →https://doi.org/10.1016/j.fertnstert.2009.11.013openalex-snapshot
Idiopathic hypogonadotropic hypogonadism in a mother and her monozygotic twins born after a single embryo transfer
inferredcites →https://doi.org/10.1016/j.fertnstert.2010.12.006openalex-snapshot
Hsp90b1 knockout targeted to male germline: a mouse model for globozoospermia
inferredcites →https://doi.org/10.1016/j.fertnstert.2013.11.128openalex-snapshot
The effect of 5α-reductase-2 deficiency on human fertility
inferredcites →https://doi.org/10.1016/j.fertnstert.2014.09.021openalex-snapshot
Genomic and genetic variation in E2F transcription factor-1 in men with nonobstructive azoospermia
inferredcites →https://doi.org/10.1016/j.fertnstert.2018.11.013openalex-snapshot
New biallelic mutations in WEE2: expanding the spectrum of mutations that cause fertilization failure or poor fertilization
inferredcites →https://doi.org/10.1016/j.fertnstert.2019.01.007openalex-snapshot
A novel homozygous FBXO43 mutation associated with male infertility and teratozoospermia in a consanguineous Chinese family
inferredcites →https://doi.org/10.1016/j.gene.2017.04.044openalex-snapshot
CFTR gene mutations and polymorphism are associated with non-obstructive azoospermia: From case-control study
inferredcites →https://doi.org/10.1016/j.gene.2017.08.033openalex-snapshot
A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF)
inferredcites →https://doi.org/10.1016/j.gene.2017.10.014openalex-snapshot
A novel mutation in HAUS7 results in severe oligozoospermia in two brothers
inferredcites →https://doi.org/10.1016/j.gene.2018.01.035openalex-snapshot
Genetic contribution of SUN5 mutations to acephalic spermatozoa in Fujian China
inferredcites →https://doi.org/10.1016/j.gene.2018.03.040openalex-snapshot
TDRD6 is associated with oligoasthenoteratozoospermia by sequencing the patient from a consanguineous family
inferredcites →https://doi.org/10.1016/j.gene.2018.11.074openalex-snapshot
A homozygous RNF220 mutation leads to male infertility with small-headed sperm
inferredcites →https://doi.org/10.1016/j.gene.2019.02.060openalex-snapshot
Identification of a homozygous GFPT2 variant in a family with asthenozoospermia
inferredcites →https://doi.org/10.1016/j.jcf.2012.01.005openalex-snapshot
Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens
inferredcites →https://doi.org/10.1016/j.jgg.2018.09.006openalex-snapshot
Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia
inferredcites →https://doi.org/10.1016/j.juro.2014.11.004openalex-snapshot
The Mutational Spectrum of WT1 in Male Infertility
inferredcites →https://doi.org/10.1016/j.mce.2006.04.021openalex-snapshot
Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes
inferredcites →https://doi.org/10.1016/j.mce.2016.05.025openalex-snapshot
Aromatase deficiency: a novel compound heterozygous mutation identified in a Chinese girl with severe phenotype and obvious maternal virilization
inferredcites →https://doi.org/10.1016/j.molcel.2012.05.048openalex-snapshot
MCM8- and MCM9-Deficient Mice Reveal Gametogenesis Defects and Genome Instability Due to Impaired Homologous Recombination
inferredcites →https://doi.org/10.1016/j.rbmo.2010.01.008openalex-snapshot
Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure
inferredcites →https://doi.org/10.1016/j.rbmo.2012.02.021openalex-snapshot
Unexplained infertility: an update and review of practice
inferredcites →https://doi.org/10.1016/j.rbmo.2017.05.017openalex-snapshot
Mutation analysis of the TUBB8 gene in nine infertile women with oocyte maturation arrest
inferredcites →https://doi.org/10.1016/j.rbmo.2018.03.009openalex-snapshot
Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest
inferredcites →https://doi.org/10.1016/j.semcdb.2016.01.013openalex-snapshot
Towards defining an ‘origin’—The case for the mammalian acrosome
inferredcites →https://doi.org/10.1016/j.tem.2018.07.002openalex-snapshot
Molecular Genetics of Premature Ovarian Insufficiency
inferredcites →https://doi.org/10.1016/j.urology.2018.06.031openalex-snapshot
Whole Exome Sequencing of a Consanguineous Turkish Family Identifies a Mutation in GTF2H3 in Brothers With Spermatogenic Failure
inferredcites →https://doi.org/10.1016/j.ydbio.2006.02.027openalex-snapshot
Sohlh1 is essential for spermatogonial differentiation
inferredcites →https://doi.org/10.1016/j.ydbio.2010.07.033openalex-snapshot
TMF/ARA160: A key regulator of sperm development
inferredcites →https://doi.org/10.1016/s0015-0282(16)50011-9openalex-snapshot
Lack of a head in human spermatozoa from sterile patients: a syndrome associated with impaired fertilization
inferredcites →https://doi.org/10.1016/s0015-0282(16)59520-xopenalex-snapshot
The ultrastructural pathology of the spermatozoon as a cause of infertility: the role of electron microscopy in the evaluation of semen quality
inferredcites →https://doi.org/10.1016/s0092-8674(00)81312-4openalex-snapshot
Meiotic Pachytene Arrest in MLH1-Deficient Mice
inferredcites →https://doi.org/10.1016/s0140-6736(03)14845-3openalex-snapshot
Azoospermia in patients heterozygous for a mutation in SYCP3
inferredcites →https://doi.org/10.1016/s0925-4773(03)00043-1openalex-snapshot
nanos1: a mouse nanos gene expressed in the central nervous system is dispensable for normal development
inferredcites →https://doi.org/10.1016/s1097-2765(00)80070-2openalex-snapshot
The Mouse RecA-like Gene Dmc1 Is Required for Homologous Chromosome Synapsis during Meiosis
inferredcites →https://doi.org/10.1016/s1097-2765(00)80404-9openalex-snapshot
The Murine SCP3 Gene Is Required for Synaptonemal Complex Assembly, Chromosome Synapsis, and Male Fertility
inferredcites →https://doi.org/10.1016/s1472-6483(10)60388-4openalex-snapshot
Screening for FOXL2 gene mutations in women with premature ovarian failure: an Indian experience
inferredcites →https://doi.org/10.1016/s1534-5807(03)00369-1openalex-snapshot
The Hop2 Protein Has a Direct Role in Promoting Interhomolog Interactions during Mouse Meiosis
inferredcites →https://doi.org/10.1038/12729openalex-snapshot
Globozoospermia in mice lacking the casein kinase II α′ catalytic subunit
inferredcites →https://doi.org/10.1038/383531a0openalex-snapshot
Growth differentiation factor-9 is required during early ovarian folliculogenesis
inferredcites →https://doi.org/10.1038/73502openalex-snapshot
The gamete fusion process is defective in eggs of Cd9-deficient mice
inferredcites →https://doi.org/10.1038/81547openalex-snapshot
Mater, a maternal effect gene required for early embryonic development in mice
inferredcites →https://doi.org/10.1038/aja.2010.47openalex-snapshot
A newly discovered mutation in PICK1 in a human with globozoospermia
inferredcites →https://doi.org/10.1038/cddis.2016.344openalex-snapshot
The control of male fertility by spermatid-specific factors: searching for contraceptive targets from spermatozoon’s head to tail
inferredcites →https://doi.org/10.1038/cddis.2016.414openalex-snapshot
Globozoospermia and lack of acrosome formation in GM130-deficient mice
inferredcites →https://doi.org/10.1038/cr.2014.70openalex-snapshot
Atg7 is required for acrosome biogenesis during spermatogenesis in mice
inferredcites →https://doi.org/10.1038/ejhg.2009.140openalex-snapshot
The CFTR frameshift mutation 3905insT and its effect at transcript and protein level
inferredcites →https://doi.org/10.1038/ejhg.2015.107openalex-snapshot
STAG3 truncating variant as the cause of primary ovarian insufficiency
inferredcites →https://doi.org/10.1038/gim.2016.225openalex-snapshot
A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes
inferredcites →https://doi.org/10.1038/gim.2017.130openalex-snapshot
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans
inferredcites →https://doi.org/10.1038/nature03362openalex-snapshot
The immunoglobulin superfamily protein Izumo is required for sperm to fuse with eggs
inferredcites →https://doi.org/10.1038/nature13203openalex-snapshot
Juno is the egg Izumo receptor and is essential for mammalian fertilization
inferredcites →https://doi.org/10.1038/ncb1135openalex-snapshot
Cohesin SMC1β is required for meiotic chromosome dynamics, sister chromatid cohesion and DNA recombination
inferredcites →https://doi.org/10.1038/ncomms5887openalex-snapshot
The subcortical maternal complex controls symmetric division of mouse zygotes by regulating F-actin dynamics
inferredcites →https://doi.org/10.1038/ng.2277openalex-snapshot
CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms
inferredcites →https://doi.org/10.1038/ng0501-82openalex-snapshot
Haploinsufficiency of protamine-1 or -2 causes infertility in mice
inferredcites →https://doi.org/10.1038/ng1907openalex-snapshot
R-spondin1 is essential in sex determination, skin differentiation and malignancy
inferredcites →https://doi.org/10.1038/ng2027openalex-snapshot
Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility
inferredcites →https://doi.org/10.1038/ng856openalex-snapshot
Cdc25b phosphatase is required for resumption of meiosis during oocyte maturation
inferredcites →https://doi.org/10.1038/nrg.2016.88openalex-snapshot
Specification and epigenetic programming of the human germ line
inferredcites →https://doi.org/10.1038/s10038-019-0568-6openalex-snapshot
Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility
inferredcites →https://doi.org/10.1038/s41431-018-0283-3openalex-snapshot
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility
inferredcites →https://doi.org/10.1038/s41467-017-02792-7openalex-snapshot
Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human
inferredcites →https://doi.org/10.1038/s41467-018-07784-9openalex-snapshot
Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9
inferredcites →https://doi.org/10.1038/s41467-018-08182-xopenalex-snapshot
Loss-of-function mutations in QRICH2 cause male infertility with multiple morphological abnormalities of the sperm flagella
inferredcites →https://doi.org/10.1038/s41598-018-28666-6openalex-snapshot
AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice
inferredcites →https://doi.org/10.1038/s41598-018-34262-5openalex-snapshot
X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family
inferredcites →https://doi.org/10.1038/s41598-019-52436-7openalex-snapshot
Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella
inferredcites →https://doi.org/10.1038/sj.cdd.4401362openalex-snapshot
E2F1 deficiency impairs murine spermatogenesis and augments testicular degeneration in SCP3-nullizygous mice
inferredcites →https://doi.org/10.1055/s-0032-1324718openalex-snapshot
The Molecular Genetics of Sex Determination and Sex Reversal in Mammals
inferredcites →https://doi.org/10.1056/nejmc1310150openalex-snapshot
Mutations in HFM1 in Recessive Primary Ovarian Insufficiency
inferredcites →https://doi.org/10.1056/nejmoa040533openalex-snapshot
A WNT4 Mutation Associated with Müllerian-Duct Regression and Virilization in a 46,XX Woman
inferredcites →https://doi.org/10.1056/nejmoa073443openalex-snapshot
A GPR54 -Activating Mutation in a Patient with Central Precocious Puberty
inferredcites →https://doi.org/10.1056/nejmoa0806228openalex-snapshot
Mutations in NR5A1 Associated with Ovarian Insufficiency
inferredcites →https://doi.org/10.1056/nejmoa1111184openalex-snapshot
InactivatingKISS1Mutation and Hypogonadotropic Hypogonadism
inferredcites →https://doi.org/10.1056/nejmoa1302160openalex-snapshot
Central Precocious Puberty Caused by Mutations in the Imprinted Gene MKRN3
inferredcites →https://doi.org/10.1056/nejmoa1308851openalex-snapshot
Mutant ZP1 in Familial Infertility
inferredcites →https://doi.org/10.1056/nejmoa1309635openalex-snapshot
Mutant Cohesin in Premature Ovarian Failure
inferredcites →https://doi.org/10.1056/nejmoa1406192openalex-snapshot
X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men
inferredcites →https://doi.org/10.1056/nejmoa1510791openalex-snapshot
Mutations in TUBB8 and Human Oocyte Meiotic Arrest
inferredcites →https://doi.org/10.1071/rd12300openalex-snapshot
Knockdown of UCHL5IP causes abnormalities in ?-tubulin localisation, spindle organisation and chromosome alignment in mouse oocyte meiotic maturation
inferredcites →https://doi.org/10.1073/pnas.0401194101openalex-snapshot
Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function
inferredcites →https://doi.org/10.1073/pnas.0401855101openalex-snapshot
Gonadotropin-regulated testicular RNA helicase (GRTH/Ddx25) is essential for spermatid development and completion of spermatogenesis
inferredcites →https://doi.org/10.1073/pnas.0506318103openalex-snapshot
An intronic insertion in KPL2 results in aberrant splicing and causes the immotile short-tail sperm defect in the pig
inferredcites →https://doi.org/10.1073/pnas.1015447108openalex-snapshot
Tudor domain containing 7 ( Tdrd7 ) is essential for dynamic ribonucleoprotein (RNP) remodeling of chromatoid bodies during spermatogenesis
inferredcites →https://doi.org/10.1073/pnas.1102284108openalex-snapshot
Heparan sulfate 6-O-sulfotransferase 1 , a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism
inferredcites →https://doi.org/10.1073/pnas.1310777111openalex-snapshot
A heterozygous mutation of GALNTL5 affects male infertility with impairment of sperm motility
inferredcites →https://doi.org/10.1073/pnas.1324025111openalex-snapshot
Lack of testicular seipin causes teratozoospermia syndrome in men
inferredcites →https://doi.org/10.1073/pnas.1424648112openalex-snapshot
Spata6 is required for normal assembly of the sperm connecting piece and tight head–tail conjunction
inferredcites →https://doi.org/10.1073/pnas.162027899openalex-snapshot
Lack of acrosome formation in mice lacking a Golgi protein, GOPC
inferredcites →https://doi.org/10.1073/pnas.212474399openalex-snapshot
Generation and characterization of androgen receptor knockout (ARKO) mice: An in vivo model for the study of androgen functions in selective tissues
inferredcites →https://doi.org/10.1073/pnas.93.11.5431openalex-snapshot
Targeted disruption of the mZP3 gene results in production of eggs lacking a zona pellucida and infertility in female mice.
inferredcites →https://doi.org/10.1074/jbc.m110.116418openalex-snapshot
Zmynd15 Encodes a Histone Deacetylase-dependent Transcriptional Repressor Essential for Spermiogenesis and Male Fertility
inferredcites →https://doi.org/10.1074/jbc.m117.784108openalex-snapshot
Loss of the Na+/H+ exchanger NHE8 causes male infertility in mice by disrupting acrosome formation
inferredcites →https://doi.org/10.1074/jbc.ra117.000861openalex-snapshot
Mechanistic insights into acephalic spermatozoa syndrome–associated mutations in the human SUN5 gene
inferredcites →https://doi.org/10.1074/jbc.ra118.002851openalex-snapshot
The histone methyltransferase SETD2 is required for expression of acrosin-binding protein 1 and protamines and essential for spermiogenesis in mice
inferredcites →https://doi.org/10.1080/09513590.2018.1464138openalex-snapshot
Mutation analysis of theTUBB8gene in primary infertile women with arrest in oocyte maturation
inferredcites →https://doi.org/10.1080/09513590802454927openalex-snapshot
A novel mutation in exon8 of the follicle-stimulating hormone receptor in a woman with primary amenorrhea
inferredcites →https://doi.org/10.1080/15548627.2016.1199300openalex-snapshot
TBC1D20 mediates autophagy as a key regulator of autophagosome maturation
inferredcites →https://doi.org/10.1083/jcb.149.6.1289openalex-snapshot
Normal Fertilization Occurs with Eggs Lacking the Integrin α6β1 and Is Cd9-Dependent
inferredcites →https://doi.org/10.1083/jcb.200709057openalex-snapshot
Mouse TEX15 is essential for DNA double-strand break repair and chromosomal synapsis during male meiosis
inferredcites →https://doi.org/10.1084/jem.20182365openalex-snapshot
A DNAH17 missense variant causes flagella destabilization and asthenozoospermia
inferredcites →https://doi.org/10.1086/422103openalex-snapshot
Hypergonadotropic Ovarian Failure Associated with an Inherited Mutation of Human Bone Morphogenetic Protein-15 (BMP15) Gene
inferredcites →https://doi.org/10.1086/521314openalex-snapshot
Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia
inferredcites →https://doi.org/10.1089/gtmb.2012.0052openalex-snapshot
Possible Association of a Novel Missense Mutation A6375G in the Mitochondrial Cytochrome C Oxidase I Gene with Asthenospermia in the Tunisian Population
inferredcites →https://doi.org/10.1091/mbc.e03-04-0226openalex-snapshot
Acroplaxome, an F-Actin–Keratin-containing Plate, Anchors the Acrosome to the Nucleus during Shaping of the Spermatid Head
inferredcites →https://doi.org/10.1091/mbc.e10-02-0170openalex-snapshot
Aurora-C Kinase Deficiency Causes Cytokinesis Failure in Meiosis I and Production of Large Polyploid Oocytes in Mice
inferredcites →https://doi.org/10.1093/biolre/ioy258openalex-snapshot
Disruption of ubiquitin specific protease 26 gene causes male subfertility associated with spermatogenesis defects in mice†
inferredcites →https://doi.org/10.1093/biosci/biu180openalex-snapshot
A Structural Basis for How Motile Cilia Beat
inferredcites →https://doi.org/10.1093/hmg/10.11.1117openalex-snapshot
Disruption of an inner arm dynein heavy chain gene results in asthenozoospermia and reduced ciliary beat frequency
inferredcites →https://doi.org/10.1093/hmg/11.14.1647openalex-snapshot
The Hook1 gene is non-functional in the abnormal spermatozoon head shape (azh) mutant mouse
inferredcites →https://doi.org/10.1093/hmg/11.19.2309openalex-snapshot
Mutations of the GREAT gene cause cryptorchidism
inferredcites →https://doi.org/10.1093/hmg/5.7.933openalex-snapshot
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
inferredcites →https://doi.org/10.1093/hmg/dds200openalex-snapshot
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots
inferredcites →https://doi.org/10.1093/hmg/dds264openalex-snapshot
An ancient founder mutation in PROKR2 impairs human reproduction
inferredcites →https://doi.org/10.1093/hmg/ddu046openalex-snapshot
Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects
inferredcites →https://doi.org/10.1093/hmg/ddv290openalex-snapshot
Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family
inferredcites →https://doi.org/10.1093/hmg/ddw186openalex-snapshot
A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development
inferredcites →https://doi.org/10.1093/hmg/ddx199openalex-snapshot
A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency
inferredcites →https://doi.org/10.1093/hmg/ddx200openalex-snapshot
Homozygous deletion of SUN5 in three men with decapitated spermatozoa
inferredcites →https://doi.org/10.1093/hmg/ddx408openalex-snapshot
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development
inferredcites →https://doi.org/10.1093/hmg/ddy034openalex-snapshot
Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia
inferredcites →https://doi.org/10.1093/hmg/ddy037openalex-snapshot
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies
inferredcites →https://doi.org/10.1093/hmg/ddy261openalex-snapshot
Basonuclin 1 deficiency is a cause of primary ovarian insufficiency
showing the first 200 of 367 · page through all 367

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4639207openalex-extracted
The Association between Multiple Metal Exposure and Semen Quality: Shanghai, China
inferred← citeshttps://doi.org/10.2139/ssrn.4777221openalex-extracted
Japanese Medaka Dmrt3a is Involved in Male Fertility
inferred← citeshttps://doi.org/10.1002/advs.202515512openalex-snapshot
Mapping the Non‐Canonical Splicing Variants: Decrypting the Hidden Genetic Architecture of Idiopathic Male Infertility
inferred← citeshttps://doi.org/10.1002/ctm2.1463openalex-snapshot
A pathogenic AKAP4 variant, p.R429H, causes male in/subfertility in humans and mice
inferred← citeshttps://doi.org/10.1002/fsn3.4258openalex-snapshot
Serum copper assessment in patients with polycystic ovary syndrome and tubal infertility: A retrospective 5‐year study
inferred← citeshttps://doi.org/10.1002/hsr2.797openalex-snapshot
Genetic correlation between female infertility and mental health and lifestyle factors: A linkage disequilibrium score regression study
inferred← citeshttps://doi.org/10.1002/humu.24355openalex-snapshot
The heterozygous mutations of SLC26A8 are not the main actors for male infertility
inferred← citeshttps://doi.org/10.1002/mco2.481openalex-snapshot
Drug development advances in human genetics‐based targets
inferred← citeshttps://doi.org/10.1002/mco2.70179openalex-snapshot
Alterations in Semen Quality and Immune‐Related Factors in Men with Infertility who Recovered from COVID‐19
inferred← citeshttps://doi.org/10.1002/mgg3.1820openalex-snapshot
Whole exome sequencing identified a rare WT1 loss‐of‐function variant in a non‐syndromic POI patient
inferred← citeshttps://doi.org/10.1002/open.202100219openalex-snapshot
NBMA Promotes Spermatogenesis by Mediating Oct4 Pathway
inferred← citeshttps://doi.org/10.1007/978-3-031-55163-5_1openalex-snapshot
Predicting Infertility: How Genetic Variants in Oocyte Spindle Genes Affect Egg Quality
inferred← citeshttps://doi.org/10.1007/978-3-031-97868-5_5openalex-snapshot
Non-systematic and Systematic Defects of Human Spermatozoon
inferred← citeshttps://doi.org/10.1007/978-981-92-0038-2_6openalex-snapshot
The Mouse as a Cornerstone of Biomedical Research: A Biological Model for Human Health and Disease
inferred← citeshttps://doi.org/10.1007/s00018-023-05025-xopenalex-snapshot
CCDC146 is required for sperm flagellum biogenesis and male fertility in mice
inferred← citeshttps://doi.org/10.1007/s00018-023-05081-3openalex-snapshot
Tektin bundle interacting protein, TEKTIP1, functions to stabilize the tektin bundle and axoneme in mouse sperm flagella
inferred← citeshttps://doi.org/10.1007/s00018-026-06225-xopenalex-snapshot
Garin3 regulates sperm-oocyte fusion and male fertility
inferred← citeshttps://doi.org/10.1007/s00438-025-02234-wopenalex-snapshot
Prevalence and molecular spectrum of thalassemia in infertile population among different ethnic groups in Hainan Province, China
inferred← citeshttps://doi.org/10.1007/s00438-025-02278-yopenalex-snapshot
A missense mutation in TCFL5 is associated with male infertility due to oligoasthenoteratozoospermia
inferred← citeshttps://doi.org/10.1007/s00439-022-02459-4openalex-snapshot
Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans
inferred← citeshttps://doi.org/10.1007/s00439-023-02606-5openalex-snapshot
Homozygous variants in CDC23 cause female infertility characterized by oocyte maturation defects
inferred← citeshttps://doi.org/10.1007/s10304-022-00494-yopenalex-snapshot
Genetische Diagnostik bei ungewollt kinderlosen Paaren oder wiederholten Fehlgeburten
inferred← citeshttps://doi.org/10.1007/s10815-021-02196-zopenalex-snapshot
Genetic factors as potential molecular markers of human oocyte and embryo quality
inferred← citeshttps://doi.org/10.1007/s10815-021-02306-xopenalex-snapshot
Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility
inferred← citeshttps://doi.org/10.1007/s10815-023-02810-2openalex-snapshot
Advances in the study of genetic factors and clinical interventions for fertilization failure
inferred← citeshttps://doi.org/10.1007/s10815-023-02873-1openalex-snapshot
A novel variant in CFAP69 causes asthenoteratozoospermia with treatable ART outcomes and a literature review
inferred← citeshttps://doi.org/10.1007/s10815-023-02897-7openalex-snapshot
Novel mutations in DNAH17 cause sperm flagellum defects and their influence on ICSI outcome
inferred← citeshttps://doi.org/10.1007/s10815-023-02961-2openalex-snapshot
Compound heterozygous mutations in TBPL2 were identified in an infertile woman with impaired ovarian folliculogenesis
inferred← citeshttps://doi.org/10.1007/s10815-024-03219-1openalex-snapshot
Identification of a novel splicing variant of thyroid hormone receptor interaction protein 13 (TRIP13) in female infertility characterized by oocyte maturation arrest
inferred← citeshttps://doi.org/10.1007/s10815-024-03294-4openalex-snapshot
Metabolomic signature of sperm in men with obesity-associated asthenozoospermia
inferred← citeshttps://doi.org/10.1007/s10815-024-03306-3openalex-snapshot
Human oocyte zona pellucida abnormalities: evaluation of clinical impact for different zona pellucida abnormalities and role of using assisted hatching
inferred← citeshttps://doi.org/10.1007/s10815-025-03626-yopenalex-snapshot
Novel homozygous variants in ASTL and WEE2 responsible for female infertility characterized by abnormal fertilization
inferred← citeshttps://doi.org/10.1007/s10815-025-03719-8openalex-snapshot
The impact of genetic variants in folliculogenesis and steroidogenesis pathways on ovarian response: a post hoc multicenter multiethnic cohort study
inferred← citeshttps://doi.org/10.1007/s10815-026-03901-6openalex-snapshot
TEX44 deficiency induces asthenoteratozoospermia by disrupting sperm axonemal integrity and mitochondrial sheath assembly, and ICSI enables successful fertility rescue
inferred← citeshttps://doi.org/10.1007/s11427-023-2408-2openalex-snapshot
Gene-knockout by iSTOP enables rapid reproductive disease modeling and phenotyping in germ cells of the founder generation
inferred← citeshttps://doi.org/10.1007/s11596-023-2704-yopenalex-snapshot
Truncating PICK1 Variant Identified in Azoospermia Affected Mitochondrial Dysfunction in Knockout Mice
inferred← citeshttps://doi.org/10.1007/s11655-022-3515-2openalex-snapshot
Efficacy of Qizi Yusi Pill on Pregnancy Outcomes in Women of Advanced Reproductive Age: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial
inferred← citeshttps://doi.org/10.1007/s12015-025-10902-yopenalex-snapshot
Transcriptome-Wide Sequencing Identifies Non-Coding RNAs and Their Competing Endogenous RNA Networks During the Stages of pPGCLCs-Induced Differentiation
inferred← citeshttps://doi.org/10.1007/s13353-025-00960-wopenalex-snapshot
Identification of lncRNA expression profiles associated with ovarian development and ageing process in mice
inferred← citeshttps://doi.org/10.1007/s43032-021-00694-0openalex-snapshot
Expanding the Genetic and Phenotypic Spectrum of Female Infertility Caused by TUBB8 Mutations
inferred← citeshttps://doi.org/10.1007/s43032-025-01851-5openalex-snapshot
Identification of the novel homozygous whole exon deletion in MEI1 underlying azoospermia and embryonic arrest in one consanguineous family
inferred← citeshttps://doi.org/10.1007/s43032-026-02159-8openalex-snapshot
Reduced and Mislocalized ACTL7A in Globozoospermia: Implications for Sperm Chromatin Integrity and Infertility
inferred← citeshttps://doi.org/10.1016/b978-0-12-822003-0.00028-0openalex-snapshot
Autophagy in germ cells, stem cells, and induced pluripotent stem cells
inferred← citeshttps://doi.org/10.1016/j.ando.2025.102481openalex-snapshot
Sertoli cell-only syndrome (Del Castillo syndrome): Past, present and future
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2024.107598openalex-snapshot
MiR-29b inhibits COC expansion and oocyte in vitro maturation via induction of ROS by targeting CYCS
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111049openalex-snapshot
The perinuclear theca protein Calicin helps shape the sperm head and maintain the nuclear structure in mice
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.113531openalex-snapshot
NLRP14 deficiency causes female infertility with oocyte maturation defects and early embryonic arrest by impairing cytoplasmic UHRF1 abundance
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2024.108105openalex-snapshot
Deciphering the comprehensive knowledgebase landscape featuring infertility with IDDB Xtra
inferred← citeshttps://doi.org/10.1016/j.cophys.2022.100611openalex-snapshot
Role of autophagy in male and female fertility
inferred← citeshttps://doi.org/10.1016/j.cub.2023.06.079openalex-snapshot
CCDC176 stabilizes microtubule doublets 1 and 9 to ensure proper sperm movement
inferred← citeshttps://doi.org/10.1016/j.ebiom.2022.104246openalex-snapshot
Genetic landscape of a large cohort of Primary Ovarian Insufficiency: New genes and pathways and implications for personalized medicine
inferred← citeshttps://doi.org/10.1016/j.ebiom.2023.104675openalex-snapshot
CFAP70 is a solid and valuable target for the genetic diagnosis of oligo-astheno-teratozoospermia in infertile men
inferred← citeshttps://doi.org/10.1016/j.ebiom.2023.104798openalex-snapshot
Deficiency in AK9 causes asthenozoospermia and male infertility by destabilising sperm nucleotide homeostasis
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118231openalex-snapshot
BDE-209 toxicity: From spermiogenesis to sexual maturity in F1 male mice
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.119561openalex-snapshot
PFOA exposure decreases acrosome reaction and increases DNA oxidative damage by impairing the sperm head shaping in mice
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115128openalex-snapshot
Overview of the development of HBV small molecule inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmg.2022.104597openalex-snapshot
EIF4ENIF1 variants in two patients with non-syndromic premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1016/j.engreg.2021.11.006openalex-snapshot
Emerging biomaterials for reproductive medicine
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2022.10.011openalex-snapshot
Is the “E” being removed from Reproductive Endocrinology to be replaced by a “G” for Genetics?
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148734openalex-snapshot
Revisiting GDF9 variants in primary ovarian insufficiency: A shift from dominant to recessive pathogenicity?
inferred← citeshttps://doi.org/10.1016/j.gene.2024.148946openalex-snapshot
Association of FOXL2 and ERCC6 variants with premature ovarian insufficiency and their potential use in clinical IVF guidance
inferred← citeshttps://doi.org/10.1016/j.gim.2022.07.027openalex-snapshot
Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrest
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e38263openalex-snapshot
WDR64, a testis-specific protein, is involved in the manchette and flagellum formation by interacting with ODF1
inferred← citeshttps://doi.org/10.1016/j.isci.2024.110366openalex-snapshot
Further evidence from DNAH12 supports favorable fertility outcomes of infertile males with dynein axonemal heavy chain gene family variants
inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104858openalex-snapshot
The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113176openalex-snapshot
LRRC71 is essential for sperm motility, fertilization, and male fertility
inferred← citeshttps://doi.org/10.1016/j.jep.2022.115867openalex-snapshot
Wuzi-Yanzong-Wan prevents oligoasthenospermia due to TAp73 suppression by affecting cellular junction remodeling in testicular tissue in mice
inferred← citeshttps://doi.org/10.1016/j.jff.2024.106451openalex-snapshot
Association of plant-based diets with odds of teratozoospermia in China: A case-control study
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.06.008openalex-snapshot
Deficiency of MFSD6L, an acrosome membrane protein, causes oligoasthenoteratozoospermia in humans and mice
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.12.010openalex-snapshot
The testis-specific gene 1700030J22Rik is essential for sperm flagellar function and male fertility in mice
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.139098openalex-snapshot
Fine particulate matter and its chemical constituents on oocyte quality in controlled ovarian hyperstimulation cycles: A prospective cohort study in China
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.141086openalex-snapshot
Environmental glyphosate exposure compromises sperm quality in mice by impairing acrosome biogenesis via GOLPH3-mediated golgiphagy
inferred← citeshttps://doi.org/10.1016/j.jri.2025.104465openalex-snapshot
Mendelian randomization reveals causal relationships between cytokines and male reproductive diseases
inferred← citeshttps://doi.org/10.1016/j.lfs.2024.123120openalex-snapshot
CRISPR innovations in tissue engineering and gene editing
inferred← citeshttps://doi.org/10.1016/j.mcpro.2023.100564openalex-snapshot
STK33 Phosphorylates Fibrous Sheath Protein AKAP3/4 to Regulate Sperm Flagella Assembly in Spermiogenesis
inferred← citeshttps://doi.org/10.1016/j.mcpro.2024.100720openalex-snapshot
TMEM225 Is Essential for Sperm Maturation and Male Fertility by Modifying Protein Distribution of Sperm in Mice
inferred← citeshttps://doi.org/10.1016/j.phymed.2024.155713openalex-snapshot
Betaine alleviates spermatogenic cells apoptosis of oligoasthenozoospermia rat model by up-regulating methyltransferases and affecting DNA methylation
inferred← citeshttps://doi.org/10.1016/j.rbmo.2022.05.016openalex-snapshot
PRSS55 is a novel potential causative gene for human male infertility
inferred← citeshttps://doi.org/10.1016/j.rbmo.2023.103765openalex-snapshot
A novel homozygous nonsense variant of AK7 is associated with multiple morphological abnormalities of the sperm flagella
inferred← citeshttps://doi.org/10.1016/j.rbmo.2024.104777openalex-snapshot
Comparing subjective indicators of health in adults aged 27–38 years conceived with and without assisted reproductive technology
inferred← citeshttps://doi.org/10.1016/j.rbmo.2025.104895openalex-snapshot
TKTL1: a new candidate gene in non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1016/j.rbmo.2025.104974openalex-snapshot
Novel homozygous variants in piRNA pathway factors lead to male infertility in humans
inferred← citeshttps://doi.org/10.1016/j.repbio.2024.100891openalex-snapshot
Identification of a novel mutation in chibby family member 2 in a non-obstructive azoospermic patient
inferred← citeshttps://doi.org/10.1016/j.repbre.2025.08.003openalex-snapshot
From bench to bedside: Mouse models in translating infertility research to clinical applications in assisted reproduction
inferred← citeshttps://doi.org/10.1016/j.scib.2022.09.026openalex-snapshot
Mutations in CCIN cause teratozoospermia and male infertility
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.09.026openalex-snapshot
MicroRNA-34b-5p targets PPP1R11 to inhibit proliferation and promote apoptosis in cattleyak Sertoli cells by regulating specific signaling pathways
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.10.011openalex-snapshot
Knockdown of Toe1 causes developmental arrest during the morula-to-blastocyst transition in mice
inferred← citeshttps://doi.org/10.1016/j.tice.2025.102879openalex-snapshot
Shikonin mitigates diabetic testicular dysfunction by improving oxidative, apoptotic, and metabolic functions in rats
inferred← citeshttps://doi.org/10.1016/j.tice.2026.103331openalex-snapshot
HSPA1A-BAG5 chaperone complex promotes spermatogenesis by driving ubiquitination-mediated degradation of ATF2
inferred← citeshttps://doi.org/10.1016/j.xfss.2025.02.002openalex-snapshot
Genetic insights into the immunological basis of male infertility: a translational perspective
inferred← citeshttps://doi.org/10.1016/j.xgen.2025.101012openalex-snapshot
Genetic landscape of human oocyte/embryo defects
inferred← citeshttps://doi.org/10.1016/j.xhgg.2021.100067openalex-snapshot
Maternal effect genes: Update and review of evidence for a link with birth defects
inferred← citeshttps://doi.org/10.1016/j.xhgg.2022.100098openalex-snapshot
Maternal effect genes as risk factors for congenital heart defects
inferred← citeshttps://doi.org/10.1038/s10038-024-01288-9openalex-snapshot
A novel homozygous nonsense variant of STX2 underlies non-obstructive azoospermia in a consanguineous Chinese family
inferred← citeshttps://doi.org/10.1038/s41378-026-01165-9openalex-snapshot
Female reproductive tract-on-a-chip for selecting sperm with ultra-low DNA fragmentation index
inferred← citeshttps://doi.org/10.1038/s41418-026-01872-wopenalex-snapshot
SMC1A is required for fate determinations of human spermatogonial stem cells and male fertility by interacting with YBX1 and stabilizing HMGA2 mRNA via an m5C modification
inferred← citeshttps://doi.org/10.1038/s41420-025-02581-yopenalex-snapshot
MCM9 deficiency impairs DNA damage repair during spermatogenesis, leading to Sertoli cell-only syndrome in humans
inferred← citeshttps://doi.org/10.1038/s41420-026-03124-9openalex-snapshot
Zona pellucida is required for oocyte actin cortex and oocyte-somatic cell interactions during oocyte growth
inferred← citeshttps://doi.org/10.1038/s41422-021-00507-8openalex-snapshot
Dominant mutations in CHK1 cause pronuclear fusion failure and zygote arrest that can be rescued by CHK1 inhibitor
inferred← citeshttps://doi.org/10.1038/s41467-025-63280-xopenalex-snapshot
The TEX44-CPT1B axis regulates mitochondrial sheath assembly and fatty acid oxidation in sperm
inferred← citeshttps://doi.org/10.1080/19396368.2026.2619009openalex-snapshot
Novel DNAH1 variants in Chinese males with MMAF-associated asthenoteratozoospermia
inferred← citeshttps://doi.org/10.1089/gtmb.2023.0263openalex-snapshot
Identification of a Homozygous Mutation of CCDC40 in a Chinese Infertile Man with MMAF and PCD-like Phenotypes
inferred← citeshttps://doi.org/10.1093/biolre/ioac076openalex-snapshot
Potential clinical value of in vitro spermatogenesis
inferred← citeshttps://doi.org/10.1093/biolre/ioac093openalex-snapshot
Genetic characterization of a missense mutation in the X-linked TAF7L gene identified in an oligozoospermic man
inferred← citeshttps://doi.org/10.1093/biolre/ioac134openalex-snapshot
Advances in studying human gametogenesis and embryonic development in China
inferred← citeshttps://doi.org/10.1093/biolre/ioad076openalex-snapshot
Experimental and molecular support for Cfap70 as a causative gene of ‘multiple morphological abnormalities of the flagella’ with male infertility
inferred← citeshttps://doi.org/10.1093/hmg/ddab163openalex-snapshot
Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging
inferred← citeshttps://doi.org/10.1093/hmg/ddab242openalex-snapshot
The mutation c.346-1G > A in SOHLH1 impairs sperm production in the homozygous but not in the heterozygous condition
inferred← citeshttps://doi.org/10.1093/hropen/hoad025openalex-snapshot
Phytochemical consumption and the risk of teratozoospermia: findings from a hospital-based case–control study in China
inferred← citeshttps://doi.org/10.1093/humrep/deab196openalex-snapshot
Potential of testis-derived circular RNAs in seminal plasma to predict the outcome of microdissection testicular sperm extraction in patients with idiopathic non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1093/humrep/deab229openalex-snapshot
Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects
inferred← citeshttps://doi.org/10.1093/humrep/deac026openalex-snapshot
Identification of a heterozygous variant of ZP2 as a novel cause of empty follicle syndrome in humans and mice
inferred← citeshttps://doi.org/10.1093/humrep/dead079openalex-snapshot
Biallelic variants inIQCNcause sperm flagellar assembly defects and male infertility
inferred← citeshttps://doi.org/10.1093/humrep/deae057openalex-snapshot
Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1093/humrep/deag071openalex-snapshot
Bi-allelic mutations of CAMSAP1 result in teratozoospermia with sperm head and flagella defects in humans
inferred← citeshttps://doi.org/10.1093/humrep/deag097openalex-snapshot
Pathogenic variants in ACTRT3 lead to male infertility characterized by fertilization defects
inferred← citeshttps://doi.org/10.1093/humupd/dmac024openalex-snapshot
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1093/humupd/dmae037openalex-snapshot
Defects in mRNA splicing and implications for infertility: a comprehensive review and in silico analysis
inferred← citeshttps://doi.org/10.1093/humupd/dmaf003openalex-snapshot
Molecular insights into sperm head shaping and its role in human male fertility
inferred← citeshttps://doi.org/10.1093/humupd/dmaf018openalex-snapshot
A comparison of spermatogenesis between flies and men—conserved processes of male gamete production
inferred← citeshttps://doi.org/10.1093/humupd/dmaf023openalex-snapshot
The intricate dance of RNA-binding proteins: unveiling the mechanisms behind male infertility
inferred← citeshttps://doi.org/10.1093/humupd/dmag008openalex-snapshot
Molecular interplay between sperm and oocyte: a narrative review
inferred← citeshttps://doi.org/10.1093/molehr/gaac021openalex-snapshot
Novel bi-allelic variants in KASH5 are associated with meiotic arrest and non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1093/molehr/gaag007openalex-snapshot
Reduced activin A levels impair urogenital system development and compromise female mouse fertility
inferred← citeshttps://doi.org/10.1093/molehr/gaag031openalex-snapshot
Investigating the role of a testis-expressed gene Tex2 in spermatogenesis in mice
inferred← citeshttps://doi.org/10.1093/nar/gkad524openalex-snapshot
RNase H1 facilitates recombinase recruitment by degrading DNA–RNA hybrids during meiosis
inferred← citeshttps://doi.org/10.1093/nar/gkag558openalex-snapshot
XPF-like domain in human SHOC1 is required for crossover formation and protecting autosome from MSUC
inferred← citeshttps://doi.org/10.1093/procel/pwae018openalex-snapshot
Discovery of CCDC188 gene as a novel genetic target for human acephalic spermatozoa syndrome
inferred← citeshttps://doi.org/10.1093/reprod/xaaf003openalex-snapshot
Asthenozoospermic spermatozoa manifest mitochondrial dysfunction and DKK3 deficiency is a pathogenic factor
inferred← citeshttps://doi.org/10.1093/sexmed/qfaf070openalex-snapshot
The effects of exercise frequency on sexual function and psychological health in infertile women
inferred← citeshttps://doi.org/10.1096/fj.202500640ropenalex-snapshot
Tmx2 Maintains Mitochondrial Function to Support Preimplantation Embryogenesis
inferred← citeshttps://doi.org/10.1097/cm9.0000000000004028openalex-snapshot
Sequencing the CCDC146 gene in a large cohort of infertile Chinese men reveals novel mutations in patients with asthenoteratozoospermia
inferred← citeshttps://doi.org/10.1097/rd9.0000000000000016openalex-snapshot
The programmed death of fetal oocytes and the correlated surveillance mechanisms
inferred← citeshttps://doi.org/10.1101/2022.01.10.475757openalex-snapshot
Ccdc38 is required for sperm flagellum biogenesis and male fertility in mouse
inferred← citeshttps://doi.org/10.1101/2023.06.21.545885openalex-snapshot
Splicing factor SRSF1 is essential for homing of precursor spermatogonial stem cells in mice
inferred← citeshttps://doi.org/10.1101/2023.10.08.561407openalex-snapshot
Identification of CFAP52 as a novel diagnostic target of male infertility with defects of sperm head-tail connection and flagella development
inferred← citeshttps://doi.org/10.1101/2025.02.23.639767openalex-snapshot
Essential role of CFAP77-CCDC105-TEX43 subcomplex in connecting axonemal A and B tubules for mammalian sperm motility
inferred← citeshttps://doi.org/10.1101/2025.05.28.656576openalex-snapshot
The XPF-like domain in SHOC1 required for homologous recombination and safeguarding autosome from meiotic silencing of unsynapsed chromatin
inferred← citeshttps://doi.org/10.1101/2025.07.28.667185openalex-snapshot
DNAH14 deficiency impairs sperm motility by reducing flagellar beat amplitude
inferred← citeshttps://doi.org/10.1111/1755-0998.13901openalex-snapshot
A framework for identifying fertility gene targets for mammalian pest control
inferred← citeshttps://doi.org/10.1111/ahg.70026openalex-snapshot
CFAP74 Variants Could Cause Male Infertility With the Asthenoteratozoospermia Phenotype
inferred← citeshttps://doi.org/10.1111/andr.13553openalex-snapshot
Novel ACTL7A variants in males lead to fertilization failure and male infertility
inferred← citeshttps://doi.org/10.1111/andr.13589openalex-snapshot
Novel variations in TENT5D lead to teratozoospermia in infertile patients
inferred← citeshttps://doi.org/10.1111/andr.13605openalex-snapshot
Whole‐exome sequencing identifies ADGB as a novel causative gene for male infertility in humans: from motility to fertilization
inferred← citeshttps://doi.org/10.1111/andr.13676openalex-snapshot
Homozygous deleterious variants in the C‐terminal of TDRD5 impair spermiogenesis, causing severe oligoasthenoteratozoospermia in humans
inferred← citeshttps://doi.org/10.1111/andr.70213openalex-snapshot
Loss‐of‐Function SSFA2 Variants Disrupt Fertility Through Impaired Acrosome Formation and Sperm Function
inferred← citeshttps://doi.org/10.1111/andr.70272openalex-snapshot
Loss‐of‐Function Variants in CCDC189 Cause Human Oligoasthenoteratozoospermia by Disrupting Sperm Flagellar and Acrosomal Architecture
inferred← citeshttps://doi.org/10.1111/andr.70280openalex-snapshot
CEP131 Deficiency Leads to Multiple Morphological Abnormalities of the Sperm Flagellum‐Associated Male Infertility via Impaired CEP290 Interaction
inferred← citeshttps://doi.org/10.1111/andr.70291openalex-snapshot
Variants in ZZS Complex‐Associated Genes TEX11 and M1AP Are Responsible for Male Infertility and Nonobstructive Azoospermia
inferred← citeshttps://doi.org/10.1111/cge.14069openalex-snapshot
A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia
inferred← citeshttps://doi.org/10.1111/cge.14383openalex-snapshot
A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns
inferred← citeshttps://doi.org/10.1111/cge.14575openalex-snapshot
A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family
inferred← citeshttps://doi.org/10.1111/cge.14604openalex-snapshot
Exploring the role of non‐canonical splice site variants in aberrant splicing associated with reproductive genetic disorders
inferred← citeshttps://doi.org/10.1111/cge.70034openalex-snapshot
Loss of Different Domains of TDRD12 Leads to Distinct Male Infertility‐Related Phenotypes
inferred← citeshttps://doi.org/10.1111/cge.70106openalex-snapshot
Identification of a Homozygous Nonsense Variant in KCTD19 Causing Meiotic Arrest and Non‐Obstructive Azoospermia in Humans
inferred← citeshttps://doi.org/10.1111/cge.70243openalex-snapshot
A Homozygous Variant in DMRTB1 Is Associated With Non‐Obstructive Azoospermia in Humans
inferred← citeshttps://doi.org/10.1111/cpr.13281openalex-snapshot
BCL2‐associated athanogene 6 exon24 contributes to testosterone synthesis and male fertility in mammals
inferred← citeshttps://doi.org/10.1126/sciadv.abn0968openalex-snapshot
Loss-of-function mutations inCEP78cause male infertility in humans and mice
inferred← citeshttps://doi.org/10.1136/jmedgenet-2021-108406openalex-snapshot
FSIP2 plays a role in the acrosome development during spermiogenesis
inferred← citeshttps://doi.org/10.1136/jmg-2022-108887openalex-snapshot
Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-101323-031045openalex-snapshot
Protein Storage in Oocytes: Implications for Oocyte Quality, Embryonic Development, and Female Fertility
inferred← citeshttps://doi.org/10.1155/2022/1269530openalex-snapshot
Therapeutic Effects of Xianlu Oral Solution on Rats with Oligoasthenozoospermia through Alleviating Apoptosis and Oxidative Stress
inferred← citeshttps://doi.org/10.1155/2022/4240490openalex-snapshot
The Activated AMPK/mTORC2 Signaling Pathway Associated with Oxidative Stress in Seminal Plasma Contributes to Idiopathic Asthenozoospermia
inferred← citeshttps://doi.org/10.1155/2023/9222954openalex-snapshot
Compound Heterozygous Mutations in FSIP2 Cause Morphological Abnormalities in Sperm Flagella Leading to Male Infertility
inferred← citeshttps://doi.org/10.1155/humu/7629729openalex-snapshot
Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility
inferred← citeshttps://doi.org/10.1155/humu/7905936openalex-snapshot
Mutation Severity of FBXO43 Determines Spermatogenic Outcome and Informs Precision ART Strategies
inferred← citeshttps://doi.org/10.1172/jci.insight.166869openalex-snapshot
Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice
inferred← citeshttps://doi.org/10.1172/jci166279openalex-snapshot
Take your mother’s ferry: preimplantation embryo development requires maternal karyopherins for nuclear transport
inferred← citeshttps://doi.org/10.1177/1934578x241264632openalex-snapshot
Hydroxytyrosol Ameliorates Busulfan-Induced Oligozoospermia in a Mouse Model
inferred← citeshttps://doi.org/10.1186/s11658-025-00826-3openalex-snapshot
Cellular osmoregulation enhances porcine embryo development by restoring zygotic genome activation via metabolic–epigenetic crosstalk
inferred← citeshttps://doi.org/10.1186/s11658-026-00971-3openalex-snapshot
IL17 signaling promotes oocyte developmental competence acquisition during maturation
inferred← citeshttps://doi.org/10.1186/s12610-023-00205-yopenalex-snapshot
Dnali1 is required for sperm motility and male fertility in mice
inferred← citeshttps://doi.org/10.1186/s12864-026-12652-8openalex-snapshot
Region-specific transcriptomic responses to CD52 deficiency in the male reproductive tract
inferred← citeshttps://doi.org/10.1186/s12870-025-06595-7openalex-snapshot
Prediction of new candidate proteins and analysis of sub-modules and protein hubs associated with seed development in rice (Oryza sativa) using an ensemble network-based systems biology approach
inferred← citeshttps://doi.org/10.1186/s12905-025-03729-9openalex-snapshot
Association between gynecological cancers and female infertility: insights from bidirectional Mendelian randomization analysis
inferred← citeshttps://doi.org/10.1186/s12920-023-01712-7openalex-snapshot
Phenotypic variability in two female siblings with oocyte maturation arrest due to a TUBB8 variant
inferred← citeshttps://doi.org/10.1186/s12958-023-01163-wopenalex-snapshot
Multi-omics study identifies that PICK1 deficiency causes male infertility by inhibiting vesicle trafficking in Sertoli cells
inferred← citeshttps://doi.org/10.1186/s12958-025-01476-yopenalex-snapshot
Colony-stimulating factor-1 as a potential therapeutic target in asthenozoospermia
inferred← citeshttps://doi.org/10.1186/s12964-025-02043-zopenalex-snapshot
IQUB mutation induces radial spoke 1 deficiency causing asthenozoospermia with normal sperm morphology in humans and mice
inferred← citeshttps://doi.org/10.1186/s12967-023-04108-4openalex-snapshot
Basic, translational and clinical studies in reproductive medicine and clinical reproductive sciences
inferred← citeshttps://doi.org/10.1186/s12967-024-05162-2openalex-snapshot
Conserved genes regulating human sex differentiation, gametogenesis and fertilization
inferred← citeshttps://doi.org/10.1186/s13048-026-02133-7openalex-snapshot
Metaphase I-arrest oocyte with agar-like zona pellucida, abandon or not abandon?
inferred← citeshttps://doi.org/10.1242/dev.200489openalex-snapshot
Loss of perinuclear theca ACTRT1 causes acrosome detachment and severe male subfertility in mice
inferred← citeshttps://doi.org/10.1242/dev.200516openalex-snapshot
CCDC38 is required for sperm flagellum biogenesis and male fertility in mice
inferred← citeshttps://doi.org/10.1360/ssv-2023-0160openalex-snapshot
Roles of primate specific genes in male reproductive system
inferred← citeshttps://doi.org/10.1360/ssv-2023-0168openalex-snapshot
The role of spermiogenesis-related genes in the occurrence of oligoasthenoteratozoospermia
inferred← citeshttps://doi.org/10.1360/ssv-2023-0169openalex-snapshot
The research progress on the role and function of manchette in spermiogenesis
inferred← citeshttps://doi.org/10.1360/ssv-2023-0172openalex-snapshot
New functions and mechanisms of RNA regulation in spermatogenesis and male infertility
inferred← citeshttps://doi.org/10.1360/ssv-2024-0230openalex-snapshot
The genetic basis of male infertility with “multiple morphological abnormalities of the flagella” and its intervention strategies
inferred← citeshttps://doi.org/10.1360/tb-2024-1401openalex-snapshot
Physiological and pathological mechanisms of human oocyte development
inferred← citeshttps://doi.org/10.1364/boe.580418openalex-snapshot
In vivo volumetric visualization and quantification of cumulus expansion in mice with intravital optical coherence tomography
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003442openalex-snapshot
The core outer junction protein CFAP77 connects A- and B-tubules within doublet microtubules of cilia and flagella
inferred← citeshttps://doi.org/10.15252/emmm.202217177openalex-snapshot
Bi‐allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility
inferred← citeshttps://doi.org/10.17650/2070-9781-2023-24-4-25-36openalex-snapshot
Genetic and spermatological aspects of acephalic sperm syndrome
inferred← citeshttps://doi.org/10.18678/dtfd.1183283openalex-snapshot
Current Approach to Genetic Causes of Male Infertility and Genetic Counseling
inferred← citeshttps://doi.org/10.19080/jgwh.2023.25.556164openalex-snapshot
What is the Molecular Link Between Infertility and Cancer?
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4121652/v1openalex-snapshot
Investigating the role of a testis-expressed gene Tex2 in spermatogenesis in mice
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4980126/v1openalex-snapshot
The Influence of Mitophagy and Apoptosis on The Embryo Development in Kartagener and Globozoospermia Cases
inferred← citeshttps://doi.org/10.21203/rs.3.rs-8214156/v1openalex-snapshot
Loss-of-function variant in TEX44 cause male infertility with asthenoteratozoospermia in humans and mice
inferred← citeshttps://doi.org/10.2174/0115680266308882240806175831openalex-snapshot
Protective Effects of Chitosan-Loaded Pomegranate Peel Extract Nanoparticles on Infertility in Diabetic Male Rats
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