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Causes and consequences of sperm mitochondrial dysfunction
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ar.1092220106openalex-snapshot
Development of mitochondrial helical sheath in the middle piece of the mouse spermatid tail: Regular dispositions and synchronized changes
inferredcites →https://doi.org/10.1002/gcc.20213openalex-snapshot
Mitochondrial DNA mutations and mitochondrial DNA depletion in gastric cancer
inferredcites →https://doi.org/10.1002/gcc.20326openalex-snapshot
Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer
inferredcites →https://doi.org/10.1006/bbrc.1998.9651openalex-snapshot
Long PCR Analysis of Human Gamete mtDNA Suggests Defective Mitochondrial Maintenance in Spermatozoa and Supports the Bottleneck Theory for Oocytes
inferredcites →https://doi.org/10.1007/978-1-4614-3573-0_2openalex-snapshot
Mitochondrial Dynamics: The Intersection of Form and Function
inferredcites →https://doi.org/10.1007/978-3-030-37972-8_8openalex-snapshot
Mitochondrial Function and Male Infertility
inferredcites →https://doi.org/10.1007/s00404-012-2440-1openalex-snapshot
Relationship of sperm DNA fragmentation, apoptosis and dysfunction of mitochondrial membrane potential with semen parameters and ART outcome after intracytoplasmic sperm injection
inferredcites →https://doi.org/10.1007/s11033-019-04861-0openalex-snapshot
Human sperm motility: a molecular study of mitochondrial DNA, mitochondrial transcription factor A gene and DNA fragmentation
inferredcites →https://doi.org/10.1007/s11626-016-0061-xopenalex-snapshot
Mitochondrial membrane potential (MMP) regulates sperm motility
inferredcites →https://doi.org/10.1016/1047-8477(90)90081-mopenalex-snapshot
Mitochondria-cytoskeleton interactions in the sperm midpiece
inferredcites →https://doi.org/10.1016/j.ab.2017.07.009openalex-snapshot
Mitochondrial membrane potential
inferredcites →https://doi.org/10.1016/j.bbamcr.2008.06.013openalex-snapshot
Cristae formation—linking ultrastructure and function of mitochondria
inferredcites →https://doi.org/10.1016/j.biochi.2013.09.017openalex-snapshot
To be or not to be a nucleoid protein: A comparison of mass-spectrometry based approaches in the identification of potential mtDNA-nucleoid associated proteins
inferredcites →https://doi.org/10.1016/j.cmet.2017.07.003openalex-snapshot
Increased Total mtDNA Copy Number Cures Male Infertility Despite Unaltered mtDNA Mutation Load
inferredcites →https://doi.org/10.1016/j.exger.2008.03.004openalex-snapshot
The 4977bp deletion of mitochondrial DNA in human skeletal muscle, heart and different areas of the brain: A useful biomarker or more?
inferredcites →https://doi.org/10.1016/j.fertnstert.2003.09.030openalex-snapshot
Activation pattern of caspases in human spermatozoa
inferredcites →https://doi.org/10.1016/j.fertnstert.2006.03.055openalex-snapshot
The functionality of mitochondria differentiates human spermatozoa with high and low fertilizing capability
inferredcites →https://doi.org/10.1016/j.fertnstert.2007.09.007openalex-snapshot
Sperm nuclear DNA fragmentation and mitochondrial activity in men with varicocele
inferredcites →https://doi.org/10.1016/j.fertnstert.2007.10.059openalex-snapshot
Mitochondrial DNA integrity and copy number in sperm from infertile men
inferredcites →https://doi.org/10.1016/j.fertnstert.2010.07.1086openalex-snapshot
Altered ultrastructure of mitochondrial membranes is strongly associated with unexplained asthenozoospermia
inferredcites →https://doi.org/10.1016/j.fertnstert.2015.11.037openalex-snapshot
Sperm DNA fragmentation and mitochondrial membrane potential combined are better for predicting natural conception than standard sperm parameters
inferredcites →https://doi.org/10.1016/j.jprot.2012.07.003openalex-snapshot
Sperm phosphoproteome profiling by ultra performance liquid chromatography followed by data independent analysis (LC–MSE) reveals altered proteomic signatures in asthenozoospermia
inferredcites →https://doi.org/10.1016/j.jri.2009.08.009openalex-snapshot
The role of mitochondrial proteins in sperm capacitation
inferredcites →https://doi.org/10.1016/j.juro.2018.03.009openalex-snapshot
Proteomic Signatures of Sperm Mitochondria in Varicocele: Clinical Use as Biomarkers of Varicocele Associated Infertility
inferredcites →https://doi.org/10.1016/j.mito.2010.05.015openalex-snapshot
Mitochondria, spermatogenesis and male infertility
inferredcites →https://doi.org/10.1016/j.redox.2013.04.005openalex-snapshot
Sites of reactive oxygen species generation by mitochondria oxidizing different substrates
inferredcites →https://doi.org/10.1016/j.semcdb.2019.10.001openalex-snapshot
Mitochondrial heteroplasmy beyond the oocyte bottleneck
inferredcites →https://doi.org/10.1016/j.tibs.2017.02.003openalex-snapshot
Regulation of Mammalian Mitochondrial Gene Expression: Recent Advances
inferredcites →https://doi.org/10.1016/j.urology.2011.12.042openalex-snapshot
Mitochondrial Respiratory Efficiency is Positively Correlated With Human Sperm Motility
inferredcites →https://doi.org/10.1016/j.urology.2012.03.005openalex-snapshot
Myoinositol: Does It Improve Sperm Mitochondrial Function and Sperm Motility?
inferredcites →https://doi.org/10.1016/s0005-2728(02)00278-5openalex-snapshot
Insight into mitochondrial structure and function from electron tomography
inferredcites →https://doi.org/10.1016/s0005-2728(98)00161-3openalex-snapshot
The mitochondrial genome: structure, transcription, translation and replication
inferredcites →https://doi.org/10.1016/s0092-8674(00)80434-1openalex-snapshot
Cytochrome c and dATP-Dependent Formation of Apaf-1/Caspase-9 Complex Initiates an Apoptotic Protease Cascade
inferredcites →https://doi.org/10.1016/s0140-6736(99)03842-8openalex-snapshot
Failure of elimination of paternal mitochondrial DNA in abnormal embryos
inferredcites →https://doi.org/10.1016/s0307-4412(98)00065-xopenalex-snapshot
The cell. A molecular approach
inferredcites →https://doi.org/10.1016/s0968-0004(00)01609-1openalex-snapshot
The internal structure of mitochondria
inferredcites →https://doi.org/10.1016/s1472-6483(10)60495-6openalex-snapshot
Degradation of paternal mitochondria after fertilization: implications for heteroplasmy, assisted reproductive technologies and mtDNA inheritance
inferredcites →https://doi.org/10.1017/s0967199418000242openalex-snapshot
Spermatic mitochondria: role in oxidative homeostasis, sperm function and possible tools for their assessment
inferredcites →https://doi.org/10.1021/pr500652yopenalex-snapshot
Identification of Proteins Involved in Human Sperm Motility Using High-Throughput Differential Proteomics
inferredcites →https://doi.org/10.1038/290457a0openalex-snapshot
Sequence and organization of the human mitochondrial genome
inferredcites →https://doi.org/10.1038/35057062openalex-snapshot
Initial sequencing and analysis of the human genome
inferredcites →https://doi.org/10.1038/nrg1606openalex-snapshot
Mitochondrial DNA mutations in human disease
inferredcites →https://doi.org/10.1038/nrm3412openalex-snapshot
Mitochondria as sensors and regulators of calcium signalling
inferredcites →https://doi.org/10.1038/sj.emboj.7600465openalex-snapshot
The mitochondrial RNA polymerase contributes critically to promoter specificity in mammalian cells
inferredcites →https://doi.org/10.1042/bj20081386openalex-snapshot
How mitochondria produce reactive oxygen species
inferredcites →https://doi.org/10.1042/bj20110114openalex-snapshot
Phosphoinositide 3-kinase signalling pathway involvement in a truncated apoptotic cascade associated with motility loss and oxidative DNA damage in human spermatozoa
inferredcites →https://doi.org/10.1042/ebc20170104openalex-snapshot
Mitochondrial dynamics: overview of molecular mechanisms
inferredcites →https://doi.org/10.1046/j.1445-5781.2002.00007.xopenalex-snapshot
Spermatozoon and mitochondrial DNA
inferredcites →https://doi.org/10.1073/pnas.0808115105openalex-snapshot
Structure of the human voltage-dependent anion channel
inferredcites →https://doi.org/10.1073/pnas.1217823110openalex-snapshot
Dimers of mitochondrial ATP synthase form the permeability transition pore
inferredcites →https://doi.org/10.1073/pnas.1810946115openalex-snapshot
Biparental Inheritance of Mitochondrial DNA in Humans
inferredcites →https://doi.org/10.1073/pnas.77.11.6715openalex-snapshot
Maternal inheritance of human mitochondrial DNA.
inferredcites →https://doi.org/10.1073/pnas.85.17.6465openalex-snapshot
Normal oxidative damage to mitochondrial and nuclear DNA is extensive.
inferredcites →https://doi.org/10.1073/pnas.93.24.13859openalex-snapshot
Misconceptions about mitochondria and mammalian fertilization: Implications for theories on human evolution
inferredcites →https://doi.org/10.1074/jbc.272.41.25409openalex-snapshot
Repair of Oxidative Damage to Nuclear and Mitochondrial DNA in Mammalian Cells
inferredcites →https://doi.org/10.1074/jbc.m112.366690openalex-snapshot
Electrophilic Aldehydes Generated by Sperm Metabolism Activate Mitochondrial Reactive Oxygen Species Generation and Apoptosis by Targeting Succinate Dehydrogenase
inferredcites →https://doi.org/10.1074/jbc.r117.789628openalex-snapshot
Mitochondrial reactive oxygen species and adipose tissue thermogenesis: Bridging physiology and mechanisms
inferredcites →https://doi.org/10.1083/jcb.200605138openalex-snapshot
Dynamic subcompartmentalization of the mitochondrial inner membrane
inferredcites →https://doi.org/10.1086/303040openalex-snapshot
Human mtDNA Haplogroups Associated with High or Reduced Spermatozoa Motility
inferredcites →https://doi.org/10.1089/ars.2012.4514openalex-snapshot
Does Prohibitin Expression Regulate Sperm Mitochondrial Membrane Potential, Sperm Motility, and Male Fertility?
inferredcites →https://doi.org/10.1093/clinchem/44.8.1616openalex-snapshot
Correlation of sperm motility with mitochondrial enzymatic activities
inferredcites →https://doi.org/10.1093/humrep/10.1.116openalex-snapshot
Asthenozoospermia and the human sperm mid-piece
inferredcites →https://doi.org/10.1093/humrep/14.4.880openalex-snapshot
X-ray microscopy of human spermatozoa shows change of mitochondrial morphology after capacitation
inferredcites →https://doi.org/10.1093/humrep/17.6.1571openalex-snapshot
A comparison of mitochondrial and nuclear DNA status in testicular sperm from fertile men and those with obstructive azoospermia
inferredcites →https://doi.org/10.1093/humrep/dem030openalex-snapshot
The expression of polymerase gamma and mitochondrial transcription factor A and the regulation of mitochondrial DNA content in mature human sperm
inferredcites →https://doi.org/10.1093/humrep/den024openalex-snapshot
Identification of proteomic differences in asthenozoospermic sperm samples
inferredcites →https://doi.org/10.1093/humrep/der200openalex-snapshot
A sperm's tail: the importance of getting it right
inferredcites →https://doi.org/10.1093/humrep/des021openalex-snapshot
Differential RNAs in the sperm cells of asthenozoospermic patients
inferredcites →https://doi.org/10.1093/humrep/dev015openalex-snapshot
Mitochondrial permeability transition increases reactive oxygen species production and induces DNA fragmentation in human spermatozoa
inferredcites →https://doi.org/10.1093/humrep/dey330openalex-snapshot
Associations of sperm mitochondrial DNA copy number and deletion rate with fertilization and embryo development in a clinical setting
inferredcites →https://doi.org/10.1093/humrep/dey335openalex-snapshot
Mitochondrial functionality modifies human sperm acrosin activity, acrosome reaction capability and chromatin integrity
inferredcites →https://doi.org/10.1093/humupd/dmp016openalex-snapshot
Mitochondrial functionality in reproduction: from gonads and gametes to embryos and embryonic stem cells
inferredcites →https://doi.org/10.1093/humupd/dmq002openalex-snapshot
Mitochondrial DNA transmission, replication and inheritance: a journey from the gamete through the embryo and into offspring and embryonic stem cells
inferredcites →https://doi.org/10.1093/humupd/dmv042openalex-snapshot
Sperm selection in natural conception: what can we learn from Mother Nature to improve assisted reproduction outcomes?
inferredcites →https://doi.org/10.1093/molehr/4.7.657openalex-snapshot
Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa
inferredcites →https://doi.org/10.1093/molehr/8.11.984openalex-snapshot
Caspase activity and apoptotic markers in ejaculated human sperm
inferredcites →https://doi.org/10.1093/molehr/8.8.719openalex-snapshot
Can mitochondrial DNA mutations cause sperm dysfunction?
inferredcites →https://doi.org/10.1093/molehr/gaq009openalex-snapshot
Proteomics-based study on asthenozoospermia: differential expression of proteasome alpha complex
inferredcites →https://doi.org/10.1093/molehr/gay010openalex-snapshot
Not every sperm is sacred; a perspective on male infertility
inferredcites →https://doi.org/10.1093/nar/gkq1224openalex-snapshot
TEFM (c17orf42) is necessary for transcription of human mtDNA
inferredcites →https://doi.org/10.1095/biolreprod.115.130989openalex-snapshot
Defective Human Sperm Cells Are Associated with Mitochondrial Dysfunction and Oxidant Production1
inferredcites →https://doi.org/10.1095/biolreprod52.4.729openalex-snapshot
Mitochondrial Deoxyribonucleic Acid 4977-bp Deletion is Associated with Diminished Fertility and Motility of Human Sperm1
inferredcites →https://doi.org/10.1095/biolreprod63.2.582openalex-snapshot
Ubiquitinated Sperm Mitochondria, Selective Proteolysis, and the Regulation of Mitochondrial Inheritance in Mammalian Embryos1
inferredcites →https://doi.org/10.1098/rspb.2008.1758openalex-snapshot
The causes of mutation accumulation in mitochondrial genomes
inferredcites →https://doi.org/10.1101/cshperspect.a012641openalex-snapshot
The Maintenance of Mitochondrial DNA Integrity--Critical Analysis and Update
inferredcites →https://doi.org/10.1111/j.1365-2605.2005.00515.xopenalex-snapshot
The impact of mitochondrial genetics on male infertility
inferredcites →https://doi.org/10.1111/j.1365-2605.2007.00768.xopenalex-snapshot
Relationship between sperm apoptosis signalling and oocyte penetration capacity
inferredcites →https://doi.org/10.1111/j.1365-2605.2010.01078.xopenalex-snapshot
Evaluation of mitochondrial respiratory efficiency during in vitro capacitation of human spermatozoa
inferredcites →https://doi.org/10.1111/j.1365-2605.2011.01218.xopenalex-snapshot
The role of mitochondria in energy production for human sperm motility
inferredcites →https://doi.org/10.1111/j.1439-0272.2008.00878.xopenalex-snapshot
Integrity of mitochondrial membrane potential reflects human sperm quality
inferredcites →https://doi.org/10.1111/j.1439-0272.2010.01117.xopenalex-snapshot
Influence of mitochondrial membrane potential of spermatozoa on in vitro fertilisation outcome
inferredcites →https://doi.org/10.1111/j.1439-0531.2010.01725.xopenalex-snapshot
‘In Vitro’ Capacitation and Acrosome Reaction are Concomitant with Specific Changes in Mitochondrial Activity in Boar Sperm: Evidence for a Nucleated Mitochondrial Activation and for the Existence of a Capacitation‐Sensitive Subpopulational Structure
inferredcites →https://doi.org/10.1111/j.1464-410x.2011.10240.xopenalex-snapshot
Effect of varicocele on sperm function and semen oxidative stress
inferredcites →https://doi.org/10.1111/j.1745-7262.2007.00280.xopenalex-snapshot
Proteomic changes in mammalian spermatozoa during epididymal maturation
inferredcites →https://doi.org/10.1111/jcmm.12945openalex-snapshot
Prohibitin involvement in the generation of mitochondrial superoxide at complex I in human sperm
inferredcites →https://doi.org/10.1128/mcb.05603-11openalex-snapshot
Mitochondrial Fission Contributes to Mitochondrial Dysfunction and Insulin Resistance in Skeletal Muscle
inferredcites →https://doi.org/10.1128/mcb.22.15.5554-5562.2002openalex-snapshot
Testis-Specific Cytochrome c-Null Mice Produce Functional Sperm but Undergo Early Testicular Atrophy
inferredcites →https://doi.org/10.1146/annurev-genet-102108-134850openalex-snapshot
The Role of Mitochondria in Apoptosis
inferredcites →https://doi.org/10.1146/annurev.biochem.76.081205.150955openalex-snapshot
Why Do We Still Have a Maternally Inherited Mitochondrial DNA? Insights from Evolutionary Medicine
inferredcites →https://doi.org/10.1155/2017/8060949openalex-snapshot
Mitochondrial Nucleoid: Shield and Switch of the Mitochondrial Genome
inferredcites →https://doi.org/10.1155/2018/5076271openalex-snapshot
Role of Mitochondria in the Oxidative Stress Induced by Electromagnetic Fields: Focus on Reproductive Systems
inferredcites →https://doi.org/10.1155/2019/6392763openalex-snapshot
The Role of the Antioxidant Response in Mitochondrial Dysfunction in Degenerative Diseases: Cross-Talk between Antioxidant Defense, Autophagy, and Apoptosis
inferredcites →https://doi.org/10.1155/2019/9825061openalex-snapshot
Mitophagy, Mitochondrial Dynamics, and Homeostasis in Cardiovascular Aging
inferredcites →https://doi.org/10.1186/1741-7007-12-34openalex-snapshot
Mitochondria as signaling organelles
inferredcites →https://doi.org/10.1186/1756-0500-2-18openalex-snapshot
Correlation of the 4977 bp mitochondrial DNA deletion with human sperm dysfunction
inferredcites →https://doi.org/10.1186/s12915-015-0129-1openalex-snapshot
Mitophagy and the mitochondrial unfolded protein response in neurodegeneration and bacterial infection
inferredcites →https://doi.org/10.1186/s12915-015-0201-xopenalex-snapshot
Structure and function of mitochondrial membrane protein complexes
inferredcites →https://doi.org/10.1196/annals.1329.050openalex-snapshot
Mitochondria of Human Spermatozoa Are Preferentially Susceptible to Apoptosis
inferredcites →https://doi.org/10.1210/jc.2006-1309openalex-snapshot
Cis -Unsaturated Fatty Acids Stimulate Reactive Oxygen Species Generation and Lipid Peroxidation in Human Spermatozoa
inferredcites →https://doi.org/10.1210/jc.2007-2616openalex-snapshot
Significance of Mitochondrial Reactive Oxygen Species in the Generation of Oxidative Stress in Spermatozoa
inferredcites →https://doi.org/10.1242/jeb.132142openalex-snapshot
A radical shift in perspective: mitochondria as regulators of reactive oxygen species
inferredcites →https://doi.org/10.1371/journal.pone.0006446openalex-snapshot
Mobile Phone Radiation Induces Reactive Oxygen Species Production and DNA Damage in Human Spermatozoa In Vitro
inferredcites →https://doi.org/10.1371/journal.pone.0018112openalex-snapshot
Not All Sperm Are Equal: Functional Mitochondria Characterize a Subpopulation of Human Sperm with Better Fertilization Potential
inferredcites →https://doi.org/10.1371/journal.pone.0168823openalex-snapshot
Mitochondrial Biomarkers Reflect Semen Quality: Results from the MARCHS Study in Chongqing, China
inferredcites →https://doi.org/10.1530/rep-13-0178openalex-snapshot
Mitochondria functionality and sperm quality
inferredcites →https://doi.org/10.1530/rep-14-0621openalex-snapshot
Human spermatozoa possess an IL4I1 l -amino acid oxidase with a potential role in sperm function
inferredcites →https://doi.org/10.26402/jpp.2018.3.05openalex-snapshot
Sperm mitochondrial dysfunction and oxidative stress as possible reasons for isolated asthenozoospermia.
inferredcites →https://doi.org/10.3389/fendo.2017.00296openalex-snapshot
Functional Mitochondria in Health and Disease
inferredcites →https://doi.org/10.3390/antiox9020134openalex-snapshot
Molecular Changes Induced by Oxidative Stress that Impair Human Sperm Motility
inferredcites →https://doi.org/10.3390/cancers10030078openalex-snapshot
New Insights into Protein Kinase B/Akt Signaling: Role of Localized Akt Activation and Compartment-Specific Target Proteins for the Cellular Radiation Response
inferredcites →https://doi.org/10.3390/jcm9020363openalex-snapshot
Evaluation of Sperm Mitochondrial Function: A Key Organelle for Sperm Motility
inferredcites →https://doi.org/10.3892/mmr.2014.2428openalex-snapshot
Oxygen free radicals and mitochondrial signaling in oligospermia and asthenospermia
inferredcites →https://doi.org/10.4103/0970-1591.40606openalex-snapshot
Mitochondrial DNA mutations in etiopathogenesis of male infertility
inferredcites →https://doi.org/10.4103/0971-6866.60183openalex-snapshot
Mitochondrial DNA mutations and male infertility
inferredcites →https://doi.org/10.4103/0974-1208.178635openalex-snapshot
Association of large scale 4977-bp "common" deletions in sperm mitochondrial DNA with asthenozoospermia and oligoasthenoteratozoospermia
inferredcites →https://doi.org/10.4161/auto.19243openalex-snapshot
Maternal inheritance of mitochondrial DNA
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.4777221openalex-extracted
Japanese Medaka Dmrt3a is Involved in Male Fertility
inferred← citeshttps://doi.org/10.1002/2211-5463.70058openalex-snapshot
Short peptide perturbs spermatogenesis via immune microenvironment dysregulation and mitochondrial imbalance
inferred← citeshttps://doi.org/10.1002/aisy.202500115openalex-snapshot
Hi‐LabSpermTracking: A Novel and High‐Quality Sperm Tracking Dataset with an Advanced Ensemble Detection and Tracking Approach for Real‐World Clinical Scenarios
inferred← citeshttps://doi.org/10.1002/cyto.a.24301openalex-snapshot
Assessment of chilling injury in hypothermic stored boar spermatozoa by multicolor flow cytometry
inferred← citeshttps://doi.org/10.1002/cyto.b.22058openalex-snapshot
Validation of a new multiparametric protocol to assess viability, acrosome integrity and mitochondrial activity in cooled and frozen thawed boar spermatozoa
inferred← citeshttps://doi.org/10.1002/rmb2.12602openalex-snapshot
Ectopic expression of the mitochondrial protein COXFA4L3 in human sperm acrosome and its potential application in the selection of male infertility treatments
inferred← citeshttps://doi.org/10.1002/smtd.202300928openalex-snapshot
Viscous Loading Regulates the Flagellar Energetics of Human and Bull Sperm
inferred← citeshttps://doi.org/10.1007/978-3-031-69962-7_6openalex-snapshot
Oxidative Stress in Infertility
inferred← citeshttps://doi.org/10.1007/978-3-031-73079-5_11openalex-snapshot
Male Effect During In Vitro Production of Bovine Embryos
inferred← citeshttps://doi.org/10.1007/978-3-031-73079-5_12openalex-snapshot
Sperm Mitochondria: Quantitative Regulation and Its Impact on Sperm Quality
inferred← citeshttps://doi.org/10.1007/s00018-022-04134-3openalex-snapshot
Mitochondrial regulation during male germ cell development
inferred← citeshttps://doi.org/10.1007/s00418-022-02111-2openalex-snapshot
Endoplasmic reticulum stress and mitochondrial injury are critical molecular drivers of AlCl3-induced testicular and epididymal distortion and dysfunction: protective role of taurine
inferred← citeshttps://doi.org/10.1007/s10565-025-10095-7openalex-snapshot
scRNA-seq deciphers molecular mechanisms of endocrine disruptor 4-nonylphenol impairing spermatogenesis in mice
inferred← citeshttps://doi.org/10.1007/s10565-026-10167-2openalex-snapshot
FBXO39 knockdown promotes spermatogenesis impairment by inducing mitochondrial dysfunction and ferroptosis via inhibiting KDM5A ubiquitination and regulating H3K4me3 demethylation
inferred← citeshttps://doi.org/10.1007/s11033-025-11158-yopenalex-snapshot
Breathing new life into male fertility: the potential of mitochondrial transplantation
inferred← citeshttps://doi.org/10.1007/s11250-025-04553-xopenalex-snapshot
Identification of sperm parameters linked to fertility and development of fertility prediction models for zebu (Bos indicus) and crossbred (Bos taurus X Bos indicus) cattle bulls
inferred← citeshttps://doi.org/10.1007/s43032-022-00953-8openalex-snapshot
Assessment of the Role of Nuclear ENDOG Gene and mtDNA Variations on Paternal Mitochondrial Elimination (PME) in Infertile Men: An Experimental Study
inferred← citeshttps://doi.org/10.1007/s43032-023-01405-7openalex-snapshot
Clinical Utility of Sperm Function Tests in Predicting Male Fertility: A Systematic Review
inferred← citeshttps://doi.org/10.1007/s43032-024-01662-0openalex-snapshot
Oxidative Stress-induced Hormonal Disruption in Male Reproduction
inferred← citeshttps://doi.org/10.1007/s44154-025-00253-6openalex-snapshot
Seminal plasma exosomes improve the motility and mitochondrial function of goat spermatozoa during liquid storage by regulating oxidative phosphorylation
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2023.107387openalex-snapshot
A comparison of the biological properties of European red deer (Cervus elaphus elaphus) spermatozoa stored in the epididymides and in a liquid state at 5 °C
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2025.108009openalex-snapshot
Seminal extracellular vesicles influence porcine spermatozoa physiology by modulating key functional parameters
inferred← citeshttps://doi.org/10.1016/j.aqrep.2024.102590openalex-snapshot
Incorporation of reduced glutathione to the extender improves frozen-thawed sperm function and fertility potential in mandarin fish (Siniperca chuatsi)
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.741332openalex-snapshot
Optimizing the post-thaw quality of cryopreserved masu salmon (Oncorhynchus masou) sperm: Evaluating the effects of antioxidant-supplemented extender
inferred← citeshttps://doi.org/10.1016/j.biopha.2022.114107openalex-snapshot
Glutathione improves testicular spermatogenesis through inhibiting oxidative stress, mitochondrial damage, and apoptosis induced by copper deposition in mice with Wilson disease
inferred← citeshttps://doi.org/10.1016/j.crtox.2026.100286openalex-snapshot
Bridging the Gap: How environmental exposures compromise male fertility and clinical Outlook
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2022.114163openalex-snapshot
Flurochloridone induced abnormal spermatogenesis by damaging testicular Sertoli cells in mice
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115262openalex-snapshot
The rare-earth yttrium induces cell apoptosis and autophagy in the male reproductive system through ROS-Ca2+-CamkII/Ampk axis
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116878openalex-snapshot
EHDPP induces proliferation inhibition and apoptosis to spermatocyte: Insights from transcriptomic and metabolomic profiles
inferred← citeshttps://doi.org/10.1016/j.envres.2022.114737openalex-snapshot
Blood trihalomethane concentrations in relation to sperm mitochondrial DNA copy number and telomere length among 958 healthy men
inferred← citeshttps://doi.org/10.1016/j.intimp.2024.112240openalex-snapshot
Donepezil and quercetin alleviate valproate-induced testicular oxidative stress, inflammation and apoptosis: Imperative roles of AMPK/SIRT1/ PGC-1α and p38-MAPK/NF-κB/ IL-1β signaling cascades
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2026.143875openalex-snapshot
Chronic heavy metal exposure drives mitochondrial remodeling and metabolic reprogramming to enhance sperm velocity in wild tree sparrows
inferred← citeshttps://doi.org/10.1016/j.jogoh.2021.102101openalex-snapshot
Relationship between nuclear DNA fragmentation, mitochondrial DNA damage and standard sperm parameters in spermatozoa of infertile patients with leukocytospermia
inferred← citeshttps://doi.org/10.1016/j.mce.2024.112393openalex-snapshot
Status of sperm mitochondrial functions and DNA methylation in infertile men with clinical varicocele before and after treatment
inferred← citeshttps://doi.org/10.1016/j.mehy.2024.111377openalex-snapshot
The effect of temperature shock on enhancing sperm motility: A new insight into molecular and cellular mechanisms through current procedures
inferred← citeshttps://doi.org/10.1016/j.repbio.2022.100652openalex-snapshot
Activation of thermogenesis pathways in testis of diet-induced obesity mice
inferred← citeshttps://doi.org/10.1016/j.repbio.2026.101249openalex-snapshot
Effect of the neonicotinoid acetamiprid on molecular events during in vitro boar spermatozoa capacitation
inferred← citeshttps://doi.org/10.1016/j.reth.2024.09.002openalex-snapshot
Calcium oscillations and mitochondrial enzymes in stem cells
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.04.024openalex-snapshot
Bimodal interplay of reactive oxygen and nitrogen species in physiology and pathophysiology of bovine sperm function
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2023.01.024openalex-snapshot
TMT-based quantitative proteomics analysis reveals the differential proteins between fresh and frozen-thawed sperm of yak (Bos grunniens)
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2023.07.027openalex-snapshot
Negative correlations of mitochondrial DNA copy number in commercial frozen bull spermatozoa with the motility parameters after thawing
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2024.12.008openalex-snapshot
Isoglycyrrhizin supplementation of frozen goat semen-extender improves post-thaw sperm quality and in vitro fertilization rates
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2024.12.012openalex-snapshot
Mitochondrial content and mtDNA copy number in spermatozoa and penetrability into oocytes
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2025.117424openalex-snapshot
SIRT5 alleviates oxidative stress of boar sperm induced by cryopreservation through IDH2 and SOD2 pathway
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2025.117462openalex-snapshot
Improvement of cryopreserved epididymal ram sperm quality and fertility through curcumin nanoparticles
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2026.117890openalex-snapshot
Non-thermal plasma enhances boar sperm quality via FOXO3-PINK1/Parkin-mediated mitophagy
inferred← citeshttps://doi.org/10.1016/j.tox.2023.153518openalex-snapshot
Quercetin protects against levetiracetam induced gonadotoxicity in rats
inferred← citeshttps://doi.org/10.1016/j.xfss.2024.10.003openalex-snapshot
Bleomycin in vitro exposure decreases markers of human male gamete competence
inferred← citeshttps://doi.org/10.1016/j.xfss.2025.02.006openalex-snapshot
Bupropion, the atypical antidepressant used in smoke cessation: an in vitro study on its effects on human sperm function
inferred← citeshttps://doi.org/10.1021/acs.analchem.4c01638openalex-snapshot
Construction of Near-Infrared Probes with Remarkable Large Stokes Shift Based on a Novel Purine Platform for the Visualization of mtG4 Upregulation during Mitochondrial Disorder in Somatic Cells and Human Sperms
inferred← citeshttps://doi.org/10.1038/s41419-022-05364-wopenalex-snapshot
Cadmium-induced apoptosis of Leydig cells is mediated by excessive mitochondrial fission and inhibition of mitophagy
inferred← citeshttps://doi.org/10.1038/s41421-021-00260-7openalex-snapshot
Spatio-temporal landscape of mouse epididymal cells and specific mitochondria-rich segments defined by large-scale single-cell RNA-seq
inferred← citeshttps://doi.org/10.1038/s41467-023-44444-zopenalex-snapshot
Leucine aminopeptidase1 controls egg deposition and hatchability in male Aedes aegypti mosquitoes
inferred← citeshttps://doi.org/10.1038/s41467-024-52319-0openalex-snapshot
Stress increases sperm respiration and motility in mice and men
inferred← citeshttps://doi.org/10.1038/s41467-025-59568-7openalex-snapshot
A nuclear-encoded endonuclease governs the paternal transmission of mitochondria in Cucumis plants
inferred← citeshttps://doi.org/10.1038/s41598-025-95820-2openalex-snapshot
Mitochondrial specific antioxidant MitoPBN mitigates oxidative stress and improves mitochondrial function in cryopreserved ram sperm
inferred← citeshttps://doi.org/10.1071/rd25069openalex-snapshot
Bacterial lipopolysaccharide (LPS) impairs sperm mitochondrial membrane potential and induces sperm apoptosis in infertile men
inferred← citeshttps://doi.org/10.1071/rd25089openalex-snapshot
Synergistic effect of glutathione and metformin mitigates testicular apoptosis by ameliorating gonadotropin hormones and gene expression in streptozotocin-induced diabetic male mice
inferred← citeshttps://doi.org/10.1080/09712119.2026.2628620openalex-snapshot
Pioneering comparative analysis of intracellular cryoprotectants on Gaga chicken sperm quality during cryopreservation
inferred← citeshttps://doi.org/10.1080/2314808x.2026.2671481openalex-snapshot
Ameliorative effect of quercetin and vitamin E against filgrastim-induced testicular deterioration in Wistar rats
inferred← citeshttps://doi.org/10.1089/ars.2021.0241openalex-snapshot
Exploring the Role of Oxidative Stress in Sperm Motility: A Proteomic Network Approach
inferred← citeshttps://doi.org/10.1089/ars.2023.0314openalex-snapshot
Building an Understanding of Proteostasis in Reproductive Cells: The Impact of Reactive Carbonyl Species on Protein Fate
inferred← citeshttps://doi.org/10.1093/biolre/ioae061openalex-snapshot
Biomarker-based human and animal sperm phenotyping: the good, the bad and the ugly
inferred← citeshttps://doi.org/10.1093/humupd/dmag013openalex-snapshot
Sperm mitochondrial DNA copy number: a marker of male fertility and reproductive success
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/10.1101/2024.06.10.597508openalex-snapshot
The zebrafish as a new model for studying chaperone-mediated autophagy unveils its role in spermatogenesis
inferred← citeshttps://doi.org/10.1101/2025.04.27.650828openalex-snapshot
Novel Fatigue Profiling Approach Highlights Temporal Dynamics of Human Sperm Motility
inferred← citeshttps://doi.org/10.1109/tase.2024.3378702openalex-snapshot
Automated Point-of-Care Semen Analysis Using Smartphone Imaging and Occlusion-Aware Multi-Object Tracking
inferred← citeshttps://doi.org/10.1111/acel.70004openalex-snapshot
Nicotinamide Riboside Supplementation Alleviates Testicular Aging Induced by Disruption of Qprt‐Dependent NAD + De Novo Synthesis in Mice
inferred← citeshttps://doi.org/10.1111/and.13741openalex-snapshot
An update on male infertility: Factors, mechanisms, and interventions
inferred← citeshttps://doi.org/10.1111/and.13752openalex-snapshot
Afterword to an update on male infertility: Factors, mechanisms, and interventions
inferred← citeshttps://doi.org/10.1111/and.14114openalex-snapshot
In vitro effects of aqueous extract of fermented rooibos (Aspalathus linearis) on human sperm function
inferred← citeshttps://doi.org/10.1111/and.14129openalex-snapshot
Can leukocytospermia predict prostate cancer via its effects on mitochondrial DNA?
inferred← citeshttps://doi.org/10.1111/and.14632openalex-snapshot
Jujing Zhuyu decoction inhibits apoptosis in rats with asthenozoospermia by regulating the mitochondrial apoptosis pathway
inferred← citeshttps://doi.org/10.1111/andr.13038openalex-snapshot
Differential impact of four sperm preparation techniques on sperm motility, morphology, DNA fragmentation, acrosome status, oxidative stress, and mitochondrial activity: A prospective study
inferred← citeshttps://doi.org/10.1111/andr.13539openalex-snapshot
The relationship between sperm nuclear DNA fragmentation, mitochondrial DNA fragmentation, and copy number in normal and abnormal human ejaculates
inferred← citeshttps://doi.org/10.1111/andr.13556openalex-snapshot
Low human sperm motility coexists with sperm nuclear DNA damage and oxidative stress in semen
inferred← citeshttps://doi.org/10.1111/rda.14291openalex-snapshot
Quercetin: Putative effects on the function of cryopreserved sperms in domestic animals
inferred← citeshttps://doi.org/10.1111/rda.14737openalex-snapshot
Damage to Mitochondria During the Cryopreservation, Causing ROS Leakage, Leading to Oxidative Stress and Decreased Quality of Ram Sperm
inferred← citeshttps://doi.org/10.1111/rda.70089openalex-snapshot
The Effect of Sodium Phytate on the Liquid Preservation of Porcine Semen
inferred← citeshttps://doi.org/10.1126/sciadv.adk2864openalex-snapshot
Making immotile sperm motile using high-frequency ultrasound
inferred← citeshttps://doi.org/10.1155/2024/2332443openalex-snapshot
Protective Effects of Astaxanthin on Post‐Thaw Sperm Quality in Normozoospermic Men
inferred← citeshttps://doi.org/10.1177/19475535251376471openalex-snapshot
Intra-Species Variation and Correlation Among Antioxidant Potential, Mitochondrial Performance, and Quality Parameters in Fresh and Cryopreserved Japanese Quail Semen
inferred← citeshttps://doi.org/10.1186/s12864-023-09329-xopenalex-snapshot
iTRAQ-based comparative proteomics reveal an enhancing role of PRDX6 in the freezability of Mediterranean buffalo sperm
inferred← citeshttps://doi.org/10.1186/s12917-023-03593-5openalex-snapshot
N-thiocarboxyanhydrides, amino acid-derived enzyme-activated H2S donors, enhance sperm mitochondrial activity in presence and absence of oxidative stress
inferred← citeshttps://doi.org/10.1186/s12917-023-03795-xopenalex-snapshot
Canine sperm motility is associated with telomere shortening and changes in expression of shelterin genes
inferred← citeshttps://doi.org/10.1186/s12958-024-01252-4openalex-snapshot
The impact of mitochondrial impairments on sperm function and male fertility: a systematic review
inferred← citeshttps://doi.org/10.1186/s40104-023-00988-0openalex-snapshot
Sperm function, mitochondrial activity and in vivo fertility are associated to their mitochondrial DNA content in pigs
inferred← citeshttps://doi.org/10.1186/s40659-024-00483-4openalex-snapshot
Embryo development is impaired by sperm mitochondrial-derived ROS
inferred← citeshttps://doi.org/10.1249/jes.0000000000000245openalex-snapshot
Physical Activity and Male Reproductive Function: A New Role for Gamete Mitochondria
inferred← citeshttps://doi.org/10.1371/journal.pone.0298697openalex-snapshot
THC and sperm: Impact on fertilization capability, pre-implantation in vitro development and epigenetic modifications
inferred← citeshttps://doi.org/10.14202/vetworld.2026.1747-1758openalex-snapshot
Effect of low-temperature stress on sperm DNA methylation and oxidative damage during cryopreservation of Tibetan pig semen
inferred← citeshttps://doi.org/10.1515/med-2025-1344openalex-snapshot
Promotion of asthenozoospermia by C9orf72 through suppression of spermatogonia activity via fructose metabolism and mitophagy
inferred← citeshttps://doi.org/10.1530/raf-23-0018openalex-snapshot
Quality of fresh and cryopreserved bovine sperm is reduced by BPA and BPF exposure
inferred← citeshttps://doi.org/10.1530/rep-21-0385openalex-snapshot
The effect and mechanism of Grim 19 on mouse sperm quality and testosterone synthesis
inferred← citeshttps://doi.org/10.1530/rep-23-0095openalex-snapshot
Characterization of bioenergetic and kinematic plasticity of bovine sperm reveals novel and dynamic temporal traits
inferred← citeshttps://doi.org/10.1590/1984-3143-ar2020-0522openalex-snapshot
Increased quality of in natura and cryopreserved semen of water buffaloes supplemented with saturated and unsaturated fatty acids from the palm oil industry
inferred← citeshttps://doi.org/10.20473/ovz.v11i3.2022.130-136openalex-snapshot
Green tea (Camellia sinensis) leaf extract maintained spermatozoa plasma membrane integrity, viability, and motility of mice (Mus musculus) exposed to cigarette smoke
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3351258/v1openalex-snapshot
C9orf72 Overexpression in Asthenozoospermia: Implications for Spermatogonia Proliferation through mitophagy and glucose metabolism
inferred← citeshttps://doi.org/10.2174/1566524022666220408104047openalex-snapshot
Sperm Mitochondria, the Driving Force Behind Human Spermatozoa Activities: Its Functions and Dysfunctions - A Narrative Review
inferred← citeshttps://doi.org/10.2174/1570159x22666240426091311openalex-snapshot
Drug Target to Alleviate Mitochondrial Dysfunctions in Alzheimer’s Disease: Recent Advances and Therapeutic Implications
inferred← citeshttps://doi.org/10.21897/rmvz.2833openalex-snapshot
Estrés oxidativo en espermatozoides epididimarios de alpaca criopreservados con diferentes concentraciones de plasma seminal
inferred← citeshttps://doi.org/10.22363/2313-0245-2024-28-3-390-402openalex-snapshot
Mitochondrial DNA copy number level in the culture medium of human embryos as a factor in predicting the onset and prolongation of pregnancy
inferred← citeshttps://doi.org/10.25259/fsr_51_2025openalex-snapshot
Beyond the Powerhouse – Unveiling Hidden Influence of Mitochondria on Reproductive Health and Fertility
inferred← citeshttps://doi.org/10.29254/2077-4214-2026-1-180-380-388openalex-snapshot
REACTIVE OXYGEN SPECIES IN EJACULATE AFFECT EMBRYO DEVELOPMENT IN VITRO WHEN ASSISTED REPRODUCTIVE TECHNOLOGIES ARE USED
inferred← citeshttps://doi.org/10.32687/1561-5936-2022-26-3-199-204openalex-snapshot
Reproductive technologies in solving the problems of infertility of the population (Part I)
inferred← citeshttps://doi.org/10.33394/bioscientist.v12i1.11295openalex-snapshot
Studi In-Vivo Antifertilitas Stigmasterol Daun Beluntas (Pluchea indica L.): Pengamatan Konsentrasi dan Motilitas Spermatozoa
inferred← citeshttps://doi.org/10.33545/gynae.2023.v7.i6a.1393openalex-snapshot
Effectiveness and tolerability of a novel blend of coq10, l-carnitine, zinc, lycopene, and astaxanthin in males with infertility: Findings from a UNESCO study
inferred← citeshttps://doi.org/10.3389/fcell.2022.926684openalex-snapshot
Mitochondrial metabolism determines the functional status of human sperm and correlates with semen parameters
inferred← citeshttps://doi.org/10.3389/fcell.2022.983993openalex-snapshot
Decoding the role of cytochrome c in metabolism of human spermatozoa by Raman imaging
inferred← citeshttps://doi.org/10.3389/fendo.2022.849534openalex-snapshot
Associations of Sperm mtDNA Copy Number, DNA Fragmentation Index, and Reactive Oxygen Species With Clinical Outcomes in ART Treatments
inferred← citeshttps://doi.org/10.3389/fendo.2026.1882458openalex-snapshot
Metabolic pathways fueling human spermatozoa capacitation and hyperactivation: a roadmap for spermatozoa bioenergetics
inferred← citeshttps://doi.org/10.3389/fphar.2025.1665356openalex-snapshot
Wuzi-Yanzong-Wan inhibits testicular mitochondrial apoptosis in rats by downregulating TAp73-Mediated P38 MAPK-ADAM17 pathway
inferred← citeshttps://doi.org/10.3389/frph.2024.1479568openalex-snapshot
Mitochondrial dysfunction signatures in idiopathic primary male infertility: a validated proteomics-based diagnostic approach
inferred← citeshttps://doi.org/10.3389/fvets.2026.1847076openalex-snapshot
Microplastics in the seminal microenvironment of boar semen: associations with sperm motility and antimicrobial susceptibility
inferred← citeshttps://doi.org/10.3390/ani10101825openalex-snapshot
Novel Low-Voltage Electro-Ejaculation Approach for Sperm Collection from Zoo Captive Lanyu Miniature Pigs (Sus barbatus sumatranus)
inferred← citeshttps://doi.org/10.3390/ani10101899openalex-snapshot
Conditioned Medium from Canine Amniotic Membrane-Derived Mesenchymal Stem Cells Improved Dog Sperm Post-Thaw Quality-Related Parameters
inferred← citeshttps://doi.org/10.3390/ani11061769openalex-snapshot
Beneficial Influence of Soybean Lecithin Nanoparticles on Rooster Frozen–Thawed Semen Quality and Fertility
inferred← citeshttps://doi.org/10.3390/ani14162406openalex-snapshot
Medaka (Oryzias latipes) Dmrt3a Is Involved in Male Fertility
inferred← citeshttps://doi.org/10.3390/ani15152246openalex-snapshot
Mitochondrial Regulation of Spermatozoa Function: Metabolism, Oxidative Stress and Therapeutic Insights
inferred← citeshttps://doi.org/10.3390/ani15192805openalex-snapshot
Repeatability of Selected Parameters Related to Stallion Sperm Quality and Cryotolerance
inferred← citeshttps://doi.org/10.3390/ani15233383openalex-snapshot
Nicotinamide Mononucleotide Enhances Boar Sperm Quality via Maintaining Mitochondrial Function During Liquid Storage
inferred← citeshttps://doi.org/10.3390/antiox10020217openalex-snapshot
Modulation of Human Sperm Mitochondrial Respiration Efficiency by Plant Polyphenols
inferred← citeshttps://doi.org/10.3390/antiox10030337openalex-snapshot
Mitochondrial Dysfunction and Oxidative Stress Caused by Cryopreservation in Reproductive Cells
inferred← citeshttps://doi.org/10.3390/antiox10081204openalex-snapshot
Mitochondria Content and Activity Are Crucial Parameters for Bull Sperm Quality Evaluation
inferred← citeshttps://doi.org/10.3390/antiox11091684openalex-snapshot
Natural Astaxanthin Improves Testosterone Synthesis and Sperm Mitochondrial Function in Aging Roosters
inferred← citeshttps://doi.org/10.3390/antiox12020514openalex-snapshot
Coenzyme Q10 and Endocrine Disorders: An Overview
inferred← citeshttps://doi.org/10.3390/antiox13060739openalex-snapshot
Exogenous Oxidative Stress in Human Spermatozoa Induces Opening of the Mitochondrial Permeability Transition Pore: Effect on Mitochondrial Function, Sperm Motility and Induction of Cell Death
inferred← citeshttps://doi.org/10.3390/antiox14010075openalex-snapshot
Effects of Essential Oils as Antioxidant and Cryoprotective Agents in Improving Frozen and Thawed Human Sperm Criteria
inferred← citeshttps://doi.org/10.3390/antiox15020174openalex-snapshot
The Gut–Extracellular Vesicle–Mitochondria Axis in Reproductive Aging: Antioxidant and Anti-Senescence Mechanisms
inferred← citeshttps://doi.org/10.3390/antiox15070795openalex-snapshot
Reactive Oxygen and Nitrogen Species in Male Reproductive Health: From Molecular Mechanisms to Clinical Consequences
inferred← citeshttps://doi.org/10.3390/biology12060827openalex-snapshot
Mitochondria Quality Control and Male Fertility
inferred← citeshttps://doi.org/10.3390/biology14050491openalex-snapshot
Efficacy and Safety of Visible and Near-Infrared Photobiomodulation Therapy on Astenospermic Human Sperm: Wavelength-Dependent Regulation of Nitric Oxide Levels and Mitochondrial Energetics
inferred← citeshttps://doi.org/10.3390/biology15100802openalex-snapshot
Association Between Oxidative Stress Biomarkers and Sperm DNA Damage in Idiopathic and Unexplained Male Infertility
inferred← citeshttps://doi.org/10.3390/biology15171562openalex-snapshot
Mitochondrial Remodeling, Cytoskeletal Dynamics, and Translational Control During Drosophila Spermatid Elongation: An Integrative Review
inferred← citeshttps://doi.org/10.3390/biomedicines11113014openalex-snapshot
Sperm Mitochondrial Content and Mitochondrial DNA to Nuclear DNA Ratio Are Associated with Body Mass Index and Progressive Motility
inferred← citeshttps://doi.org/10.3390/cells11050797openalex-snapshot
The Role of Mitochondria in Human Fertility and Early Embryo Development: What Can We Learn for Clinical Application of Assessing and Improving Mitochondrial DNA?
inferred← citeshttps://doi.org/10.3390/cells15020149openalex-snapshot
Mitochondrial Metabolic Checkpoints in Human Fertility: Reactive Oxygen Species as Gatekeepers of Gamete Competence
inferred← citeshttps://doi.org/10.3390/ijms25073980openalex-snapshot
Mitochondrial Differentiation during Spermatogenesis: Lessons from Drosophila melanogaster
inferred← citeshttps://doi.org/10.3390/ijms252313064openalex-snapshot
Sperm-Borne Mitochondrial Activity Influenced by Season and Age of Holstein Bulls
inferred← citeshttps://doi.org/10.3390/medicina59101769openalex-snapshot
Oxidative Stress and Male Infertility: The Protective Role of Antioxidants
inferred← citeshttps://doi.org/10.3390/metabo15060379openalex-snapshot
Dietary and Lifestyle Interventions to Mitigate Oxidative Stress in Male and Female Fertility: Practical Insights for Infertility Management—A Narrative Review
inferred← citeshttps://doi.org/10.3390/oxygen2040036openalex-snapshot
Oxidative Stress as an Underlying Mechanism of Bacteria-Inflicted Damage to Male Gametes
inferred← citeshttps://doi.org/10.3390/ph15050519openalex-snapshot
Age-Related Decline of Male Fertility: Mitochondrial Dysfunction and the Antioxidant Interventions
inferred← citeshttps://doi.org/10.3390/reprodmed6030016openalex-snapshot
HSP60 Reduction Causes an Abnormal Genotype and Sex Distribution and Impairs Mitochondrial Activity in Mouse Spermatozoa
inferred← citeshttps://doi.org/10.3390/vetsci9080403openalex-snapshot
Green Tea Extract in the Extender Improved the Post-Thawed Semen Quality and Decreased Amino Acid Mutation of Kacang Buck Sperm
inferred← citeshttps://doi.org/10.34172/jlms.2022.75openalex-snapshot
Preclinical and Clinical Applications of Photobiomodulation Therapy in Sperm Motility: A Narrative Review
inferred← citeshttps://doi.org/10.34172/mj.2024.004openalex-snapshot
Sperm DNA damage in men with severe asthenozoospermia
inferred← citeshttps://doi.org/10.3791/63790openalex-snapshot
Flow Cytometric Analysis of Biomarkers for Detecting Human Sperm Functional Defects
inferred← citeshttps://doi.org/10.4081/aiua.2024.12837openalex-snapshot
How much does mitochondrial dysfunction affect male infertility?
inferred← citeshttps://doi.org/10.4103/mjbl.mjbl_1259_23openalex-snapshot
Isolation and Purification of Acrosin (ACR) from the Human Seminal Fluid of Infertility Patients
inferred← citeshttps://doi.org/10.55787/jtams.23.53.2.182openalex-snapshot
SINGLE SPERMATOZOON HEAD TRACKING FOR ROBOTIC INTRACYTOPLASMIC SPERM INJECTION (ICSI)
inferred← citeshttps://doi.org/10.5582/bst.2026.01002openalex-snapshot
Implications of mitochondrial function in embryonic development
inferred← citeshttps://doi.org/10.5772/intechopen.107774openalex-snapshot
Reactive Oxygen Species - Advances and Developments
inferred← citeshttps://doi.org/10.5772/intechopen.112304openalex-snapshot
Oxidative Stress and Male Fertility: Promising Role of Nutraceuticals
inferred← citeshttps://doi.org/10.6084/m9.figshare.22774360openalex-snapshot
Additional file 1 of iTRAQ-based comparative proteomics reveal an enhancing role of PRDX6 in the freezability of Mediterranean buffalo sperm
inferred← citeshttps://doi.org/10.6084/m9.figshare.22774363openalex-snapshot
Additional file 2 of iTRAQ-based comparative proteomics reveal an enhancing role of PRDX6 in the freezability of Mediterranean buffalo sperm
inferred← citeshttps://doi.org/10.6084/m9.figshare.25123957openalex-snapshot
Additional file 1 of Sperm function, mitochondrial activity and in vivo fertility are associated to their mitochondrial DNA content in pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.25124052openalex-snapshot
Additional file 2 of Sperm function, mitochondrial activity and in vivo fertility are associated to their mitochondrial DNA content in pigs
inferred← citeshttps://doi.org/10.6084/m9.figshare.26568970openalex-snapshot
Additional file 1 of N-thiocarboxyanhydrides, amino acid-derived enzyme-activated H2S donors, enhance sperm mitochondrial activity in presence and absence of oxidative stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.26568973openalex-snapshot
Additional file 2 of N-thiocarboxyanhydrides, amino acid-derived enzyme-activated H2S donors, enhance sperm mitochondrial activity in presence and absence of oxidative stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.26568976openalex-snapshot
Additional file 3 of N-thiocarboxyanhydrides, amino acid-derived enzyme-activated H2S donors, enhance sperm mitochondrial activity in presence and absence of oxidative stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.26568979openalex-snapshot
Additional file 4 of N-thiocarboxyanhydrides, amino acid-derived enzyme-activated H2S donors, enhance sperm mitochondrial activity in presence and absence of oxidative stress
inferred← citeshttps://doi.org/10.6084/m9.figshare.26568982openalex-snapshot
Additional file 5 of N-thiocarboxyanhydrides, amino acid-derived enzyme-activated H2S donors, enhance sperm mitochondrial activity in presence and absence of oxidative stress
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