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Hypergonadotropic Ovarian Failure Associated with an Inherited Mutation of Human Bone Morphogenetic Protein-15 (BMP15) Gene
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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/(sici)1096-8628(19991229)89:4<186::aid-ajmg3>3.0.co;2-5openalex-snapshot
Ovarian differentiation and gonadal failure
inferredcites →https://doi.org/10.1007/s004390000364openalex-snapshot
Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure
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/s0015-0282(00)01539-9openalex-snapshot
Mutation analysis of the growth differentiation factor-9 and -9B genes in patients with premature ovarian failure and polycystic ovary syndrome
inferredcites →https://doi.org/10.1016/s0015-0282(16)59467-9openalex-snapshot
Regulation of human granulosa-luteal cell progesterone production and proliferation by gonadotropins and growth factors
inferredcites →https://doi.org/10.1016/s0015-0282(97)00480-9openalex-snapshot
The finnish follicle-stimulating hormone receptor gene mutation is rare in North american women with 46,xx ovarian failure
inferredcites →https://doi.org/10.1016/s0021-9258(18)47087-1openalex-snapshot
The type 1 repeats of thrombospondin 1 activate latent transforming growth factor-beta.
inferredcites →https://doi.org/10.1016/s0021-9258(18)80047-3openalex-snapshot
Site-directed Mutagenesis of Cysteine Residues in the Pro Region of the Transforming Growth Factor β1 Precursor
inferredcites →https://doi.org/10.1016/s0889-8545(03)00027-5openalex-snapshot
Contemporary issues in primary amenorrhea
inferredcites →https://doi.org/10.1016/s1359-6101(99)00010-6openalex-snapshot
Latent transforming growth factor-β binding proteins (LTBPs)—structural extracellular matrix proteins for targeting TGF-β action
inferredcites →https://doi.org/10.1038/35006129openalex-snapshot
Betaglycan binds inhibin and can mediate functional antagonism of activin signalling
inferredcites →https://doi.org/10.1038/77033openalex-snapshot
Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner
inferredcites →https://doi.org/10.1038/ng0997-58openalex-snapshot
Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1
inferredcites →https://doi.org/10.1074/jbc.m207362200openalex-snapshot
Molecular Basis of Bone Morphogenetic Protein-15 Signaling in Granulosa Cells
inferredcites →https://doi.org/10.1074/jbc.m210598200openalex-snapshot
Effect of Intracellular Interactions on the Processing and Secretion of Bone Morphogenetic Protein-15 (BMP-15) and Growth and Differentiation Factor-9
inferredcites →https://doi.org/10.1086/302152openalex-snapshot
Evidence for a Turner Syndrome Locus or Loci at Xp11.2-p22.1
inferredcites →https://doi.org/10.1095/biolreprod.103.023093openalex-snapshot
Mutations in the Genes for Oocyte-Derived Growth Factors GDF9 and BMP15 Are Associated with Both Increased Ovulation Rate and Sterility in Cambridge and Belclare Sheep (Ovis aries)1
inferredcites →https://doi.org/10.1128/mcb.8.10.4162openalex-snapshot
Molecular Events in the Processing of Recombinant Type 1 Pre-Pro-Transforming Growth Factor Beta to the Mature Polypeptide
inferredcites →https://doi.org/10.1210/en.2002-220929openalex-snapshot
A Novel Function of Bone Morphogenetic Protein-15 in the Pituitary: Selective Synthesis and Secretion of FSH by Gonadotropes
inferredcites →https://doi.org/10.1210/er.2002-0003openalex-snapshot
Genetic Analysis of the Mammalian Transforming Growth Factor-β Superfamily
inferredcites →https://doi.org/10.1210/er.2003-0007openalex-snapshot
The Bone Morphogenetic Protein System In Mammalian Reproduction
inferredcites →https://doi.org/10.1210/jc.84.8.2744openalex-snapshot
Human Growth Differentiation Factor 9 (GDF-9) and Its Novel Homolog GDF-9B Are Expressed in Oocytes during Early Folliculogenesis
inferredcites →https://doi.org/10.1210/jcem-21-11-1440openalex-snapshot
CLINICAL ASSESSMENT OF BODY HAIR GROWTH IN WOMEN
inferredcites →https://doi.org/10.1210/jcem.84.8.5921openalex-snapshot
Human Growth Differentiation Factor 9 (GDF-9) and Its Novel Homolog GDF-9B Are Expressed in Oocytes during Early Folliculogenesis1
inferredcites →https://doi.org/10.1210/me.12.12.1809openalex-snapshot
The Bone Morphogenetic Protein 15 Gene Is X-Linked and Expressed in Oocytes
inferredcites →https://doi.org/10.1210/mend.15.6.0662openalex-snapshot
Synergistic Roles of Bone Morphogenetic Protein 15 and Growth Differentiation Factor 9 in Ovarian Function
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/pharmacia.72.e147149zenodo-depositor-declared
BMP15 genetic variations in patients with premature ovarian insufficiency – correlation with clinical and laboratory parameters
inferred← citeshttps://doi.org/10.1002/9780470015902.a0026636openalex-snapshot
Genetics of Primary Ovarian Insufficiency
inferred← citeshttps://doi.org/10.1002/ajmg.a.36807openalex-snapshot
Phenotype–genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature
inferred← citeshttps://doi.org/10.1002/ajmg.c.31684openalex-snapshot
A hypothesis: Could telomere length and/or epigenetic alterations contribute to infertility in females with Turner syndrome?
inferred← citeshttps://doi.org/10.1002/humu.20961openalex-snapshot
BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1002/humu.23988openalex-snapshot
Fundamental role of BMP15 in human ovarian folliculogenesis revealed by null and missense mutations associated with primary ovarian insufficiency
inferred← citeshttps://doi.org/10.1002/mgg3.1165openalex-snapshot
Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1002/mrd.20661openalex-snapshot
Follicular growth in vitro: detection of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) during in vitro culture of ovine cortical slices
inferred← citeshttps://doi.org/10.1002/mrd.20912openalex-snapshot
Fibroblast growth factor 7 stimulates in vitro growth of oocytes originating from bovine early antral follicles
inferred← citeshttps://doi.org/10.1002/mrd.21265openalex-snapshot
Integral role of GDF‐9 and BMP‐15 in ovarian function
inferred← citeshttps://doi.org/10.1002/mrd.22131openalex-snapshot
Kit ligand and glial‐derived neurotrophic factor as alternative supplements for activation and development of ovine preantral follicles in vitro
inferred← citeshttps://doi.org/10.1002/mrd.22285openalex-snapshot
Cytokines in ovarian folliculogenesis, oocyte maturation and luteinisation
inferred← citeshttps://doi.org/10.1002/rmb2.12371openalex-snapshot
The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review
inferred← citeshttps://doi.org/10.1002/rmb2.12538openalex-snapshot
Paracrine regulation of granulosa cell development in the antral follicles in mammals
inferred← citeshttps://doi.org/10.1002/wsbm.21openalex-snapshot
Regulatory roles of transforming growth factor beta family members in folliculogenesis
inferred← citeshttps://doi.org/10.1007/978-0-85729-826-3_6openalex-snapshot
How the Oocyte Influences Follicular Cell Function and Why
inferred← citeshttps://doi.org/10.1007/978-1-4939-0659-8_3openalex-snapshot
Genetics of Female Infertility Due to Anomalies of the Ovary and Mullerian Ducts
inferred← citeshttps://doi.org/10.1007/978-1-59745-292-2_27openalex-snapshot
Bone Morphogenetic Proteins/Growth Differentiation Factors and Smad Activation in Ovarian Granulosa Cells and Carcinoma
inferred← citeshttps://doi.org/10.1007/978-2-287-87855-8_4openalex-snapshot
Syndrome de Turner: Corrélations entre phénotypes et défauts cytogénétiques du chromosome X
inferred← citeshttps://doi.org/10.1007/978-2-8178-0061-5_2openalex-snapshot
Dialogue ovocyte-cumulus: concept et applications cliniques
inferred← citeshttps://doi.org/10.1007/978-2-8178-0061-5_38openalex-snapshot
Impacts morphologiques et moléculaires de la qualité ovocytaire en assistance médicale à la procréation
inferred← citeshttps://doi.org/10.1007/978-3-030-18901-3_29-1openalex-snapshot
Disorders of the Ovary
inferred← citeshttps://doi.org/10.1007/978-3-030-34150-3_2openalex-snapshot
The Genetics of Turner Syndrome
inferred← citeshttps://doi.org/10.1007/978-3-030-49984-6_16openalex-snapshot
Amenorrhea in Adolescents
inferred← citeshttps://doi.org/10.1007/978-3-031-83979-5_3openalex-snapshot
Premature Ovarian Insufficiency
inferred← citeshttps://doi.org/10.1007/978-3-319-22491-6_5openalex-snapshot
Mechanisms of Primary Ovarian Insufficiency
inferred← citeshttps://doi.org/10.1007/978-3-319-47507-3_4openalex-snapshot
BMP and BMP Regulation: Structure and Function
inferred← citeshttps://doi.org/10.1007/978-3-319-59318-0_3openalex-snapshot
Primary Ovarian Insufficiency
inferred← citeshttps://doi.org/10.1007/978-3-642-02062-9_1openalex-snapshot
New Insights into Ovarian Function
inferred← citeshttps://doi.org/10.1007/978-3-642-02062-9_4openalex-snapshot
Contraception Targets in Mammalian Ovarian Development
inferred← citeshttps://doi.org/10.1007/978-981-99-7028-5_7openalex-snapshot
Genetic Testing in Premature Ovarian Failure
inferred← citeshttps://doi.org/10.1007/bf03347073openalex-snapshot
Genetic defects of ovarian TGF-β-like factors and premature ovarian failure
inferred← citeshttps://doi.org/10.1007/s00018-005-5394-7openalex-snapshot
Genetics of early mammalian folliculogenesis
inferred← citeshttps://doi.org/10.1007/s00109-021-02055-5openalex-snapshot
Premature ovarian insufficiency: pathogenesis and therapeutic potential of mesenchymal stem cell
inferred← citeshttps://doi.org/10.1007/s00335-014-9537-8openalex-snapshot
A high resolution map of mammalian X chromosome fragile regions assessed by large-scale comparative genomics
inferred← citeshttps://doi.org/10.1007/s00404-010-1815-4openalex-snapshot
Genetic aspects of premature ovarian failure: a literature review
inferred← citeshttps://doi.org/10.1007/s00431-011-1561-zopenalex-snapshot
Mutation screening of BMP4 and Id2 genes in Chinese patients with congenital ureteropelvic junction obstruction
inferred← citeshttps://doi.org/10.1007/s00439-005-0081-1openalex-snapshot
A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletions
inferred← citeshttps://doi.org/10.1007/s00439-006-0150-0openalex-snapshot
Missense mutations in the BMP15 gene are associated with ovarian failure
inferred← citeshttps://doi.org/10.1007/s00439-013-1330-3openalex-snapshot
Characterization of a novel missense mutation in the prodomain of GDF5, which underlies brachydactyly type C and mild Grebe type chondrodysplasia in a large Pakistani family
inferred← citeshttps://doi.org/10.1007/s00467-009-1287-6openalex-snapshot
Functional analysis of BMP4 mutations identified in pediatric CAKUT patients
inferred← citeshttps://doi.org/10.1007/s10304-006-0171-8openalex-snapshot
Genetik ovarieller Störungen
inferred← citeshttps://doi.org/10.1007/s10545-010-9221-4openalex-snapshot
Ovarian function in girls and women with GALT‐deficiency galactosemia
inferred← citeshttps://doi.org/10.1007/s10735-010-9294-2openalex-snapshot
Expression of GDF-9, BMP-15 and their receptors in mammalian ovary follicles
inferred← citeshttps://doi.org/10.1007/s10815-015-0494-2openalex-snapshot
Effect of Anti-Müllerian hormone (AMH) and bone morphogenetic protein 15 (BMP-15) on steroidogenesis in primary-cultured human luteinizing granulosa cells through Smad5 signalling
inferred← citeshttps://doi.org/10.1007/s10815-017-0930-6openalex-snapshot
Age-related expression of TGF beta family receptors in human cumulus oophorus cells
inferred← citeshttps://doi.org/10.1007/s10815-018-1305-3openalex-snapshot
Connecting links between genetic factors defining ovarian reserve and recurrent miscarriages
inferred← citeshttps://doi.org/10.1007/s10815-019-01548-0openalex-snapshot
Association of BMP15 and GDF9 variants to premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1007/s10815-022-02574-1openalex-snapshot
Identification of novel biallelic variants in BMP15 in two siblings with premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1007/s11427-012-4355-2openalex-snapshot
An update on primary ovarian insufficiency
inferred← citeshttps://doi.org/10.1007/s11427-024-2606-6openalex-snapshot
Deleterious variants in RNF111 impair female fertility and induce premature ovarian insufficiency in humans and mice
inferred← citeshttps://doi.org/10.1007/s11825-011-0270-3openalex-snapshot
Genetische Ursachen der prämaturen Ovarialinsuffizienz und Ovardysgenesie
inferred← citeshttps://doi.org/10.1007/s12020-011-9477-yopenalex-snapshot
Relationship between Sloan-Kettering virus expression and mouse follicular development
inferred← citeshttps://doi.org/10.1007/s12098-013-1266-6openalex-snapshot
Etiological Evaluation of Adolescents with Primary Amenorrhea
inferred← citeshttps://doi.org/10.1007/s12210-015-0418-1openalex-snapshot
Mutations and sequence variants in GDF9, BMP15, and BMPR1B genes in Maremmana cattle breed with single and twin births
inferred← citeshttps://doi.org/10.1007/s12522-011-0082-9openalex-snapshot
Unique bioactivities of bone morphogenetic proteins in regulation of reproductive endocrine functions
inferred← citeshttps://doi.org/10.1007/s40142-013-0027-1openalex-snapshot
The Genetics of Infertility: Current Status of the Field
inferred← citeshttps://doi.org/10.1007/s42000-019-00141-5openalex-snapshot
Premature ovarian insufficiency in adolescence: a chance for early diagnosis?
inferred← citeshttps://doi.org/10.1007/s43032-019-00137-xopenalex-snapshot
Luteinizing Hormone Action in Human Oocyte Maturation and Quality: Signaling Pathways, Regulation, and Clinical Impact
inferred← citeshttps://doi.org/10.1007/s43032-023-01370-1openalex-snapshot
Implication of Novel BMP15 and GDF9 Variants in Unexpected Poor Ovarian Response
inferred← citeshttps://doi.org/10.1007/s43032-024-01467-1openalex-snapshot
Understanding the Mechanisms of Diminished Ovarian Reserve: Insights from Genetic Variants and Regulatory Factors
inferred← citeshttps://doi.org/10.1007/s43032-025-01831-9openalex-snapshot
From Dominant Assumptions to Recessive Trait: Rethinking BMP15 in Ovarian Dysfunction
inferred← citeshttps://doi.org/10.1016/b978-0-12-374430-2.00019-5openalex-snapshot
Genetic Considerations in the Evaluation of Menstrual Cycle Irregularities
inferred← citeshttps://doi.org/10.1016/b978-0-12-375097-6.10030-7openalex-snapshot
Disorders of the Hypothalamic–Pituitary–Gonadal Axis
inferred← citeshttps://doi.org/10.1016/b978-0-12-383834-6.00040-9openalex-snapshot
Genetics of Female Infertility in Humans
inferred← citeshttps://doi.org/10.1016/b978-0-12-383834-6.00092-6openalex-snapshot
Disorders of the Gonads, Genital Tract, and Genitalia
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00021-1openalex-snapshot
Follicular Development
inferred← citeshttps://doi.org/10.1016/b978-0-12-420196-5.00016-2openalex-snapshot
Genetics and Genomics of Reproductive Medicine and Health
inferred← citeshttps://doi.org/10.1016/b978-0-12-800892-8.00018-xopenalex-snapshot
Genetic Considerations in the Evaluation of Menstrual Cycle Irregularities
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64644-5openalex-snapshot
Follistatin and Transforming Growth Factor β (TGFβ) Family
inferred← citeshttps://doi.org/10.1016/b978-0-12-813209-8.00007-8openalex-snapshot
Cell-Cell Interactions in Ovarian Follicles: Role of TGF-β Superfamily Members
inferred← citeshttps://doi.org/10.1016/b978-0-12-813570-9.00019-xopenalex-snapshot
Genetics and Genomics of Primary Ovarian Insufficiency
inferred← citeshttps://doi.org/10.1016/b978-0-12-815236-2.00005-9openalex-snapshot
Hypogonadotropic and Hypergonadotropic Hypogonadism in Females: Disorders of Reproductive Ducts
inferred← citeshttps://doi.org/10.1016/b978-0-12-816561-4.00011-9openalex-snapshot
Genetics of premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1016/b978-0-323-18907-1.00119-0openalex-snapshot
Diagnosis and Treatment of Disorders of Sexual Development
inferred← citeshttps://doi.org/10.1016/b978-0-323-29738-7.00017-4openalex-snapshot
Physiology and Pathology of the Female Reproductive Axis
inferred← citeshttps://doi.org/10.1016/b978-0-323-29738-7.00023-xopenalex-snapshot
Pediatric Disorders of Sex Development
inferred← citeshttps://doi.org/10.1016/b978-0-323-65399-2.00010-3openalex-snapshot
Fertilization and embryogenesis
inferred← citeshttps://doi.org/10.1016/b978-0-323-91380-5.00015-0openalex-snapshot
Premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1016/b978-0-323-91380-5.00027-7openalex-snapshot
Update on the genetics and genomics of premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1016/b978-0-443-07477-6.50026-3openalex-snapshot
Normal ovaries, inflammatory and non-neoplastic conditions
inferred← citeshttps://doi.org/10.1016/b978-0-443-13825-6.00170-9openalex-snapshot
Genetic control of fetal sex development
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00067-5openalex-snapshot
Follistatin and Transforming Growth Factor β (TGFβ) Family
inferred← citeshttps://doi.org/10.1016/b978-012369443-0/50005-3openalex-snapshot
Genetic Programming in Ovarian Development and Oogenesis
inferred← citeshttps://doi.org/10.1016/b978-012369443-0/50010-7openalex-snapshot
Premature Ovarian Failure
inferred← citeshttps://doi.org/10.1016/b978-1-4160-2911-3.50018-2openalex-snapshot
10.1016/b978-1-4160-2911-3.50018-2
inferred← citeshttps://doi.org/10.1016/b978-1-4160-2911-3.50024-8openalex-snapshot
10.1016/b978-1-4160-2911-3.50024-8
inferred← citeshttps://doi.org/10.1016/b978-1-4160-4907-4.00008-5openalex-snapshot
The Ovarian Life Cycle
inferred← citeshttps://doi.org/10.1016/b978-1-4160-5583-9.00119-2openalex-snapshot
Diagnosis and Treatment of Disorders of Sexual Development
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0324-5.00017-1openalex-snapshot
Physiology and Pathology of the Female Reproductive Axis
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0324-5.00023-7openalex-snapshot
Disorders of Sex Development
inferred← citeshttps://doi.org/10.1016/b978-1-4557-2758-2.00009-3openalex-snapshot
The Ovarian Life Cycle
inferred← citeshttps://doi.org/10.1016/b978-1-4557-4858-7.00014-7openalex-snapshot
Ambiguous genitalia
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.01.005openalex-snapshot
Translating genomics to the clinical diagnosis of disorders/differences of sex development
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2022.01.001openalex-snapshot
Sheep as a model for neuroendocrinology research
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.12.003openalex-snapshot
Molecular Aspects and Clinical Relevance of GDF9 and BMP15 in Ovarian Function
inferred← citeshttps://doi.org/10.1016/j.ajhg.2008.04.018openalex-snapshot
Transcription Factor FIGLA is Mutated in Patients with Premature Ovarian Failure
inferred← citeshttps://doi.org/10.1016/j.ajhg.2009.08.001openalex-snapshot
Complex Segmental Duplications Mediate a Recurrent dup(X)(p11.22-p11.23) Associated with Mental Retardation, Speech Delay, and EEG Anomalies in Males and Females
inferred← citeshttps://doi.org/10.1016/j.ajhg.2012.04.016openalex-snapshot
Genome-wide Association Study Identifies Candidate Genes for Male Fertility Traits in Humans
inferred← citeshttps://doi.org/10.1016/j.ajhg.2013.03.007openalex-snapshot
Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome
inferred← citeshttps://doi.org/10.1016/j.ajog.2007.05.029openalex-snapshot
BMP15 mutations in XX gonadal dysgenesis and premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2006.12.017openalex-snapshot
Differential gene expression of bone morphogenetic protein 15 and growth differentiation factor 9 during in vitro maturation of porcine oocytes and early embryos
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2016.02.005openalex-snapshot
Differential expression of GDF-9 and BMP- 15 during follicular development in canine ovaries evaluated by flow cytometry
inferred← citeshttps://doi.org/10.1016/j.bbadis.2008.01.006openalex-snapshot
Role of transforming growth factor-β superfamily signaling pathways in human disease
inferred← citeshttps://doi.org/10.1016/j.bbadis.2012.05.013openalex-snapshot
Molecular control of oogenesis
inferred← citeshttps://doi.org/10.1016/j.beem.2009.12.002openalex-snapshot
Control of sex development
inferred← citeshttps://doi.org/10.1016/j.beem.2021.101594openalex-snapshot
Genetics of ovarian insufficiency and defects of folliculogenesis
inferred← citeshttps://doi.org/10.1016/j.biopha.2018.03.056openalex-snapshot
Current approaches for the treatment of premature ovarian failure with stem cell therapy
inferred← citeshttps://doi.org/10.1016/j.bpobgyn.2017.05.003openalex-snapshot
Genetic basis of eugonadal and hypogonadal female reproductive disorders
inferred← citeshttps://doi.org/10.1016/j.cbpa.2008.09.034openalex-snapshot
Potential role of bone morphogenetic protein-15 in zebrafish follicle development and oocyte maturation
inferred← citeshttps://doi.org/10.1016/j.cca.2018.06.041openalex-snapshot
Interfering effects of bisphenol A on in vitro growth of preantral follicles and maturation of oocyes
inferred← citeshttps://doi.org/10.1016/j.ctmp.2026.200288openalex-snapshot
Yijing Tang for premature ovarian insufficiency: A systematic review and methodological appraisal
inferred← citeshttps://doi.org/10.1016/j.ecl.2005.07.002openalex-snapshot
Mechanisms of Premature Menopause
inferred← citeshttps://doi.org/10.1016/j.ejmg.2018.10.012openalex-snapshot
Sex chromosomes-linked single-gene disorders involved in human infertility
inferred← citeshttps://doi.org/10.1016/j.emcend.2005.08.002openalex-snapshot
Actualités en endocrinologie de la reproduction
inferred← citeshttps://doi.org/10.1016/j.fct.2025.115719openalex-snapshot
Decoding premature ovarian insufficiency: A full spectrum review from epidemiology to management with emphasis on cyclophosphamide-evoked ovarian injury
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2004.11.059openalex-snapshot
An update: spontaneous premature ovarian failure is not an early menopause
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2005.10.071openalex-snapshot
Investigation of the human stem cell factor KIT ligand gene, KITLG, in women with 46,XX spontaneous premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2006.02.107openalex-snapshot
Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2006.05.079openalex-snapshot
Growth differentiating factor-9 mutations may be associated with premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2006.05.080openalex-snapshot
Mutational analysis of betaglycan/TGF-βRIII in premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2007.06.083openalex-snapshot
Association of genetic markers within the BMP15 gene with anovulation and infertility in women with polycystic ovary syndrome
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2007.08.053openalex-snapshot
Glycolytic enzyme expression in human granulosa cells
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2007.11.085openalex-snapshot
Premature ovarian failure and androgen receptor gene CAG repeat lengths weighted by X chromosome inactivation patterns
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2008.08.119openalex-snapshot
Bone morphogenetic protein 15 expression in human ovaries from fetuses, girls, and women
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2010.06.040openalex-snapshot
Sequence variation analysis of the prolactin receptor C-terminal region in women with premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2011.03.045openalex-snapshot
Influence of follicular fluid GDF9 and BMP15 on embryo quality
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2011.04.045openalex-snapshot
Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2012.08.021openalex-snapshot
Genetic considerations in the patient with Turner syndrome—45,X with or without mosaicism
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2012.10.026openalex-snapshot
NR5A1 (SF-1) gene variants in a group of 26 young women with XX primary ovarian insufficiency
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2015.04.016openalex-snapshot
Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.03.007openalex-snapshot
Trimethylamine N-oxide (TMAO) treatment triggers premature ovarian insufficiency (POI) via the activation of mitochondrial pathway apoptosis in granulosa cells
inferred← citeshttps://doi.org/10.1016/j.gde.2006.04.005openalex-snapshot
X-linked premature ovarian failure: a complex disease
inferred← citeshttps://doi.org/10.1016/j.gene.2026.150104openalex-snapshot
Distinct BNC1 variants contribute to premature ovarian insufficiency through different molecular mechanisms
inferred← citeshttps://doi.org/10.1016/j.gyobfe.2008.07.002openalex-snapshot
Analyse génétique des insuffisances ovariennes prématurées : implication des gènes forkhead et TGF-β
inferred← citeshttps://doi.org/10.1016/j.gyobfe.2008.07.011openalex-snapshot
Syndrome de Turner et procréation
inferred← citeshttps://doi.org/10.1016/j.ijgo.2010.03.023openalex-snapshot
Genetic abnormalities in Turkish women with premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.jaut.2009.03.004openalex-snapshot
Primary ovarian insufficiency: X chromosome defects and autoimmunity
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.11.009openalex-snapshot
Advances in monogenic female infertility
inferred← citeshttps://doi.org/10.1016/j.jpag.2012.05.017openalex-snapshot
Precocious Puberty in Turner Syndrome Variant
inferred← citeshttps://doi.org/10.1016/j.jpag.2020.04.002openalex-snapshot
Spontaneous Sexual Development and Heavy Menstrual Bleeding in 45,X Monosomy and 45,X/47,XXX Mosaic Turner Syndrome and a Review of the Literature
inferred← citeshttps://doi.org/10.1016/j.jpp.2013.09.002openalex-snapshot
Aménorrhée de l’adolescente
inferred← citeshttps://doi.org/10.1016/j.mad.2026.112186openalex-snapshot
Embryonic stem cell-derived extracellular vesicles alleviate ovarian dysfunction
inferred← citeshttps://doi.org/10.1016/j.maturitas.2012.09.017openalex-snapshot
Clinical characteristics and genetic analysis in women with premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1016/j.maturitas.2019.09.010openalex-snapshot
Turner syndrome and osteoporosis
inferred← citeshttps://doi.org/10.1016/j.maturitas.2024.108153openalex-snapshot
Genetic associations of miRNA variants (miR-10a, miR-30c, miR-181a, miR-499b) with primary ovarian insufficiency in Korean women
inferred← citeshttps://doi.org/10.1016/j.mce.2004.08.013openalex-snapshot
Oocyte-expressed genes affecting ovulation rate
inferred← citeshttps://doi.org/10.1016/j.mce.2004.10.012openalex-snapshot
Molecular biology and physiological role of the oocyte factor, BMP-15
inferred← citeshttps://doi.org/10.1016/j.mce.2007.11.005openalex-snapshot
Recent advances in the study of genes involved in non-syndromic premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.mce.2008.11.004openalex-snapshot
Aging of the human ovary and testis
inferred← citeshttps://doi.org/10.1016/j.mce.2009.07.016openalex-snapshot
Genetically modified mouse models for premature ovarian failure (POF)
inferred← citeshttps://doi.org/10.1016/j.mce.2010.05.017openalex-snapshot
Impaired production of BMP-15 and GDF-9 mature proteins derived from proproteins WITH mutations in the proregion
inferred← citeshttps://doi.org/10.1016/j.mce.2010.10.002openalex-snapshot
The bioactivity of human bone morphogenetic protein-15 is sensitive to C-terminal modification: Characterization of the purified untagged processed mature region
inferred← citeshttps://doi.org/10.1016/j.mce.2011.02.007openalex-snapshot
Steady-state level of bone morphogenetic protein-15 in goat ovaries and its influence on in vitro development and survival of preantral follicles
inferred← citeshttps://doi.org/10.1016/j.mce.2011.07.031openalex-snapshot
Mutations in inhibin and activin genes associated with human disease
inferred← citeshttps://doi.org/10.1016/j.mce.2011.07.049openalex-snapshot
Oogenesis: Transcriptional regulators and mouse models
inferred← citeshttps://doi.org/10.1016/j.mce.2013.02.016openalex-snapshot
The genetic basis of female reproductive disorders: Etiology and clinical testing
inferred← citeshttps://doi.org/10.1016/j.mce.2015.05.005openalex-snapshot
Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing
inferred← citeshttps://doi.org/10.1016/j.mce.2017.07.021openalex-snapshot
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing
inferred← citeshttps://doi.org/10.1016/j.mce.2017.11.002openalex-snapshot
The effect of ovarian reserve and receptor signalling on granulosa cell apoptosis during human follicle development
inferred← citeshttps://doi.org/10.1016/j.mefs.2010.06.002openalex-snapshot
Genetic screening for infertility: When should it be done?
inferred← citeshttps://doi.org/10.1016/j.mefs.2014.02.005openalex-snapshot
Investigation of some genetic variations in BMP15 accompanied with premature ovarian failure (POF) in Syrian women
inferred← citeshttps://doi.org/10.1016/j.ogc.2012.09.007openalex-snapshot
A New Approach to Primary Ovarian Insufficiency
inferred← citeshttps://doi.org/10.1016/j.omtn.2021.10.015openalex-snapshot
lncRNA DDGC participates in premature ovarian insufficiency through regulating RAD51 and WT1
inferred← citeshttps://doi.org/10.1016/j.rbmo.2010.02.018openalex-snapshot
Genes governing premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.rbmo.2011.01.002openalex-snapshot
Low-level X chromosome mosaicism in women with sporadic premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.rbmo.2011.02.015openalex-snapshot
A single nucleotide polymorphism in BMP15 is associated with high response to ovarian stimulation
inferred← citeshttps://doi.org/10.1016/j.rbmo.2014.07.018openalex-snapshot
BMP15 c.-9C>G promoter sequence variant may contribute to the cause of non-syndromic premature ovarian failure
inferred← citeshttps://doi.org/10.1016/j.rbmo.2022.05.003openalex-snapshot
Homozygous missense variants in BMPR15 can result in primary ovarian insufficiency
inferred← citeshttps://doi.org/10.1016/j.sjbs.2021.05.061openalex-snapshot
Two novel mutations in exon 2 of bone morphogenetic protein (BMP) 15 gene in Pakistani infertile females
inferred← citeshttps://doi.org/10.1016/j.steroids.2017.07.002openalex-snapshot
BMP15 in catfish testis: Cellular distribution, seasonal variation, and its role in steroidogenesis
inferred← citeshttps://doi.org/10.1016/j.tem.2006.03.010openalex-snapshot
Mining the oocyte transcriptome
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2019.02.012openalex-snapshot
Cellular localization and seasonal variation in BMP15 expression in ovary of the catfish Clarias batrachus and its role in ovarian steroidogenesis
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2020.08.019openalex-snapshot
PI3K inhibitor reduces in vitro maturation and developmental competence of porcine oocytes
inferred← citeshttps://doi.org/10.1016/j.xfnr.2020.06.001openalex-snapshot
New perspectives on the genetic causes of diminished ovarian reserve and opportunities for genetic screening: systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.03.002openalex-snapshot
Bone Morphogenetic Protein (BMP) signaling in animal reproductive system development and function
inferred← citeshttps://doi.org/10.1016/j.ygcen.2010.10.024openalex-snapshot
The hypothalamic–pituitary–ovarian axis and manipulations of the oestrous cycle in the brushtail possum
inferred← citeshttps://doi.org/10.1016/s0003-4266(06)73007-4openalex-snapshot
L’insuffisance ovarienne prématurée
inferred← citeshttps://doi.org/10.1016/s0246-1064(09)44360-3openalex-snapshot
Insuffisance ovarienne prématurée
inferred← citeshttps://doi.org/10.1016/s0246-1064(12)54741-9openalex-snapshot
Infertilités féminines d’origine endocrinienne
inferred← citeshttps://doi.org/10.1016/s0246-1064(15)43123-8openalex-snapshot
10.1016/s0246-1064(15)43123-8
inferred← citeshttps://doi.org/10.1016/s0246-1064(18)67529-2openalex-snapshot
10.1016/s0246-1064(18)67529-2
inferred← citeshttps://doi.org/10.1016/s0246-1064(23)47380-xopenalex-snapshot
10.1016/s0246-1064(23)47380-x
inferred← citeshttps://doi.org/10.1016/s1155-1941(03)00068-4openalex-snapshot
Insuffisance ovarienne prématurée
inferred← citeshttps://doi.org/10.1016/s1155-1941(12)53097-0openalex-snapshot
Insuffisance ovarienne prématurée
inferred← citeshttps://doi.org/10.1016/s1155-1941(13)50291-5openalex-snapshot
10.1016/s1155-1941(13)50291-5
inferred← citeshttps://doi.org/10.1016/s1245-1789(11)71058-7openalex-snapshot
Amenorrea de la adolescente
inferred← citeshttps://doi.org/10.1016/s1283-081x(09)70782-9openalex-snapshot
Insuficiencia ovárica prematura
inferred← citeshttps://doi.org/10.1016/s1283-081x(12)63398-0openalex-snapshot
Infertilidad femenina de origen endocrino
inferred← citeshttps://doi.org/10.1016/s1283-081x(19)41709-8openalex-snapshot
Insuficiencia ovárica prematura
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)60041-7openalex-snapshot
Genetics of ovarian hyperstimulation syndrome
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)60679-7openalex-snapshot
An oocentric view of folliculogenesis and embryogenesis
inferred← citeshttps://doi.org/10.1016/s1637-5017(11)72482-6openalex-snapshot
Aménorrhée de l'adolescente
inferred← citeshttps://doi.org/10.1016/s1937-6448(08)00807-1openalex-snapshot
Chapter 7 Oocyte Quality and Maternal Control of Development
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