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Genetics of primary ovarian insufficiency: new developments and opportunities

Genetics of primary ovarian insufficiency: new developments and opportunities

http://www.wikidata.org/entity/Q26798895

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Oocyte-somatic cell interactions in the human ovary-novel role of bone morphogenetic proteins and growth differentiation factors Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency Impaired protein stability and nuclear localization of NOBOX variants associated with premature ovarian insufficiency Role of microRNAs in premature ovarian insufficiency.Environmental pollutants, a possible etiology for premature ovarian insufficiency: a narrative review of animal and human data.Primary ovarian insufficiency: different approaches in three cases and a review of literature Mutation analysis of NANOS3 in Brazilian women with primary ovarian failure A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family.Dormancy and activation of human oocytes from primordial and primary follicles: molecular clues to oocyte regulation.Environmentally Induced Epigenetic Transgenerational Inheritance of Reproductive Disease.New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing.NOBOX is a strong autosomal candidate gene in Tunisian patients with primary ovarian insufficiency.Primary ovarian insufficiency with t(5;13): a case report and literature review on disrupted genes.Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women.Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).A potential functional association between mutant BMPR2 and primary ovarian insufficiency.BMP15 "knockout-like" effect in familial premature ovarian insufficiency with persistent ovarian reserve.Premature Ovarian Insufficiency - an update on recent advances in understanding and management.Menstrual cycle characteristics of young females with occult primary ovarian insufficiency at initial diagnosis and one-year follow-up with serum amh level and antral follicle count.Variation analysis of PUM1 gene in Chinese women with primary ovarian insufficiency.Reproductive ovarian testing and the alphabet soup of diagnoses: DOR, POI, POF, POR, and FOR.Primary ovarian insufficiency in classic galactosemia: current understanding and future research opportunities.TBP2 gene may not be associated with primary ovarian insufficiency.Bioengineering Strategies to Treat Female Infertility.Acquisition of oocyte competence to develop as an embryo: integrated nuclear and cytoplasmic events.A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency.POLR2C Mutations Are Associated With Primary Ovarian Insufficiency in Women.Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency.Recent developments in genetics and medically assisted reproduction: from research to clinical applications Scans for signatures of selection in Russian cattle breed genomes reveal new candidate genes for environmental adaptation and acclimation Complex genetics of female fertility Environmental toxicant induced epigenetic transgenerational inheritance of ovarian pathology and granulosa cell epigenome and transcriptome alterations: ancestral origins of polycystic ovarian syndrome and primary ovarian insufiency

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Genetics of primary ovarian insufficiency: new developments and opportunities

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Genetics of primary ovarian insufficiency: new developments and opportunities

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Human Reproduction Update

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Genetics of primary ovarian insufficiency: new developments and opportunities

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Joe Leigh Simpson

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Yingying Qin

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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

A review of trisomy X (47,XXX)

Transcription factor FIGLA is mutated in patients with premature ovarian failure

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

An integrated encyclopedia of DNA elements in the human genome

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome

Identification of novel mutations in FOXL2 associated with premature ovarian failure

FOXL2 mutation screening in a large panel of POF patients and XX males

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

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genetic variation

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