Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice - Test2 - elhamkhani - TriplyDB

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

http://www.wikidata.org/entity/Q36375813

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Use of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI)The FMR1 gene, infertility, and reproductive decision-making: a review Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene Genomic markers of ovarian reserve Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian age.FMR1 premutation is an uncommon explanation for premature ovarian failure in Han Chinese.Approaches to identify genetic variants that influence the risk for onset of fragile X-associated primary ovarian insufficiency (FXPOI): a preliminary study.Understanding decreased fertility in women carriers of the FMR1 premutation: a possible mechanism for Fragile X-Associated Primary Ovarian Insufficiency (FXPOI).How the FMR1 gene became relevant to female fertility and reproductive medicine.Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegeneration Curvilinear association of CGG repeats and age at menopause in women with FMR1 premutation expansions.FMRP Associates with Cytoplasmic Granules at the Onset of Meiosis in the Human Oocyte.Presence of inclusions positive for polyglycine containing protein, FMRpolyG, indicates that repeat-associated non-AUG translation plays a role in fragile X-associated primary ovarian insufficiency.Granulosa cell and oocyte mitochondrial abnormalities in a mouse model of fragile X primary ovarian insufficiency.Length of FMR1 repeat alleles within the normal range does not substantially affect the risk of early menopause.FMR1 CGG expansions: prevalence and sex ratios.Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms.Molecular insights into the aetiology of female reproductive ageing.The impact of FMR1 gene mutations on human reproduction and development: a systematic review.Fragile X syndrome: an overview and update of the FMR1 gene.Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).FMR1 gene mutation screening by TP-PCR in patients with premature ovarian failure and fragile-X.Ovarian Follicular Theca Cell Recruitment, Differentiation, and Impact on Fertility: 2017 Update.Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome.

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P2860

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

http://www.wikidata.org/entity/Q36375813

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

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2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

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2012年學術文章

@zh-hant

name

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

@ast

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

@en

type

label

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

@ast

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

@en

prefLabel

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

@ast

Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

@en

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Human Molecular Genetics

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Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice

@en

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Cuiling Lu

http://www.w3.org/2001/XMLSchema#string

Dahua Chen

http://www.w3.org/2001/XMLSchema#string

Fei Gao

http://www.w3.org/2001/XMLSchema#string

Huiping Tan

http://www.w3.org/2001/XMLSchema#string

Li Lin

http://www.w3.org/2001/XMLSchema#string

Peng Jin

http://www.w3.org/2001/XMLSchema#string

Stephanie L Sherman

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P2860

Binding of ras to phosphoinositide 3-kinase p110alpha is required for ras-driven tumorigenesis in mice

Clinical practice. Primary ovarian insufficiency

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome

Targeted disruption of Pten in ovarian granulosa cells enhances ovulation and extends the life span of luteal cells

Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data

Premature ovarian failure among fragile X premutation carriers: parent-of-origin effect?

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

The fragile X premutation: into the phenotypic fold.

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5039-5047

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10.1093/HMG/DDS348

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23

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21

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2012-08-21T00:00:00Z

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22914733

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3490511

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