How the FMR1 gene became relevant to female fertility and reproductive medicine. - Wikidata - wikimedia - TriplyDB

How the FMR1 gene became relevant to female fertility and reproductive medicine.

How the FMR1 gene became relevant to female fertility and reproductive medicine.

http://www.wikidata.org/entity/Q34106386

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Association of skewed X-chromosome inactivation with FMR1 CGG repeat length and anti-Mullerian hormone levels: a cohort study.Effect of race and ethnicity on utilization and outcomes of assisted reproductive technology in the USA.Length of FMR1 repeat alleles within the normal range does not substantially affect the risk of early menopause.The importance of redundancy of functional ovarian reserve when investigating potential genetic effects on ovarian function.FMR6 may play a role in the pathogenesis of fragile X-associated premature ovarian insufficiency.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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2014 nî lūn-bûn

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2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

How the FMR1 gene became relevant to female fertility and reproductive medicine.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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FGENE.2014.00284

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Frontiers in Genetics

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How the FMR1 gene became relevant to female fertility and reproductive medicine.

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Andrea Weghofer

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David H Barad

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Norbert Gleicher

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Vitaly A Kushnir

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FMR1 genotype with autoimmunity-associated polycystic ovary-like phenotype and decreased pregnancy chance

FMRP targets distinct mRNA sequence elements to regulate protein expression

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

Utilizing FMR1 gene mutations as predictors of treatment success in human in vitro fertilization

Expression of fragile X mental retardation protein and Fmr1 mRNA during folliculogenesis in the rat

The impact in older women of ovarian FMR1 genotypes and sub-genotypes on ovarian reserve

Association of FMR1 genotypes with in vitro fertilization (IVF) outcomes based on ethnicity/race

Elevated prevalence of 35-44 FMR1 trinucleotide repeats in women with diminished ovarian reserve

Can egg donor selection be improved?--A pilot study

The (CGG)n repeat element within the 5' untranslated region of the FMR1 message provides both positive and negative cis effects on in vivo translation of a downstream reporter.

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10.3389/FGENE.2014.00284

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2014-08-29T00:00:00Z

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