Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency. - Wikidata - awgldk - TriplyDB

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

http://www.wikidata.org/entity/Q36085633

about

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 Skin-derived mesenchymal stem cells help restore function to ovaries in a premature ovarian failure mouse model Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene Association of skewed X-chromosome inactivation with FMR1 CGG repeat length and anti-Mullerian hormone levels: a cohort study.RNA-binding proteins in human oogenesis: Balancing differentiation and self-renewal in the female fetal germline Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian age.Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome Expression of an expanded CGG-repeat RNA in a single pair of primary sensory neurons impairs olfactory adaptation in Caenorhabditis elegans.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.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.Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice Somatic expansion in mouse and human carriers of fragile X premutation alleles.Granulosa cell and oocyte mitochondrial abnormalities in a mouse model of fragile X primary ovarian insufficiency.FMR1-dependent variability of ovarian aging patterns is already apparent in young oocyte donors.FMR1 CGG expansions: prevalence and sex ratios.Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms.Quantifying growing versus non-growing ovarian follicles in the mouse.Molecular insights into the aetiology of female reproductive ageing.Fragile X syndrome: an overview and update of the FMR1 gene.Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).Newborn screening for fragile X syndrome.The importance of redundancy of functional ovarian reserve when investigating potential genetic effects on ovarian function.Premature recruitment of oocyte pool and increased mTOR activity in Fmr1 knockout mice and reversal of phenotype with rapamycin.The Stage- and Cell Type-Specific Localization of Fragile X Mental Retardation Protein in Rat Ovaries.Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome.

P2860

Q21198724-54A130C6-7871-4CFD-AD28-FDDCF8D8745D Q27026782-301640BF-21E8-4076-8F9C-393C415B427C Q27324731-E77F5DCE-B379-47B6-8ED5-50B5899D06A2 Q28077015-B626C629-FAE8-43B2-97FD-9D84134897EE Q33617701-A1B60EF4-FE76-4A0C-A9E5-4E2F2262A1F0 Q33732476-22CAE412-6B9C-4326-A686-6690F311DE1F Q33786496-94B36B9A-9C82-4381-BFF5-41F5A9723CAA Q34055453-17877DE2-A4CC-4D8A-91AA-7F18098E6066 Q34074523-1F8F7B30-70F5-4F48-90CA-C9F7317366E0 Q34077084-C06F1FEE-1440-4E48-8FBC-8442409D084D Q34106386-FF775771-F83C-47F3-B886-F53573B0C6E3 Q35541848-7126244E-E217-44B6-B29A-565D37BC1746 Q36151280-2075BBFE-CA6C-4746-A165-8C253CC10F54 Q36368705-6F19961B-0DBF-4E8E-A24F-615EFA6D50F5 Q36375813-6EE663E1-AF70-44DA-A2AE-0B8DBF91394B Q36472667-B82C9ABE-5A1B-4B31-8741-350F38A0E68B Q36946491-346F5105-317F-4260-BAC5-C0B00611F5F0 Q37115382-325F4818-4F48-48D2-ACB2-D159D6936CB5 Q37451133-A3DCBDDE-06E1-4BC1-969F-939FA5C1AE3D Q37524454-F696B380-2AEE-4CB2-9C2F-4F25F0CD966C Q37586512-D2301628-7FB1-431A-B142-E4C8A0305A07 Q38605681-5937EB9D-8055-4008-B519-F7BD9CA3ECAE Q39375765-6B347771-BE17-4D39-93FF-80ABD99E3EF6 Q41144516-450B338F-B8EF-4A05-AB08-491C59CB81F7 Q41258345-D039C416-E86A-4A62-969A-0CEBF4CD4D8B Q42398270-9AD58DCC-C473-4759-A020-AD234776768C Q47556307-5DE4AEB5-4044-4187-8726-5C9B186B1F21 Q48577134-2E8AD6E7-F216-46B8-A0D3-9458A517A469 Q49905433-99D4353C-A748-4EB6-99FF-47AC6608E9A5

P2860

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

http://www.wikidata.org/entity/Q36085633

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

@ast

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

@en

type

label

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

@ast

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

@en

prefLabel

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

@ast

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

@en

P1433

Q36085633-2BE375FE-B502-46CC-902E-9BDF4202624B

P1476

Q36085633-BFACD4BD-97F1-4444-A4CE-388E9C5E9940

P2093

Q36085633-4C3A8673-A41E-494F-B213-860BFC7D7B01

Q36085633-536AE777-57C6-4D55-90BD-C6B1D93D6BDD

Q36085633-7E5C5919-7FE3-45B4-AC03-1E9EEE59B060

Q36085633-825B6CC1-4432-4F07-980F-6CE841E88ACD

Q36085633-9072B39B-E669-47D1-9E78-47872DE929F6

Q36085633-9CDAF52F-7DFF-41AB-873C-D213BBB2D532

Q36085633-9E7B0054-50AE-4D2D-9DA7-130B9EFE5126

Q36085633-CE642EAB-484B-4B99-B18E-BFC682DCDECC

Q36085633-D53D7A83-C798-4BC0-8242-D653CB2E8947

Q36085633-E2664E9A-1897-43A1-9DFE-E4A9BE6DABC0

P2860

Q36085633-108B2380-A9B9-4034-8627-32D37D8FD55C

Q36085633-178A494C-88A1-4227-82AD-A65F988E4119

Q36085633-1BC75BDE-9299-4EEB-A784-28890BC74AD7

Q36085633-1CC7363C-447D-4917-9BD2-CE6C90001D4D

Q36085633-1F5FBF1E-CEAF-4514-8565-E163148EFCBC

Q36085633-27322216-2D21-41D5-9BFF-9A6DE17F0159

Q36085633-340E07FF-1C4E-4F25-9137-D741D8680BCD

Q36085633-37153105-128D-4521-B16E-4F5686964492

Q36085633-37E943E4-F309-445C-BE53-8B23A0C3BCFB

Q36085633-3D03EA62-9923-4DB2-AB77-B3F72F6377FB

P304

Q36085633-D742EF0E-898A-4177-AD5C-8F3F5ACF9DC9

P31

Q36085633-A767FA27-21AD-4E31-BBC4-B3ECBB0C1106

P356

Q36085633-C8707577-417C-45D3-96AB-27FB880DBCA9

P433

Q36085633-45941382-A829-40B9-BAD8-D6B682CFC30E

P478

Q36085633-29F26F45-264A-49C4-AA52-B313BF88E18F

P577

Q36085633-16CF4103-129E-4621-8C63-D72D1AAB194A

P5875

Q36085633-63B28ECB-3D37-4AC2-AB8E-0F2C2310F704

P698

Q36085633-2767A5D3-840D-4682-9192-78761B17B253

P932

Q36085633-F9173841-9003-4B95-A9E6-1596B77EE6DE

P356

0022155412441002

P1433

Journal of Histochemistry & Cytochemistry

P1476

Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency.

@en

P2093

Ali Entezam

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

Gloria E Hoffman

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

Jodi A Flaws

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

John H McDonald

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

Karen Usdin

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

Lawrence Nelson

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

Noriyuki Otsuka

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

Sanjeeda Jafar

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

Wei Wei Le

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

Zhi-Bin Tong

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

P2860

The zona pellucida: using molecular genetics to study the mammalian egg coat

From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome

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

Ablation of the Sam68 gene impairs female fertility and gonadotropin-dependent follicle development

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

Impairing follicle-stimulating hormone (FSH) signaling in vivo: targeted disruption of the FSH receptor leads to aberrant gametogenesis and hormonal imbalance

Hormone-induced proliferation and differentiation of granulosa cells: a coordinated balance of the cell cycle regulators cyclin D2 and p27Kip1

The zona pellucida: using molecular genetics to study the mammalian egg coat

Isolation of a human DNA sequence which spans the fragile X.

Studies of FRAXA and FRAXE in women with premature ovarian failure.

P304

439-456

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

P31

scholarly article

P356

10.1369/0022155412441002

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

P433

6

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

P478

60

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

P577

2012-04-02T00:00:00Z

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

P5875

223982722

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

P698

22470123

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

P932

3393073

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