Genes and premature ovarian failure (Q40827034)

24 September 2017

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title

Genes and premature ovarian failure (English)

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24 September 2017

Christin-Maitre S

1

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24 September 2017

Vasseur C

series ordinal

2

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24 September 2017

Portnoï MF

series ordinal

3

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24 September 2017

Bouchard P

series ordinal

4

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24 September 2017

publication date

1 October 1998

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Molecular and Cellular Endocrinology

24 September 2017

published in

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24 September 2017

volume

145

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24 September 2017

issue

1-2

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24 September 2017

page(s)

75-80

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

24 September 2017

cites work

1 reference

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7 January 2021

A gene for blepharophimosis-ptosis-epicanthus inversus syndrome maps to chromosome 3q23

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7 January 2021

Atm-deficient mice: a paradigm of ataxia telangiectasia

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7 January 2021

A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility

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7 January 2021

Premature gonadal failure

1 reference

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7 January 2021

Growth differentiation factor-9 is required during early ovarian folliculogenesis

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7 January 2021

Developmental expression and regulation of the gap junction protein and transcript in rat ovaries.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Linkage analysis in blepharophimosis-ptosis syndrome confirms localisation to 3q21-24

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Follicle stimulating hormone is required for ovarian follicle maturation but not male fertility

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Brief report: testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene

1 reference

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7 January 2021

Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone beta-subunit gene

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

The Finnish follicle-stimulating hormone receptor gene mutation is rare in North American women with 46,XX ovarian failure

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Oocyte-specific expression of growth/differentiation factor-9

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7 January 2021

An analysis of Xq deletions

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Primary amenorrhoea and infertility due to a mutation in the beta-subunit of follicle-stimulating hormone

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Ovarian Changes in Ataxia Telangiectasia

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7 January 2021

Positional cloning of the APECED gene

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7 January 2021

Apoptosis-associated signaling pathways are required for chemotherapy-mediated female germ cell destruction

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https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature

1 reference

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7 January 2021

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

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7 January 2021

Follicular depletion during the menopausal transition: evidence for accelerated loss and ultimate exhaustion

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Functional disomies of the X chromosome influence the cell selection and hence the X inactivation pattern in females with balanced X-autosome translocations: A review of 122 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Obstetrical and gynecological complications in fragile X carriers: a multicenter study

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https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Female infertility in mice lacking connexin 37

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7 January 2021

The anatomy and histology of XO human embryos and fetuses

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https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Blepharophimosis plus ovarian failure: a likely candidate for a contiguous gene syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Aod2, the locus controlling development of atrophy in neonatal thymectomy-induced autoimmune ovarian dysgenesis, co-localizes with Il2, Fgfb, and Idd3

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

The critical region on the human Xq.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

Aod1, the immunoregulatory locus controlling abrogation of tolerance in neonatal thymectomy-induced autoimmune ovarian dysgenesis, maps to mouse chromosome 16.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

The connexin family of intercellular channel forming proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2898%2900172-5

7 January 2021

10.1016/S0303-7207(98)00172-5

Identifiers

DOI

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24 September 2017

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