Genetic defects of ovarian TGF-β-like factors and premature ovarian failure (Q37836267)

24 August 2017

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title

Genetic defects of ovarian TGF-β-like factors and premature ovarian failure (English)

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24 August 2017

L Persani

1

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24 August 2017

R Rossetti

series ordinal

2

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24 August 2017

C Cacciatore

series ordinal

3

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24 August 2017

S Fabre

series ordinal

4

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24 August 2017

language of work or name

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4 February 2011

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Journal of Endocrinological Investigation

24 August 2017

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24 August 2017

34

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24 August 2017

3

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24 August 2017

244-251

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https://scigraph.springernature.com/pub.10.1007/bf03347073

24 August 2017

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https://api.crossref.org/works/10.1007%2FBF03347073

Primary ovarian insufficiency: a more accurate term for premature ovarian failure.

21 January 2018

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Clinical practice. Primary ovarian insufficiency

21 January 2018

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Number of ovarian follicles in human fetuses with the 45,X karyotype.

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

Differences in follicle-stimulating hormone secretion between 45,X monosomy Turner syndrome and 45,X/46,XX mosaicism are evident at an early age.

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

Premature ovarian failure

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

Genome-wide association studies identify loci associated with age at menarche and age at natural menopause

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Female sex preponderance for idiopathic familial premature ovarian failure suggests an X chromosome defect: opinion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Thyroid-stimulating hormone and thyroid-stimulating hormone receptor structure-function relationships

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Genetic analysis of the mammalian transforming growth factor-beta superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

The bone morphogenetic protein system in mammalian reproduction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

The bone morphogenetic protein 15 gene is X-linked and expressed in oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

The oocyte and its role in regulating ovulation rate: a new paradigm in reproductive biology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Mutations in an oocyte-derived growth factor gene (BMP15) cause increased ovulation rate and infertility in a dosage-sensitive manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

21 January 2018

Fecundity genes in sheep

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https://api.crossref.org/works/10.1007%2FBF03347073

Mutations in the genes for oocyte-derived growth factors GDF9 and BMP15 are associated with both increased ovulation rate and sterility in Cambridge and Belclare sheep (Ovis aries).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

A novel mutation in the bone morphogenetic protein 15 gene causing defective protein secretion is associated with both increased ovulation rate and sterility in Lacaune sheep.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Regulation of ovulation rate in mammals: contribution of sheep genetic models

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Oocytes prevent cumulus cell apoptosis by maintaining a morphogenic paracrine gradient of bone morphogenetic proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Oocyte-secreted factors enhance oocyte developmental competence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Posttranslational processing of mouse and human BMP-15: potential implication in the determination of ovulation quota

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Turner syndrome and haploinsufficiency

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

Primary Ovarian Insufficiency: X chromosome defects and autoimmunity

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure.

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

Missense mutations in the BMP15 gene are associated with ovarian failure

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03347073

BMP15 mutations associated with primary ovarian insufficiency cause a defective production of bioactive protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Variants of the BMP15 gene in a cohort of patients with premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Association study of four key folliculogenesis genes in polycystic ovary syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Variation in bone morphogenetic protein 15 is not associated with spontaneous human dizygotic twinning

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Evidence for a Turner syndrome locus or loci at Xp11.2-p22.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

The X chromosome and the ovary

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Growth differentiation factor-9 is required during early ovarian folliculogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Homozygosity for a single base-pair mutation in the oocyte-specific GDF9 gene results in sterility in Thoka sheep.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

A new polymorphism in the Growth and Differentiation Factor 9 (GDF9) gene is associated with increased ovulation rate and prolificacy in homozygous sheep.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Mutational screening of the coding region of growth differentiation factor 9 gene in Indian women with ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Growth differentiating factor-9 mutations may be associated with premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

A Deletion Mutation in GDF9 in Sisters with Spontaneous DZ Twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

HLA and genomewide allele sharing in dizygotic twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Novel variants in growth differentiation factor 9 in mothers of dizygotic twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Aberrant expression of growth differentiation factor-9 in oocytes of women with polycystic ovary syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Alpha-inhibin is a tumour-suppressor gene with gonadal specificity in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Development of cancer cachexia-like syndrome and adrenal tumors in inhibin-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Autosomal translocation associated with premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Mutational analysis of the mature peptide region of inhibin genes in Indian women with ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Mutational analysis of inhibin alpha gene revealed three novel variations in Indian women with premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

A large-scale association study to assess the impact of known variants of the human INHA gene on premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

G769A variation of inhibin alpha-gene in korean women with premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Inhibin and premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Functional analysis of the human inhibin alpha subunit variant A257T and its potential role in premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Genetic disorders of the skeleton: a developmental approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Mutation in bone morphogenetic protein receptor-IB is associated with increased ovulation rate in Booroola Mérino ewes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Highly prolific Booroola sheep have a mutation in the intracellular kinase domain of bone morphogenetic protein IB receptor (ALK-6) that is expressed in both oocytes and granulosa cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

The type I BMP receptor BmprIB is essential for female reproductive function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

X-linked premature ovarian failure: a complex disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Genes involved in human premature ovarian failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Heritability of Age at Natural Menopause in the Framingham Heart Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Investigating the association between inhibin alpha gene promoter polymorphisms and premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03347073

Editorial: BMP15--the first true ovarian determinant gene on the X-chromosome?

21 January 2018

1 reference

12 December 2020

Inhibin: a candidate gene for premature ovarian failure

1 reference

12 December 2020

Polymorphisms in GDF9 and BMP15 associated with fertility and ovulation rate in Moghani and Ghezel sheep in Iran

1 reference

12 December 2020

BMP15 mutations in XX gonadal dysgenesis and premature ovarian failure

1 reference

12 December 2020

Synergistic roles of bone morphogenetic protein 15 and growth differentiation factor 9 in ovarian function.

1 reference

12 December 2020

Family history as a predictor of early menopause.

1 reference

12 December 2020

Mutation analysis of the growth differentiation factor-9 and -9B genes in patients with premature ovarian failure and polycystic ovary syndrome

1 reference

12 December 2020

Paracrine actions of growth differentiation factor-9 in the mammalian ovary.

1 reference

12 December 2020

Physiological effects of major genes affecting ovulation rate in sheep

1 reference

12 December 2020

Controversial role of inhibin alpha-subunit gene in the aetiology of premature ovarian failure

1 reference

12 December 2020

INHA promoter polymorphisms are associated with premature ovarian failure

1 reference

12 December 2020

Incidence of premature ovarian failure.

1 reference

12 December 2020

Inheritance in idiopathic premature ovarian failure: analysis of 71 cases

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12 December 2020

Identifiers

DOI

10.1007/BF03347073

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24 August 2017

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