(Q34145023)

31 July 2017

title

Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations (English)

1 reference

premature ovarian failure

31 July 2017

main subject

1 reference

Hundscheid RD

1

1 reference

31 July 2017

Sistermans EA

2

1 reference

31 July 2017

Thomas CM

3

1 reference

31 July 2017

Braat DD

4

1 reference

31 July 2017

Straatman H

5

1 reference

31 July 2017

Kiemeney LA

6

1 reference

31 July 2017

Oostra BA

7

1 reference

31 July 2017

Smits AP

8

1 reference

31 July 2017

language of work or name

English

0 references

publication date

1 February 2000

1 reference

American Journal of Human Genetics

31 July 2017

published in

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31 July 2017

volume

66

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31 July 2017

issue

2

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31 July 2017

page(s)

413-418

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Premature ovarian failure (POF) and fragile X premutation females: from POF to to fragile X carrier identification, from fragile X carrier diagnosis to POF association data

31 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Studies of FRAXA and FRAXE in women with premature ovarian failure

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Fragile X premutation screening in women with premature ovarian failure

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Fragile X premutations are not a major cause of early menopause

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Enhanced expression of the murine FMR1 gene during germ cell proliferation suggests a special function in both the male and the female gonad

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Quantitative comparison of FMR1 gene expression in normal and premutation alleles

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Directed Genetic Change Model for X Chromosome Inactivation in Eutherian Mammals

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Incidence of premature ovarian failure.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Chapter 2 Biochemistry of Male Germ Cell Differentiation in Mammals: RNA Synthesis in Meiotic and Postmeiotic Cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Genetics of oocyte ageing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

General ageing and ovarian ageing

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Biological bases of premature ovarian failure.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Characterization of the full fragile X syndrome mutation in fetal gametes

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

A model conforming the decline in follicle numbers to the age of menopause in women.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288093

Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease?

28 October 2018

1 reference

12 December 2020

Assessment of unconjugated oestradiol and progesterone serum levels throughout pregnancy in normal women and in women with hyperprolactinaemia, who conceived after bromocriptine treatment

1 reference

12 December 2020

Preferential expression of the maternally derived X chromosome in the mouse yolk sac

1 reference

12 December 2020

Both X chromosomes function before visible X-chromosome inactivation in female mouse embryos

1 reference

12 December 2020

Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium

1 reference

12 December 2020

Prenatal diagnosis of fragile X syndrome

1 reference

12 December 2020

Confirmation of early menopause in fragile X carriers

1 reference

12 December 2020

Identifiers

DOI

10.1086/302774

1 reference

31 July 2017

1 reference

31 July 2017

1 reference