(Q24309202)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

title

Screening for known mutations in EIF2B genes in a large panel of patients with premature ovarian failure (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

obstetrics and gynaecology

4 January 2020

main subject

0 references

Eukaryotic translation initiation factor 2B subunit epsilon

1 reference

Eukaryotic translation initiation factor 2B subunit delta

1 reference

Eukaryotic translation initiation factor 2B subunit beta

1 reference

ovarian follicle development

1 reference

premature ovarian failure

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

3

Raphael Schiffmann

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

author name string

Fernande Gauthier-Barichard

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Vien H Vanderhoof

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Vladimir K Bakalov

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Lawrence M Nelson

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Odile Boespflug-Tanguy

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

language of work or name

English

0 references

publication date

26 October 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

volume

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

page(s)

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

Ovarian failure related to eukaryotic initiation factor 2B mutations

4 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=529454

Identification of novel mutations in FOXL2 associated with premature ovarian failure

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=529454

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=529454

Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=529454

Genes and translocations involved in POF.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=529454

Incidence of premature ovarian failure.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=529454

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

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1472-6874-4-8

The effect of genotype on the natural history of eIF2B-related leukodystrophies

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1472-6874-4-8

Inhibin: a candidate gene for premature ovarian failure

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15507143

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Premature ovarian failure

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15507143

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

X chromosome defects and premature ovarian failure

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15507143

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1472-6874-4-8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

4 January 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15507143%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

PubMed publication ID

15507143

1 reference