The study of MED12 gene mutations in uterine leiomyomas from Iranian patients (Q50993068)

26 March 2018

http://europepmc.org/abstract/MED/26298726

title

The study of MED12 gene mutations in uterine leiomyomas from Iranian patients (English)

1 reference

26 March 2018

http://europepmc.org/abstract/MED/26298726

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Samaneh Sadeghi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Mandana Khorrami

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Mona Amin-Beidokhti

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Maryam Abbasi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Zeeba Kamalian

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Mirdavood Omrani

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

Ozra Azmoodeh

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

publication date

23 August 2015

1 reference

26 March 2018

http://europepmc.org/abstract/MED/26298726

published in

Tumor Biology

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1 June 2020

volume

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1 June 2020

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

page(s)

1567-1571

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

The associations between the polymorphisms of the ER-α gene and the risk of uterine leiomyoma (ULM).

1 June 2020

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

MED12 exon 2 mutations in histopathological uterine leiomyoma variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

MED12 exon 2 mutations are common in uterine leiomyomas from South African patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Uterine leiomyoma-linked MED12 mutations disrupt mediator-associated CDK activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

CDK8: a positive regulator of transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Mediator is a transducer of Wnt/beta-catenin signaling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

MED12 mutation frequency in unselected sporadic uterine leiomyomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Novel MED12 gene somatic mutations in women from the Southern United States with symptomatic uterine fibroids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Risk factors for surgically removed fibroids in a large cohort of teachers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Risk of uterine leiomyomata in relation to tobacco, alcohol and caffeine consumption in the Black Women's Health Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Prevalence of uterine leiomyomas in the first trimester of pregnancy: an ultrasound-screening study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

MED12 and HMGA2 mutations: two independent genetic events in uterine leiomyoma and leiomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Mutational analysis of MED12 exon 2 in uterine leiomyoma and other common tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Missense mutations in exon 2 of the MED12 gene are involved in IGF-2 overexpression in uterine leiomyoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Mutations in Exon 1 highlight the role of MED12 in uterine leiomyomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

A mediator lost in the war on cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Molecular topography of the MED12-deleted region in smooth muscle tumors: a possible link between non-B DNA structures and hypermutability

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Use of X-chromosome inactivation pattern to determine the clonal origins of uterine leiomyoma and leiomyosarcoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

Single-strand conformation polymorphism and heteroduplex analysis for gel-based mutation detection

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS13277-015-3943-8

MED12 mutations in uterine fibroids--their relationship to cytogenetic subgroups

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26298726

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/26298726

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26298726

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S13277-015-3943-8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26298726%20AND%20SRC:MED&resulttype=core&format=json