MED12 exon 2 mutations are common in uterine leiomyomas from South African patients-Reference-Cited by-同舟云学术

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

Published:2011-12-19 Issue:12 Volume:2 Page:966-969
ISSN:1949-2553
Container-title:Oncotarget
language:en
Short-container-title:Oncotarget

Author:

Mäkinen Netta¹,Heinonen Hanna-Riikka¹,Moore Shane²,Tomlinson Ian P.M.³,van der Spuy Zephne M.²,Aaltonen Lauri A.¹

Affiliation:

1. Department of Medical Genetics, Genome-Scale Biology Research Program, University of Helsinki, Helsinki, Finland

2. Department of Obstetrics and Gynaecology, Faculty of Health Sciences, University of Cape Town, South Africa

3. Wellcome Trust Centre for Human Genetics and NIHR Comprehensive Biomedical Research Centre, Nuffield Department of Clinical Medicine, Roosevelt Drive, University of Oxford, Oxford OX3 7BN, UK

Publisher

Impact Journals, LLC

Subject

Oncology

Cited by 79 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Gene variants polymorphisms and uterine leiomyoma: an updated review;Frontiers in Genetics;2024-03-20

2. Racial disparity in uterine leiomyoma: new insights of genetic and environmental burden in myometrial cells;Molecular Human Reproduction;2024-01-30

3. Current and Emerging Treatment Options for Uterine Fibroids;Drugs;2023-11-03

4. The Influence of Race/Ethnicity on the Transcriptomic Landscape of Uterine Fibroids;International Journal of Molecular Sciences;2023-08-30

5. The Mediator Complex Subunit 12 (MED-12) Gene and Uterine Fibroids: a Systematic Review;Reproductive Sciences;2023-07-29

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