4.6 Article

MED12 mutations in leiomyosarcoma and extrauterine leiomyoma

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Oncology

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

Eun Mi Je et al.

INTERNATIONAL JOURNAL OF CANCER (2012)

Article Oncology

MED12 mutations in uterine fibroids-their relationship to cytogenetic subgroups

Dominique Nadine Markowski et al.

INTERNATIONAL JOURNAL OF CANCER (2012)

Article Genetics & Heredity

Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer

Christopher E. Barbieri et al.

NATURE GENETICS (2012)

Editorial Material Medicine, General & Internal

Uterine Fibroids and Evidence-Based Medicine - Not an Oxymoron

Elizabeth A. Stewart

NEW ENGLAND JOURNAL OF MEDICINE (2012)

Article Multidisciplinary Sciences

MED12 Alterations in Both Human Benign and Malignant Uterine Soft Tissue Tumors

Gaelle Perot et al.

PLOS ONE (2012)

Article Genetics & Heredity

A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome)

P. Rump et al.

CLINICAL GENETICS (2011)

Review Oncology

Genetic aberrations in soft tissue leiomyosarcoma

Jilong Yang et al.

CANCER LETTERS (2009)

Article Obstetrics & Gynecology

Uterine leiomyosarcoma arising from a fibroid

M. Bukar et al.

JOURNAL OF OBSTETRICS AND GYNAECOLOGY (2009)

Article Biochemistry & Molecular Biology

The Human CDK8 Subcomplex Is a Histone Kinase That Requires Med12 for Activity and Can Function Independently of Mediator

Matthew T. Knuesel et al.

MOLECULAR AND CELLULAR BIOLOGY (2009)

Review Oncology

Clinical management of uterine sarcomas

Frederic Amant et al.

LANCET ONCOLOGY (2009)

Article Oncology

Uterine Sarcoma 2008

Jeff F. Lin et al.

CURRENT ONCOLOGY REPORTS (2008)

Article Biochemistry & Molecular Biology

Cdk8 is essential for preimplantation mouse development

Thomas Westerling et al.

MOLECULAR AND CELLULAR BIOLOGY (2007)

Article Genetics & Heredity

The original Lujan syndrome family has a novel missense mutation (p. N1007S) in the MED12 gene

Charles E. Schwartz et al.

JOURNAL OF MEDICAL GENETICS (2007)

Review Biochemistry & Molecular Biology

Genetic heterogeneity among uterine leiomyomata: insights into malignant progression

Jennelle C. Hodge et al.

HUMAN MOLECULAR GENETICS (2007)

Article Genetics & Heredity

A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome

Hiba Risheg et al.

NATURE GENETICS (2007)

Review Multidisciplinary Sciences

Uterine fibroids: The elephant in the room

CL Walker et al.

SCIENCE (2005)

Article Pathology

Uterine myxoid leiomyosarcoma within a leiomyoma

K Mittal et al.

HUMAN PATHOLOGY (2000)