Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis-Reference-Cited by-同舟云学术

Alteration of DNA binding, dimerization, and nuclear translocation of SHOX homeodomain mutations identified in idiopathic short stature and Leri-Weill dyschondrosteosis

Published:2005 Issue:1 Volume:26 Page:44-52
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Schneider Katja U.,Marchini Antonio,Sabherwal Nitin,Röth Ralph,Niesler Beate,Marttila Tiina,Blaschke Rüdiger J.,Lawson Margaret,Dumic Miroslav,Rappold Gudrun

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference45 articles.

1. Mutations in PAX3 that cause Waardenburg syndrome type I: Ten new mutations and review of the literature

2. Molecular evolution of the homeodomain family of transcription factors

3. SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

4. Dimerization of SOX9 is required for chondrogenesis, but not for sex determination

5. Determination of the Nuclear Magnetic Resonance Solution Structure of an Antennapedia Homeodomain-DNA Complex

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