Transcriptional and Translational Regulation of the Léri-Weill and Turner Syndrome Homeobox Gene SHOX-Reference-Cited by-同舟云学术

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Transcriptional and Translational Regulation of the Léri-Weill and Turner Syndrome Homeobox Gene SHOX

Published:2003-11 Issue:48 Volume:278 Page:47820-47826
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Blaschke Rüdiger J.,Töpfer Christine,Marchini Antonio,Steinbeisser Herbert,Janssen Johannes W.G.,Rappold Gudrun A.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference40 articles.

1. The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator

2. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

3. PHOG, a candidate gene for involvement in the short stature of Turner syndrome

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

5. Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis

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3. Clinical impact of variants in non-coding regions of SHOX – Current knowledge;Gene;2022-04

4. Variants in the 5′UTR reduce SHOX expression and contribute to SHOX haploinsufficiency;European Journal of Human Genetics;2020-07-09

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