Molecular basis of the human ribosomopathy Shwachman-Diamond syndrome-Reference-Cited by-同舟云学术

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Molecular basis of the human ribosomopathy Shwachman-Diamond syndrome

Published:2018-01 Issue: Volume:67 Page:109-127
ISSN:2212-4926
Container-title:Advances in Biological Regulation
language:en
Short-container-title:Advances in Biological Regulation

Author:

Warren Alan J.^ORCID

Funder

Specialist Programme from Bloodwise

UK Medical Research Council

Wellcome Trust strategic award to the Cambridge Institute for Medical Research

Wellcome Trust

MRC

Connor Wright Shwachman-Diamond Project

Cambridge National Institute for Health Research Biomedical Research Centre

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology,Molecular Medicine

Reference187 articles.

1. Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations;Ajore;EMBO Mol. Med.,2017

2. Mutation of a gene essential for ribosome biogenesis, EMG1, causes Bowen-Conradi syndrome;Armistead;Am. J. Hum. Genet.,2009

3. Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome;Austin;J. Clin. Invest.,2008

4. The Shwachman-Diamond SBDS protein localizes to the nucleolus;Austin;Blood,2005

5. Shwachman-Bodian Diamond syndrome is a multi-functional protein implicated in cellular stress responses;Ball;Hum. Mol. Genet.,2009

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