Mysterious Ribosomopathies-Reference-Cited by-同舟云学术

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Mysterious Ribosomopathies

Published:2013-08-23 Issue:6148 Volume:341 Page:849-850
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

McCann Kathleen L.¹,Baserga Susan J.¹²³

Affiliation:

1. Department of Genetics, Yale University School of Medicine, New Haven, CT 06520, USA.

2. Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, CT 06520, USA.

3. Department of Therapeutic Radiology, Yale University School of Medicine, New Haven, CT 06520, USA.

Abstract

Ribosomes are essential in all cell types, yet mutations to ribosomal proteins or assembly factors cause tissue-specific disease.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference13 articles.

1. Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

2. Raiser D. M., Narla A., Ebert B. L., Leuk. Lymphoma 1 (2013).

3. When ribosomes go bad: diseases of ribosome biogenesis

4. Non–Diamond Blackfan Anemia Disorders of Ribosome Function: Shwachman Diamond Syndrome and 5q- Syndrome

5. Ribosomal Protein SA Haploinsufficiency in Humans with Isolated Congenital Asplenia

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