Differential Gene Expression Reveals Mitochondrial Dysfunction in an Imprinting Center Deletion Mouse Model of Prader-Willi Syndrome-Reference-Cited by-同舟云学术

Differential Gene Expression Reveals Mitochondrial Dysfunction in an Imprinting Center Deletion Mouse Model of Prader-Willi Syndrome

Published:2013-07-29 Issue:5 Volume:6 Page:347-355
ISSN:1752-8054
Container-title:Clinical and Translational Science
language:en
Short-container-title:Clinical And Translational Science

Author:

Yazdi Puya G.¹,Su Hailing¹,Ghimbovschi Svetlana²,Fan Weiwei,Coskun Pinar E.,Nalbandian Angèle¹,Knoblach Susan²,Resnick James L.³,Hoffman Eric²,Wallace Douglas C.,Kimonis Virginia E.¹

Affiliation:

1. Division of Genetics and Metabolism; Department of Pediatrics; University of California; Irvine; California; USA

2. Children's National Medical Center; Research Center Genetic Medicine; Washington; DC; USA

3. Department of Molecular Genetics and Microbiology; University of Florida College of Medicine; Gainesville; Florida; USA

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference30 articles.

1. Imprinting in Angelman and Prader-Willi syndromes;Jiang;Curr Opin Genet Dev.,1998

2. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes;Nicholls;Ann Rev Genom and Human Genet.,2001

3. Prader-Willi syndrome;Cassidy;Genet Med.,2011

4. Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization;Cavaille;Proc Natl Acad Sci USA.,2000

5. Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain;los Santos;Am J Human Genet.,2000

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