Cockayne Syndrome: The many challenges and approaches to understand a multifaceted disease
Author:
Affiliation:
1. Washington University School of Medicine, USA
2. Universidade Federal de Ouro Preto, Brazil
3. Universidade Federal de Ouro Preto, Brazil; Universidade de São Paulo, Brazil
4. Universidade de São Paulo, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v43n1s1/1415-4757-GMB-43-1-s1-e20190085.pdf
Reference199 articles.
1. Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane;Aamann MD;FASEB J,2010
2. Cockayne Syndrome group B protein stimulates NEIL2 DNA glycosylase activity
3. Molecular pathophysiology of impaired glucose metabolism, mitochondrial dysfunction, and oxidative DNA damage in Alzheimer’s disease brain;Abolhassani N;Mech Ageing Dev,2017
4. Loss of proteostasis is a pathomechanism in Cockayne syndrome;Alupei MC;Cell Rep,2018
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