Scratching the Surface of Werner Syndrome and Human Ageing.
作者信息
Poot Martin
出版信息
Mol Syndromol. 2017 Dec;9(1):1-4. doi: 10.1159/000484424. Epub 2017 Nov 23.
Abstract
摘要
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Scratching the Surface of Werner Syndrome and Human Ageing.
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1
Genes, Proteins, and Biological Pathways Preventing Chromothripsis.
Methods Mol Biol. 2018;1769:231-251. doi: 10.1007/978-1-4939-7780-2_15.
2
Genome-wide DNA methylation analysis in blood cells from patients with Werner syndrome.
Clin Epigenetics. 2017 Aug 30;9:92. doi: 10.1186/s13148-017-0389-4. eCollection 2017.
3
Accelerated epigenetic aging in Werner syndrome.
Aging (Albany NY). 2017 Apr;9(4):1143-1152. doi: 10.18632/aging.101217.
4
Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype.
Sci Rep. 2017 Mar 9;7:44081. doi: 10.1038/srep44081.
5
DNA methylation levels at individual age-associated CpG sites can be indicative for life expectancy.
Aging (Albany NY). 2016 Feb;8(2):394-401. doi: 10.18632/aging.100908.
6
Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements.
Mol Syndromol. 2015 Sep;6(3):110-34. doi: 10.1159/000438812. Epub 2015 Aug 15.
7
Aging stem cells. A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging.
Science. 2015 Jun 5;348(6239):1160-3. doi: 10.1126/science.aaa1356. Epub 2015 Apr 30.
8
Nonenzymatic role for WRN in preserving nascent DNA strands after replication stress.
Cell Rep. 2014 Nov 20;9(4):1387-401. doi: 10.1016/j.celrep.2014.10.025. Epub 2014 Nov 6.
9
DNA2 cooperates with the WRN and BLM RecQ helicases to mediate long-range DNA end resection in human cells.
J Biol Chem. 2014 Sep 26;289(39):27314-27326. doi: 10.1074/jbc.M114.578823. Epub 2014 Aug 13.
10
DNA methylation age of human tissues and cell types.
Genome Biol. 2013;14(10):R115. doi: 10.1186/gb-2013-14-10-r115.
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