Functional deficit associated with a missense Werner syndrome mutation-Reference-Cited by-同舟云学术

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Functional deficit associated with a missense Werner syndrome mutation

Published:2013-06 Issue:6 Volume:12 Page:414-421
ISSN:1568-7864
Container-title:DNA Repair
language:en
Short-container-title:DNA Repair

Author:

Tadokoro Takashi,Rybanska-Spaeder Ivana,Kulikowicz Tomasz,Dawut Lale,Oshima Junko,Croteau Deborah L.,Bohr Vilhelm A.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference56 articles.

1. Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process;Epstein;Medicine (Baltimore),1966

2. Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing;Goto;Mech. Ageing Dev.,1997

3. Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey;Takemoto;Geriatr. Gerontol. Int.,2012

4. Werner syndrome;Oshima,1993

5. The spectrum of WRN mutations in Werner syndrome patients;Huang;Hum. Mutat.,2006

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1. RecQ dysfunction contributes to social and depressive-like behavior and affects aldolase activity in mice;Neurobiology of Disease;2023-05

2. Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases;Journal of Medical Genetics;2022-05-09

3. Studying Werner syndrome to elucidate mechanisms and therapeutics of human aging and age-related diseases;Biogerontology;2019-01-21

4. Werner Syndrome as a Model of Human Aging;Conn's Handbook of Models for Human Aging;2018

5. Werner syndrome ( WRN ) gene variants and their association with altered function and age-associated diseases;Ageing Research Reviews;2018-01

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