Literature DB >> 11138345

Werner's syndrome: from clinics to genetics.

M Goto1.   

Abstract

Werner's syndrome (WS), a representative progeroid syndrome with chromosomal instability caused by the mutation of RecQ type DNA/RNA helicase, manifests skin changes similar to those observed in systemic sclerosis (SSc). In addition, patients with WS show a variety of the signs and symptoms of normal ageing at an early stage of their life; gray hair, alopecia, muscle atrophy, osteoporosis, cataracts, hypogonadism, diabetes mellitus, hyperlipidemia, atherosclerosis, malignancy, brain atrophy, and senile dementia. Although no direct evidence has been presented linking RecQ type DNA/RNA helicase dysfunction with the occurrence of premature ageing symptoms in WS, WS may give us a unique model to analyze the skin changes and the mechanisms of fibrosis in SSc.

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Mesh:

Year:  2000        PMID: 11138345

Source DB:  PubMed          Journal:  Clin Exp Rheumatol        ISSN: 0392-856X            Impact factor:   4.473


  19 in total

1.  Werner's syndrome: a quite rare disease for differential diagnosis of scleroderma.

Authors:  Cemal Bes; Seref Vardi; Melih Güven; Mehmet Soy
Journal:  Rheumatol Int       Date:  2009-06-03       Impact factor: 2.631

2.  Loss of Werner syndrome protein function promotes aberrant mitotic recombination.

Authors:  P R Prince; M J Emond; R J Monnat
Journal:  Genes Dev       Date:  2001-04-15       Impact factor: 11.361

Review 3.  Mitochondrial involvement in brain function and dysfunction: relevance to aging, neurodegenerative disorders and longevity.

Authors:  V Calabrese; G Scapagnini; A M Giuffrida Stella; T E Bates; J B Clark
Journal:  Neurochem Res       Date:  2001-06       Impact factor: 3.996

4.  Mechanism of Werner DNA helicase: POT1 and RPA stimulates WRN to unwind beyond gaps in the translocating strand.

Authors:  Byungchan Ahn; Jae Wan Lee; Hana Jung; Gad Beck; Vilhelm A Bohr
Journal:  PLoS One       Date:  2009-03-05       Impact factor: 3.240

5.  Cooperation of DNA-PKcs and WRN helicase in the maintenance of telomeric D-loops.

Authors:  Rika Kusumoto-Matsuo; Patricia L Opresko; Dale Ramsden; Hidetoshi Tahara; Vilhelm A Bohr
Journal:  Aging (Albany NY)       Date:  2010-05       Impact factor: 5.682

6.  The eye as a window to rare endocrine disorders.

Authors:  Rupali Chopra; Ashish Chander; Jubbin J Jacob
Journal:  Indian J Endocrinol Metab       Date:  2012-05

7.  Reprogramming suppresses premature senescence phenotypes of Werner syndrome cells and maintains chromosomal stability over long-term culture.

Authors:  Akira Shimamoto; Harunobu Kagawa; Kazumasa Zensho; Yukihiro Sera; Yasuhiro Kazuki; Mitsuhiko Osaki; Mitsuo Oshimura; Yasuhito Ishigaki; Kanya Hamasaki; Yoshiaki Kodama; Shinsuke Yuasa; Keiichi Fukuda; Kyotaro Hirashima; Hiroyuki Seimiya; Hirofumi Koyama; Takahiko Shimizu; Minoru Takemoto; Koutaro Yokote; Makoto Goto; Hidetoshi Tahara
Journal:  PLoS One       Date:  2014-11-12       Impact factor: 3.240

Review 8.  Structural mechanisms of human RecQ helicases WRN and BLM.

Authors:  Ken Kitano
Journal:  Front Genet       Date:  2014-10-29       Impact factor: 4.599

Review 9.  Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming.

Authors:  Akira Shimamoto; Koutaro Yokote; Hidetoshi Tahara
Journal:  Front Genet       Date:  2015-01-29       Impact factor: 4.599

10.  Serines 440 and 467 in the Werner syndrome protein are phosphorylated by DNA-PK and affects its dynamics in response to DNA double strand breaks.

Authors:  Rika Kusumoto-Matsuo; Deblina Ghosh; Parimal Karmakar; Alfred May; Dale Ramsden; Vilhelm A Bohr
Journal:  Aging (Albany NY)       Date:  2014-01       Impact factor: 5.682

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