Literature DB >> 12526788

DNA single-strand break repair and spinocerebellar ataxia.

Keith W Caldecott1.   

Abstract

DNA single-strand break repair (SSBR) is critical for the survival and genetic stability of mammalian cells. Three papers have recently associated mutations in putative human SSBR genes with hereditary spinocerebellar ataxia. The emerging links between SSBR and neurodegenerative disorders are discussed.

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Year:  2003        PMID： 12526788     DOI： 10.1016/s0092-8674(02)01247-3

Source DB:  PubMed          Journal:  Cell        ISSN： 0092-8674            Impact factor:   41.582


  44 in total

1.  Sensing DNA damage by PARP-like fingers.

Authors:  Stefania Petrucco
Journal:  Nucleic Acids Res       Date:  2003-12-01       Impact factor: 16.971

2.  In vitro complementation of Tdp1 deficiency indicates a stabilized enzyme-DNA adduct from tyrosyl but not glycolate lesions as a consequence of the SCAN1 mutation.

Authors:  Amy J Hawkins; Mark A Subler; Konstantin Akopiants; Jenny L Wiley; Shirley M Taylor; Ann C Rice; Jolene J Windle; Kristoffer Valerie; Lawrence F Povirk
Journal:  DNA Repair (Amst)       Date:  2009-02-10

3.  A novel locus for autosomal recessive spastic ataxia on chromosome 17p.

Authors:  Naima Bouslam; Ahmed Bouhouche; Ali Benomar; Sylvain Hanein; Stephan Klebe; Hamid Azzedine; Silvia Di Giandomenico; Anne Boland-Augé; Filippo M Santorelli; Alexandra Durr; Alexis Brice; Mohamed Yahyaoui; Giovanni Stevanin
Journal:  Hum Genet       Date:  2007-02-02       Impact factor: 4.132

Review 4.  Accumulation of nuclear DNA damage or neuron loss: molecular basis for a new approach to understanding selective neuronal vulnerability in neurodegenerative diseases.

Authors:  Ivona Brasnjevic; Patrick R Hof; Harry W M Steinbusch; Christoph Schmitz
Journal:  DNA Repair (Amst)       Date:  2008-05-23

5.  p53 Deficiency rescues neuronal apoptosis but not differentiation in DNA polymerase beta-deficient mice.

Authors:  Noriyuki Sugo; Naoko Niimi; Yasuaki Aratani; Keiko Takiguchi-Hayashi; Hideki Koyama
Journal:  Mol Cell Biol       Date:  2004-11       Impact factor: 4.272

Review 6.  DNA Damage and Associated DNA Repair Defects in Disease and Premature Aging.

Authors:  Vinod Tiwari; David M Wilson
Journal:  Am J Hum Genet       Date:  2019-08-01       Impact factor: 11.025

7.  Xrcc4 physically links DNA end processing by polynucleotide kinase to DNA ligation by DNA ligase IV.

Authors:  Christine Anne Koch; Roger Agyei; Sarah Galicia; Pavel Metalnikov; Paul O'Donnell; Andrei Starostine; Michael Weinfeld; Daniel Durocher
Journal:  EMBO J       Date:  2004-09-23       Impact factor: 11.598

8.  Autosomal recessive spinocerebellar ataxia and peripheral neuropathy with raised alpha-fetoprotein.

Authors:  Louise Izatt; Andrea H Németh; Anjela Meesaq; Kerry R Mills; A Malcolm R Taylor; Christopher E Shaw
Journal:  J Neurol       Date:  2004-07       Impact factor: 4.849

9.  The genesis of cerebellar interneurons and the prevention of neural DNA damage require XRCC1.

Authors:  Youngsoo Lee; Sachin Katyal; Yang Li; Sherif F El-Khamisy; Helen R Russell; Keith W Caldecott; Peter J McKinnon
Journal:  Nat Neurosci       Date:  2009-07-26       Impact factor: 24.884

10.  CK2 phosphorylation-dependent interaction between aprataxin and MDC1 in the DNA damage response.

Authors:  Olivier J Becherel; Burkhard Jakob; Amy L Cherry; Nuri Gueven; Markus Fusser; Amanda W Kijas; Cheng Peng; Sachin Katyal; Peter J McKinnon; Junjie Chen; Bernd Epe; Stephen J Smerdon; Gisela Taucher-Scholz; Martin F Lavin
Journal:  Nucleic Acids Res       Date:  2009-12-14       Impact factor: 16.971
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