Literature DB >> 3276189

Diseases with DNA damage-processing defects.

T L Timme1, R E Moses.   

Abstract

Xeroderma pigmentosum, Cockayne's syndrome, ataxia telangiectasia, Fanconi anemia, and Bloom's syndrome are autosomal recessive diseases with cellular defects in the ability to process DNA damage. Although these diseases are rare, they are seen occasionally in practice and provide insight into the mechanisms of DNA repair and replication in humans. The authors will review the clinical and cytological presentation of each disease, the genetic heterogeneity, as inferred by complementation analysis, and the differentiating characteristics of each. The authors will conclude with a discussion of the state of current research on each disease and possible directions for future research.

Entities:  

Mesh:

Year:  1988        PMID: 3276189     DOI: 10.1097/00000441-198801000-00009

Source DB:  PubMed          Journal:  Am J Med Sci        ISSN: 0002-9629            Impact factor:   2.378


  8 in total

Review 1.  The mammalian Mre11-Rad50-nbs1 protein complex: integration of functions in the cellular DNA-damage response.

Authors:  J H Petrini
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

2.  Cranial CT and MRI in diseases with DNA repair defects.

Authors:  P Demaerel; B E Kendall; D Kingsley
Journal:  Neuroradiology       Date:  1992       Impact factor: 2.804

3.  Cranial MRI in ataxia-telangiectasia.

Authors:  F Sardanelli; R C Parodi; C Ottonello; P Renzetti; S Saitta; E Lignana; G L Mancardi
Journal:  Neuroradiology       Date:  1995-01       Impact factor: 2.804

4.  Xeroderma pigmentosum and Cockayne syndrome: overlapping clinical and biochemical phenotypes.

Authors:  G A Greenhaw; A Hebert; M E Duke-Woodside; I J Butler; J T Hecht; J E Cleaver; G H Thomas; W A Horton
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

5.  Characterization of the mus308 gene in Drosophila melanogaster.

Authors:  E A Leonhardt; D S Henderson; J E Rinehart; J B Boyd
Journal:  Genetics       Date:  1993-01       Impact factor: 4.562

6.  Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype.

Authors:  T Itoh; J E Cleaver; M Yamaizumi
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

Review 7.  Immunodeficiency, centromeric region instability, facial anomalies syndrome (ICF).

Authors:  Melanie Ehrlich; Kelly Jackson; Corry Weemaes
Journal:  Orphanet J Rare Dis       Date:  2006-03-01       Impact factor: 4.123

Review 8.  Cell cycle control, checkpoint mechanisms, and genotoxic stress.

Authors:  R E Shackelford; W K Kaufmann; R S Paules
Journal:  Environ Health Perspect       Date:  1999-02       Impact factor: 9.031

  8 in total

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