Literature DB >> 8451764

Human genetic instability syndromes: single gene defects with increased risk of cancer.

M Digweed1.   

Abstract

The experimental findings of the last 5 years are reviewed for the genetic instability syndromes: Xeroderma pigmentosum, Fanconi's anaemia, Ataxia telangiectasia and Bloom's syndrome. In these autosomal recessive genetic diseases, single gene defects lead to genetic instability, increased mutation rates and cancer. Deficiencies in the ability to effectively repair DNA lesions have been suggested for all of these syndromes. The status of characterization of these DNA repair defects is presented and the possible mechanisms of lesion fixation as mutation are discussed. The four known human genes whose mutation leads to inherited genetic instability are described.

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Year:  1993        PMID: 8451764     DOI: 10.1016/0378-4274(93)90061-2

Source DB:  PubMed          Journal:  Toxicol Lett        ISSN: 0378-4274            Impact factor:   4.372


  10 in total

1.  Aspergillus nidulans uvsBATR and scaANBS1 genes show genetic interactions during recovery from replication stress and DNA damage.

Authors:  Marcia Regina von Zeska Kress Fagundes; Camile P Semighini; Iran Malavazi; Marcela Savoldi; Joel Fernandes de Lima; Maria Helena de Souza Goldman; Steven D Harris; Gustavo Henrique Goldman
Journal:  Eukaryot Cell       Date:  2005-07

Review 2.  Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study Group.

Authors: 
Journal:  Arch Dis Child       Date:  2000-05       Impact factor: 3.791

Review 3.  Cancer risk and oxidative DNA damage in man.

Authors:  S Loft; H E Poulsen
Journal:  J Mol Med (Berl)       Date:  1996-06       Impact factor: 4.599

4.  Recombination and its roles in DNA repair, cellular immortalization and cancer.

Authors:  M A Shammas; R J Shmookler Reis
Journal:  Age (Omaha)       Date:  1999-04

5.  Analysis of genetic instability during mammary tumor progression using a novel selection-based assay for in vivo mutations in a bacteriophage lambda transgene target.

Authors:  J L Jakubczak; G Merlino; J E French; W J Muller; B Paul; S Adhya; S Garges
Journal:  Proc Natl Acad Sci U S A       Date:  1996-08-20       Impact factor: 11.205

6.  An inherited NBN mutation is associated with poor prognosis prostate cancer.

Authors:  C Cybulski; D Wokołorczyk; W Kluźniak; A Jakubowska; B Górski; J Gronwald; T Huzarski; A Kashyap; T Byrski; T Dębniak; A Gołąb; B Gliniewicz; A Sikorski; J Switała; T Borkowski; A Borkowski; A Antczak; L Wojnar; J Przybyła; M Sosnowski; B Małkiewicz; R Zdrojowy; P Sikorska-Radek; J Matych; J Wilkosz; W Różański; J Kiś; K Bar; P Bryniarski; A Paradysz; K Jersak; J Niemirowicz; P Słupski; P Jarzemski; M Skrzypczyk; J Dobruch; P Domagała; S A Narod; J Lubiński
Journal:  Br J Cancer       Date:  2012-11-13       Impact factor: 7.640

Review 7.  Telomeres, chromosome instability and cancer.

Authors:  Susan M Bailey; John P Murnane
Journal:  Nucleic Acids Res       Date:  2006-05-08       Impact factor: 16.971

Review 8.  Mechanisms of spontaneous human cancers.

Authors:  S Venitt
Journal:  Environ Health Perspect       Date:  1996-05       Impact factor: 9.031

Review 9.  Whole-body MRI in pediatric patients with cancer.

Authors:  Marcos Duarte Guimarães; Julia Noschang; Sara Reis Teixeira; Marcel Koenigkam Santos; Henrique Manoel Lederman; Vivian Tostes; Vikas Kundra; Alex Dias Oliveira; Bruno Hochhegger; Edson Marchiori
Journal:  Cancer Imaging       Date:  2017-02-10       Impact factor: 3.909

Review 10.  Ionizing Radiation Protein Biomarkers in Normal Tissue and Their Correlation to Radiosensitivity: Protocol for a Systematic Review.

Authors:  Anne Dietz; Maria Gomolka; Simone Moertl; Prabal Subedi
Journal:  J Pers Med       Date:  2020-12-22
  10 in total

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