Literature DB >> 11701643

DNA damage processing defects and disease.

R E Moses1.   

Abstract

Inherited defects in DNA repair or the processing of DNA damage can lead to disease. Both autosomal recessive and autosomal dominant modes of inheritance are represented. The diseases as a group are characterized by genomic instability, with eventual appearance of cancer. The inherited defects frequently have a specific DNA damage sensitivity, with cells from affected individuals showing normal resistance to other genotoxic agents. The known defects are subtle alterations in transcription, replication, or recombination, with alternate pathways of processing permitting cellular viability. Distinct diseases may arise from different mutations in one gene; thus, clinical phenotypes may reflect the loss of different partial functions of a gene. The findings indicate that partial defects in transcription or recombination lead to genomic instability, cancer, and characteristic disease phenotypes.

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Year:  2001        PMID: 11701643     DOI: 10.1146/annurev.genom.2.1.41

Source DB:  PubMed          Journal:  Annu Rev Genomics Hum Genet        ISSN: 1527-8204            Impact factor:   8.929


  11 in total

Review 1.  Fanconi anaemia.

Authors:  M D Tischkowitz; S V Hodgson
Journal:  J Med Genet       Date:  2003-01       Impact factor: 6.318

2.  Chronic myeloid leukemia 2011: successes, challenges, and strategies--proceedings of the 5th annual BCR-ABL1 positive and BCR-ABL1 negative myeloproliferative neoplasms workshop.

Authors:  Tariq I Mughal; Jerald P Radich; Richard A Van Etten; Alfonso Quintás-Cardama; Tomasz Skorski; Farhad Ravandi; Daniel J DeAngelo; Carlo Gambacorti-Passerini; Giovanni Martinelli; Ayalew Tefferi
Journal:  Am J Hematol       Date:  2011-09       Impact factor: 10.047

3.  Polymorphisms in DNA repair genes and breast cancer risk in Russian population: a case-control study.

Authors:  Alexandra S Shadrina; Natalia A Ermolenko; Uljana A Boyarskikh; Tatiana V Sinkina; Alexandr F Lazarev; Valentina D Petrova; Maxim L Filipenko
Journal:  Clin Exp Med       Date:  2014-12-24       Impact factor: 3.984

Review 4.  Chronic myeloid leukemia cells refractory/resistant to tyrosine kinase inhibitors are genetically unstable and may cause relapse and malignant progression to the terminal disease state.

Authors:  Tomasz Skorski
Journal:  Leuk Lymphoma       Date:  2011-02

5.  Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents.

Authors:  A W Hemphill; Y Akkari; A H Newell; R A Schultz; M Grompe; P S North; I D Hickson; P M Jakobs; S Rennie; D Pauw; J Hejna; S B Olson; R E Moses
Journal:  Cytogenet Genome Res       Date:  2009-09-04       Impact factor: 1.636

6.  Multiple-pathway analysis of double-strand break repair mutations in Drosophila.

Authors:  Dena M Johnson-Schlitz; Carlos Flores; William R Engels
Journal:  PLoS Genet       Date:  2007-02-21       Impact factor: 5.917

7.  Gly322Asp and Asn127Ser single nucleotide polymorphisms (SNPs) of hMSH2 mismatch repair gene and the risk of triple-negative breast cancer in Polish women.

Authors:  Beata Smolarz; Marianna Makowska; Dariusz Samulak; Magdalena M Michalska; Hanna Romanowicz
Journal:  Fam Cancer       Date:  2015-03       Impact factor: 2.375

8.  Association of common variants in mismatch repair genes and breast cancer susceptibility: a multigene study.

Authors:  João Conde; Susana N Silva; Ana P Azevedo; Valdemar Teixeira; Julieta Esperança Pina; José Rueff; Jorge F Gaspar
Journal:  BMC Cancer       Date:  2009-09-25       Impact factor: 4.430

9.  Triplex-induced DNA damage response.

Authors:  Faye A Rogers; Meetu Kaushik Tiwari
Journal:  Yale J Biol Med       Date:  2013-12-13

10.  X-ray repair cross-complementing protein 1 and 3 polymorphisms and susceptibility of breast cancer in a Jordanian population.

Authors:  Mazhar S Al Zoubi
Journal:  Saudi Med J       Date:  2015-10       Impact factor: 1.484

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