Literature DB >> 10699050

Detecting low penetrance genes in cancer: the way ahead.

R S Houlston1, I P Tomlinson.   

Abstract

The search for the genes responsible for many complex genetic diseases is well under way and has already been successful in some cases. The study of cancer as a complex genetic disease has lagged behind other conditions, largely because of particular problems that are associated with malignant disease. Cancer also, however, presents specific opportunities for gene identification, which are not found in many other diseases. While the methods of genetic mapping and gene cloning used for other complex diseases will be applied to cancer, these must almost certainly be complemented by other methods, such as the study of somatic mutations, cancer associated phenotypes, and modifier genes for Mendelian cancers. Here, we review the strategies available for identifying cancer predisposition genes of low and moderate penetrance.

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Year:  2000        PMID: 10699050      PMCID: PMC1734538          DOI: 10.1136/jmg.37.3.161

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  62 in total

Review 1.  Incidence, risk factors and prevention of melanoma.

Authors:  R M MacKie
Journal:  Eur J Cancer       Date:  1998-07       Impact factor: 9.162

2.  Genomewide transmission/disequilibrium testing--consideration of the genotypic relative risks at disease loci.

Authors:  N J Camp
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

3.  Tissues of MSH2-deficient mice demonstrate hypermutability on exposure to a DNA methylating agent.

Authors:  S E Andrew; M McKinnon; B S Cheng; A Francis; J Penney; A H Reitmair; T W Mak; F R Jirik
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-03       Impact factor: 11.205

4.  Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.

Authors:  D G Wang; J B Fan; C J Siao; A Berno; P Young; R Sapolsky; G Ghandour; N Perkins; E Winchester; J Spencer; L Kruglyak; L Stein; L Hsie; T Topaloglou; E Hubbell; E Robinson; M Mittmann; M S Morris; N Shen; D Kilburn; J Rioux; C Nusbaum; S Rozen; T J Hudson; R Lipshutz; M Chee; E S Lander
Journal:  Science       Date:  1998-05-15       Impact factor: 47.728

5.  Association of malaria parasite population structure, HLA, and immunological antagonism.

Authors:  S C Gilbert; M Plebanski; S Gupta; J Morris; M Cox; M Aidoo; D Kwiatkowski; B M Greenwood; H C Whittle; A V Hill
Journal:  Science       Date:  1998-02-20       Impact factor: 47.728

6.  Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair.

Authors:  T A Prolla; S M Baker; A C Harris; J L Tsao; X Yao; C E Bronner; B Zheng; M Gordon; J Reneker; N Arnheim; D Shibata; A Bradley; R M Liskay
Journal:  Nat Genet       Date:  1998-03       Impact factor: 38.330

7.  Evidence for a novel osteosarcoma tumor-suppressor gene in the chromosome 18 region genetically linked with Paget disease of bone.

Authors:  M J Nellissery; S S Padalecki; Z Brkanac; F R Singer; G D Roodman; K K Unni; R J Leach; M F Hansen
Journal:  Am J Hum Genet       Date:  1998-09       Impact factor: 11.025

8.  Meta-analysis of studies of the CYP2D6 polymorphism in relation to lung cancer and Parkinson's disease.

Authors:  A Rostami-Hodjegan; M S Lennard; H F Woods; G T Tucker
Journal:  Pharmacogenetics       Date:  1998-06

Review 9.  Genetics of inflammatory bowel disease.

Authors:  J Satsangi; M Parkes; D P Jewell; J I Bell
Journal:  Clin Sci (Lond)       Date:  1998-05       Impact factor: 6.124

10.  Radiation-induced micronucleus induction in lymphocytes identifies a high frequency of radiosensitive cases among breast cancer patients: a test for predisposition?

Authors:  D Scott; J B Barber; E L Levine; W Burrill; S A Roberts
Journal:  Br J Cancer       Date:  1998-02       Impact factor: 7.640

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  2 in total

1.  Genetic variants of EGFR (142285G>A) and ESR1 (2014G>A) gene polymorphisms and risk of breast cancer.

Authors:  Ranbir Chander Sobti; Marjan Askari; Mohsen Nikbakht; Neha Singh; Suresh C Sharma; Abayneh Munshea Abitew
Journal:  Mol Cell Biochem       Date:  2012-07-19       Impact factor: 3.396

2.  Rule-based induction method for haplotype comparison and identification of candidate disease loci.

Authors:  Sirkku Karinen; Silva Saarinen; Rainer Lehtonen; Pasi Rastas; Pia Vahteristo; Lauri A Aaltonen; Sampsa Hautaniemi
Journal:  Genome Med       Date:  2012-03-19       Impact factor: 11.117

  2 in total

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