A polymorphism in the hMSH2 gene (gIVS12-6T>C) associated with non-Hodgkin lymphomas

Cancer Genetics and Cytogenetics

Volumn 133, Issue 1, 2002, Pages 29-33

  Paz y Mio, César ^a   Pérez, J Christian ^a   Fiallo, B Fernanda ^a   Leone, Paola E ^a  

^a PONTIFICIA UNIVERSIDAD CATÓLICA DEL ECUADOR   (Ecuador)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BASE MISPAIRING; BINDING SITE; CANCER RISK; CANCER SUSCEPTIBILITY; CARCINOGENESIS; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA POLYMORPHISM; DNA REPAIR; DNA SEQUENCE; EXON; GENE FREQUENCY; GENETIC RISK; GENETIC SCREENING; GENETIC STABILITY; GENETIC VARIABILITY; HUMAN; HUMAN TISSUE; INTRON; NONHODGKIN LYMPHOMA; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SINGLE STRAND CONFORMATION POLYMORPHISM;

ALLELES; DNA-BINDING PROTEINS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LYMPHOMA, NON-HODGKIN; MUTS HOMOLOG 2 PROTEIN; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTO-ONCOGENE PROTEINS; RISK FACTORS;

EID: 0036125079     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(01)00547-7     Document Type: Article

References (34)

1. Involvement of nucleotide-excision repair in msh2 pms1- independent mismatch repair
2. Cancer-susceptibility genes. Gatekeepers and caretakers
3. Mismatch repair: Mechanisms and relationship to cancer susceptibility
4. Lessons from hereditary colorectal cancer
5. Mismatch repair in replication fidelity, genetic recombination and cancer biology
6. Microsatellite instability, mismatch repair deficiency, and genetic defects in human cancer cell lines
7. Mismatch repair defects in cancer
8. MSH2 deficient mice are viable and susceptible to lymphoid tumors
9. Mouse models for hereditary nonpolyposis colorectal cancer
10. Defects of the mismatch repair gene MSH2 are implicated in the development of murine and human lymphoblastic lymphomas and are associated with the aberrant expression of rhombotin-2 (Lmo-2) and Tal-1 (SLC)
11. Mutator phenotype in human hematopoietic neoplasms and its association with deletions disabling DNA repair genes and bcl-2 rearrangements
12. Mutation of the hMSH2 gene in two families with hereditary nonpolyposis colorectal cancer
13. Extraction of nucleic acids from clinical samples and cultured cells
14. Single nucleotide polymorphisms as tools in human genetics
15. Mutations of a MutS homolog in hereditary non-polyposis colorectal cancer
16. Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations
17. Hereditary nonpolyposis colorectal cancer (HNPCC): Eight novel germline mutations in hMSH2 or hMLH1 genes
18. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
19. A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitis
20. The future of genetic studies of complex human diseases
21. The new genomics: Global views of biology
22. Variations on a theme: Cataloging human DNA sequence variation
23. Drug metabolism polymorphisms as modulators of cancer susceptibility
24. Characterization of single-nucleotide polymorphisms in coding regions of human genes
25. How many diseases does it take to map a gene with SNPs?
26. The ΔF508 mutation in Ecuador, South America
27. BCR-ABL rearrangement frequencies in CML and ALL in Ecuador, South America
28. MSH2-deficient murine lymphomas harbor insertion/deletion mutations in the transforming growth factor beta receptor type 2 gene and display low not high frequency microsatellite instability
29. Frameshift mutations of the hMSH6 gene in human leukemia cell lines
30. Eukaryotic mismatch repair: An update
31. Polymorphisms in the human DNA repair gene XPF
32. Identification of single nucleotide polymorphisms in human DNA repair genes