A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitis
- 31 July 1995
- journal article
- Published by Elsevier in Gastroenterology
- Vol. 109 (1) , 151-155
- https://doi.org/10.1016/0016-5085(95)90280-5
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Transcription-Coupled Repair and Human DiseaseScience, 1994
- Mismatch Repair, Genetic Stability, and CancerScience, 1994
- Binding of Mismatched Microsatellite DNA Sequences by the Human MSH2 ProteinScience, 1994
- MLH1, PMS1, and MSH2 Interactions During the Initiation of DNA Mismatch Repair in YeastScience, 1994
- Are the associations between Alzheimer's disease and polymorphisms in the apolipoprotein E and the apolipoprotein CII genes due to linkage disequilibrium?Annals of Neurology, 1994
- Molecular basis of human hypertension: Role of angiotensinogenCell, 1992
- MECHANISMS AND BIOLOGICAL EFFECTS OF MISMATCH REPAIRAnnual Review of Genetics, 1991
- Identification of intronic point mutations as an alternative mechanism for p53 inactivation in lung cancer.Journal of Clinical Investigation, 1990
- Oncogenic Point Mutations in the Human Retinoblastoma Gene: Their Application to Genetic CounselingNew England Journal of Medicine, 1989
- Purification of DNA from formaldehyde fixed and paraffin embedded human tissueBiochemical and Biophysical Research Communications, 1985