| scholarly article | Q13442814 |
| P50 | author | Gareth Evans | Q29642643 |
| Cecilia Brassett | Q48504849 | ||
| P2093 | author name string | E R Maher | |
| R D Kolodner | |||
| L Verma | |||
| M F Kane | |||
| J Schmeits | |||
| P2860 | cites work | Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis | Q22122362 |
| hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6 | Q24323176 | ||
| The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations | Q27935158 | ||
| Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
| Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer | Q28253384 | ||
| The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer | Q28256988 | ||
| Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer | Q28257360 | ||
| Biochemistry and genetics of eukaryotic mismatch repair | Q28282377 | ||
| A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer | Q28289377 | ||
| Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells | Q28292781 | ||
| Mutations of GTBP in genetically unstable cells | Q28292802 | ||
| Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair | Q28508905 | ||
| Mouse models for hereditary nonpolyposis colorectal cancer | Q28585761 | ||
| Mutation in the mismatch repair gene Msh6 causes cancer susceptibility | Q28592583 | ||
| Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair | Q29615027 | ||
| Microsatellite instability in cancer of the proximal colon | Q29620692 | ||
| Microsatellite instability in early onset and familial colorectal cancer. | Q33678081 | ||
| Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
| Functional overlap in mismatch repair by human MSH3 and MSH6. | Q34603929 | ||
| Mutator phenotypes in human colorectal carcinoma cell lines | Q35568305 | ||
| Mechanisms and biological effects of mismatch repair | Q37041860 | ||
| Genetic instability occurs in the majority of young patients with colorectal cancer | Q38297232 | ||
| Germline mutations in a polycytosine repeat of the hMSH6 gene in Korean hereditary nonpolyposis colorectal cancer | Q38328724 | ||
| Microsatellite instability in yeast: dependence on repeat unit size and DNA mismatch repair genes | Q40022200 | ||
| Characterization of distinct human endometrial carcinoma cell lines deficient in mismatch repair that originated from a single tumor | Q41005472 | ||
| Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer | Q42005199 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
| Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation | Q46049171 | ||
| Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred | Q48044118 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| Microsatellite instability in colorectal cancer: different mutator phenotypes and the principal involvement of hMLH1. | Q50893078 | ||
| Diagnostic microsatellite instability: definition and correlation with mismatch repair protein expression. | Q53439660 | ||
| Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients | Q57570041 | ||
| Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer | Q61946741 | ||
| The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) | Q62978412 | ||
| Colorectal cancer screening | Q68194974 | ||
| Molecular analysis of mutations in mutator colorectal carcinoma cell lines | Q70972736 | ||
| Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes | Q71733947 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | colorectal cancer | Q188874 |
| microsatellite | Q265193 | ||
| colorectal carcinoma | Q25493920 | ||
| P304 | page(s) | 678-682 | |
| P577 | publication date | 1999-09-01 | |
| P1433 | published in | Journal of Medical Genetics | Q14640281 |
| P1476 | title | Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer | |
| P478 | volume | 36 |
| Q48252170 | Accuracy of four mononucleotide-repeat markers for the identification of DNA mismatch-repair deficiency in solid tumors |
| Q79832402 | An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation |
| Q33535820 | An optimized pentaplex PCR for detecting DNA mismatch repair-deficient colorectal cancers |
| Q37108779 | Association of MSH6 mutation with glioma susceptibility, drug resistance and progression |
| Q45741007 | Colorectal cancer in Iran: immunohistochemical profiles of four mismatch repair proteins |
| Q35748966 | Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors |
| Q88766390 | Delineating a new feature of constitutional mismatch repair deficiency (CMMRD) syndrome: breast cancer |
| Q35869219 | Detection of microsatellite instability by fluorescence multiplex polymerase chain reaction |
| Q90679214 | Immune checkpoint inhibitors for the treatment of MSI-H/MMR-D colorectal cancer and a perspective on resistance mechanisms |
| Q36734614 | Immunohistochemistry versus microsatellite instability testing for screening colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome. Part II. The utility of microsatellite instability testing |
| Q36246487 | Lynch syndrome genes |
| Q36611645 | MSH6 germline mutations in early-onset colorectal cancer patients without family history of the disease |
| Q49959979 | MSH6 haploinsufficiency at relapse contributes to the development of thiopurine resistance in pediatric B-lymphoblastic leukemia |
| Q37331928 | MSH6 mutations arise in glioblastomas during temozolomide therapy and mediate temozolomide resistance. |
| Q90749821 | Microsatellite Instability: Diagnosis, Heterogeneity, Discordance, and Clinical Impact in Colorectal Cancer |
| Q33918755 | Microsatellite instability and mutational analysis of transforming growth factor beta receptor type II gene (TGFBR2) in sporadic ovarian cancer. |
| Q43864989 | Milestones of Lynch syndrome: 1895-2015. |
| Q37360286 | Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant |
| Q80597703 | Muir-Torre Syndrome: expanding the genotype and phenotype--a further family with a MSH6 mutation |
| Q81602162 | Mutational analysis of hMsh6 in Israeli HNPCC and HNPCC-like families |
| Q79198177 | Mutations of the 'minor' mismatch repair gene MSH6 in typical and atypical hereditary nonpolyposis colorectal cancer |
| Q38937353 | Novel hMSH2, hMSH6 and hMLH1 gene mutations and microsatellite instability in sporadic colorectal cancer |
| Q35022384 | Prevalence of defective DNA mismatch repair and MSH6 mutation in an unselected series of endometrial cancers |
| Q34785026 | Role of microsatellite instability-low as a diagnostic biomarker of Lynch syndrome in colorectal cancer |
| Q34433799 | Tumours with loss of MSH6 expression are MSI-H when screened with a pentaplex of five mononucleotide repeats |
| Q36246500 | Use of microsatellite instability and immunohistochemistry testing for the identification of individuals at risk for Lynch syndrome |
| Q36612580 | Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability |
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