about
Current hypotheses on how microsatellite instability leads to enhanced survival of Lynch Syndrome patientsMED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1Genome sequence of the hyperthermophilic crenarchaeon Pyrobaculum aerophilum.Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2Gene expression profile in BALB/c-3T3 cells transformed with beryllium sulfateHuman exonuclease I is required for 5' and 3' mismatch repairEpigenetic silencing of AXIN2 in colorectal carcinoma with microsatellite instabilityMSH2 and ATR form a signaling module and regulate two branches of the damage response to DNA methylationCharacterization of a mammalian homolog of the Escherichia coli MutY mismatch repair proteinHuman stanniocalcin: a possible hormonal regulator of mineral metabolismCloning and characterization of a functional human homolog of Escherichia coli endonuclease IIIDNA polymerase delta is required for human mismatch repair in vitroMethylator-induced, mismatch repair-dependent G2 arrest is activated through Chk1 and Chk2Simple tandem DNA repeats and human genetic diseaseA catalogue of genes in the cardiovascular system as identified by expressed sequence tagsReview of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramificationsTumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancerMolecular origins of cancer: Molecular basis of colorectal cancerGene expression profiling in human fetal liver and identification of tissue- and developmental-stage-specific genes through compiled expression profiles and efficient cloning of full-length cDNAsMicrosatellite instability in colorectal cancerMutations affecting a putative MutLalpha endonuclease motif impact multiple mismatch repair functionsDNA mismatch repair: molecular mechanism, cancer, and ageingThe homeobox gene CDX2 in colorectal carcinoma: a genetic analysis3pK, a new mitogen-activated protein kinase-activated protein kinase located in the small cell lung cancer tumor suppressor gene regionChromatid cohesion defects may underlie chromosome instability in human colorectal cancersA multiprotein nuclear complex connects Fanconi anemia and Bloom syndromehMLH1 promoter hypermethylation is an early event in human endometrial tumorigenesisSeven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresisHepatitis B virus X protein interacts with a probable cellular DNA repair proteinSomatic frameshift mutations in the Bloom syndrome BLM gene are frequent in sporadic gastric carcinomas with microsatellite mutator phenotypeDiscovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies.Human AP endonuclease suppresses DNA mismatch repair activity leading to microsatellite instability.Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesisMouse models for the discovery of colorectal cancer driver genesPMS2 monoallelic mutation carriers: the known unknownFunctional studies on the candidate ATPase domains of Saccharomyces cerevisiae MutLalpha.The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs.Increased mutagenesis and unique mutation signature associated with mitotic gene conversionOpportunities for immunotherapy in microsatellite instable colorectal cancerThe genetic heterogeneity of colorectal cancer predisposition - guidelines for gene discovery
P2860
Q21328691-2E2272E2-1018-41C9-931D-E82888A1DFCAQ22009114-54B0A59F-42B5-47A2-AEB2-E0C7B2595CA8Q22066214-9079C7F3-F692-45DD-B837-439595D76261Q22248073-59535AD5-24BC-4647-9F82-9E2265708D9EQ23919603-B9276AE9-5E83-4D49-853E-F487204C523DQ24292224-2BB9D91B-85BE-421B-B8DC-88F07A9C8622Q24292772-323A122F-7CFE-47A2-A2E0-5C4277BFF446Q24301197-C1A025E2-5DA4-48C1-B308-85D59C824B5DQ24309547-24A15597-9506-41DE-814F-19B1839D8E15Q24310829-2F27D143-6152-4FE6-BA26-E8DC85AF1DA2Q24311942-D8BF5865-1968-4EE9-AAFE-34074297BC67Q24313002-D7FF5C9E-D282-48AE-B7B4-BF19EC32A790Q24556572-C0A5CE1F-509D-4972-A8B5-E73B229432B2Q24561717-B81B5FF4-87DE-4A4F-8B81-0E8A274BF70FQ24562782-AD423C87-EA68-4444-B888-8EFEC1878376Q24610838-F7392EFE-B7B4-4ECB-A562-62246B1034CBQ24614511-D92E93D8-2BAE-4DBA-8A8B-0245AFAC951AQ24617331-8BE8AA85-A833-4C26-A921-9F774361D093Q24620270-F5236D18-5B0D-4BE1-8A53-6211BB71EECEQ24627393-97E94919-676D-4F50-AD10-6012C23C9011Q24646969-27138BB2-04AA-4A1F-96CD-CFF77539934DQ24647002-73D28F3E-7A08-41C1-9572-9B0280B3E73DQ24648834-5D399A5F-5185-4D93-915E-42F0AE2E1E28Q24650774-EC8DC48D-C36D-41D6-94C2-1678774BDA65Q24656162-2B7BC348-AB61-439E-B367-21ACB3162BF0Q24669612-11EAAB05-264C-42F5-8AEA-AE42B17B30FBQ24670424-6B44D214-1499-478E-8685-206B672E02E2Q24671692-86E973AB-5D11-4EB0-8D42-B42A3AD2408BQ24676695-F188621C-8185-4964-BD61-4417C86F1021Q24803238-8FC3C511-B0BA-4825-95C3-85F34EDE7A78Q24811003-A0E3A80D-BBFA-4B24-97F8-DA5D4A5440FBQ24812717-10A899A0-4DB0-4609-BA7A-ACC4DA67238CQ25257401-82CE4D5E-6489-4331-8070-4C52E94EF2BCQ26774627-B86360A6-FAF3-4BF2-B964-71E6B0E70CC4Q27024662-063D703D-CEF6-4495-9214-F68CFF839E45Q27929951-3AB1D24B-BCEB-4CAA-B810-C6F4493D2D76Q27930815-C0467F77-7880-4E12-8EEC-4942882B59A1Q27934880-080D6F05-26AE-4BB1-8439-DF27B8CF65F3Q28066110-4932AC14-712B-41FF-BC57-98773269071AQ28077234-C457B5CD-B816-481B-8EA5-AABEE035E4BD
P2860
description
1994 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի մարտին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Science
@fr
artículu científicu espublizáu en 1994
@ast
im März 1994 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1994/03/18)
@sk
vědecký článek publikovaný v roce 1994
@cs
wetenschappelijk artikel (gepubliceerd op 1994/03/18)
@nl
наукова стаття, опублікована в березні 1994
@uk
name
Mutation of a mutL homolog in hereditary colon cancer
@ast
Mutation of a mutL homolog in hereditary colon cancer
@en
Mutation of a mutL homolog in hereditary colon cancer
@nl
type
label
Mutation of a mutL homolog in hereditary colon cancer
@ast
Mutation of a mutL homolog in hereditary colon cancer
@en
Mutation of a mutL homolog in hereditary colon cancer
@nl
prefLabel
Mutation of a mutL homolog in hereditary colon cancer
@ast
Mutation of a mutL homolog in hereditary colon cancer
@en
Mutation of a mutL homolog in hereditary colon cancer
@nl
P2093
P3181
P356
P1433
P1476
Mutation of a mutL homolog in hereditary colon cancer
@en
P2093
C. A. Rosen
C. M. Fraser
K. C. Carter
M. D. Adams
N. C. Nicolaides
N. Papadopoulos
R. D. Fleischmann
S. M. Ruben
P304
P3181
P356
10.1126/SCIENCE.8128251
P407
P577
1994-03-18T00:00:00Z