| scholarly article | Q13442814 |
| P50 | author | Bert Vogelstein | Q827502 |
| Kenneth W. Kinzler | Q28031580 | ||
| P2093 | author name string | N C Nicolaides | |
| P Modrich | |||
| S J Littman | |||
| P2860 | cites work | Mutations of two PMS homologues in hereditary nonpolyposis colon cancer | Q24318484 |
| Positive autoregulation of c-myb expression via Myb binding sites in the 5' flanking region of the human c-myb gene | Q24595119 | ||
| Mutation of a mutL homolog in hereditary colon cancer | Q28114939 | ||
| 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 | ||
| Molecular cloning of the N-terminus of GTBP | Q28292000 | ||
| Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells | Q28292781 | ||
| GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells | Q28292790 | ||
| Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer | Q28294774 | ||
| Meiotic pachytene arrest in MLH1-deficient mice | Q28510650 | ||
| Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair | Q29618879 | ||
| A versatile in vivo and in vitro eukaryotic expression vector for protein engineering | Q29620181 | ||
| Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines | Q33720790 | ||
| Genomic organization of the human PMS2 gene family. | Q34373629 | ||
| Analysis of the 5' region of PMS2 reveals heterogeneous transcripts and a novel overlapping gene | Q34385102 | ||
| Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs | Q34554581 | ||
| The molecular basis of Turcot's syndrome | Q34662365 | ||
| Functional domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA mismatch repair proteins and their relevance to human hereditary nonpolyposis colorectal cancer-associated mutations | Q36570003 | ||
| Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
| The Jun family members, c-Jun and JunD, transactivate the human c-myb promoter via an Ap1-like element. | Q38325809 | ||
| Mismatch repair, genetic stability, and cancer | Q40556409 | ||
| Cisplatin and adriamycin resistance are associated with MutLalpha and mismatch repair deficiency in an ovarian tumor cell line | Q41174585 | ||
| Cancer of the microsatellite mutator phenotype. | Q41263775 | ||
| Mismatch Repair Deficiency in Phenotypically Normal Human Cells | Q41347026 | ||
| Hypermutability and mismatch repair deficiency in RER+ tumor cells | Q41508298 | ||
| MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast | Q42427955 | ||
| Mispair specificity of methyl-directed DNA mismatch correction in vitro | Q44909730 | ||
| Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer | Q48084125 | ||
| Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients | Q57570041 | ||
| Mismatch repair and cancer | Q57956407 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | phenotype | Q104053 |
| P304 | page(s) | 1635-1641 | |
| P577 | publication date | 1998-03-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype | |
| P478 | volume | 18 |
| Q52712904 | An Organismal CNV Mutator Phenotype Restricted to Early Human Development. |
| Q36835972 | Constitutive deficiency in DNA mismatch repair |
| Q40744193 | Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair |
| Q34568596 | DNA mismatch repair defects: role in colorectal carcinogenesis |
| Q28478209 | Down-regulation of DNA mismatch repair enhances initiation and growth of neuroblastoma and brain tumour multicellular spheroids |
| Q77753605 | Eukaryotic mismatch repair: an update |
| Q33898040 | Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene |
| Q57204279 | Expression of a truncated Brca1 protein delays lactational mammary development in transgenic mice |
| Q36641429 | Extensive molecular screening for hereditary non-polyposis colorectal cancer |
| Q38755812 | Functional and physical interaction between the mismatch repair and FA-BRCA pathways |
| Q27929951 | Functional studies on the candidate ATPase domains of Saccharomyces cerevisiae MutLalpha. |
| Q35069957 | Fusion tyrosine kinase NPM-ALK Deregulates MSH2 and suppresses DNA mismatch repair function novel insights into a potent oncoprotein |
| Q35663759 | Gene expression analysis of tumor spheroids reveals a role for suppressed DNA mismatch repair in multicellular resistance to alkylating agents |
| Q28214754 | Genetic instability in human mismatch repair deficient cancers |
| Q35930688 | Genetic predisposition to colorectal cancer |
| Q64917220 | Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations |
| Q93493049 | HNPCC (Lynch Syndrome): Differential Diagnosis, Molecular Genetics and Management - a Review |
| Q60934518 | Human Exonuclease 1 (EXO1) Regulatory Functions in DNA Replication with Putative Roles in Cancer |
| Q33234976 | Human antibodies for immunotherapy development generated via a human B cell hybridoma technology |
| Q40947848 | Identification of new tumor suppressor genes based on in vivo functional inactivation of a candidate gene |
| Q34012877 | Isolation and characterization of point mutations in mismatch repair genes that destabilize microsatellites in yeast |
| Q55467573 | Low level of microsatellite instability in paediatric malignant astrocytomas. |
| Q49111534 | Low-level microsatellite instability phenotype in sporadic glioblastoma multiforme |
| Q22009114 | MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1 |
| Q22010995 | MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability |
| Q33270665 | Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach |
| Q42112990 | Microsatellite instability and mismatch repair gene inactivation in sporadic pancreatic and colon tumours |
| Q36529711 | Microsatellite instability in the peripheral blood leukocytes of HNPCC patients |
| Q38337751 | Mismatch-, MutS-, MutL-, and helicase II-dependent unwinding from the single-strand break of an incised heteroduplex |
| Q33230453 | Morphogenics as a tool for target discovery and drug development |
| Q40762457 | Mutation frequency in coding and non-coding repeat sequences in mismatch repair deficient cells derived from normal human tissue |
| Q38874456 | NPM-ALK mediates phosphorylation of MSH2 at tyrosine 238, creating a functional deficiency in MSH2 and the loss of mismatch repair |
| Q61811779 | New Phenotypes of Potato Co-induced by Mismatch Repair Deficiency and Somatic Hybridization |
| Q33909895 | Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome |
| Q33959136 | Polymorphisms of the human UDP-glucuronosyltransferase (UGT) 1A7 gene in colorectal cancer |
| Q37444790 | Protein and genome evolution in Mammalian cells for biotechnology applications |
| Q39608661 | Rapid generation of rice mutants via the dominant negative suppression of the mismatch repair protein OsPMS1. |
| Q40969083 | Repair of large insertion/deletion heterologies in human nuclear extracts is directed by a 5' single-strand break and is independent of the mismatch repair system |
| Q27938377 | Separation-of-function mutations in Saccharomyces cerevisiae MSH2 that confer mismatch repair defects but do not affect nonhomologous-tail removal during recombination |
| Q34786141 | The "comparative growth assay": examining the interplay of anti-cancer agents with cells carrying single gene alterations |
| Q40222264 | The E705K mutation in hPMS2 exerts recessive, not dominant, effects on mismatch repair |
| Q34989790 | The genetic pathogenesis of colorectal cancer |
| Q36447028 | The hMSH2(M688R) Lynch syndrome mutation may function as a dominant negative |
| Q24621737 | Unbalanced replication as a major source of genetic instability in cancer cells |
| Q49043239 | Yeast mutator phenotype enforced by Arabidopsis PMS1 expression |
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