(Q36246487)

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Lynch syndrome genes

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

1 reference

Europe PubMed Central

Lynch syndrome genes (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

1 reference

based on heuristic

inferred from title

Päivi Peltomäki

object named as

Päivi Peltomäki

1

0 references

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

Familial Cancer

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

227-232

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database

1 reference

https://api.crossref.org/works/10.1007%2FS10689-004-7993-0

21 January 2018

Germline and somatic mutation analysis of MLH3 in MSI-positive colorectal cancer

1 reference

https://api.crossref.org/works/10.1007%2FS10689-004-7993-0

21 January 2018

Methylation-induced G2/M arrest requires a full complement of the mismatch repair protein hMLH1

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ-line mutation of the hMSH6/GTBP gene in an atypical hereditary nonpolyposis colorectal cancer kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of human MLH1 and MSH2 missense variants and hybrid human-yeast MLH1 proteins in Saccharomyces cerevisiae

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Little evidence for involvement of MLH3 in colorectal cancer predisposition

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The selection for mismatch repair defects in hereditary nonpolyposis colorectal cancer: revising the mutator hypothesis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of hMSH2 and hMSH6 expression is frequent in sporadic endometrial carcinomas with microsatellite instability: a population-based study

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline and somatic mutations in hMSH6 and hMSH3 in gastrointestinal cancers of the microsatellite mutator phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A role for MLH3 in hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of MSH2 and MSH6 characterizes endometrial but not colon carcinomas in hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch Repair Deficiency in Phenotypically Normal Human Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of hMLH3 in familial colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA mismatch repair and mutation avoidance pathways

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frameshift mutator mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional interactions and signaling properties of mammalian DNA mismatch repair proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clues to the pathogenesis of familial colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of hPMS1 and hPMS2 in predisposing to colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bacterial mutator genes and the control of spontaneous mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability in cancer of the proximal colon

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Meiotic arrest and aneuploidy in MLH3-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Eukaryotic DNA mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of Turcot's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of cDNA clones derived from the divergently transcribed gene in the region upstream from the human dihydrofolate reductase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refined chromosomal localization of the mismatch repair and hereditary nonpolyposis colorectal cancer genes hMSH2 and hMSH6

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of a mutL homolog in hereditary colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning and characterization of the human and Caenorhabditis elegans homologs of the Saccharomyces cerevisiae MSH5 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of a locus predisposing to human colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumour susceptibility and spontaneous mutation in mice deficient in Mlh1, Pms1 and Pms2 DNA mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Probable involvement of a germ-line mutation of an unknown mismatch repair gene in a Japanese Muir-Torre syndrome phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Redundancy of Saccharomyces cerevisiae MSH3 and MSH6 in MSH2-dependent mismatch repair

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic organization and expression of the human MSH3 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sublocalization of a locus at 3p21.3?23 predisposing to hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA mismatch repair and genetic instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of MSH3 protein expression is frequent in MLH1-deficient colorectal cancer and is associated with disease progression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Steady-state regulation of the human DNA mismatch repair system.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single gene complementation of the hPMS2 defect in HEC-1-A endometrial carcinoma cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Drastic genetic instability of tumors and normal tissues in Turcot syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional analysis of MSH6 mutations linked to kindreds with putative hereditary non-polyposis colorectal cancer syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair activity in mammalian mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair defects in cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline and somatic mutation analyses in the DNA mismatch repair gene MLH3: Evidence for somatic mutation in colorectal cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/16136382

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10689-004-7993-0

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 August 2017

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