Patients with bi-allelic germline mutations in mismatch repair (MMR) genes (MLH1, MSH2, MSH6, or PMS2) develop a rare but severe variant of Lynch syndrome called constitutional MMR deficiency (CMMRD). This syndrome is characterized by early-onset colorectal cancers, lymphomas or leukemias, and brain tumors. There is no satisfactory method for diagnosis of CMMRD because screens for mutations in MMR genes are non-informative for 30% of patients. MMR-deficient cancer cells are resistant to genotoxic agents and have microsatellite instability (MSI), due to accumulation of errors in repetitive DNA sequences. We investigated whether these features could be used to identify patients with CMMRD.publisher: Elsevier articletitle: Diagnosis of Constit...
Heterozygous carriers of a pathogenic variant in the mismatch repair genes have an increased risk to...
Monoallelic PMS2 germline mutations cause 5-15% of Lynch syndrome, a midlife cancer predisposition, ...
Biallelic germline mismatch repair (MMR) gene (MLH1, MSH2, MSH6, and PMS2) mutations are an extremel...
Purpose: Diagnosis of Mismatch Repair Deficiency (MMRD) is crucial for tumor management and early de...
PURPOSE: Constitutional mismatch repair deficiency (CMMRD) is a highly penetrant cancer predispositi...
International audienceDNA mismatch repair (MMR) deficiency is one of the best understood forms of ge...
BackgroundLynch syndrome is a genetic disease characterized by abnormal DNA replication caused by ge...
DNA mismatch repair (MMR) deficiency is one of the best understood forms of genetic instability in c...
Patients with bi-allelic germline mutations in mismatch repair (MMR) genes (MLH1, MSH2, MSH6, or PMS...
Purpose: Constitutional mismatch repair deficiency (CMMRD) is a highly penetrant cancer predispositi...
Contains fulltext : 136846pub.pdf (publisher's version ) (Closed access)Lynch synd...
Item does not contain fulltextMonoallelic germline mutations in one of the DNA mismatch repair (MMR)...
Biallelic germline mismatch repair (MMR) gene (MLH1, MSH2, MSH6, and PMS2) mutations are an extremel...
peer reviewedConstitutional mismatch repair deficiency (CMMRD) is caused by germline pathogenic vari...
BACKGROUND & AIMS: Patients with bi-allelic germline mutations in mismatch repair (MMR) genes (MLH1,...
Heterozygous carriers of a pathogenic variant in the mismatch repair genes have an increased risk to...
Monoallelic PMS2 germline mutations cause 5-15% of Lynch syndrome, a midlife cancer predisposition, ...
Biallelic germline mismatch repair (MMR) gene (MLH1, MSH2, MSH6, and PMS2) mutations are an extremel...
Purpose: Diagnosis of Mismatch Repair Deficiency (MMRD) is crucial for tumor management and early de...
PURPOSE: Constitutional mismatch repair deficiency (CMMRD) is a highly penetrant cancer predispositi...
International audienceDNA mismatch repair (MMR) deficiency is one of the best understood forms of ge...
BackgroundLynch syndrome is a genetic disease characterized by abnormal DNA replication caused by ge...
DNA mismatch repair (MMR) deficiency is one of the best understood forms of genetic instability in c...
Patients with bi-allelic germline mutations in mismatch repair (MMR) genes (MLH1, MSH2, MSH6, or PMS...
Purpose: Constitutional mismatch repair deficiency (CMMRD) is a highly penetrant cancer predispositi...
Contains fulltext : 136846pub.pdf (publisher's version ) (Closed access)Lynch synd...
Item does not contain fulltextMonoallelic germline mutations in one of the DNA mismatch repair (MMR)...
Biallelic germline mismatch repair (MMR) gene (MLH1, MSH2, MSH6, and PMS2) mutations are an extremel...
peer reviewedConstitutional mismatch repair deficiency (CMMRD) is caused by germline pathogenic vari...
BACKGROUND & AIMS: Patients with bi-allelic germline mutations in mismatch repair (MMR) genes (MLH1,...
Heterozygous carriers of a pathogenic variant in the mismatch repair genes have an increased risk to...
Monoallelic PMS2 germline mutations cause 5-15% of Lynch syndrome, a midlife cancer predisposition, ...
Biallelic germline mismatch repair (MMR) gene (MLH1, MSH2, MSH6, and PMS2) mutations are an extremel...