Germline mutations in PMS2 and MLH1 in individuals with solitary loss of PMS2 expression in colorectal carcinomas from the Colon Cancer Family Registry Cohort | BMJ Open
MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study | European Journal of Human Genetics
Silencing of the DNA Mismatch Repair Gene MLH1 Induced by Hypoxic Stress in a Pathway Dependent on the Histone Demethylase LSD1: Cell Reports
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population
Meiotic Pachytene Arrest in MLH1-Deficient Mice: Cell
Mismatch repair defects and Lynch syndrome: The role of the basic scientist in the battle against cancer. - Abstract - Europe PMC
High prevalence of the MLH1 V384D germline mutation in patients with HER2-positive luminal B breast cancer | Scientific Reports
MLH1 c.199G>A, a Known Mutation for Lynch Syndrome, Is Also Associated with Sebaceous Neoplasm | International Journal of Dermatology and Venereology
The role of DNA mismatch repair in immunotherapy of human cancer
Update on Lynch syndrome genomics | Familial Cancer
Cancer risk and MLH1 gene mutations
MLH1 and MSH2 protein domains annotated with somatic non-synonymous... | Download Scientific Diagram
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome | eLife
Why a Tumor MMR Sequencing Test? - Impact Genetics - Impact Genetics
MLH1 (human mutL homolog 1)
MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years | BMC Medical Genetics | Full Text
Frontiers | A Pediatric Case of Glioblastoma Multiforme Associated With a Novel Germline p.His112CysfsTer9 Mutation in the MLH1 Gene Accompanied by a p.Arg283Cys Mutation in the TP53 Gene: A Case Report
IJMS | Free Full-Text | DNA Mismatch Repair Gene Variants in Sporadic Solid Cancers
DNA methylation changes and somatic mutations as tumorigenic events in Lynch syndrome-associated adenomas retaining mismatch repair protein expression - eBioMedicine
Gene Mutation MLH1 and Cancer Risk
Frontiers | Lynch Syndrome Germline Mutations in Breast Cancer: Next Generation Sequencing Case-Control Study of 1,263 Participants
Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree
Promoter region of the MLH1 gene. ( a ) Genomic region of MLH1 and... | Download Scientific Diagram
Expression of ectopic MLH1 protein increases the level of pre-miR-422a... | Download Scientific Diagram
PMS2 - an overview | ScienceDirect Topics
Cancer risk and MLH1 gene mutations
