Expression of ectopic MLH1 protein increases the level of pre-miR-422a... | Download Scientific Diagram
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome | eLife
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
Promoter region of the MLH1 gene. ( a ) Genomic region of MLH1 and... | Download Scientific Diagram
Cancers | Free Full-Text | Lynch-like Syndrome: Potential Mechanisms and Management
Schematic representation of partial LOH in the MLH1 gene. A: The... | Download Scientific Diagram
Silencing of the DNA Mismatch Repair Gene MLH1 Induced by Hypoxic Stress in a Pathway Dependent on the Histone Demethylase LSD1: Cell Reports
Genetics, diagnosis and treatment of Lynch syndrome: Old lessons and current challenges (Review)
MLH1 - Wikipedia
MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years | BMC Medical Genetics | Full Text
Gene Mutation MLH1 and Cancer Risk
Meiotic Pachytene Arrest in MLH1-Deficient Mice: Cell
MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years | BMC Medical Genetics | Full Text
High prevalence of the MLH1 V384D germline mutation in patients with HER2-positive luminal B breast cancer | Scientific Reports
Defective DNA mismatch repair and MLH1, MSH2 mutations in endometrial cancers
Cancer risk and MLH1 gene mutations
Oncotarget Does breast carcinoma belong to the Lynch syndrome tumor spectrum? | Oncotarget
Study reveals somatic mutation profile of colorectal tumor with simultaneous APC and MLH1 germline mutations
Why a Tumor MMR Sequencing Test? - Impact Genetics - Impact Genetics
MLH1 - an overview | ScienceDirect Topics
DNA methylation changes and somatic mutations as tumorigenic events in Lynch syndrome-associated adenomas retaining mismatch repair protein expression - eBioMedicine
MLH1 (human mutL homolog 1)
Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree
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
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome | eLife
