Pages that link to "Q37385768"

The following pages link to Comprehensive molecular analysis of mismatch repair gene defects in suspected Lynch syndrome (hereditary nonpolyposis colorectal cancer) cases (Q37385768):

Displaying 20 items.

• Modulation of mismatch repair and genomic stability by miR-155 (Q24612859) (← links)
• Inter-individual variation in DNA repair capacity: a need for multi-pathway functional assays to promote translational DNA repair research (Q28388726) (← links)
• Down-regulation of DNA mismatch repair enhances initiation and growth of neuroblastoma and brain tumour multicellular spheroids (Q28478209) (← links)
• Lynch syndrome among gynecologic oncology patients meeting Bethesda guidelines for screening (Q33653935) (← links)
• Clinical relevance of microsatellite instability in colorectal cancer (Q33990921) (← links)
• Prevalence of Alterations in DNA Mismatch Repair Genes in Patients With Young-Onset Colorectal Cancer (Q34677794) (← links)
• Integrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms (Q35053925) (← links)
• Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results (Q35925275) (← links)
• Comparison of the clinical prediction model PREMM(1,2,6) and molecular testing for the systematic identification of Lynch syndrome in colorectal cancer (Q36315747) (← links)
• MLH1 methylation screening is effective in identifying epimutation carriers (Q36403949) (← links)
• Mammalian Exo1 encodes both structural and catalytic functions that play distinct roles in essential biological processes (Q36991032) (← links)
• De novo constitutional MLH1 epimutations confer early-onset colorectal cancer in two new sporadic Lynch syndrome cases, with derivation of the epimutation on the paternal allele in one (Q37224356) (← links)
• A Novel Chemotherapeutic Agent to Treat Tumors with DNA Mismatch Repair Deficiencies (Q37276892) (← links)
• Molecular and prognostic heterogeneity of microsatellite-unstable colorectal cancer. (Q37708015) (← links)
• Preparing pathology for personalized medicine: possibilities for improvement of the pre-analytical phase. (Q37863222) (← links)
• Inappropriate gene expression in human cancer and its far-reaching biological and clinical significance (Q37964451) (← links)
• Towards the lean lab: the industry challenge (Q38337903) (← links)
• Evidence for ATP-dependent structural rearrangement of nuclease catalytic site in DNA mismatch repair endonuclease MutL. (Q39712247) (← links)
• A systematic review of test accuracy studies evaluating molecular micro-satellite instability testing for the detection of individuals with lynch syndrome. (Q47155477) (← links)
• Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation (Q60023148) (← links)