Genotype to phenotype: analyzing the effects of inherited mutations in colorectal cancer families.
about
Current status of familial gastrointestinal polyposis syndromesFamilial colon cancer syndromes: an update of a rapidly evolving fieldThe genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.Molecular genetics of supernumerary tooth formation.Nuclear signaling from cadherin adhesion complexesAnticipation in lynch syndrome: where we are where we goThe predicted truncation from a cancer-associated variant of the MSH2 initiation codon alters activity of the MSH2-MSH6 mismatch repair complexENIGMA--evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genesTALEN-mediated apc mutation in Xenopus tropicalis phenocopies familial adenomatous polyposis.Genetic screens to identify pathogenic gene variants in the common cancer predisposition Lynch syndrome.Extra nuchal-type fibroma associated with elastosis, traumatic neuroma, a rare APC gene missense mutation, and a very rare MUTYH gene polymorphism: a case report and review of the literature*.Molecular classification of colorectal carcinomas: the genotype-to-phenotype relation.Multiple factors insulate Msh2-Msh6 mismatch repair activity from defects in Msh2 domain I.Tumor suppressor genes in familial adenomatous polyposisDetermining the functional significance of mismatch repair gene missense variants using biochemical and cellular assays.Distinct requirements within the Msh3 nucleotide binding pocket for mismatch and double-strand break repair.Inactivation of MSH3 by promoter methylation correlates with primary tumor stage in nasopharyngeal carcinoma.Modifier-concept of colorectal carcinogenesis: lipidomics as a technical tool in pathway analysis.The Changing Landscape of Lynch Syndrome due to PMS2 Mutations.Clinical Impact of Mismatch Repair Protein Testing on Outcome of Early Staged Colorectal Carcinomas.A rapid and cell-free assay to test the activity of lynch syndrome-associated MSH2 and MSH6 missense variants.Detection of a heterozygous germline APC mutation in a three-generation family with familial adenomatous polyposis using targeted massive parallel sequencing in Vietnam
P2860
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P2860
Genotype to phenotype: analyzing the effects of inherited mutations in colorectal cancer families.
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genotype to phenotype: analyzi ...... in colorectal cancer families.
@ast
Genotype to phenotype: analyzi ...... in colorectal cancer families.
@en
type
label
Genotype to phenotype: analyzi ...... in colorectal cancer families.
@ast
Genotype to phenotype: analyzi ...... in colorectal cancer families.
@en
prefLabel
Genotype to phenotype: analyzi ...... in colorectal cancer families.
@ast
Genotype to phenotype: analyzi ...... in colorectal cancer families.
@en
P2860
P1433
P1476
Genotype to phenotype: analyzi ...... in colorectal cancer families.
@en
P2093
Christopher D Heinen
P2860
P356
10.1016/J.MRFMMM.2009.09.004
P407
P577
2009-09-17T00:00:00Z