about
Familial adenomatous polyposisElevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2Secreted Frizzled-related proteins inhibit motility and promote growth of human malignant glioma cellsFamilial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 gene.Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatinMolecular subgroups of medulloblastoma: the current consensusThe miR-17~92 cluster collaborates with the Sonic Hedgehog pathway in medulloblastomaThe links between axin and carcinogenesisNeurology and the skin.Uroplakin IIIb, a urothelial differentiation marker, dimerizes with uroplakin Ib as an early step of urothelial plaque assemblyRole of APC and DNA mismatch repair genes in the development of colorectal cancers.Microtubule plus-end tracking proteins in neuronal developmentMolecular approach to genetic and epigenetic pathogenesis of early-onset colorectal cancerCurrent Understanding on EGFR and Wnt/β-Catenin Signaling in Glioma and Their Possible CrosstalkMedulloblastoma-biology and microenvironment: a reviewPMS2 monoallelic mutation carriers: the known unknownTurcot syndrome confirmed with molecular analysisParental exposure to pesticides and childhood brain cancer: U.S. Atlantic coast childhood brain cancer studyMSH2 deficient mice are viable and susceptible to lymphoid tumoursColocalization of APC and PSD-95 in the nerve fiber as well as in the post-synapse of matured neurons.Advances in the genetics of glioblastoma: are we reaching critical mass?Neurodevelopment in schizophrenia: the role of the wnt pathways.Inherited predisposition to glioma.Low frequency of replication errors in primary nervous system tumours.Targeted deletion of the C-terminus of the mouse adenomatous polyposis coli tumor suppressor results in neurologic phenotypes related to schizophrenia.Colorectal cancer: molecules and populations.Colorectal cancer in adolescents.Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes.Familial adenomatous polyposis in a 5 year old child: a clinical, pathological, and molecular genetic studyGenetic susceptibility to non-polyposis colorectal cancer.A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype.Molecular heterogeneity in medulloblastoma with implications for differing tumor biology.The adenomatous polyposis coli protein.Loss of the mismatch repair protein MSH6 in human glioblastomas is associated with tumor progression during temozolomide treatment.Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene.Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome.Lower gastrointestinal tract cancer predisposition syndromesDNA mismatch repair genes and colorectal cancer.Wnt/β-catenin signalling is active in a highly dynamic pattern during development of the mouse cerebellum.
P2860
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P2860
description
1995 nî lūn-bûn
@nan
1995 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի մարտին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
The molecular basis of Turcot's syndrome.
@ast
The molecular basis of Turcot's syndrome.
@en
The molecular basis of Turcot's syndrome.
@nl
type
label
The molecular basis of Turcot's syndrome.
@ast
The molecular basis of Turcot's syndrome.
@en
The molecular basis of Turcot's syndrome.
@nl
prefLabel
The molecular basis of Turcot's syndrome.
@ast
The molecular basis of Turcot's syndrome.
@en
The molecular basis of Turcot's syndrome.
@nl
P2093
P1476
The molecular basis of Turcot's syndrome.
@en
P2093
Hamilton SR
Papadopoulos N
Parsons RE
P304
P356
10.1056/NEJM199503303321302
P407
P577
1995-03-01T00:00:00Z