BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency.
about
Lynch syndrome and Lynch syndrome mimics: The growing complex landscape of hereditary colon cancerGermline mutation of RPS20, encoding a ribosomal protein, causes predisposition to hereditary nonpolyposis colorectal carcinoma without DNA mismatch repair deficiencyEarly-onset colorectal cancer: a sporadic or inherited disease?Germline Mutations in the Polyposis-Associated Genes BMPR1A, SMAD4, PTEN, MUTYH and GREM1 Are Not Common in Individuals with Serrated Polyposis Syndrome.Integrative analysis of hereditary nonpolyposis colorectal cancer: the contribution of allele-specific expression and other assays to diagnostic algorithms.Exome sequencing in one family with gastric- and rectal cancer.Update on Lynch syndrome genomics.Evolving approach and clinical significance of detecting DNA mismatch repair deficiency in colorectal carcinoma.New genes emerging for colorectal cancer predisposition.Expanding the genotype-phenotype spectrum in hereditary colorectal cancer by gene panel testing.Familial colorectal cancer type X: genetic profiles and phenotypic features.Signaling Receptors for TGF-β Family Members.Recent discoveries in the molecular genetics of Lynch syndrome.Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancerFamilial Colorectal Cancer Type X in Central Iran: A New Clinicopathologic Description.Correspondence: Reply to 'SEMA4A variation and risk of colorectal cancer'.Screening of BMPR1a for pathogenic mutations in familial colorectal cancer type X families from Newfoundland.Candidate predisposing germline copy number variants in early onset colorectal cancer patients.Familial Colorectal Cancer Type X.Two novel colorectal cancer risk loci in the region on chromosome 9q22.32.BMPR1A mutations in early-onset colorectal cancer with mismatch repair proficiency.The TGFβ-signaling pathway and colorectal cancer: associations between dysregulated genes and miRNAs.
P2860
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P2860
BMPR1A mutations in hereditary nonpolyposis colorectal cancer without mismatch repair deficiency.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
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2011年學術文章
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2011年學術文章
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name
BMPR1A mutations in hereditary ...... ut mismatch repair deficiency.
@en
BMPR1A mutations in hereditary ...... ut mismatch repair deficiency.
@nl
type
label
BMPR1A mutations in hereditary ...... ut mismatch repair deficiency.
@en
BMPR1A mutations in hereditary ...... ut mismatch repair deficiency.
@nl
prefLabel
BMPR1A mutations in hereditary ...... ut mismatch repair deficiency.
@en
BMPR1A mutations in hereditary ...... ut mismatch repair deficiency.
@nl
P2093
P50
P1433
P1476
BMPR1A mutations in hereditary ...... ut mismatch repair deficiency.
@en
P2093
Ari Ristimäki
Heikki J Järvinen
Maarit Lappalainen
Päivi Lahermo
Wael M Abdel-Rahman
P356
10.1053/J.GASTRO.2011.03.063
P407
P577
2011-06-01T00:00:00Z