Genetic conditions associated with intestinal juvenile polyps.
about
Germline PTEN mutations are rare and highly penetrantHereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood.Monogenic and chromosomal causes of isolated speech and language impairment.A review of juvenile polyposis syndrome.Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes.Mutation analysis of 13 driver genes of colorectal cancer-related pathways in Taiwanese patientsSMAD4 mutations found in unselected HHT patients.Postnatal ablation of osteoblast Smad4 enhances proliferative responses to canonical Wnt signaling through interactions with β-catenin.Colorectal polyps: sporadic and syndromic.The LKB1 complex-AMPK pathway: the tree that hides the forestHereditary colorectal cancer syndromes and genetic testing.Aggressive juvenile polyposis in children with chromosome 10q23 deletion.Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposis.Deletion of PTEN and BMPR1A on chromosome 10q23 is not always associated with juvenile polyposis of infancy.Matrix metalloproteinases in the urine and tissue of patients with juvenile polyps: potential biomarkers for the presence of polyps.Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function.The classification of intestinal polyposis.Epithelial Pten is dispensable for intestinal homeostasis but suppresses adenoma development and progression after Apc mutation.Mosaic partial deletion of the PTEN gene in a patient with Cowden syndrome.Germline bone morphogenesis protein receptor 1A mutation causes colorectal tumorigenesis in hereditary mixed polyposis syndrome.Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutationHamartomatous polyposis syndromes
P2860
Q33722586-C9C4A39E-01A5-48BB-B9A0-8DC458BE943BQ33916338-38C5052A-08E7-474D-8316-3C57D9B5AA8DQ34483411-D16ABAB0-0781-496D-8395-62A664B7C4CAQ34562065-093A6F68-1E71-4993-8F5F-AC4E1D293E4EQ34658313-E0CFA9A5-6F6E-44EB-B45B-4CC762AD53C0Q36526325-81E3FC25-993E-4A4A-B4CC-E902B49BD482Q36927105-D2562676-8478-448B-BD3F-3B4584834E14Q37386131-96061842-9596-4541-8710-51A99AA3842CQ37756369-F6FA6C81-225D-468E-8B6C-0F8C27831399Q37886809-0314F57F-4A93-4D44-A464-56367DBC0F94Q38224227-3890391E-271C-41E9-AA65-D74163A1CA20Q39883895-CE042A7E-4B07-41F6-9A51-4DD37559ED3EQ42844340-3C1BB056-04C4-4747-8455-21CC5D5453A7Q43085621-5C409FB0-461F-4FBC-A8F0-37373B2240A7Q43086863-D0716ED6-1737-47D0-957F-1E7493B1113AQ43146864-D366B305-D0C5-487B-8E93-127E55C4609EQ45162633-FD49DC25-C7D7-4AAD-82CC-0029F513B9E3Q46244569-373F499E-6239-4FBD-9127-A9445E1CED16Q51155217-D04076A0-27A7-4CD8-98CB-C7A975A9E9C8Q54398293-4FD3CFBD-C460-4E34-976E-B626F446CECFQ57735460-E822DCD8-40D3-42E5-85D1-4C1476F718E1Q59303125-C315DFB1-5D4D-45F2-BD5E-C23EE3E2CA47
P2860
Genetic conditions associated with intestinal juvenile polyps.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Genetic conditions associated with intestinal juvenile polyps.
@ast
Genetic conditions associated with intestinal juvenile polyps.
@en
type
label
Genetic conditions associated with intestinal juvenile polyps.
@ast
Genetic conditions associated with intestinal juvenile polyps.
@en
prefLabel
Genetic conditions associated with intestinal juvenile polyps.
@ast
Genetic conditions associated with intestinal juvenile polyps.
@en
P2860
P356
P1476
Genetic conditions associated with intestinal juvenile polyps.
@en
P2093
Anders Merg
James R Howe
P2860
P356
10.1002/AJMG.C.30020
P577
2004-08-01T00:00:00Z