Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
about
Characterisation of the human GFRalpha-3 locus and investigation of the gene in Hirschsprung diseaseGenome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's diseaseGenetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysisDifferential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liabilityThe sensitivity of activated Cys Ret mutants to glial cell line-derived neurotrophic factor is mandatory to rescue neuroectodermic cells from apoptosis.Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis.A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma.Effect of RET c.2307T>G Polymorphism on the Outcomes of Posterior Sagittal Neurectomy for Hirschsprung Disease Procedure in Indonesian Population.Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease.Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma.Multiple endocrine neoplasias type 2B and RET proto-oncogene.Association of RET codon 691 polymorphism in radiation-induced human thyroid tumours with C-cell hyperplasia in peritumoural tissue.Allele-specific expression at the RET locus in blood and gut tissue of individuals carrying risk alleles for Hirschsprung disease.Genetic analysis of RET, GFR alpha 1 and GDNF genes in Spanish families with multiple endocrine neoplasia type 2A.Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles.Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.Cys611Ser mutation in RET proto-oncogene in a kindred with medullary thyroid carcinoma and Hirschsprung's disease.Localizing a putative mutation as the major contributor to the development of sporadic Hirschsprung disease to the RET genomic sequence between the promoter region and exon 2.Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease?TheRETC620S mutation causes multiple endocrine neoplasia type 2A (MEN2A) but not Hirschsprung disease (HSCR) in a family cosegregating both phenotypesGermline sequence variant S836S in the RET proto-oncogene is associated with low level predisposition to sporadic medullary thyroid carcinoma in the Spanish population
P2860
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P2860
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
@en
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
@nl
type
label
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
@en
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
@nl
prefLabel
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
@en
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
@nl
P2093
P2860
P356
P1476
Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease.
@en
P2093
Kuhlisch E
Schackert HK
Schreiber M
P2860
P304
P356
10.1086/302618
P407
P577
1999-11-01T00:00:00Z