Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles.
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Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.Complex pathogenesis of Hirschsprung's disease in a patient with hydrocephalus, vesico-ureteral reflux and a balanced translocation t(3;17)(p12;q11).Effect of RET c.2307T>G Polymorphism on the Outcomes of Posterior Sagittal Neurectomy for Hirschsprung Disease Procedure in Indonesian Population.Induction of RET dependent and independent pro-inflammatory programs in human peripheral blood mononuclear cells from Hirschsprung patients.Effects of RET and NRG1 polymorphisms in Indonesian patients with Hirschsprung diseaseRET and PHOX2B genetic polymorphisms and Hirschsprung's disease susceptibility: a meta-analysisEffect of 3'UTR RET Variants on RET mRNA Secondary Structure and Disease Presentation in Medullary Thyroid Carcinoma.Heparin-binding epidermal growth factor-like growth factor promotes murine enteric nervous system development and enteric neural crest cell migration.Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation.Genetic and epigenetic factors affect RET gene expression in breast cancer cell lines and influence survival in patients.Advances in molecular genetics of Hirschsprung's disease.Total colonic aganglionosis and Hirschsprung's disease: a review.Allele-specific expression at the RET locus in blood and gut tissue of individuals carrying risk alleles for Hirschsprung disease.The microenvironment in the Hirschsprung's disease gut supports myenteric plexus growth.The involvement of the RET variant G691S in medullary thyroid carcinoma enlightened by a meta-analysis study.
P2860
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P2860
Haplotypes of the human RET proto-oncogene associated with Hirschsprung disease in the Italian population derive from a single ancestral combination of alleles.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Haplotypes of the human RET pr ...... estral combination of alleles.
@en
Haplotypes of the human RET pr ...... estral combination of alleles.
@nl
type
label
Haplotypes of the human RET pr ...... estral combination of alleles.
@en
Haplotypes of the human RET pr ...... estral combination of alleles.
@nl
prefLabel
Haplotypes of the human RET pr ...... estral combination of alleles.
@en
Haplotypes of the human RET pr ...... estral combination of alleles.
@nl
P2093
P2860
P1476
Haplotypes of the human RET pr ...... estral combination of alleles.
@en
P2093
F Lantieri
G Martucciello
R Ravazzolo
P2860
P356
10.1111/J.1529-8817.2005.00196.X
P407
P577
2006-01-01T00:00:00Z