NOD2 gene polymorphism rs2066844 associates with need for combined liver-intestine transplantation in children with short-gut syndrome.
about
Nucleotide oligomerization domain 2 polymorphisms in patients with intestinal failure.Recipient's genetic R702W NOD2 variant is associated with an increased risk of bacterial infections after orthotopic liver transplantation.A non-interventional study of the genetic polymorphisms of NOD2 associated with increased mortality in non-alcoholic liver transplant patients.Increased expression of peripheral blood leukocyte genes implicate CD14+ tissue macrophages in cellular intestine allograft rejection.Impact of Single Nucleotide Polymorphisms (SNPs) on Immunosuppressive Therapy in Lung Transplantation.Crohn disease risk prediction-Best practices and pitfalls with exome data.Collecting Biospecimens From an Internet-Based Prospective Cohort Study of Inflammatory Bowel Disease (CCFA Partners): A Feasibility Study.A CARD9 polymorphism is associated with decreased likelihood of persistent conjugated hyperbilirubinemia in intestinal failure.Intestinal Transplant Inflammation: the Third Inflammatory Bowel Disease.Management of Crohn's Disease in the New Era of Gut Rehabilitation and Intestinal Transplantation.Polymorphisms in the Mannose-Binding Lectin Gene are Associated with Defective Mannose-Binding Lectin Functional Activity in Crohn's Disease PatientsNOD2 and pouch complications in UC patients: old-world clinical dogmas give way to biological definitions.The current therapeutic options for Crohn's disease: from medical therapy to intestinal transplantation.Current treatment paradigms in pediatric short bowel syndrome.Pre-emptive Intestinal Transplant: The Surgeon's Point of View.Feasibility of salivary DNA collection in a population-based case-control study: a pilot study of pediatric Crohn's disease.Abnormal CX3CR1⁺ lamina propria myeloid cells from intestinal transplant recipients with NOD2 mutations.Visceral transplantation in patients with intestinal-failure associated liver disease: Evolving indications, graft selection, and outcomes.
P2860
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P2860
NOD2 gene polymorphism rs2066844 associates with need for combined liver-intestine transplantation in children with short-gut syndrome.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
NOD2 gene polymorphism rs20668 ...... ldren with short-gut syndrome.
@en
type
label
NOD2 gene polymorphism rs20668 ...... ldren with short-gut syndrome.
@en
prefLabel
NOD2 gene polymorphism rs20668 ...... ldren with short-gut syndrome.
@en
P2093
P2860
P50
P356
P1476
NOD2 gene polymorphism rs20668 ...... ldren with short-gut syndrome.
@en
P2093
Chethan Ashokkumar
Feras Alissa
Geoffrey J Bond
Hakon Hakonarson
Jeffrey Rudolph
Kareem Abu-Elmagd
Kyle A Soltys
Marcus Rivera
Mylarappa Ningappa
P2860
P304
P356
10.1038/AJG.2010.322
P407
P577
2010-10-19T00:00:00Z