Cargando…
A CARD9 Polymorphism Is Associated with Decreased Likelihood of Persistent Conjugated Hyperbilirubinemia in Intestinal Failure
Recently, genetic associations have been described in intestinal transplants. Namely, Crohn's disease susceptibility gene NOD2 polymorphisms have been reported to be more prevalent in patients with graft failure following intestinal transplantation (IT). Therefore, we sought to determine if pol...
Autores principales: | Burghardt, Karolina Maria, Avinashi, Vishal, Kosar, Christina, Xu, Wei, Wales, Paul W., Avitzur, Yaron, Muise, Aleixo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897546/ https://www.ncbi.nlm.nih.gov/pubmed/24465786 http://dx.doi.org/10.1371/journal.pone.0085915 |
Ejemplares similares
-
TTC7A: Steward of Intestinal Health
por: Jardine, Sasha, et al.
Publicado: (2018) -
Positive interactions within and between populations decrease the likelihood of evolutionary rescue
por: Goldberg, Yaron, et al.
Publicado: (2021) -
Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and Hypertriglyceridemia
por: Elkadri, Abdul, et al.
Publicado: (2015) -
Conjugated Hyperbilirubinemia in Infants: Is There Still a Role for ERCP?
por: Stovicek, Jan, et al.
Publicado: (2021) -
Conjugated hyperbilirubinemia presenting in first fourteen days in term neonates
por: Chiou, Fang Kuan, et al.
Publicado: (2017)