Cargando…
HOXB5 Cooperates with NKX2-1 in the Transcription of Human RET
The enteric nervous system (ENS) regulates peristaltic movement of the gut, and abnormal ENS causes Hirschsprung's disease (HSCR) in newborns. HSCR is a congenital complex genetic disorder characterised by a lack of enteric ganglia along a variable length of the intestine. The receptor tyrosine...
Autores principales: | Zhu, Jiang, Garcia-Barcelo, Maria-Mercedes, Tam, Paul Kwong Hang, Lui, Vincent Chi Hang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3108997/ https://www.ncbi.nlm.nih.gov/pubmed/21677782 http://dx.doi.org/10.1371/journal.pone.0020815 |
Ejemplares similares
-
Pathogenesis of Choledochal Cyst: Insights from Genomics and Transcriptomics
por: Ye, Yongqin, et al.
Publicado: (2022) -
RET Mutational Spectrum in Hirschsprung Disease: Evaluation of 601 Chinese Patients
por: So, Man-Ting, et al.
Publicado: (2011) -
Pathological role of methionine in the initiation and progression of biliary atresia
por: Jiachen, Zheng, et al.
Publicado: (2023) -
Whole genome sequencing reveals epistasis effects within RET for Hirschsprung disease
por: Wang, Yanbing, et al.
Publicado: (2022) -
Gene Network Analysis of Candidate Loci for Human Anorectal Malformations
por: Wong, Emily H. M., et al.
Publicado: (2013)