Cargando…
Immunohistochemical differentiation between chronic enteropathy associated with SLCO2A1 gene and other inflammatory bowel diseases
BACKGROUND/AIMS: We recently identified recessive mutations in the solute carrier organic anion transporter family member 2A1 gene (SLCO2A1) as causative variants of chronic enteropathy associated with SLCO2A1 (CEAS). The aim of this study was to evaluate SLCO2A1 protein expression in the intestinal...
Autores principales: | Yamaguchi, Satoko, Yanai, Shunichi, Nakamura, Shotaro, Kawasaki, Keisuke, Eizuka, Makoto, Uesugi, Noriyuki, Sugai, Tamotsu, Umeno, Junji, Esaki, Motohiro, Matsumoto, Takayuki |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Association for the Study of Intestinal Diseases
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077302/ https://www.ncbi.nlm.nih.gov/pubmed/30090038 http://dx.doi.org/10.5217/ir.2018.16.3.393 |
Ejemplares similares
-
Distinction between Chronic Enteropathy Associated with the SLCO2A1 Gene and Crohn’s Disease
por: Yanai, Shunichi, et al.
Publicado: (2019) -
SLCO2A1 gene is the causal gene for both primary hypertrophic osteoarthropathy and hereditary chronic enteropathy
por: Umeno, Junji, et al.
Publicado: (2021) -
Association between white opaque substance under magnifying colonoscopy and lipid droplets in colorectal epithelial neoplasms
por: Kawasaki, Keisuke, et al.
Publicado: (2017) -
Chronic Enteropathy Associated with SLCO2A1 with Pachydermoperiostosis
por: Tsuzuki, Yoshikazu, et al.
Publicado: (2020) -
A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter
por: Umeno, Junji, et al.
Publicado: (2015)