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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...

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書目詳細資料
發表在:Intest Res
Main Authors: Yamaguchi, Satoko, Yanai, Shunichi, Nakamura, Shotaro, Kawasaki, Keisuke, Eizuka, Makoto, Uesugi, Noriyuki, Sugai, Tamotsu, Umeno, Junji, Esaki, Motohiro, Matsumoto, Takayuki
格式: Artigo
語言:Inglês
出版: Korean Association for the Study of Intestinal Diseases 2018
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6077302/
https://ncbi.nlm.nih.gov/pubmed/30090038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5217/ir.2018.16.3.393
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