Slco2a1 deficiency exacerbates experimental colitis via inflammasome activation in macrophages: a possible mechanism of chronic enteropathy associated with SLCO2A1 gene

Loss-of-function mutations in the solute carrier organic anion transporter family, member 2a1 gene (SLCO2A1), which encodes a prostaglandin (PG) transporter, have been identified as causes of chronic nonspecific multiple ulcers in the small intestine; however, the underlying mechanisms have not been...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Nakata, Rieko, Nakamura, Yoshinobu, Hosomi, Shuhei, Okuda, Hiroaki, Nishida, Yu, Sugita, Naoko, Itani, Shigehiro, Nadatani, Yuji, Otani, Koji, Tanaka, Fumio, Kamata, Noriko, Taira, Koichi, Nagami, Yasuaki, Tanigawa, Tetsuya, Watanabe, Toshio, Yamagami, Hirokazu, Nakanishi, Takeo, Fujiwara, Yasuhiro
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2020
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7078201/
https://ncbi.nlm.nih.gov/pubmed/32184453
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-61775-9
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados