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pro vyhledávání: '"S M, Curristin"'
Autor:
C, Montrose-Rafizadeh, D L, Blackmon, A, Hamosh, M M, Oliva, A L, Hawkins, S M, Curristin, C A, Griffin, V W, Yang, W B, Guggino, G R, Cutting
Publikováno v:
The Journal of biological chemistry. 267(27)
Transcriptional and post-transcriptional regulation of CFTR (cystic fibrosis transmembrane conductance regulator) gene expression was studied in HT29 cells. It is known that the abundance of CFTR mRNA increases during differentiation of pluripotent H
Cystic fibrosis (CF) is a recessive hereditary disorder, requiring both parental cystic fibrosis conductance transmembrane regulator (CFTR) genes to carry mutations for clinical disease to manifest, i.e., only 50% of normal CFTR gene expression is re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc83ba685f355b69347c73c77618ee14
https://europepmc.org/articles/PMC329931/
https://europepmc.org/articles/PMC329931/