Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A

Những quyển sách tương tự

• The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells
  Bằng: Stanke, Frauke, et al.
  Được phát hành: (2014)
• Identification of SNPs in the cystic fibrosis interactome influencing pulmonary progression in cystic fibrosis
  Bằng: Gisler, Franziska M, et al.
  Được phát hành: (2013)
• Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1B
  Bằng: Becker, Tim, et al.
  Được phát hành: (2020)
• A regulatory SNP modifies cystic fibrosis by disrupting NFκB complex binding on FAS
  Bằng: Awah, Chidiebere U, et al.
  Được phát hành: (2015)
• An association study on contrasting cystic fibrosis endophenotypes recognizes KRT8 but not KRT18 as a modifier of cystic fibrosis disease severity and CFTR mediated residual chloride secretion
  Bằng: Stanke, Frauke, et al.
  Được phát hành: (2011)