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

Samankaltaisia teoksia

• Initial interrogation, confirmation and fine mapping of modifying genes: STAT3, IL1B and IFNGR1 determine cystic fibrosis disease manifestation
  Tekijä: Labenski, Heike, et al.
  Julkaistu: (2011)
• CLCA4 variants determine the manifestation of the cystic fibrosis basic defect in the intestine
  Tekijä: Kolbe, Ernst-Wolfgang, et al.
  Julkaistu: (2013)
• A regulatory SNP modifies cystic fibrosis by disrupting NFκB complex binding on FAS
  Tekijä: Awah, Chidiebere U, et al.
  Julkaistu: (2015)
• Differential decay of parent-of-origin-specific genomic sharing in cystic fibrosis-affected sib pairs maps a paternally imprinted locus to 7q34
  Tekijä: Stanke, Frauke, et al.
  Julkaistu: (2010)
• The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cells
  Tekijä: Stanke, Frauke, et al.
  Julkaistu: (2014)