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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 21, 2007
CFTR protein analysis of splice site mutation 2789+5 G-AAndrea van Barneveld, Frauke Stanke, Andreas Claass, et al.
Biochimica Et Biophysica Acta|March 1, 2006
Ex vivo biochemical analysis of CFTR in human rectal biopsiesAndrea van Barneveld, Frauke Stanke, Manfred Ballmann, et al.
European Journal of Human Genetics : EJHG|October 18, 2012
CLCA4 variants determine the manifestation of the cystic fibrosis basic defect in the intestineErnst-Wolfgang Kolbe, Stephanie Tamm, Silke Hedtfeld, et al.
European Journal of Human Genetics : EJHG|April 5, 2007
Transmission ratio distortion and maternal effects confound the analysis of modulators of cystic fibrosis disease severity on 19q13Tim Becker, Silke Jansen, Stephanie Tamm, et al.
European Journal of Human Genetics : EJHG|October 10, 2013
The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cellsFrauke Stanke, Andrea van Barneveld, Silke Hedtfeld, et al.
BMC Genetics|June 26, 2007
Genetic variants of chemokine receptor CCR7 in patients with systemic lupus erythematosus, Sjogren's syndrome and systemic sclerosisDaniel Kahlmann, Ana Clara Marques Davalos-Misslitz, Lars Ohl, et al.
Molecules (Basel, Switzerland)|May 5, 2021
Effect of Alpha-1 Antitrypsin on CFTR Levels in Primary Human Airway Epithelial Cells Grown at the Air-Liquid-InterfaceFrauke Stanke, Sabina Janciauskiene, Stephanie Tamm, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Ex vivo CF diagnosis by intestinal current measurements (ICM) in small aperture, circulating Ussing chambersHugo R De Jonge, Manfred Ballmann, Henk Veeze, et al.
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