Horst Fischer
Affiliations: | Research | Children's Hospital Oakland |
Area:
cystic fibrosis, epithelial transportGoogle:
"https://scholar.google.com/citations?hl=en&user=WyJPX7YAAAAJ"Parents
Sign in to add mentorWolfgang Clauss | grad student | FU Berlin | |
Willy Van Driessche | grad student | KU Leuven Medical School | |
Terry Machen | post-doc | UC Berkeley | |
Jonathan Widdicombe | research scientist | Children's Hospital Oakland (Neurotree) |
Collaborators
Sign in to add collaboratorMark Joseph Kurth | collaborator | UC Davis (Chemistry Tree) | |
Michael H. Nantz | collaborator | UC Davis (Chemistry Tree) |
BETA: Related publications
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Publications
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Illek B, Fischer H, Machen TE, et al. (2023) Protective role of CFTR during fungal infection of cystic fibrosis bronchial epithelial cells with . Frontiers in Cellular and Infection Microbiology. 13: 1196581 |
Sellers ZM, Illek B, Figueira MF, et al. (2017) Impaired PGE2-stimulated Cl- and HCO3- secretion contributes to cystic fibrosis airway disease. Plos One. 12: e0189894 |
Schwarzer C, Fischer H, Machen TE. (2016) Chemotaxis and Binding of Pseudomonas aeruginosa to Scratch-Wounded Human Cystic Fibrosis Airway Epithelial Cells. Plos One. 11: e0150109 |
Suzuki S, Sargent RG, Illek B, et al. (2016) TALENs Facilitate Single-step Seamless SDF Correction of F508del CFTR in Airway Epithelial Submucosal Gland Cell-derived CF-iPSCs. Molecular Therapy. Nucleic Acids. 5: e273 |
Schwagerus E, Sladek S, Buckley ST, et al. (2015) Expression and function of the epithelial sodium channel δ-subunit in human respiratory epithelial cells in vitro. Pflugers Archiv : European Journal of Physiology |
Fischer H. (2014) The G551D CFTR chloride channel spurs the development of personalized medicine. The Journal of Physiology. 592: 1907-8 |
Schwarzer C, Ravishankar B, Patanwala M, et al. (2014) Thapsigargin blocks Pseudomonas aeruginosa homoserine lactone-induced apoptosis in airway epithelia. American Journal of Physiology. Cell Physiology. 306: C844-55 |
Cho DY, Hwang PH, Illek B, et al. (2011) Acid and base secretion in freshly excised nasal tissue from cystic fibrosis patients with ΔF508 mutation International Forum of Allergy and Rhinology. 1: 123-127 |
Sweeney RM, Fischer H, McAuley DF. (2011) Nasal potential difference to detect Na+ channel dysfunction in acute lung injury. American Journal of Physiology-Lung Cellular and Molecular Physiology. 300 |
Illek B, Lei D, Fischer H, et al. (2010) Sensitivity of Chloride Efflux vs. Transepithelial Measurements in Mixed CF and Normal Airway Epithelial Cell Populations Cellular Physiology and Biochemistry. 26: 983-990 |