Karl Kunzelmann

CFTR: interacting with everything?

K. Kunzelmann, Karl Kunzelmann, 2001, News in physiological sciences : an international journal of physiology produced jointly by the International Union of Physiological Sciences and the American Physiological Society.

Cl− transport by cystic fibrosis transmembrane conductance regulator (CFTR) contributes to the inhibition of epithelial Na+ channels (ENaCs) in Xenopus oocytes co‐expressing CFTR and ENaC

K. Kunzelmann, R. Greger, M. Briel, 1998, The Journal of physiology.

ATP-induced Ca2+ signals in bronchial epithelial cells

G. Verleden, L. Missiaen, J. Parys, 1998, Pflügers Archiv.

Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)

S. Lalani, K. Chayama, M. Vikkula, 1999, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Culture-dependent expression of Na+ conductances in airway epithelial cells

K. Kunzelmann, D. Gruenert, R. Greger, 1996, Pflügers Archiv.

No evidence for inhibition of ENaC through CFTR-mediated release of ATP.

R. Schreiber, K. Kunzelmann, M. Mall, 2002, Biochimica et biophysica acta.

Defective cholinergic Cl(-) secretion and detection of K(+) secretion in rectal biopsies from cystic fibrosis patients.

A. Wissner, K. Kunzelmann, R. Greger, 2000, American journal of physiology. Gastrointestinal and liver physiology.

Targeted replacement of normal and mutant CFTR sequences in human airway epithelial cells using DNA fragments.

K. Kunzelmann, K. Goncz, D. Gruenert, 1998, Human molecular genetics.

CFTR-mediated inhibition of epithelial Na+ conductance in human colon is defective in cystic fibrosis.

K. Kunzelmann, R. Greger, M. Bleich, 1999, American journal of physiology. Gastrointestinal and liver physiology.

Inhibition of amiloride-sensitive epithelial Na(+) absorption by extracellular nucleotides in human normal and cystic fibrosis airways.

A. Wissner, K. Kunzelmann, T. Gonska, 2000, American journal of respiratory cell and molecular biology.

Epithelial cell specific properties and genetic complementation in a ΔF508 cystic fibrosis nasal polyp cell line

K. Kunzelmann, D. Gruenert, L. C. Escobar, 1995, In Vitro Cellular & Developmental Biology - Animal.

Benzbromarone as adjuvant therapy for cystic fibrosis lung disease: a pilot clinical trial.

F. Friedrich, L. Petry, Amanda da Silva Meneses, 2024, Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia.

Inhibition of epithelial Na+ currents by intracellular domains of the cystic fibrosis transmembrane conductance regulator

J. Riordan, G. Kiser, R. Schreiber, 1997, FEBS letters.