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Results: 1-25 | 26-34
Results: 1-25/34
The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentration
Authors: Konig, J Schreiber, R Voelcker, T Mall, M Kunzelmann, K
Citation: J. Konig et al., The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentration, EMBO REP, 2(11), 2001, pp. 1047-1051
CFTR: Interacting with everything?
Authors: Kunzelmann, K
Citation: K. Kunzelmann, CFTR: Interacting with everything?, NEWS PHYSL, 16, 2001, pp. 167-170
Expression and function of colonic epithelial K(v)LQT1 K+ channels
Authors: Kunzelmann, K Bleich, M Warth, R Levy-Holzman, R Garty, H Schreiber, R
Citation: K. Kunzelmann et al., Expression and function of colonic epithelial K(v)LQT1 K+ channels, CLIN EXP PH, 28(1-2), 2001, pp. 79-83
Mechanisms of the inhibition of epithelial Na+ channels by CFTR and purinergic stimulation
Authors: Kunzelmann, K Schreiber, R Boucherot, A
Citation: K. Kunzelmann et al., Mechanisms of the inhibition of epithelial Na+ channels by CFTR and purinergic stimulation, KIDNEY INT, 60(2), 2001, pp. 455-461
Properties and function of KCNQ1 K+ channels isolated from the rectal gland of Squalus acanthias
Authors: Kerst, G Beschorner, U Unsold, B von Hahn, T Schreiber, R Greger, R Gerlach, U Lang, HJ Kunzelmann, K Bleich, M
Citation: G. Kerst et al., Properties and function of KCNQ1 K+ channels isolated from the rectal gland of Squalus acanthias, PFLUG ARCH, 443(1), 2001, pp. 146-154
Cystic fibrosis and CFTR
Authors: Greger, R Schreiber, R Mall, M Wissner, A Hopf, A Briel, M Bleich, M Warth, R Kunzelmann, K
Citation: R. Greger et al., Cystic fibrosis and CFTR, PFLUG ARCH, 443, 2001, pp. S3-S7
Regulation and properties of KCNQ1 (K(v)LQT1) and impact of the cystic fibrosis transmembrane conductance regulator
Authors: Boucherot, A Schreiber, R Kunzelmann, K
Citation: A. Boucherot et al., Regulation and properties of KCNQ1 (K(v)LQT1) and impact of the cystic fibrosis transmembrane conductance regulator, J MEMBR BIO, 182(1), 2001, pp. 39-47
Cloning and function of the rat colonic epithelial K+ channel K(V)LQT1
Authors: Kunzelmann, K Hubner, M Schreiber, R Levy-Holzman, R Garty, H Bleich, M Warth, R Slavik, M von Hahn, T Greger, R
Citation: K. Kunzelmann et al., Cloning and function of the rat colonic epithelial K+ channel K(V)LQT1, J MEMBR BIO, 179(2), 2001, pp. 155-164
Control of cystic fibrosis transmembrane conductance regulator expression by BAP31
Authors: Lambert, G Becker, B Schreiber, R Boucherot, A Reth, M Kunzelmann, K
Citation: G. Lambert et al., Control of cystic fibrosis transmembrane conductance regulator expression by BAP31, J BIOL CHEM, 276(23), 2001, pp. 20340-20345
Control of the cystic fibrosis transmembrane conductance regulator by alpha G(i) and RGS proteins
Authors: Schreiber, R Kindle, P Benzing, T Walz, G Kunzelmann, K
Citation: R. Schreiber et al., Control of the cystic fibrosis transmembrane conductance regulator by alpha G(i) and RGS proteins, BIOC BIOP R, 281(4), 2001, pp. 917-923
Role of CFTR's PDZ1-binding domain, NBF1 and Cl- conductance in inhibitionof epithelial Na+ channels in Xenopus oocytes
Authors: Boucherot, A Schreiber, R Kunzelmann, K
Citation: A. Boucherot et al., Role of CFTR's PDZ1-binding domain, NBF1 and Cl- conductance in inhibitionof epithelial Na+ channels in Xenopus oocytes, BBA-BIOMEMB, 1515(1), 2001, pp. 64-71
Inhibition of amiloride-sensitive epithelial Na+ absorption by extracellular nucleotides in human normal and cystic fibrosis airways
Authors: Mall, M Wissner, A Gonska, T Calenborn, D Kuehr, J Brandis, M Kunzelmann, K
Citation: M. Mall et al., Inhibition of amiloride-sensitive epithelial Na+ absorption by extracellular nucleotides in human normal and cystic fibrosis airways, AM J RESP C, 23(6), 2000, pp. 755-761
Role of K(v)LQT1 in cyclic adenosine monophosphate-mediated Cl- secretion in human airway epithelia
Authors: Mall, M Wissner, A Schreiber, R Kuehr, J Seydewitz, HH Brandis, M Greger, R Kunzelmann, K
Citation: M. Mall et al., Role of K(v)LQT1 in cyclic adenosine monophosphate-mediated Cl- secretion in human airway epithelia, AM J RESP C, 23(3), 2000, pp. 283-289
Defects in processing and trafficking of cystic fibrosis transmembrane conductance regulator
Authors: Kunzelmann, K Nitschke, R
Citation: K. Kunzelmann et R. Nitschke, Defects in processing and trafficking of cystic fibrosis transmembrane conductance regulator, EXP NEPHROL, 8(6), 2000, pp. 332-342
A Bartter's syndrome mutation of ROMK1 exerts dominant negative effects onK+ conductance
Authors: Kunzelmann, K Hubner, M Vollmer, M Ruf, R Hildebrandt, F Greger, R Schreiber, R
Citation: K. Kunzelmann et al., A Bartter's syndrome mutation of ROMK1 exerts dominant negative effects onK+ conductance, CELL PHYS B, 10(3), 2000, pp. 117-124
Unexpected effects of pathogens on epithelial Na+ channels
Authors: Kunzelmann, K Beesley, A King, N Karupiah, G Young, J Cook, D
Citation: K. Kunzelmann et al., Unexpected effects of pathogens on epithelial Na+ channels, J KOR MED S, 15, 2000, pp. S59-S60
Transfer and expression of foreign genes in mammalian cells
Authors: Colosimo, A Goncz, KK Holmes, AR Kunzelmann, K Novelli, G Malone, RW Bennett, MJ Gruenert, DC
Citation: A. Colosimo et al., Transfer and expression of foreign genes in mammalian cells, BIOTECHNIQU, 29(2), 2000, pp. 314
Amino acid transport in podocytes
Authors: Gloy, J Reitinger, S Fischer, KG Schreiber, R Boucherot, A Kunzelmann, K Mundel, P Pavenstadt, H
Citation: J. Gloy et al., Amino acid transport in podocytes, AM J P-REN, 278(6), 2000, pp. F999-F1005
Defective cholinergic Cl- secretion and detection of K+ secretion in rectal biopsies from cystic fibrosis patients
Authors: Mall, M Wissner, A Seydewitz, HH Kuehr, J Brandis, M Greger, R Kunzelmann, K
Citation: M. Mall et al., Defective cholinergic Cl- secretion and detection of K+ secretion in rectal biopsies from cystic fibrosis patients, AM J P-GAST, 278(4), 2000, pp. G617-G624
Control of epithelial Na+ conductance by the cystic fibrosis transmembraneconductance regulator
Authors: Kunzelmann, K Schreiber, R Nitschke, R Mall, M
Citation: K. Kunzelmann et al., Control of epithelial Na+ conductance by the cystic fibrosis transmembraneconductance regulator, PFLUG ARCH, 440(2), 2000, pp. 193-201
Influenza virus inhibits amiloride-sensitive Na+ channels in respiratory epithelia
Authors: Kunzelmann, K Beesley, AH King, NJ Karupiah, G Young, JA Cook, DI
Citation: K. Kunzelmann et al., Influenza virus inhibits amiloride-sensitive Na+ channels in respiratory epithelia, P NAS US, 97(18), 2000, pp. 10282-10287
14-3-3 Interacts with regulator of G protein signaling proteins and modulates their activity
Authors: Benzing, T Yaffe, MB Arnould, T Sellin, L Schermer, B Schilling, B Schreiber, R Kunzelmann, K Leparc, GG Kim, E Walz, G
Citation: T. Benzing et al., 14-3-3 Interacts with regulator of G protein signaling proteins and modulates their activity, J BIOL CHEM, 275(36), 2000, pp. 28167-28172
Aquaporin 3 cloned from Xenopus laevis is regulated by the cystic fibrosistransmembrane conductance regulator
Authors: Schreiber, R Pavenstadt, H Greger, R Kunzelmann, K
Citation: R. Schreiber et al., Aquaporin 3 cloned from Xenopus laevis is regulated by the cystic fibrosistransmembrane conductance regulator, FEBS LETTER, 475(3), 2000, pp. 291-295
Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes
Authors: Mall, M Wissner, A Seydewitz, HH Hubner, M Kuehr, J Brandis, M Greger, R Kunzelmann, K
Citation: M. Mall et al., Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes, BR J PHARM, 130(8), 2000, pp. 1884-1892
Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotype
Authors: Beck, S Kuhr, J Schutz, VV Seydewitz, HH Brandis, M Greger, R Kunzelmann, K
Citation: S. Beck et al., Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotype, PEDIAT PULM, 27(4), 1999, pp. 251-259
Risultati: 1-25 | 26-34