 |
 |
|
|
|
|
Kunzelmann K and Mall M.
Cystic Fibrosis.
Encyclopedic Reference of Molecular Mechanisms of Disease. Springer, Berlin 1: 1224 (2009).
Koehl GE, Spitzner M, Ousingsawat J, Schreiber R, Geissler EK, and Kunzelmann K.
Rapamycin Inhibits Oncogenic Intestinal Ion Channels and Neoplasia in APCMin/+ Mice.
Clin.Cancer Res (in press).
Treharne KJ, Xu Z, Chen J-H, Best OG, Cassidy D, Gruenert DC, Hegyi P, Gray L, Sheppard D, Kunzelmann K, and Mehta A.
Inhibition of protein kinase CK2 closes the CFTR Cl- channel, but has no effect on the cystic fibrosis mutant F508-CFTR.
J Physiol (Lond.) (in press).
Rotte A, Bhandaru M, Föller M, Biswas R, Mack AF, Friedrich B, Rexhepaj R, Nasir O, Ackermann TF, Boini KM, Kunzelmann K, Behrens J, Lang F.
APC sensitive gastric acid secretion.
Cell Physiol Biochem. 2009;23(1-3):133-42.
[Pubmed]
Milenkovic VM, Soria RB, Aldehni F, Schreiber R, Kunzelmann K.
Functional assembly and purinergic activation of bestrophins.
Pflugers Arch. 2009 Jun;458(2):431-41.
[Pubmed]
Kongsuphol P, Cassidy D, Hieke B, Treharne KJ, Schreiber R, Mehta A, Kunzelmann K.
Mechanistic insight into control of CFTR by AMPK.
J Biol Chem. 2009 Feb 27;284(9):5645-53.
[Pubmed]
Faria D, Schreiber R, Kunzelmann K.
CFTR is activated through stimulation of purinergic P2Y2 receptors.
Pflugers Arch. 2009 Apr;457(6):1373-80.
[Pubmed]
Almaça J, Kongsuphol P, Hieke B, Ousingsawat J, Viollet B, Schreiber R, Amaral MD, Kunzelmann K.
AMPK controls epithelial Na(+) channels through Nedd4-2 and causes an epithelial phenotype when mutated.
Pflugers Arch. 2009 Aug;458(4):713-21.
[Pubmed]
Aldehni F, Spitzner M, Martins JR, Barro-Soria R, Schreiber R, Kunzelmann K.
Bestrophin 1 promotes epithelial-to-mesenchymal transition of renal collecting duct cells.
J Am Soc Nephrol. 2009 Jul;20(7):1556-64.
[Pubmed]
Kongsuphol P, Hieke B, Ousingsawat J, Almaca J, Viollet B, Schreiber R, Kunzelmann K.
Regulation of Cl(-) secretion by AMPK in vivo.
Pflugers Arch. 2009 Mar;457(5):1071-8.
[Pubmed]
Spitzner M, Martins JR, Soria RB, Ousingsawat J, Scheidt K, Schreiber R, Kunzelmann K.
Eag1 and Bestrophin 1 are up-regulated in fast-growing colonic cancer cells.
J Biol Chem. 2008 Mar 21;283(12):7421-8.
[Pubmed]
Schreiber R, Castrop H, Kunzelmann K.
Allergen-induced airway hyperresponsiveness is absent in ecto-5'-nucleotidase (CD73)-deficient mice.
Pflugers Arch. 2008 Nov;457(2):431-40.
[Pubmed]
Ousingsawat J, Spitzner M, Schreiber R, Kunzelmann K.
Upregulation of colonic ion channels in APC ( Min/+ ) mice.
Pflugers Arch. 2008 Aug;456(5):847-55.
[Pubmed]
Milenkovic VM, Langmann T, Schreiber R, Kunzelmann K, Weber BH.
Molecular evolution and functional divergence of the bestrophin protein family.
BMC Evol Biol. 2008 Feb 28;8:72.
[Pubmed]
Illek B, Maurisse R, Wahler L, Kunzelmann K, Fischer H, Gruenert DC.
Cl transport in complemented CF bronchial epithelial cells correlates with CFTR mRNA expression levels.
Cell Physiol Biochem. 2008;22(1-4):57-68.
[Pubmed]
Hennig B, Schultheiss G, Kunzelmann K, Diener M.
Ca2+-induced Cl- efflux at rat distal colonic epithelium.
J Membr Biol. 2008 Jan;221(2):61-72.
[Pubmed]
Hennig B, Schultheiss G, Kunzelmann K, Diener M.
Ca2+-induced Cl- efflux at rat distal colonic epithelium.
J Membr Biol. 2008 Jan;221(2):61-72.
[Pubmed]
Grangeia A, Barro-Soria R, Carvalho F, Damas AM, Maurício AC, Kunzelmann K, Barros A, Sousa M.
Molecular and functional characterization of CBAVD-causing mutations located in CFTR nucleotide-binding domains.
Cell Physiol Biochem. 2008;22(1-4):79-92.
[Pubmed]
Barro-Soria R, Schreiber R, Kunzelmann K.
Bestrophin 1 and 2 are components of the Ca(2+) activated Cl(-) conductance in mouse airways.
Biochim Biophys Acta. 2008 Oct;1783(10):1993-2000.
[Pubmed]
Bachhuber T, Almaça J, Aldehni F, Mehta A, Amaral MD, Schreiber R, Kunzelmann K.
Regulation of the epithelial Na+ channel by the protein kinase CK2.
J Biol Chem. 2008 May 9;283(19):13225-32.
[Pubmed]
Amaral MD, Kunzelmann K.
Molecular targeting of CFTR as a therapeutic approach to cystic fibrosis.
Trends Pharmacol Sci. 2007 Jul;28(7):334-41.
[Pubmed]
Kunzelmann K, Milenkovic VM, Spitzner M, Soria RB, Schreiber R.
Calcium-dependent chloride conductance in epithelia: is there a contribution by Bestrophin?
Pflugers Arch. 2007 Sep;454(6):879-89.
[Pubmed]
Puntheeranurak S, Schreiber R, Spitzner M, Ousingsawat J, Krishnamra N, Kunzelmann K.
Control of ion transport in mouse proximal and distal colon by prolactin.
Cell Physiol Biochem. 2007;19(1-4):77-88.
[Pubmed]
Ousingsawat J, Spitzner M, Puntheeranurak S, Terracciano L, Tornillo L, Bubendorf L, Kunzelmann K, Schreiber R.
Expression of voltage-gated potassium channels in human and mouse colonic carcinoma.
Clin Cancer Res. 2007 Feb 1;13(3):824-31.
[Pubmed]
Kunzelmann K, Sun J, Meanger J, King NJ, Cook DI.
Inhibition of airway Na+ transport by respiratory syncytial virus.
J Virol. 2007 Apr;81(8):3714-20.
[Pubmed]
Sousa M, Ousingsawat J, Seitz R, Puntheeranurak S, Regalado A, Schmidt A, Grego T, Jansakul C, Amaral MD, Schreiber R, Kunzelmann K.
An extract from the medicinal plant Phyllanthus acidus and its isolated compounds induce airway chloride secretion: A potential treatment for cystic fibrosis.
Mol Pharmacol. 2007 Jan;71(1):366-76.
[Pubmed]
Spitzner M, Ousingsawat J, Scheidt K, Kunzelmann K, Schreiber R.
Voltage-gated K+ channels support proliferation of colonic carcinoma cells.
FASEB J. 2007 Jan;21(1):35-44.
[Pubmed]
Bloch M, Ousingsawat J, Simon R, Schraml P, Gasser TC, Mihatsch MJ, Kunzelmann K, Bubendorf L.
KCNMA1 gene amplification promotes tumor cell proliferation in human prostate cancer.
Oncogene. 2007 Apr 12;26(17):2525-34.
[Pubmed]
Amaral,M.D. and K.Kunzelmann.
Molecular Targeting of CFTR as a Therapeutic Approach to Cystic Fibrosis.
Trends Pharmacol Sci.(in press).
Crawford,R.M., K.J.Treharne, M.Foretz, B.Viollet, B.Hieke, K.Kunzelmann, R.Schreiber, and A.Mehta.
Identification of two novel in vivo AMPK targets in the nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator.
FASEB J (in press).
Kunzelmann,K., V.M.Milenkovic, M.Spitzner, R.Barro Soria, and R.Schreiber.
Calcium dependent chloride conductance in epithelia: Is there a contribution by Bestrophin?
Pflügers Arch (in press).
Kunzelmann,K., J.Meanger, N.J.King, and D.I.Cook.
Inhibition of airway Na+ transport by respiratory syncytial virus.
J Virology (in press).
Kunzelmann,K. and M.Mall.
Cystic Fibrosis. Encyclopedic Reference of Molecular Mechanisms of Disease.
Springer (in press)
Ousingsawat,J., M.Spitzner, S.Puntheeranurak, L.Terracciano, L.Tornillo, L.Bubendorf, K.Kunzelmann, and R.Schreiber.
Expression of voltage gated potassium channels in human and mouse colonic carcinoma.
Clinical Cancer Research 13:824-831.
Puntheeranurak,S., R.Schreiber, K.Kunzelmann, and N.Krishnamra.
Control of ion transport in mouse proximal and distal colon by prolactin.
Cell Physiol Biochem 19:77-88.
Spitzner,M., J.Ousingsawat, K.Scheidt, K.Kunzelmann, and R.Schreiber.
Role of voltage gated K+ channels for proliferation of colonic cancer cells.
FASEB J 21:35-44.
Treharne,K.J., R.M.Crawford, O.G.Best, E.A.Schulte, J.-H.Chen, D.C.Gruenert, S.M.Wilson, K.Kunzelmann, D.N.Sheppard, and A.Mehta.
Protein kinase CK2, CFTR and the deltaF508 mutation - deltaF508 deletion disrupts a kinase binding site.
J Biol Chem 282:10804-10813.
Barro Soria,R., M.Spitzner, R.Schreiber, and K.Kunzelmann.
Bestrophin 1 enables Ca2+ activated Cl- conductance in epithelia.
J Biol Chem (in press).
Kunzelmann, K., Spitzner M., Ousingsawat J., Martins J. R. and Schreiber R.
Expression von Ionenkanälen beim Kolonkarzinom: Neue diagnostische und therapeutische Möglichkeiten?
Onkologie heute 2, 18-21 (2006).
Dawson PA, Pirlo KJ, Steane SE, Kunzelmann K, Chien YJ, Markovich D.
Molecular cloning and characterization of the mouse Na+ sulfate cotransporter gene (Slc13a4): Structure and expression.
Genes Genet Syst. 2006 Aug;81(4):265-72.
[Pubmed]
Stumpf A, Almaca J, Kunzelmann K, Wenners-Epping K, Huber SM, Haberle J, Falk S, Duebbers A, Walte M, Oberleithner H, Schillers H.
IADS, a decomposition product of DIDS activates a cation conductance in Xenopus oocytes and human erythrocytes: new compound for the diagnosis of cystic fibrosis.
Cell Physiol Biochem. 2006;18(4-5):243-52.
[Pubmed]
Huber TB, Schermer B, Müller RU, Höhne M, Bartram M, Calixto A, Hagmann H, Reinhardt C, Koos F, Kunzelmann K, Shirokova E, Krautwurst D, Harteneck C, Simons M, Pavenstädt H, Kerjaschki D, Thiele C, Walz G, Chalfie M, Benzing T.
Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channels.
Proc Natl Acad Sci U S A. 2006 Nov 14;103(46):17079-86.
[Pubmed]
Barro Soria R, Spitzner M, Schreiber R, Kunzelmann K.
Bestrophin 1 enables Ca2+ activated Cl- conductance in epithelia.
J Biol Chem. 2006 Sep 26.
[Pubmed]
Kunzelmann K, Scheidt K, Scharf B, Ousingsawat J, Schreiber R, Wainwright B, McMorran B.
Flagellin of Pseudomonas aeruginosa inhibits Na+ transport in airway epithelia.
FASEB J. 2006 Mar;20(3):545-6.
[Pubmed]
Dawson,P.A., K.J.Pirlo, S.E.Steane, K.Kunzelmann, Y.J.Chien, and D.Markovich.
Molecular cloning and characterization of the mouse Na+ sulfate cotransporter gene (Slc13a4): structure and expression.
Genes Genet Syst 81:265-272.
Huber,T.B., B.Schermer, R.U.Muller, M.Hohne, M.Bartram, A.Calixto, H.Hagmann, C.Reinhardt, F.Koos, K.Kunzelmann, E.Shirokova, D.Krautwurst, C.Harteneck, M.Simons, H.Pavenstadt, D.Kerjaschki, C.Thiele, G.Walz, M.Chalfie, and T.Benzing.
Podocin and MEC-2 bind cholesterol to regulate the activity of associated ion channels.
Proc.Natl.Acad.Sci.U.S.A..
Kunzelmann,K., K.Scheidt, B.Scharf, J.Ousingsawat, R.Schreiber, B.J.Wainwright, and B.McMorran.
Pseudomonas flagellin inhibits Na+ transport in airway epithelia.
FASEB J 20:545-546.
Kunzelmann,K., M.Spitzner, J.Ousingsawat, J.R.Martins, and R.Schreiber.
Expression von Ionenkanälen beim Kolonkarzinom: Neue diagnostische und therapeutische Möglichkeiten?
Onkologie heute 2:18-21.
Sousa,M., J.Ousingsawat, R.Seitz, S.Puntheeranurak, A.Regalado, A.Schmidt, T.Grego, C.Jansakul, M.D.Amaral, R.Schreiber, and K.Kunzelmann.
Thai medical plant extract from Phyllanthus acidus as a potential treatment for cystic fibrosis.
Mol.Pharmacol 71:366-376.
Stumpf,A., J.R.Martins, K.Kunzelmann, K.Wenners-Epping, S.Huber, J.Häberle, S.Falk, A.Dübbers, M.Walte, H.Oberleithner, and H.Schillers.
IADS, a decomposition product of DIDS, activates a cation conductance in human erythrocytes and Xenopus laevis oocytes.
Cell Physiol Biochem (in press) 18:243-252.
Adam,G., J.Ousingsawat, R.Schreiber, and K.Kunzelmann.
Increase in intracellular Cl- concentration by cAMP and Ca2+ dependent stimulation of M1 collecting duct cells.
Pflügers Arch 449:470-478.
Bachhuber,T., J.König, T.Voelcker, B.Mürle, R.Schreiber, and K.Kunzelmann.
Chloride interference with the epithelial Na+ channel ENaC.
J Biol Chem 280:31587-31594.
Bloch,M., J.Ousingsawat, R.Simon, T.C.Gasser, M.J.Mihatsch, K.Kunzelmann, and L.Bubendorf.
KCNMA1 gene amplification promotes tumor cell proliferation in prostate cancer.
Oncogen 459:443-447.
da Paula,A.C., A.Ramalho, C.Farinha, J.Cheng, R.Maurisse, D.C.Gruenert, J.Ousingsawat, K.Kunzelmann, and M.D.Amaral.
Characterization of a novel airway submucosal gland cellular model for cystic fibrosis studies.
Cell Physiol Biochem 15:251-262.
Dawson,P.A., K.J.Pirlo, S.E.Steane, K.A.Nguyen, K.Kunzelmann, Y.J.Chien, and D.Markovich.
The rat Na + sulfate cotransporter rNaS2: Functional characterisation, tissue distribution and gene (slc13a4) structure.
Pflügers Arch 450:262-268.
Kunzelmann,K.
Ion channels and cancer.
J Membr.Biol 205:159-173.
Kunzelmann,K., T.Bachhuber, G.Adam, T.Voelcker, B.Mürle, M.Mall, and R.Schreiber.
Role of CFTR and other ion channels in cystic fibrosis. In: Defects of Secretion in Cystci Fibrosis.
Carsten Schultz (Ed). Adv Exp Med Biol. 558.:23-41.
Kunzelmann,K., J.Sun, D.Markovich, J.König, B.Mürle, M.Mall, and R.Schreiber.
Control of ion transport in mammalian airways by protease activated receptors type 2 (PAR-2).
FASEB J 19:969-970.
Mall,M. and K.Kunzelmann.
Correction of the CF defect by curcumin: Hypes and disappointments.
BioEssays 27:9-13.
Markovich,D., R.R.Regeer, K.Kunzelmann, and P.A.Dawson.
Functional characterization and genomic organization of the human Na(+)-sulfate cotransporter hNaS2 gene (SLC13A4).
Biochem Biophys.Res.Commun. 326:729-734.
Mendes,F., J.Wakefield, T.Bachhuber, M.Barroso, Z.Bebok, D.Penque, K.Kunzelmann, and M.Amaral.
Establishment and Characterization of a novel polarized MDCK epithelial cellular model for CFTR studies.
Cell Physiol Biochemc 16:281-290.
Schreiber,R. and K.Kunzelmann.
Purinergic P2Y6 receptors induce Ca2+ and CFTR dependent Cl- secretion in mouse trachea.
Cell Physiol Biochem 16:99-108.
Gruenert,D.C., K.Kunzelmann, G.Novelli, A.Colosimo, R.Kapsa, and E.Bruscia.
Letter to the editors.
Oligonucleotides 14:157-158.
Hirtz,S., T.Gonska, H.H.Seydewitz, J.Thomas, P.Greiner, J.Kuehr, M.Brandis, I.eichler, H.Rocha, A.-I.Lopes, C.Barreto, A.Ramalho, M.Amaral, K.Kunzelmann, and M.Mall.
CFTR Cl- channel function in native human colon correlates with the genotype and the phenotype in cystic fibrosis.
Gastroenterology 127:1085-1095.
Kunzelmann,K., J.König, D.Markovich, N.King, G.Karupiah, and D.I.Cook.
Acute effects of parainfluenza virus on epithelial electrolyte transport.
J Biol Chem 279:48760-48766.
Kunzelmann,K., D.Sun, and J.König.
Effect of dietary lectins on ion transport in epithelia.
Br.J.Pharmacol 142:1-8.
Kunzelmann,K. and B.McMorran.
First encounter: How pathogens compromise epithelial transport.
Physiology 19: 240-244.
Kunzelmann,K., T.Bachhuber, R.R.Regeer, D.Markovich, J.Sun, and R.Schreiber.
Purinergic inhibition of the epithelial Na+ channel ENaC via hydrolysis of PIP2.
FASEB J 18:142-163.
Kunzelmann,K., J.Sun, D.Markovich, J.König, B.Mürle, T.Voelcker, M.Mall, and R.Schreiber.
Inhibition of epithelial Na+ channels by CFTR and purinergic agonists: Mechanisms and significance for CF.
Am J Physiol Regul Integr Comp Physiol. 2002 Mar;282(3):R639-48.
Mall,M., S.Hirtz, T.Gonska, and K.Kunzelmann.
Assessment of CFTR function in rectal biopsies for the diagnosis of cystic fibrosis.
Journal of Cystic Fibrosis 3:165-169.
Mall,M., S.M.Kreda, A.Mengos, T.J.Jensen, S.Hirtz, H.H.Seydewitz, J.Yankaskas, K.Kunzelmann, J.R.Riordan, and R.C.Boucher.
The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon.
Gastroenterology 126:32-41.
Schreiber,R., A.Boucherot, B.Mürle, J.Sun, and K.Kunzelmann.
Control of epithelial ion transport by Cl- and PDZ proteins.
J Membr.Biol 199:89-98.
Schreiber,R., G.D.Bartoszyk, and K.Kunzelmann.
The k-opioid receptor agonist asimadoline inhibits epithelial transport in mouse trachea and colon.
Eur.J Pharmacol 503:185-190.
Kunzelmann,K.
ENaC is inhibited by an increase in the intracellular Cl- concentration mediated through activation of Cl- channels.
Pflügers Arch 445:505-512.
Kunzelmann,K.
Control of membrane transport by the cystic fibrosis transmembrane conductance regulator (CFTR). In: Kirk KL and Dawson DC, eds.The Cystic Fibrosis Transmembrane Conductance Regulator.
Landes Bioscience USA.Kluwer Academic / Plenum Publisher, 1:55-93.
Kunzelmann,K. and M.Mall.
Pharmacotherapy of the ion transport defect in cystic fibrosis: role of purinergic receptor agonists and other potential therapeutics.
American Journal of Respiratory Medicine 2:299-309.
Mall,M., T.Gonska, J.Thomas, R.Schreiber, H.H.Seydewitz, J.Kuehr, M.Brandis, and K.Kunzelmann.
Role of basolateral K+ channels in Ca2+ activated Cl- secretion in human normal and cystic fibrosis airway epithelia.
Pediatric Research 53:608-618.
Oceandy,D., B.J.McMorran, R.Schreiber, B.Wainwright, and K.Kunzelmann.
GFP-tagged CFTR transgene is functional in the G551D Cystic Fibrosis mouse colon.
J Membr.Biol 192:159-167.
Schreiber,M., B.Mürle, J.Sun, and K.Kunzelmann.
Electrolyte transport in the mouse trachea: role of luminal K+ conductance.
J Membr.Biol 189:143-151.
Schreiber,R., J.König, J.Sun, D.Markovich, and K.Kunzelmann.
Impact of Cl- but not osmotic swelling on inhibition of Na+ absorption by purinergic stimulation and activation of CFTR.
J Membr.Biol 192:101-110.
Boucherot,A., R.Schreiber, H.Pavenstädt, and K.Kunzelmann.
Cloning and expression of the mouse glomerular podoplanin homologue gp38P.
Nephrol.Dial.Transplant 17:978-984.
König,J., R.Schreiber, M.Mall, and K.Kunzelmann.
No evidence for inhibition of ENaC through CFTR mediated release of ATP.
Biochim Biophys Acta 1565:17-28.
Kunzelmann,K., R.Schreiber, J.König, and M.Mall.
Activation of ion secretion via proteinase activated receptors (PAR2) in colon and airways.
Cell Biochem Biophys 26:1-6
Kunzelmann,K. and M.Mall.
Electrolyte transport in the colon: Mechanisms and implications for disease.
Physiological Reviews 82: 245-289.
Kunzelmann,K., R.Schreiber, and D.I.Cook.
Mechanisms for inhibition of amiloride-sensitive Na+ absorption by extracellular nuceotides in mouse trachea.
Pflügers Arch 444:220-226.
Mall,M., T.Gonska, J.Thomas, S.Hirtz, R.Schreiber, and K.Kunzelmann.
Activation of ion secretion via proteinase activated receptors (PAR2) in the human colon.
Am.J.Physiol 282:200-210.
Oceandy,D., B.J.McMorran, S.N.Smith, R.Schreiber, K.Kunzelmann, E.W.F.Alten, D.A.Hume, and B.J.Wainwright.
Gene complementation of airway epithelium in the cystic fibrosis mouse in necessary and sufficient to correct the pathogen clearance and inflammatory abnormalities.
Hum.Mol.Genet. 11:1059-1067
Boucherot,A., R.Schreiber, and K.Kunzelmann.
Regulation and properties of KCNQ1 (KVLQT1) and impact of the cystic fibrosis transmembrane conductance regulator.
J Membr.Biol 182:39-47.
Boucherot,A., R.Schreiber, and K.Kunzelmann.
Role of CFTR's PDZ- binding domain, NBF1 and Cl- conductance in inhibition of epithelial Na+ channels in Xenopus oocytes.
BBA 1515:64-71.
Greger,R., R.Schreiber, M.Mall, A.Wissner, A.Hopf, M.Briel, M.Bleich, R.Warth, and K.Kunzelmann.
Cystic Fibrosis and CFTR.
Pflügers Arch 443:S3-S7.
Kerst,G., U.Beschorner, B.Unsöld, T.vonHahn, R.Schreiber, R.Greger, U.Gerlach, H.-J.Lang, K.Kunzelmann, and M.Bleich.
Properties and function of KCNQ1 K+ channels isolated from the rectal gland of Squalus Acanthias.
Pflügers Arch 443:146-154.
König,J., R.Schreiber, T.Voelcker, M.Mall, and K.Kunzelmann.
CFTR inhibits ENaC through an increase in the intracellular Cl- concentration.
EMBO Reports 2:1-5.
Kunzelmann,K. and M.Mall.
Pharmacotherapy of the ion transport defect in cystic fibrosis.
Clin Exp Pharmacol Physiol 28: 857-867.
Kunzelmann,K., M.Bleich, R.Warth, and R.Schreiber.
Expression and function of the rat colonic epithelial K+ channel KVLQT1.
Clin.and Exp.Pharmacol.and Physiol. 28:79-83.
Kunzelmann,K., R.Schreiber, and A.Boucherot.
Mechanism of the inhibition of epithelial Na+ channels by CFTR and purinergic stimulation.
Kidney International 60:455-461.
Kunzelmann,K., M.Hübner, R.Schreiber, R.Levy-Holzman, H.Garty, M.Bleich, R.Warth, M.Slavik, T.von Hahn, and R.Greger.
Cloning and function of the rat colonic epithelial KVLQT1 (KCNQ1).
J Membr.Biol. 179:155-164.
Kunzelmann,K.
Patch - Clamp Studien zur Charakterisierung der CFTR-Funktion. In: Reinhardt D, Götz M.,Kraemer R.,Schöni M. (eds).
Mukoviszidose.Springer Berlin/Heidelberg42-47.
Kunzelmann,K., J.König, and R.Schreiber.
Interaction of the epithelial Na+ channel ENaC and CFTR: Crosstalk via Cl-?
Kidney and Blood Press Res 24:399-402.
Kunzelmann,K.
CFTR: Interacting with everything?
News Physiol Sciences 17: 167-170.
Lambert,G., B.Becker, R.Schreiber, A.Boucherot, M.Reth, and K.Kunzelmann.
BAP31 dependent expression of CFTR.
J Biol Chem 276:20340-20345.
Mall,M. and K.Kunzelmann.
CFTR:A regulator of the amiloride - sensitive epithelial Na+ channel ENaC. In: Cystic Fibrosis European Network, ed.European Working Group on CFTR Expression.
Springer Berlin 2:23-26.
Schreiber,R., P.Kindle, T.Benzing, G.Walz, and K.Kunzelmann.
Control of the Cystic Fibrosis Transmembrane Conductance Regulator by alphaGi and RGS proteins.
BBRC 281:917-923.
Benzing,T., M.B.Yaffe, T.Arnould, L.Sellin, B.Schermer, B.Schilling, R.Schreiber, K.Kunzelmann, G.G.Leparc, E.Kim, and G.Walz.
14-3-3 interacts with regulator of G protein signaling proteins and modulates their activity.
J Biol Chem 275:28167-28172.
Colosimo,A., K.K.Goncz, A.R.Holmes, K.Kunzelmann, G.Novelli, R.W.Malone, M.J.Bennet, and D.C.Gruenert.
Transfere and expression of foreign genes in epithelial cells.
BioTechniques 29:314-322.
Gloy,J., S.Reitinger, K.-G.Fischer, R.Schreiber, A.Boucherot, K.Kunzelmann, P.Mundel, and H.Pavenstädt.
Amino acid transport in mouse podocytes.
Am.J.Physiol. 278:F999-F1005.
Kunzelmann,K., R.Schreiber, R.Nitschke, and M.Mall.
Control of epithelial Na+ conductance by the Cystic Fibrosis Transmembrane Conductance Regulator.
Pflügers Arch 440:193-201.
Kunzelmann,K., A.H.Beesley, N.J.King, G.Karupiah, J.A.Young, and D.I.Cook.
Influenza virus inhibits amiloride- sensitive Na+ channels in respiratory epithelia.
Proc.Natl.Acad Sci.U.S.A. 97:10282-10287.
Kunzelmann,K. and R.Nitschke.
Defects in processing and trafficking of CFTR.
Experimental Nephrology 8: 332-342.
Kunzelmann,K., A.Beesley, N.King, G.Karupiah, J.Young, and D.I.Cook.
Unexpected effects of pathogens on epithelial Na+ channels.
J Korean.Med Sci. 15:S59-S60.
Kunzelmann,K., M.Hübner, M.Vollmer, R.Ruf, F.Hildebrandt, R.Greger, and R.Schreiber.
A Bartter's syndrome mutation of ROMK1 exerts dominant negative effects on K+ conductance.
Cell Physiol Biochem 10:117-124.
Mall,M., A.Wissner, M.Hübner, J.Kühr, M.Brandis, R.Greger, and K.Kunzelmann.
Effect of genistein on native epithelial tissues from normal individuals and CF patients and on CFTR expressed in Xenopus oocytes.
Br.J Pharmacol 130:1884-1892.
Mall,M., A.Wissner, R.Schreiber, J.Kühr, H.H.Seydewitz, M.Brandis, R.Greger, and K.Kunzelmann.
Role of KVLQT1 in cAMP mediated Cl- secretion in human airways.
Am J Respir.Cell Mol.Biol 23:283-289.
Mall,M., A.Wissner, J.Kühr, T.Gonska, M.Brandis, and K.Kunzelmann.
Inhibition of amiloride sensitive epithelial Na+ absorption by extracellular nucleotides in human normal and CF airways.
Am J Respir.Cell Mol.Biol. 23:755-761.
Mall,M., A.Wissner, H.H.Seydewitz, J.Kühr, M.Brandis, R.Greger, and K.Kunzelmann.
Defective cholinergic Cl- secretion and detection of K+ secretion in rectal biopsies from cystic fibrosis patients.
Am.J.Physiol. 278:G617-G624.
Schreiber,R., H.Pavenstädt, R.Greger, and K.Kunzelmann.
Aquaporin 3 cloned from Xenopus laevis is regulated by the cystic fibrosis transmembrane conductance regulator.
FEBS Letters 475:291-295.
