Studies on human porin XXII: cell membrane integrated human porin channels are involved in regulatory volume decrease (RVD) of HeLa cells.
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N. Hilschmann | F. Thinnes | H. Götz | G. Walter | C. Schwarzer | K. Hellmann | T. Hellmann | R. Merker | U. Brockhaus-Pruchniewicz | Norbert Hilschmann | Hilde Götz | Friedrich P. Thinnes | Rolf Merker | Ulrike Brockhaus-Pruchniewicz | Christian Schwarzer | Götz Walter
[1] N. Hilschmann,et al. Studies on human porin XXI: gadolinium opens Up cell membrane standing porin channels making way for the osmolytes chloride or taurine-A putative approach to activate the alternate chloride channel in cystic fibrosis. , 2000, Molecular genetics and metabolism.
[2] N. Hilschmann,et al. The plasma membrane of Xenopus laevis oocytes contains voltage-dependent anion-selective porin channels. , 2000, The international journal of biochemistry & cell biology.
[3] A. Messina,et al. Porin Is Present in the Plasma Membrane Where It Is Concentrated in Caveolae and Caveolae-related Domains* , 1999, The Journal of Biological Chemistry.
[4] N. Hilschmann,et al. Purification procedure and monoclonal antibodies: two instruments for research on vertebrate porins. , 1999, Analytical biochemistry.
[5] C. Remacle,et al. Caveolin‐1 modulates the activity of the volume‐regulated chloride channel , 1999, The Journal of physiology.
[6] Ana Luisa Eguiguren,et al. Separate taurine and chloride efflux pathways activated during regulatory volume decrease. , 1999, American journal of physiology. Cell physiology.
[7] M. Valverde. ClC channels: leaving the dark ages on the verge of a new millennium. , 1999, Current opinion in cell biology.
[8] R. Kinne,et al. Osmoregulation in the mammalian kidney: the role of organic osmolytes. , 1999, The Journal of experimental zoology.
[9] L. Goldstein,et al. Organic osmolyte channels in cell volume regulation in vertebrates. , 1999, The Journal of experimental zoology.
[10] T. Friedrich,et al. The CLC chloride channel family , 1999, Pflügers Archiv.
[11] N. Hilschmann,et al. Mitochondria-Derived and Extra-Mitochondrial Human Type-1 Porin Are Identical as Revealed by Amino Acid Sequencing and Electrophysiological Characterisation , 1999, Biological chemistry.
[12] D. Duan,et al. A Serine Residue in ClC-3 Links Phosphorylation–Dephosphorylation to Chloride Channel Regulation by Cell Volume , 1999, The Journal of general physiology.
[13] N. Hilschmann,et al. Lentil Lectin Enriched Microsomes from the Plasma Membrane of the Human B-Lymphocyte Cell Line H2LCL Carry a Heavy Load of Type-1 Porin , 1998, Biological chemistry.
[14] A. Gruber,et al. Genomic cloning, molecular characterization, and functional analysis of human CLCA1, the first human member of the family of Ca2+-activated Cl- channel proteins. , 1998, Genomics.
[15] W. Craigen,et al. A Novel Isoform of the Mitochondrial Outer Membrane Protein VDAC3 via Alternative Splicing of a 3-Base Exon , 1998, The Journal of Biological Chemistry.
[16] B. Nilius,et al. Modulation of volume-regulated anion channels by extra- and intracellular pH , 1998, Pflügers Archiv.
[17] F. Lang,et al. Tyrosine kinase-dependent activation of a chloride channel in CD95-induced apoptosis in T lymphocytes. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[18] F. Lang,et al. The Tyrosine Kinase p56lck Mediates Activation of Swelling-induced Chloride Channels in Lymphocytes , 1998, The Journal of cell biology.
[19] F. Thinnes,et al. New Findings Concerning Vertebrate Porin , 1997, Naturwissenschaften.
[20] Y. Okada. Volume expansion-sensing outward-rectifier Cl- channel: fresh start to the molecular identity and volume sensor. , 1997, The American journal of physiology.
[21] K. Kirk,et al. Swelling-activated Organic Osmolyte Channels , 1997, The Journal of Membrane Biology.
[22] K. Strange,et al. Swelling-activated organic osmolyte efflux: a new role for anion channels. , 1995, Kidney international.
[23] R. Olsen,et al. Functional domains of GABAA receptors. , 1995, Trends in pharmacological sciences.
[24] F. Thinnes,et al. Further evidence for multitopological localization of mammalian porin (VDAC) in the plasmalemma forming part of a chloride channel complex affected in cystic fibrosis and encephalomyopathy. , 1995, Biochemical and molecular medicine.
[25] F. Thinnes,et al. Studies on human porin. XII. Eight monoclonal mouse anti-"porin 31HL" antibodies discriminate type 1 and type 2 mammalian porin channels/VDACs in western blotting and enzyme-linked immunosorbent assays. , 1994, Biochemical medicine and metabolic biology.
[26] A. Baldini,et al. Human genes encoding the voltage-dependent anion channel (VDAC) of the outer mitochondrial membrane: mapping and identification of two new isoforms. , 1994, Genomics.
[27] G. Fishman,et al. Cloning and in situ localization of a brain-derived porin that constitutes a large-conductance anion channel in astrocytic plasma membranes. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[28] R. Frizzell,et al. Ca(2+)-dependent Cl- channels in undifferentiated human colonic cells (HT-29). II. Regulation and rundown. , 1993, The American journal of physiology.
[29] W. Guggino. Outwardly rectifying chloride channels and CF: A divorce and remarriage , 1993, Journal of bioenergetics and biomembranes.
[30] J. Adelman,et al. Cloning and functional expression in yeast of two human isoforms of the outer mitochondrial membrane channel, the voltage-dependent anion channel. , 1993, The Journal of biological chemistry.
[31] H. Betz,et al. Structure and function of inhibitory glycine receptors , 1992, Quarterly Reviews of Biophysics.
[32] R. Olsen,et al. Isolation and cloning of a voltage-dependent anion channel-like Mr 36,000 polypeptide from mammalian brain. , 1992, The Journal of biological chemistry.
[33] J. Wine,et al. Swelling-induced and depolarization-induced C1-channels in normal and cystic fibrosis epithelial cells. , 1991, The American journal of physiology.
[34] N. Hilschmann,et al. Studies on human porin. IV. The primary structures of "Porin 31HM" purified from human skeletal muscle membranes and of "Porin 31HL" derived from human B lymphocyte membranes are identical. , 1991, Biological chemistry Hoppe-Seyler.
[35] N. Hilschmann,et al. Studies on human porin. III. Does the voltage-dependent anion channel "Porin 31HL" form part of the chloride channel complex, which is observed in different cells and thought to be affected in cystic fibrosis? , 1990, Biological chemistry Hoppe-Seyler.
[36] W. Breuer. Reconstitution of a kidney chloride channel and its identification by covalent labeling. , 1990, Biochimica et biophysica acta.
[37] D. Häussinger,et al. Functional significance of cell volume regulatory mechanisms. , 1998, Physiological reviews.
[38] N. Hilschmann,et al. Channel active mammalian porin, purified from crude membrane fractions of human B lymphocytes or bovine skeletal muscle, reversibly binds the stilbene-disulfonate group of the chloride channel blocker DIDS. , 1994, Biological chemistry Hoppe-Seyler.
[39] J. Riordan,et al. The cystic fibrosis transmembrane conductance regulator. , 1993, Annual review of physiology.