The K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients von Roth, Eva K, Hirtz, Stephanie, Duerr, Julia, Wenning, Daniel, Eichler, Irmgard, Seydewitz, Hans H, Amaral, Margarida D, Mall, Marcus A

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CFTR Cl − channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis von Hirtz, Stephanie, Gonska, Tanja, Seydewitz, Hans H., Thomas, Jörg, Greiner, Peter, Kuehr, Joachim, Brandis, Matthias, Eichler, Irmgard, Rocha, Herculano, Lopes, Ana—Isabel, Barreto, Celeste, Ramalho, Anabela, Amaral, Margarida D., Kunzelmann, Karl, Mall, Marcus

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Modulation of Ca2+-activated Cl- secretion by basolateral K+ channels in human normal and cystic fibrosis airway epithelia von MALL, Marcus, GONSKA, Tanja, THOMAS, Jörg, SCHREIBER, Rainer, SEYDEWITZ, Hans H, KUEHR, Joachim, BRANDIS, Matthias, KUNZELMANN, Karl

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Effect of genistein on native epithelial tissue from normal individuals and CF patients and on ion channels expressed in Xenopus oocytes von Mall, Marcus, Wissner, Andreas, Seydewitz, Hans H, Hübner, Martin, Kuehr, Joachim, Brandis, Matthias, Greger, Rainer, Kunzelmann, Karl

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Molecular genetic analysis of 40 patients with glycogen storage disease type Ia: 100% mutation detection rate and 5 novel mutations von Seydewitz, Hans H., Matern, Dietrich

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Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype von WESTON, B. W, LIN, J.-L, CHEN, Y. T, MUENZER, J, CAMERON, H. S, ARNOLD, R. R, SEYDEWITZ, H. H, MAYATEPEK, E, VAN SCHAFTINGEN, E, VEIGA-DA-CUNHA, M, MATERN, D

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Pediatric Reference Ranges for Osteocalcin Measured by the Immulite Analyzer von Seydewitz, Hans H., Henschen, Matthias, Kühnel, Werner, Brandis, Matthias

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The ΔF508 mutation results in loss of CFTR function and mature protein in native human colon von Mall, Marcus, Kreda, Silvia M., Mengos, April, Jensen, Timothy J., Hirtz, Stephanie, Seydewitz, Hans H., Yankaskas, James, Kunzelmann, Karl, Riordan, John R., Boucher, Richard C.

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Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens von DÖRK, T, DWORNICZAK, B, PANDER, H.-J, SPERLING, H, RATJEN, F, PASSARGE, E, SCHMIDTKE, J, STUHRMANN, M, AULEHLA-SCHOLZ, C, WIECZOREK, D, BÖHM, I, MAYEROVA, A, SEYDEWITZ, H. H, NIESCHLAG, E, MESCHEDE, D, HORST, J

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The K.sup.+ Channel Opener 1-EBIO Potentiates Residual Function of Mutant CFTR in Rectal Biopsies from Cystic Fibrosis Patients von Roth, Eva K, Hirtz, Stephanie, Duerr, Julia, Wenning, Daniel, Eichler, Irmgard, Seydewitz, Hans H, Amaral, Margarida D, Mall, Marcus A

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The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon von Mall, Marcus, Kreda, Silvia M, Mengos, April, Jensen, Timothy J, Hirtz, Stephanie, Seydewitz, Hans H, Yankaskas, James, Kunzelmann, Karl, Riordan, John R, Boucher, Richard C

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Primary treatment of propionic acidemia complicated by acute thiamine deficiency von Matern, Dietrich, Seydewitz, Hans H., Lehnert, Willy, Niederhoff, Helmut, Leititis, Jekabs U., Brandis, Matthias

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Isolation and complete amino‐acid sequence of the small polypeptide from light‐harvesting pigment‐protein complex I (B870) of Rhodopseudomonas capsulata von TADROS, Monier H., SUTER, Franz, SEYDEWITZ, Hans H., WITT, Irene, ZUBER, Herbert, DREWS, Gerhart

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Role of K V LQT1 in Cyclic Adenosine Monophosphate–Mediated Cl − Secretion in Human Airway Epithelia von Mall, Marcus, Wissner, Andreas, Schreiber, Rainer, Kuehr, Joachim, Seydewitz, Hans H., Brandis, Matthias, Greger, Rainer, Kunzelmann, Karl

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Role of KVLQT1 in Cyclic Adenosine Monophosphate-Mediated Cl- Secretion in Human Airway Epithelia von Mall, Marcus, Wissner, Andreas, Schreiber, Rainer, Kuehr, Joachim, Seydewitz, Hans H, Brandis, Matthias, Greger, Rainer, Kunzelmann, Karl

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Validation of treatment strategies for enterohaemorrhagic Escherichia coli O104:H4 induced haemolytic uraemic syndrome: case-control study von Menne, Jan, Nitschke, Martin, Stingele, Robert, Abu-Tair, Mariam, Beneke, Jan, Bramstedt, Jörn, Bremer, Jan P, Brunkhorst, Reinhard, Busch, Veit, Dengler, Reinhard, Deuschl, Günther, Fellermann, Klaus, Fickenscher, Helmut, Gerigk, Christoph, Goettsche, Alexander, Greeve, Jobst, Hafer, Carsten, Hagenmüller, Friedrich, Haller, Hermann, Herget-Rosenthal, Stefan, Hertenstein, Bernd, Hofmann, Christina, Lang, Melanie, Kielstein, Jan T, Klostermeier, Ulrich C, Knobloch, Johannes, Kuehbacher, Markus, Kunzendorf, Ulrich, Lehnert, Hendrik, Manns, Michael P, Menne, Tobias F, Meyer, Tobias N, Michael, Claus, Münte, Thomas, Neumann-Grutzeck, Christine, Nuernberger, Jens, Pavenstaedt, Hermann, Ramazan, Leyla, Renders, Lutz, Repenthin, Jonas, Ries, Wolfgang, Rohr, Axel, Rump, Lars Christian, Samuelsson, Ola, Sayk, Friedhelm, Schmidt, Bernhard M W, Schnatter, Sabine, Schöcklmann, Harald, Schreiber, Stefan, von Seydewitz, Cay U, Steinhoff, Jürgen, Stracke, Sylvia, Suerbaum, Sebastian, van de Loo, Andreas, Vischedyk, Martin, Weissenborn, Karin, Wellhöner, Peter, Wiesner, Monika, Zeissig, Sebastian, Büning, Jürgen, Schiffer, Mario, Kuehbacher, Tanja

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Glycogen storage disease type I: diagnosis and phenotype/genotype correlation von Matern, Dietrich, Seydewitz, Hans, Bali, Deeksha, Lang, Christine, Chen, Yuan-Tsong

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A novel missense mutation, S1159F, in exon 19 of the CFTR gene von Seydewitz, Hans Hermann, Mall, Marcus, Kuehr, Joachim

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Expression of CNTF Receptor-{alpha} in Chick Violet-Sensitive Cones with Unique Morphologic Properties von Seydewitz, Vera, Rothermel, Andree, Fuhrmann, Sabine, Schneider, Aniko, DeGrip, Willem J, Layer, Paul G, Hofmann, Hans-Dieter

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A novel frameshift mutation, c.1870delG, in exon 12 of the CFTR gene von Seydewitz, Hans Hermann, Gonska, Tanja, Mall, Marcus, Kueh, Joachim

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