Physiologic cold shock of <it>Moraxella catarrhalis </it>affects the expression of genes involved in the iron acquisition, serum resistance and immune evasion

Por Schaller André, Troller Rolf, Spaniol Violeta, Aebi Christoph
Publicado em 2011-08-01

Physiologic cold shock of Moraxella catarrhalis affects the expression of genes involved in the iron acquisition, serum resistance and immune evasion

Por Spaniol, Violeta, Troller, Rolf, Schaller, André, Aebi, Christoph
Publicado em 2011

Outer membrane porin M35 of Moraxella catarrhalis mediates susceptibility to aminopenicillins

Por Jetter, Marion, Heiniger, Nadja, Spaniol, Violeta, Troller, Rolf, Schaller, André, Aebi, Christoph
Publicado em 2009

Identification of SNPs in the cystic fibrosis interactome influencing pulmonary progression in cystic fibrosis

Por Gisler, Franziska M, von Kanel, Thomas, Kraemer, Richard, Schaller, André, Gallati, Sabina
Publicado em 2013

The stem–loop binding protein stimulates histone translation at an early step in the initiation pathway

Por GORGONI, BARBARA, ANDREWS, STUART, SCHALLER, ANDRÉ, SCHÜMPERLI, DANIEL, GRAY, NICOLA K., MÜLLER, BERNDT
Publicado em 2005

The CFTR frameshift mutation 3905insT and its effect at transcript and protein level

Por Sanz, Javier, von Känel, Thomas, Schneider, Mircea, Steiner, Bernhard, Schaller, André, Gallati, Sabina
Publicado em 2010

Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimic

Por Pröbstel, Anne-Katrin, Schaller, André, Lieb, Johanna, Hench, Juergen, Frank, Stephan, Fuhr, Peter, Kappos, Ludwig, Sinnreich, Michael
Publicado no Neurol Genet (2016)

Characterization of two novel intronic OPA1 mutations resulting in aberrant pre-mRNA splicing

Por Bolognini, Ramona, Gerth-Kahlert, Christina, Abegg, Mathias, Bartholdi, Deborah, Mathis, Nicolas, Sturm, Veit, Gallati, Sabina, Schaller, André
Publicado no BMC Med Genet (2017)

Molecular and biochemical characterisation of a novel mutation in POLG associated with Alpers syndrome

Por Schaller, André, Hahn, Dagmar, Jackson, Christopher B, Kern, Ilse, Chardot, Christophe, Belli, Dominique C, Gallati, Sabina, Nuoffer, Jean-Marc
Publicado em 2011

Clinical and molecular characterization of the potential CF disease modifier syntaxin 1A

Por von Kanel, Thomas, Stanke, Frauke, Weber, Melanie, Schaller, Andre, Racine, Julien, Kraemer, Richard, Chanson, Marc, Tümmler, Burkhard, Gallati, Sabina
Publicado em 2013

The Vacuolar H(+)-ATPase B1 Subunit Polymorphism p.E161K Associates with Impaired Urinary Acidification in Recurrent Stone Formers

Por Dhayat, Nasser A., Schaller, Andre, Albano, Giuseppe, Poindexter, John, Griffith, Carolyn, Pasch, Andreas, Gallati, Sabina, Vogt, Bruno, Moe, Orson W., Fuster, Daniel G.
Publicado no J Am Soc Nephrol (2016)

Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients

Por Mueller, Sandro Manuel, Gehrig, Saskia Maria, Petersen, Jens A., Frese, Sebastian, Mihaylova, Violeta, Ligon-Auer, Maria, Khmara, Natalia, Nuoffer, Jean-Marc, Schaller, André, Lundby, Carsten, Toigo, Marco, Jung, Hans H.
Publicado no Orphanet J Rare Dis (2017)

Neutrophil extracellular trap formation requires OPA1-dependent glycolytic ATP production

Por Amini, Poorya, Stojkov, Darko, Felser, Andrea, Jackson, Christopher B., Courage, Carolina, Schaller, André, Gelman, Laurent, Soriano, Maria Eugenia, Nuoffer, Jean-Marc, Scorrano, Luca, Benarafa, Charaf, Yousefi, Shida, Simon, Hans-Uwe
Publicado no Nat Commun (2018)

Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy

Por Nair, Anil V., Hocher, Berthold, Verkaart, Sjoerd, van Zeeland, Femke, Pfab, Thiemo, Slowinski, Torsten, Chen, You-Peng, Schlingmann, Karl Peter, Schaller, André, Gallati, Sabina, Bindels, René J., Konrad, Martin, Hoenderop, Joost G.
Publicado em 2012

CLDN16 Genotype Predicts Renal Decline in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

Por Konrad, Martin, Hou, Jianghui, Weber, Stefanie, Dötsch, Jörg, Kari, Jameela A., Seeman, Tomas, Kuwertz-Bröking, Eberhard, Peco-Antic, Amira, Tasic, Velibor, Dittrich, Katalin, Alshaya, Hammad O., von Vigier, Rodo O., Gallati, Sabina, Goodenough, Daniel A., Schaller, André
Publicado em 2008

Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement

Por Konrad, Martin, Schaller, André, Seelow, Dominik, Pandey, Amit V., Waldegger, Siegfried, Lesslauer, Annegret, Vitzthum, Helga, Suzuki, Yoshiro, Luk, John M., Becker, Christian, Schlingmann, Karl P., Schmid, Marcel, Rodriguez-Soriano, Juan, Ariceta, Gema, Cano, Francisco, Enriquez, Ricardo, Jüppner, Harald, Bakkaloglu, Sevcan A., Hediger, Matthias A., Gallati, Sabina, Neuhauss, Stephan C. F., Nürnberg, Peter, Weber, Stefanie
Publicado em 2006

Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement

Por Haack, Tobias B, Jackson, Christopher B, Murayama, Kei, Kremer, Laura S, Schaller, André, Kotzaeridou, Urania, de Vries, Maaike C, Schottmann, Gudrun, Santra, Saikat, Büchner, Boriana, Wieland, Thomas, Graf, Elisabeth, Freisinger, Peter, Eggimann, Sandra, Ohtake, Akira, Okazaki, Yasushi, Kohda, Masakazu, Kishita, Yoshihito, Tokuzawa, Yoshimi, Sauer, Sascha, Memari, Yasin, Kolb-Kokocinski, Anja, Durbin, Richard, Hasselmann, Oswald, Cremer, Kirsten, Albrecht, Beate, Wieczorek, Dagmar, Engels, Hartmut, Hahn, Dagmar, Zink, Alexander M, Alston, Charlotte L, Taylor, Robert W, Rodenburg, Richard J, Trollmann, Regina, Sperl, Wolfgang, Strom, Tim M, Hoffmann, Georg F, Mayr, Johannes A, Meitinger, Thomas, Bolognini, Ramona, Schuelke, Markus, Nuoffer, Jean-Marc, Kölker, Stefan, Prokisch, Holger, Klopstock, Thomas
Publicado no Ann Clin Transl Neurol (2015)