نتائج البحث - Franz Zimmermann
- يعرض 1 - 12 نتائج من 12
-
1
ORTHOTOPIC LIVER ALLOGRAFTS IN THE RAT حسب Franz Zimmermann, HUGH FF. S. DAVIES, PETER P. KNOLL, J. M. Gokel, Traudel Schmidt
منشور في 1984Artigo -
2
Lipoic Acid Synthetase Deficiency Causes Neonatal-Onset Epilepsy, Defective Mitochondrial Energy Metabolism, and Glycine Elevation حسب Johannes A. Mayr, Franz Zimmermann, Christine Fauth, Christa Bergheim, David Meierhofer, Doris Radmayr, Johannes Zschocke, Johannes Koch, Wolfgang Sperl
منشور في 2011Artigo -
3
-
4
-
5
Low aerobic mitochondrial energy metabolism in poorly- or undifferentiated neuroblastoma حسب René G. Feichtinger, Franz Zimmermann, Johannes A. Mayr, Daniel Neureiter, Cornelia Hauser‐Kronberger, Freimut H. Schilling, Neil D. Jones, Wolfgang Sperl, Barbara Kofler
منشور في 2010Artigo -
6
Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway حسب Johannes A. Mayr, Peter Freisinger, Kurt Schlachter, Boris Rolinski, Franz Zimmermann, T Scheffner, Tobias B. Haack, Johannes Koch, Uwe Ahting, Holger Prokisch, Wolfgang Sperl
منشور في 2011Artigo -
7
Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 subunit حسب Johannes A. Mayr, Vendula Havlíčková, Franz Zimmermann, I. Magler, Vilma Kaplanová, Pavel Ješina, Alena Pecinová, Hana Nůsková, Johannes Koch, Wolfgang Sperl, J Houštěk
منشور في 2010Artigo -
8
Spectrum of combined respiratory chain defects حسب Johannes A. Mayr, Tobias B. Haack, Peter Freisinger, Daniela Karall, Christine Makowski, Johannes Koch, René G. Feichtinger, Franz Zimmermann, Boris Rolinski, Uwe Ahting, Thomas Meitinger, Holger Prokisch, Wolfgang Sperl
منشور في 2015Revisão -
9
Mitochondrial DNA haplogroup T is associated with coronary artery disease and diabetic retinopathy: a case control study حسب Barbara Kofler, Edith E. Mueller, Waltraud Eder, Olaf Stanger, Richard Maier, Martin Weger, Anton Haas, Robert Winker, O. Schmut, Bernhard Paulweber, Bernhard Iglseder, Wilfried Renner, Martina Wiesbauer, Irene Aigner, Danijela Šantić, Franz Zimmermann, Johannes A. Mayr, Wolfgang Sperl
منشور في 2009Artigo -
10
Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome حسب Johannes A. Mayr, Tobias B. Haack, Elisabeth Graf, Franz Zimmermann, Thomas Wieland, Birgit Haberberger, Andrea Superti‐Furga, Janbernd Kirschner, Beat Steinmann, Matthias R. Baumgartner, Isabella Moroni, Eleonora Lamantea, Massimo Zeviani, Richard J. Rodenburg, Jan Smeitink, Tim M. Strom, Thomas Meitinger, Wolfgang Sperl, Holger Prokisch
منشور في 2012Artigo -
11
ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy حسب Tobias B. Haack, Robert Kopajtich, Peter Freisinger, Thomas Wieland, Joanna Rorbach, Thomas J. Nicholls, Enrico Baruffini, Anett Walther, Katharina Danhauser, Franz Zimmermann, Ralf A. Husain, Jessica Schum, Helen Mundy, Ileana Ferrero, Tim M. Strom, Thomas Meitinger, Robert W. Taylor, Michal Minczuk, Johannes A. Mayr, Holger Prokisch
منشور في 2013Artigo -
12
Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency حسب Uwe Ahting, Johannes A. Mayr, Arnaud Vanlander, Steven Hardy, Saikat Santra, Christine Makowski, Charlotte L. Alston, Franz Zimmermann, Lucia Abela, Barbara Plecko, Marianne Rohrbach, Stephanie Spranger, Sara Seneca, Boris Rolinski, Angela Hagendorff, Maja Hempel, Wolfgang Sperl, Thomas Meitinger, Joél Smet, Robert W. Taylor, Rudy Van Coster, Peter Freisinger, Holger Prokisch, Tobias B. Haack
منشور في 2015Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Biochemistry
Gene
Mitochondrion
Genetics
Mitochondrial DNA
Medicine
Molecular biology
Endocrinology
Internal medicine
Mitochondrial disease
Mitochondrial respiratory chain
Oxidative phosphorylation
Pathology
Respiratory chain
Amino acid
Carcinogenesis
Cell biology
Chemistry
Enzyme
Glycine
Mutation
Succinate dehydrogenase
ATP hydrolysis
ATP synthase
ATP synthase gamma subunit
ATPase
Allele
Andrology
Antigen