Resultados de procura - Johannes A. Mayr

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  1. 1
    Choline‐related‐inherited metabolic diseases—A mini review

    Choline‐related‐inherited metabolic diseases—A mini review por Saskia B. Wortmann, Johannes A. Mayr

    Publicado 2019
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  2. 2
    Treatable mitochondrial diseases: cofactor metabolism and beyond

    Treatable mitochondrial diseases: cofactor metabolism and beyond por Felix Distelmaier, Tobias B. Haack, Saskia B. Wortmann, Johannes A. Mayr, Holger Prokisch

    Publicado 2016
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  3. 3
    Functional Differences between Mitochondrial Haplogroup T and Haplogroup H in HEK293 Cybrid Cells

    Functional Differences between Mitochondrial Haplogroup T and Haplogroup H in HEK293 Cybrid Cells por Edith E. Mueller, Susanne M. Brunner, Johannes A. Mayr, Olaf Stanger, Wolfgang Sperl, Barbara Kofler

    Publicado 2012
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  4. 4
    The mitochondrial phosphate carrier: Role in oxidative metabolism, calcium handling and mitochondrial disease

    The mitochondrial phosphate carrier: Role in oxidative metabolism, calcium handling and mitochondrial disease por Erin L. Seifert, Erzsébet Ligeti, Johannes A. Mayr, Neal Sondheimer, Gyӧrgy Hajnόczky

    Publicado 2015
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  5. 5
    Characterization and Function in Vivo of Two Novel Phospholipases B/Lysophospholipases fromSaccharomyces cerevisiae

    Characterization and Function in Vivo of Two Novel Phospholipases B/Lysophospholipases fromSaccharomyces cerevisiae por Olaf Merkel, Markus Fido, Johannes A. Mayr, Hermann Prüger, Florian Raab, Gerhild Zandonella, Sepp D. Kohlwein, Fritz Paltauf

    Publicado 1999
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  6. 6
    Lipoic Acid Synthetase Deficiency Causes Neonatal-Onset Epilepsy, Defective Mitochondrial Energy Metabolism, and Glycine Elevation

    Lipoic Acid Synthetase Deficiency Causes Neonatal-Onset Epilepsy, Defective Mitochondrial Energy Metabolism, and Glycine Elevation por Johannes A. Mayr, Franz Zimmermann, Christine Fauth, Christa Bergheim, David Meierhofer, Doris Radmayr, Johannes Zschocke, Johannes Koch, Wolfgang Sperl

    Publicado 2011
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  7. 7
    Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma

    Loss of Complex I due to Mitochondrial DNA Mutations in Renal Oncocytoma por Johannes A. Mayr, David Meierhofer, Franz Zimmermann, René G. Feichtinger, Christian Kögler, Manfred Ratschek, N. Schmeller, Wolfgang Sperl, Barbara Kofler

    Publicado 2008
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  8. 8
    Inhibition of Neuroblastoma Tumor Growth by Ketogenic Diet and/or Calorie Restriction in a CD1-Nu Mouse Model

    Inhibition of Neuroblastoma Tumor Growth by Ketogenic Diet and/or Calorie Restriction in a CD1-Nu Mouse Model por Raphael J. Morscher, Sepideh Aminzadeh-Gohari, René G. Feichtinger, Johannes A. Mayr, Roland Lang, Daniel Neureiter, Wolfgang Sperl, Barbara Kofler

    Publicado 2015
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  9. 9
    Lack of complex I is associated with oncocytic thyroid tumours

    Lack of complex I is associated with oncocytic thyroid tumours por Franz Zimmermann, Johannes A. Mayr, Daniel Neureiter, René G. Feichtinger, Beate Alinger, N. D. Jones, Waltraud Eder, Wolfgang Sperl, Barbara Kofler

    Publicado 2009
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  10. 10
    Severe depletion of mitochondrial DNA in spinal muscular atrophy

    Severe depletion of mitochondrial DNA in spinal muscular atrophy por Alexandra Berger, Johannes A. Mayr, David Meierhofer, Ulrike Fötschl, Reginald E. Bittner, Herbert Budka, Claude Grethen, Michael Huemer, Barbara Kofler, Wolfgang Sperl

    Publicado 2003
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  11. 11
    Low aerobic mitochondrial energy metabolism in poorly- or undifferentiated neuroblastoma

    Low aerobic mitochondrial energy metabolism in poorly- or undifferentiated neuroblastoma por René G. Feichtinger, Franz Zimmermann, Johannes A. Mayr, Daniel Neureiter, Cornelia Hauser‐Kronberger, Freimut H. Schilling, Neil D. Jones, Wolfgang Sperl, Barbara Kofler

    Publicado 2010
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  12. 12
    Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway

    Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway por Johannes A. Mayr, Peter Freisinger, Kurt Schlachter, Boris Rolinski, Franz Zimmermann, T Scheffner, Tobias B. Haack, Johannes Koch, Uwe Ahting, Holger Prokisch, Wolfgang Sperl

    Publicado 2011
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  13. 13
    Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 subunit

    Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 subunit por Johannes A. Mayr, Vendula Havlíčková, Franz Zimmermann, I. Magler, Vilma Kaplanová, Pavel Ješina, Alena Pecinová, Hana Nůsková, Johannes Koch, Wolfgang Sperl, J Houštěk

    Publicado 2010
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  14. 14
    Mitochondrial Haplogroups, Control Region Polymorphisms and Malignant Melanoma: A Study in Middle European Caucasians

    Mitochondrial Haplogroups, Control Region Polymorphisms and Malignant Melanoma: A Study in Middle European Caucasians por Sabine Ebner, Roland Lang, Edith E. Mueller, Waltraud Eder, Michaela Oeller, Alexandra Moser, Josef Koller, Bernhard Paulweber, Johannes A. Mayr, Wolfgang Sperl, Barbara Kofler

    Publicado 2011
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  15. 15
    A ketogenic diet supplemented with medium-chain triglycerides enhances the anti-tumor and anti-angiogenic efficacy of chemotherapy on neuroblastoma xenografts in a CD1-nu mouse model

    A ketogenic diet supplemented with medium-chain triglycerides enhances the anti-tumor and anti-angiogenic efficacy of chemotherapy on neuroblastoma xenografts in a CD1-nu mouse mod... por Sepideh Aminzadeh-Gohari, René G. Feichtinger, Silvia Vidali, Felix Locker, Tricia Rutherford, Maura O’Donnel, Andrea Stöger-Kleiber, Johannes A. Mayr, Wolfgang Sperl, Barbara Kofler

    Publicado 2017
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  16. 16
    Mitochondrial Phosphate–Carrier Deficiency: A Novel Disorder of Oxidative Phosphorylation

    Mitochondrial Phosphate–Carrier Deficiency: A Novel Disorder of Oxidative Phosphorylation por Johannes A. Mayr, Olaf Merkel, Sepp D. Kohlwein, Boris Gebhardt, Hansjosef Böhles, Ulrike Fötschl, Johannes Koch, Michaela Jaksch, Hanns Lochmüller, Rita Horváth, Peter Freisinger, Wolfgang Sperl

    Publicado 2007
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  17. 17
    Mitochondrial DNA mutation analysis from exome sequencing—A more holistic approach in diagnostics of suspected mitochondrial disease

    Mitochondrial DNA mutation analysis from exome sequencing—A more holistic approach in diagnostics of suspected mitochondrial disease por Matias Wagner, Riccardo Berutti, Bettina Lorenz‐Depiereux, Elisabeth Graf, Gertrud Eckstein, Johannes A. Mayr, Thomas Meitinger, Uwe Ahting, Holger Prokisch, Tim M. Strom, Saskia B. Wortmann

    Publicado 2019
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  18. 18
    Mitochondrial Haplogroups and Control Region Polymorphisms in Age-Related Macular Degeneration: A Case-Control Study

    Mitochondrial Haplogroups and Control Region Polymorphisms in Age-Related Macular Degeneration: A Case-Control Study por Edith E. Mueller, Elena Schaier, Susanne M. Brunner, Waltraud Eder, Johannes A. Mayr, Stefan Egger, C. Nischler, Hannes Oberkofler, Herbert A. Reitsamer, Wolfgang Patsch, Wolfgang Sperl, Barbara Kofler

    Publicado 2012
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  19. 19
    Biliary Atresia: Swiss National Study, 1994–2004

    Biliary Atresia: Swiss National Study, 1994–2004 por Barbara E. Wildhaber, Pietro Majno, Johannes A. Mayr, Zacharias Zachariou, Judith Hohlfeld, Marcus Schwoebel, Walter Kistler, Martin Meuli, Claude Le Coultre, Gilles Mentha, Dominique C. Belli, Christophe Chardot

    Publicado 2008
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  20. 20
    Spectrum of combined respiratory chain defects

    Spectrum of combined respiratory chain defects por 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

    Publicado 2015
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