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Neurogenetics
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January 22, 2013
Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis
Dennis Lal, Kerstin Becker, Susanne Motameny, et al.
Mitochondrion
|
October 11, 2016
Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNA
Claudia B Catarino, Uwe Ahting, Mirjana Gusic, et al.
American Journal of Human Genetics
|
December 14, 2011
Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway
Johannes A Mayr, Peter Freisinger, Kurt Schlachter, et al.
Journal of Neurology
|
February 21, 2008
Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation
Jügen Prestel, Klaus Gempel, Till-Karsten Hauser, et al.
Journal of Inherited Metabolic Disease
|
May 7, 2019
Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial disease
Matias Wagner, Riccardo Berutti, Bettina Lorenz-Depiereux, et al.
Molecular Biology of the Cell
|
December 12, 2003
Reconstituted TOM core complex and Tim9/Tim10 complex of mitochondria are sufficient for translocation of the ADP/ATP carrier across membranes
Andreja Vasiljev, Uwe Ahting, Frank E Nargang, et al.
Proteomics
|
November 19, 2005
Proteome analysis of mitochondrial outer membrane from Neurospora crassa
Simone Schmitt, Holger Prokisch, Tilman Schlunck, et al.
Journal of Inherited Metabolic Disease
|
March 18, 2015
Spectrum of combined respiratory chain defects
Johannes A Mayr, Tobias B Haack, Peter Freisinger, et al.
Plos One
|
October 8, 2013
Alterations of red cell membrane properties in neuroacanthocytosis
Claudia Siegl, Patricia Hamminger, Herbert Jank, et al.
Biochimica Et Biophysica Acta
|
December 30, 2008
Neurological phenotype and reduced lifespan in heterozygous Tim23 knockout mice, the first mouse model of defective mitochondrial import
Uwe Ahting, Thomas Floss, Nikolas Uez, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 36) with videos related to
Sort By:
Page
of 4
Neurogenetics
|
January 22, 2013
Homozygous missense mutation of NDUFV1 as the cause of infantile bilateral striatal necrosis
Dennis Lal, Kerstin Becker, Susanne Motameny, et al.
Mitochondrion
|
October 11, 2016
Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNA
Claudia B Catarino, Uwe Ahting, Mirjana Gusic, et al.
American Journal of Human Genetics
|
December 14, 2011
Thiamine pyrophosphokinase deficiency in encephalopathic children with defects in the pyruvate oxidation pathway
Johannes A Mayr, Peter Freisinger, Kurt Schlachter, et al.
Journal of Neurology
|
February 21, 2008
Clinical and molecular characterisation of a Parkinson family with a novel PINK1 mutation
Jügen Prestel, Klaus Gempel, Till-Karsten Hauser, et al.
Journal of Inherited Metabolic Disease
|
May 7, 2019
Mitochondrial DNA mutation analysis from exome sequencing-A more holistic approach in diagnostics of suspected mitochondrial disease
Matias Wagner, Riccardo Berutti, Bettina Lorenz-Depiereux, et al.
Molecular Biology of the Cell
|
December 12, 2003
Reconstituted TOM core complex and Tim9/Tim10 complex of mitochondria are sufficient for translocation of the ADP/ATP carrier across membranes
Andreja Vasiljev, Uwe Ahting, Frank E Nargang, et al.
Proteomics
|
November 19, 2005
Proteome analysis of mitochondrial outer membrane from Neurospora crassa
Simone Schmitt, Holger Prokisch, Tilman Schlunck, et al.
Journal of Inherited Metabolic Disease
|
March 18, 2015
Spectrum of combined respiratory chain defects
Johannes A Mayr, Tobias B Haack, Peter Freisinger, et al.
Plos One
|
October 8, 2013
Alterations of red cell membrane properties in neuroacanthocytosis
Claudia Siegl, Patricia Hamminger, Herbert Jank, et al.
Biochimica Et Biophysica Acta
|
December 30, 2008
Neurological phenotype and reduced lifespan in heterozygous Tim23 knockout mice, the first mouse model of defective mitochondrial import
Uwe Ahting, Thomas Floss, Nikolas Uez, et al.
Page
of 4