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P Seibel

Showing results (41-50 of 49) with videos related to

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Journal of Cellular and Molecular Medicine|June 23, 2009
Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic studyJ Müller-Höcker, R Horvath, S Schäfer, et al.
Hepatology (Baltimore, Md.)|September 26, 1997
Defects of the respiratory chain in the normal human liver and in cirrhosis during agingJ Müller-Höcker, D Aust, H Rohrbach, et al.
Topics in Companion Animal Medicine|October 29, 2021
Trichloroacetic Acid Injection for Treatment of Eyelid Apocrine Hidrocystomas in a CatJoão A T Pigatto, Alessandra F Silva, Maiara P Seibel, et al.
Journal of the Neurological Sciences|October 1, 1991
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)P Seibel, F Degoul, G Bonne, et al.
Neurology|May 1, 1994
Multiple symmetric lipomatosis: abnormalities in complex IV and multiple deletions in mitochondrial DNAT Klopstock, M Naumann, B Schalke, et al.
Arquivos Brasileiros De Cardiologia|March 23, 2001
Calcified aneurysms in coronary arteries of a 48-year-old patientM K Momolli, J L Castro e Silva Pretto, D Sato, et al.
Journal of Virology|January 21, 2011
Involvement of p32 and microtubules in alteration of mitochondrial functions by rubella virusC Claus, S Chey, S Heinrich, et al.
Journal of Neuropathology and Experimental Neurology|July 11, 2000
New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscleR Schröder, S Vielhaber, F R Wiedemann, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chainI Wittig, P Augstein, G K Brown, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Journal of Cellular and Molecular Medicine|June 23, 2009
Mitochondrial DNA depletion and fatal infantile hepatic failure due to mutations in the mitochondrial polymerase γ (POLG) gene: a combined morphological/enzyme histochemical and immunocytochemical/biochemical and molecular genetic studyJ Müller-Höcker, R Horvath, S Schäfer, et al.
Hepatology (Baltimore, Md.)|September 26, 1997
Defects of the respiratory chain in the normal human liver and in cirrhosis during agingJ Müller-Höcker, D Aust, H Rohrbach, et al.
Topics in Companion Animal Medicine|October 29, 2021
Trichloroacetic Acid Injection for Treatment of Eyelid Apocrine Hidrocystomas in a CatJoão A T Pigatto, Alessandra F Silva, Maiara P Seibel, et al.
Journal of the Neurological Sciences|October 1, 1991
Genetic biochemical and pathophysiological characterization of a familial mitochondrial encephalomyopathy (MERRF)P Seibel, F Degoul, G Bonne, et al.
Neurology|May 1, 1994
Multiple symmetric lipomatosis: abnormalities in complex IV and multiple deletions in mitochondrial DNAT Klopstock, M Naumann, B Schalke, et al.
Arquivos Brasileiros De Cardiologia|March 23, 2001
Calcified aneurysms in coronary arteries of a 48-year-old patientM K Momolli, J L Castro e Silva Pretto, D Sato, et al.
Journal of Virology|January 21, 2011
Involvement of p32 and microtubules in alteration of mitochondrial functions by rubella virusC Claus, S Chey, S Heinrich, et al.
Journal of Neuropathology and Experimental Neurology|July 11, 2000
New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscleR Schröder, S Vielhaber, F R Wiedemann, et al.
Journal of Inherited Metabolic Disease|April 5, 2001
Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chainI Wittig, P Augstein, G K Brown, et al.
Pageof 5