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Journal of Cell Science
|
March 10, 2011
Depletion of PINK1 affects mitochondrial metabolism, calcium homeostasis and energy maintenance
Bavo Heeman, Chris Van den Haute, Sarah-Ann Aelvoet, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 18, 2017
Statins Affect Skeletal Muscle Performance: Evidence for Disturbances in Energy Metabolism
Neeltje A E Allard, Tom J J Schirris, Rebecca J Verheggen, et al.
Neurology
|
February 19, 2024
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children
Jamie I Verhoeven, Jasper Kramer, Juergen Seeger, et al.
Molecular Genetics and Metabolism
|
March 14, 2016
Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis
Saikat Santra, Jessie M Cameron, Casper Shyr, et al.
Journal of Inherited Metabolic Disease
|
December 21, 2014
The spectrum of pyruvate oxidation defects in the diagnosis of mitochondrial disorders
Wolfgang Sperl, Leanne Fleuren, Peter Freisinger, et al.
American Journal of Human Genetics
|
July 6, 2010
Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect
Hana Antonicka, Elsebet Ostergaard, Florin Sasarman, et al.
International Journal of Molecular Sciences
|
July 13, 2024
Characterisation of an Adult Zebrafish Model for <i>SDHB</i>-Associated Phaeochromocytomas and Paragangliomas
Jasmijn B Miltenburg, Marnix Gorissen, Inge van Outersterp, et al.
European Journal of Heart Failure
|
February 28, 2018
Iron deficiency impairs contractility of human cardiomyocytes through decreased mitochondrial function
Martijn F Hoes, Niels Grote Beverborg, J David Kijlstra, et al.
Analytical Biochemistry
|
May 21, 2009
Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome
Riekelt H Houtkooper, Richard J Rodenburg, Charlotte Thiels, et al.
Human Mutation
|
April 23, 2009
Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency
Saskia J G Hoefs, Cindy E J Dieteren, Richard J Rodenburg, et al.
Page
of 14
Search research articles
Search
Showing results (51-60 of 137) with videos related to
Sort By:
Page
of 14
Journal of Cell Science
|
March 10, 2011
Depletion of PINK1 affects mitochondrial metabolism, calcium homeostasis and energy maintenance
Bavo Heeman, Chris Van den Haute, Sarah-Ann Aelvoet, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 18, 2017
Statins Affect Skeletal Muscle Performance: Evidence for Disturbances in Energy Metabolism
Neeltje A E Allard, Tom J J Schirris, Rebecca J Verheggen, et al.
Neurology
|
February 19, 2024
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 Children
Jamie I Verhoeven, Jasper Kramer, Juergen Seeger, et al.
Molecular Genetics and Metabolism
|
March 14, 2016
Cytosolic phosphoenolpyruvate carboxykinase deficiency presenting with acute liver failure following gastroenteritis
Saikat Santra, Jessie M Cameron, Casper Shyr, et al.
Journal of Inherited Metabolic Disease
|
December 21, 2014
The spectrum of pyruvate oxidation defects in the diagnosis of mitochondrial disorders
Wolfgang Sperl, Leanne Fleuren, Peter Freisinger, et al.
American Journal of Human Genetics
|
July 6, 2010
Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect
Hana Antonicka, Elsebet Ostergaard, Florin Sasarman, et al.
International Journal of Molecular Sciences
|
July 13, 2024
Characterisation of an Adult Zebrafish Model for <i>SDHB</i>-Associated Phaeochromocytomas and Paragangliomas
Jasmijn B Miltenburg, Marnix Gorissen, Inge van Outersterp, et al.
European Journal of Heart Failure
|
February 28, 2018
Iron deficiency impairs contractility of human cardiomyocytes through decreased mitochondrial function
Martijn F Hoes, Niels Grote Beverborg, J David Kijlstra, et al.
Analytical Biochemistry
|
May 21, 2009
Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome
Riekelt H Houtkooper, Richard J Rodenburg, Charlotte Thiels, et al.
Human Mutation
|
April 23, 2009
Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency
Saskia J G Hoefs, Cindy E J Dieteren, Richard J Rodenburg, et al.
Page
of 14