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BioFactors, ISSN 0951-6433, 09/2011, Volume 37, Issue 5, pp. 361 - 365
Journal Article
Biochimica et Biophysica Acta - General Subjects, ISSN 0304-4165, 05/2012, Volume 1820, Issue 5, pp. 625 - 631
Background: Although causative mutations have been identified for numerous mitochondrial disorders, few disease-modifying treatments are available. Two... 
Coenzyme Q | Mitochondria | Mitochondrial DNA | MNGIE | Ubiquinone | Thymidine phosphorylase
Journal Article
American Journal of Human Genetics, ISSN 0002-9297, 2006, Volume 79, Issue 6, pp. 1125 - 1129
Journal Article
Thorax, ISSN 0040-6376, 9/2019, p. thoraxjnl-2019-213621
Muscle mitochondrial dysfunction is implicated in intensive care unit-acquired weakness, but there is no serum biomarker of muscle mitochondrial function for... 
Journal Article
Brain : a journal of neurology, ISSN 0006-8950, 09/2019, Volume 142, Issue 9, pp. 2756 - 2774
Multiple sclerosis is an autoimmune demyelinating disorder of the CNS, characterized by inflammatory lesions and an underlying neurodegenerative process, which... 
Index Medicus | Abridged Index Medicus
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 11/2018, Volume 24, Issue 21, pp. 5392 - 5406
Purpose: The goal of this study is to enhance the efficacy of imipridones, a novel class of AKT/ERK inhibitors that displayed limited therapeutic efficacy... 
ANTICANCER ACTIVITY | SERINE SYNTHESIS | CELLS | ENHANCED LETHALITY | ONCOLOGY | STRESS-RESPONSE | SENSITIVITY | BCL-2/BCL-XL | COMBINATION | APOPTOSIS IN-VITRO | REVEALS
Journal Article
PLoS ONE, 02/2012, Volume 7, Issue 2
Journal Article
BBA - General Subjects, ISSN 0304-4165, 05/2012, Volume 1820, Issue 5, p. 625
Although causative mutations have been identified for numerous mitochondrial disorders, few disease-modifying treatments are available. Two examples of... 
Enzymes | Mitochondrial DNA
Journal Article
NEW ENGLAND JOURNAL OF MEDICINE, ISSN 0028-4793, 07/2014, Volume 371, Issue 1, pp. 81 - 82
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 03/2007, Volume 117, Issue 3, pp. 587 - 589
Although it was first described in 1989, our understanding of coenzyme Q10 (CoQ10) deficiency is only now coming of age with the recent first description of... 
Mitochondria - enzymology | Coenzymes | Humans | Mitochondrial Encephalomyopathies - genetics | Ubiquinone - analogs & derivatives | Ubiquinone - deficiency | Mitochondrial Encephalomyopathies - enzymology | Child, Preschool | Infant | Ubiquinone - genetics | Mutation | Ubiquinone - biosynthesis
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2012, Volume 7, Issue 2, p. e30606
Journal Article
Cell metabolism, ISSN 1550-4131, 3/2014, Volume 19, Issue 3, pp. 470 - 483
In growing tissues, cell fitness disparities provoke interactions that promote stronger cells at the expense of the weaker in a process called cell... 
Journal Article
Journal of Neurology, ISSN 0340-5354, 11/2014, Volume 261, Issue 11, p. 2192
Inherited ataxias are heterogeneous disorders affecting both children and adults, with over 40 different causative genes, making molecular genetic diagnosis... 
Complications and side effects | Care and treatment | Gene mutations | Analysis | Ataxia | Ubiquinones | Influence | Research
Journal Article
Journal of Neurology, ISSN 0340-5354, 11/2014, Volume 261, Issue 11, pp. 2192 - 2198
Inherited ataxias are heterogeneous disorders affecting both children and adults, with over 40 different causative genes, making molecular genetic diagnosis... 
Journal Article
Developmental Disabilities Research Reviews, ISSN 1940-5510, 2010, Volume 16, Issue 2, pp. 183 - 188
Coenzyme Q(10) (CoQ(10)) is an essential electron carrier in the mitochondrial respiratory chain and an important antioxidant. Deficiency of CoQ(10) is a... 
Oxidative stress | Respiratory chain activity | Coenzyme Q10 | ROS | PERMEABILITY TRANSITION PORE | coenzyme Q10 | DIPHOSPHATE SYNTHASE SUBUNIT-2 | PSYCHIATRY | respiratory chain activity | COQ DEFICIENCY | Q DEFICIENCY | SACCHAROMYCES-CEREVISIAE | NEUROSCIENCES | CLINICAL NEUROLOGY | CEREBELLAR-ATAXIA | MYOPATHIC FORM | PEDIATRICS | OCULOMOTOR APRAXIA-1 | RESPIRATORY-CHAIN DYSFUNCTION | oxidative stress | UBIQUINONE DEFICIENCY | Neurological Impairments | Brain | Pathology | Therapy | Genetics | Disabilities | Molecular Structure | Genetic Disorders | Clinical Diagnosis | Siblings | Humans | Kidney Diseases - diagnosis | Ubiquinone - deficiency | Spinocerebellar Degenerations - diagnosis | Developmental Disabilities - genetics | Kidney Diseases - genetics | Spinocerebellar Degenerations - therapy | Mitochondrial Myopathies - therapy | Atrophy | DNA Mutational Analysis | Mitochondrial Diseases - therapy | Mitochondrial Myopathies - diagnosis | Child | Developmental Disabilities - diagnosis | Infant, Newborn | Mitochondrial Diseases - genetics | Mitochondrial Encephalomyopathies - genetics | Ubiquinone - analogs & derivatives | Mitochondrial Encephalomyopathies - diagnosis | Ubiquinone - genetics | Spinocerebellar Degenerations - genetics | Genes, Recessive | Developmental Disabilities - therapy | Disease Progression | Cerebellum - pathology | Mitochondrial Myopathies - genetics | Mitochondrial Encephalomyopathies - therapy | Chromosome Aberrations | Kidney Diseases - therapy | Mitochondrial Diseases - diagnosis | Kidney Glomerulus
Journal Article
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