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aspartic acid and Electron Transport Chain Deficiencies, Mitochondrial

aspartic acid has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 20 studies

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's10 (50.00)29.6817
2010's10 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fukuda, M; Nagao, Y1
Beyrath, J; Iannetti, EF; Koopman, WJH; Smeitink, JAM; Willems, PHGM1
Aoki, I; Barkovich, AJ; Iwasaki, N; Nitta, N; Saito, S; Takanashi, J; Tanaka, R1
Agrimi, G; Castegna, A; Corricelli, M; Danese, A; Fiermonte, G; Giannuzzi, G; Giorgi, C; Lasorsa, FM; Massenzio, F; Monti, B; Palmieri, EM; Palmieri, F; Palmieri, L; Peña-Altamira, LE; Petralla, S; Pinton, P; Porcelli, V; Profilo, E; Sbano, L; Virgili, M; Viscomi, C; Zeviani, M1
Chandrashekar, KN1
Aygok, GA; Bullock, RM; Fatouros, P; Kettenmann, B; Marmarou, A1
Haller, RG; Vissing, J1
Friedman, SD; Gropman, AL; Ishak, G; Saneto, RP; Shaw, DW1
Dolan, PJ; Jin, YN; Johnson, GV; Quintanilla, RA1
Anglin, RE; Mazurek, MF; Noseworthy, MD; Rosebush, PI; Tarnopolsky, M1
Casarejos, MJ; Contreras, L; Dierssen, M; Grau, JM; Llorente-Folch, I; Mena, MA; Pardo, B; Saheki, T; Sahún, I; Satrústegui, J1
Angebault, C; Bielicki, G; Boddaert, N; Brabet, P; Cazevieille, C; Chaix, B; Delettre, C; Gueguen, N; Hamel, CP; Lenaers, G; Mausset-Bonnefont, AL; Puel, JL; Renou, JP; Reynier, P; Rigau, V; Sarzi, E; Seveno, M; Wang, J1
Boutron, A; Brivet, M; de Villemeur, TB; Guiochon-Mantel, A; Haut, S; Legrand, A; Rustin, P; Slama, A1
Alhassoon, OM; Brown, GG; Ellis, RJ; Gonzalez, R; Grant, I; Letendre, S; McCutchan, JA; Patterson, TL; Schweinsburg, BC; Taylor, MJ; Videen, JS1
Cecil, KM; deGrauw, T; Dinopoulos, A; Egelhoff, JC; Hadjigeorgiou, GM; Papadimitriou, A; Schapiro, MB; Wong, B1
Aygok, GA; Bullock, R; Fatouros, P; Marmarou, A; Signoretti, S1
Almeida, J; Ataíde, A; Borges, L; Correia, C; Coutinho, AM; Diogo, L; Grazina, M; Marques, C; Miguel, T; Oliveira, C; Oliveira, G; Vicente, AM1
Debska-Vielhaber, G; Elger, CE; Fendrich, R; Heinze, HJ; Kaufmann, J; Kudin, AP; Kunz, WS; Leibfritz, D; Niessen, HG; Schönfeld, MA; Schramm, J; Vielhaber, S; Wellmer, J; Willker, W1
Aygok, GA; Bullock, RM; Fatouros, PP; Marmarou, A; Portella, G; Signoretti, S1
Barker, PB; Bizzi, A; Bugiani, M; Castelli, G; Danesi, U; Erbetta, A; Farina, L; Herskovits, EH; Moroni, I; Uziel, G1

Reviews

1 review(s) available for aspartic acid and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
The use of neuroimaging in the diagnosis of mitochondrial disease.
    Developmental disabilities research reviews, 2010, Volume: 16, Issue:2

    Topics: Adenosine Triphosphate; Aspartic Acid; Brain; Child; Developmental Disabilities; Diagnosis, Differential; Humans; Image Processing, Computer-Assisted; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mitochondrial Diseases; Phosphocreatine

2010

Trials

3 trial(s) available for aspartic acid and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
Brain mitochondrial injury in human immunodeficiency virus-seropositive (HIV+) individuals taking nucleoside reverse transcriptase inhibitors.
    Journal of neurovirology, 2005, Volume: 11, Issue:4

    Topics: Adult; Aspartic Acid; Brain; Cell Respiration; Didanosine; Female; HIV Infections; Humans; Lamivudine; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mitochondria; Mitochondrial Diseases; Reverse Transcriptase Inhibitors; Stavudine; Treatment Outcome; Zidovudine

2005
Mitochondrial injury measured by proton magnetic resonance spectroscopy in severe head trauma patients.
    Acta neurochirurgica. Supplement, 2005, Volume: 95

    Topics: Adult; Aspartic Acid; Biomarkers; Brain; Brain Ischemia; Choline; Craniocerebral Trauma; Creatine; Female; Humans; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Mitochondria; Mitochondrial Diseases; Prognosis; Protons; Trauma Severity Indices

2005
Assessment of mitochondrial impairment in traumatic brain injury using high-resolution proton magnetic resonance spectroscopy.
    Journal of neurosurgery, 2008, Volume: 108, Issue:1

    Topics: Adolescent; Adult; Aspartic Acid; Brain Injuries; Choline; Creatine; Female; Follow-Up Studies; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mitochondrial Diseases; Outcome Assessment, Health Care; Predictive Value of Tests; Time Factors

2008

Other Studies

16 other study(ies) available for aspartic acid and Electron Transport Chain Deficiencies, Mitochondrial

ArticleYear
Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.
    Journal of medical case reports, 2019, Oct-21, Volume: 13, Issue:1

    Topics: Arginine; Aspartic Acid; Biomarkers; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondrial; Growth Differentiation Factor 15; Humans; Male; MELAS Syndrome; Middle Aged; Mitochondrial Diseases; Mutation

2019
Rescue from galactose-induced death of Leigh Syndrome patient cells by pyruvate and NAD
    Cell death & disease, 2018, 11-14, Volume: 9, Issue:11

    Topics: Adenosine Triphosphate; Aspartic Acid; Cell Death; Culture Media; Electron Transport Complex I; Fibroblasts; Galactose; Gene Expression; Glycolysis; Humans; Ketoglutaric Acids; Leigh Disease; Malates; Mitochondria; Mitochondrial Diseases; Mutation; NAD; NADH Dehydrogenase; Oxaloacetic Acid; Primary Cell Culture; Pyruvic Acid; Skin

2018
Neurochemistry in shiverer mouse depicted on MR spectroscopy.
    Journal of magnetic resonance imaging : JMRI, 2014, Volume: 39, Issue:6

    Topics: Amino Acid Transport Systems, Acidic; Analysis of Variance; Animals; Antiporters; Aspartic Acid; Brain; Cerebral Cortex; Choline; Disease Models, Animal; Hereditary Central Nervous System Demyelinating Diseases; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mice; Mice, Inbred ICR; Mice, Neurologic Mutants; Mitochondrial Diseases; Myelin Basic Protein; Neurochemistry; Psychomotor Disorders; Thalamus; White Matter

2014
Down-regulation of the mitochondrial aspartate-glutamate carrier isoform 1 AGC1 inhibits proliferation and N-acetylaspartate synthesis in Neuro2A cells.
    Biochimica et biophysica acta. Molecular basis of disease, 2017, Volume: 1863, Issue:6

    Topics: Amino Acid Transport Systems; Amino Acid Transport Systems, Acidic; Antiporters; Aspartic Acid; Cell Line; Cell Proliferation; Down-Regulation; Hereditary Central Nervous System Demyelinating Diseases; Humans; Mitochondrial Diseases; Mitochondrial Proteins; Neurons; Psychomotor Disorders

2017
D-Aspartic acid induced oxidative stress and mitochondrial dysfunctions in testis of prepubertal rats.
    Amino acids, 2010, Volume: 38, Issue:3

    Topics: Animals; Aspartic Acid; Biomarkers; Calcium Signaling; Dose-Response Relationship, Drug; Lipid Peroxidation; Male; Membrane Potential, Mitochondrial; Mitochondrial Diseases; Mitochondrial Membranes; Organ Size; Oxidative Stress; Permeability; Random Allocation; Rats; Rats, Wistar; Sexual Maturation; Stereoisomerism; Subcellular Fractions; Testis; Time Factors

2010
Assessment of mitochondrial impairment and cerebral blood flow in severe brain injured patients.
    Acta neurochirurgica. Supplement, 2008, Volume: 102

    Topics: Aspartic Acid; Blood Flow Velocity; Brain Injuries; Cerebrovascular Circulation; Diffusion Magnetic Resonance Imaging; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Spectroscopy; Mitochondrial Diseases; Protons; Regional Blood Flow

2008
Drilling for energy in mitochondrial disease.
    Archives of neurology, 2009, Volume: 66, Issue:8

    Topics: Adenosine Triphosphate; Animals; Apoptosis; Aspartic Acid; Cell Survival; Cells, Cultured; DNA Mutational Analysis; DNA, Mitochondrial; Energy Metabolism; Genetic Therapy; Glycolysis; Humans; Ketoglutaric Acids; Mitochondrial Diseases; Oxidative Phosphorylation

2009
Truncated tau and Aβ cooperatively impair mitochondria in primary neurons.
    Neurobiology of aging, 2012, Volume: 33, Issue:3

    Topics: Alzheimer Disease; Amyloid beta-Peptides; Animals; Aspartic Acid; Cell Line, Transformed; Down-Regulation; Humans; Mitochondria; Mitochondrial Diseases; Neurons; Primary Cell Culture; Prosencephalon; Rats; tau Proteins

2012
Psychiatric symptoms correlate with metabolic indices in the hippocampus and cingulate in patients with mitochondrial disorders.
    Translational psychiatry, 2012, Nov-13, Volume: 2

    Topics: Adult; Aged; Anxiety; Aspartic Acid; Case-Control Studies; Caudate Nucleus; Creatine; Female; Glutamic Acid; Glutamine; Glycerylphosphorylcholine; Gyrus Cinguli; Hippocampus; Humans; Inositol; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mitochondrial Diseases; Psychiatric Status Rating Scales

2012
AGC1-malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway.
    Journal of neurochemistry, 2013, Volume: 124, Issue:3

    Topics: Amino Acid Transport Systems, Acidic; Animals; Antiporters; Aspartic Acid; Corpus Striatum; Dopamine; Emotions; Exploratory Behavior; Female; Hereditary Central Nervous System Demyelinating Diseases; Malates; Male; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Diseases; Mitochondrial Membrane Transport Proteins; Motor Skills Disorders; Neural Pathways; Oxidative Stress; Pregnancy; Psychomotor Disorders; Substantia Nigra

2013
The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.
    Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12

    Topics: Acoustic Stimulation; Age Factors; Aging, Premature; Animals; Aspartic Acid; Chi-Square Distribution; Creatine; Disease Models, Animal; Disease Progression; Electron Transport Chain Complex Proteins; Electron Transport Complex IV; Electroretinography; Evoked Potentials, Auditory, Brain Stem; Evoked Potentials, Visual; Gene Expression Regulation; Glycolysis; GTP Phosphohydrolases; Humans; Lactic Acid; Locomotion; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Membrane Proteins; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mitochondrial Diseases; Muscle, Skeletal; Nervous System; Optic Atrophy, Autosomal Dominant; Optic Nerve; Phenotype; Physical Conditioning, Animal; Psychoacoustics; Psychomotor Performance; Reaction Time; Retina; Retinal Ganglion Cells; Sequence Deletion

2012
The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers.
    European journal of human genetics : EJHG, 2004, Volume: 12, Issue:3

    Topics: Amino Acid Sequence; Aspartic Acid; Child, Preschool; Cytochromes b; DNA, Mitochondrial; Electron Transport; Electron Transport Complex III; Fibroblasts; Genotype; Glycine; Humans; Lymphocytes; Male; Mitochondrial Diseases; Molecular Sequence Data; Mutation, Missense; Phenotype

2004
Brain MRI and proton MRS findings in infants and children with respiratory chain defects.
    Neuropediatrics, 2005, Volume: 36, Issue:5

    Topics: Aspartic Acid; Brain; Brain Chemistry; Brain Mapping; Child; Child, Preschool; Female; Humans; Infant; Infant, Newborn; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Mitochondrial Diseases; Protons

2005
Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.
    Journal of autism and developmental disorders, 2006, Volume: 36, Issue:8

    Topics: Aspartic Acid; Autistic Disorder; Chromosome Mapping; DNA Mutational Analysis; DNA Primers; DNA, Mitochondrial; Gene Expression; Gene Frequency; Glutamic Acid; Haplotypes; Humans; Lactic Acid; Membrane Transport Proteins; Mitochondrial Diseases; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Pyruvic Acid

2006
Subfield-specific loss of hippocampal N-acetyl aspartate in temporal lobe epilepsy.
    Epilepsia, 2008, Volume: 49, Issue:1

    Topics: Aconitate Hydratase; Adult; Aged; Aspartic Acid; Cell Count; Electroencephalography; Epilepsy, Temporal Lobe; Female; Glucose; Hippocampus; Humans; Lactates; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mitochondria; Mitochondrial Diseases; Parahippocampal Gyrus; Preoperative Care; Pyramidal Cells; Sclerosis; Succinates

2008
Classification of childhood white matter disorders using proton MR spectroscopic imaging.
    AJNR. American journal of neuroradiology, 2008, Volume: 29, Issue:7

    Topics: Adrenoleukodystrophy; Adult; Alexander Disease; Aspartic Acid; Brain; Child; Child, Preschool; Choline; Creatine; Diagnosis, Differential; DNA Mutational Analysis; Dominance, Cerebral; Female; Hereditary Central Nervous System Demyelinating Diseases; Humans; Image Processing, Computer-Assisted; Infant; Intracellular Signaling Peptides and Proteins; Lactic Acid; Linear Models; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Membrane Proteins; Mitochondrial Diseases; Muscular Dystrophies; Pelizaeus-Merzbacher Disease; Prospective Studies

2008