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index medicus (178) 178
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ii citrullinemia (36) 36
mitochondrial membrane transport proteins (36) 36
urea cycle (36) 36
citrin deficiency (34) 34
citrullinemia - genetics (34) 34
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infant, newborn (30) 30
identification (29) 29
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medicine, research & experimental (26) 26
membrane transport proteins - genetics (26) 26
mitochondrial proteins - genetics (26) 26
molecular sequence data (26) 26
calcium-binding proteins - deficiency (25) 25
citrin (25) 25
citrullinemia (24) 24
liver - metabolism (24) 24
infant (23) 23
liver (23) 23
organic anion transporters - deficiency (23) 23
adult-onset type ii citrullinemia (21) 21
carnitine - deficiency (21) 21
hyperammonemia (21) 21
middle aged (21) 21
argininosuccinate synthase - genetics (20) 20
base sequence (19) 19
biophysics (19) 19
disease models, animal (19) 19
gastroenterology & hepatology (19) 19
neurosciences (19) 19
messenger-rna (18) 18
slc25a13 (17) 17
calcium-binding proteins - genetics (16) 16
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kinetics (16) 16
liver-transplantation (16) 16
mice, mutant strains (16) 16
amino acid sequence (15) 15
analysis (15) 15
argininosuccinate synthase - metabolism (15) 15
carnitine deficiency (15) 15
cell biology (15) 15
mice, knockout (15) 15
mitochondrial membrane transport proteins - genetics (15) 15
mouse (15) 15
polymerase chain reaction (15) 15
protein (15) 15
urea - metabolism (15) 15
adolescent (14) 14
ammonia - blood (14) 14
argininosuccinate synthase - deficiency (14) 14
dna mutational analysis (14) 14
expression (14) 14
mitochondria (14) 14
aspartate-glutamate carrier (13) 13
cholestasis, intrahepatic - genetics (13) 13
rna, messenger - genetics (13) 13
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arginine (12) 12
aspartate glutamate carrier (12) 12
biochemistry (12) 12
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membrane transport proteins - deficiency (11) 11
metabolism (11) 11
mice, inbred c57bl (11) 11
mitochondrial proteins - deficiency (11) 11
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calcium - metabolism (10) 10
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Journal Article
Molecular Therapy, ISSN 1525-0016, 07/2019, Volume 27, Issue 7, pp. 1242 - 1251
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, pp. e74544 - e74544
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 6/2008, Volume 53, Issue 6, pp. 534 - 545
Journal Article
Journal Article
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 02/2013, Volume 124, Issue 3, pp. 347 - 362
The mitochondrial transporter of aspartate‐glutamate Aralar/ AGC 1 is a regulatory component of the malate‐aspartate shuttle. Aralar deficiency in mouse and... 
B | VMAT | 2 | global cerebral hypomyelination | malate‐aspartate shuttle | mni | 1 deficiency | AGC | dopamine | ® | O | ank | malate-aspartate shuttle | AGC-1 deficiency | OmniBank | VMAT2 | NICOTINAMIDE NUCLEOTIDE TRANSHYDROGENASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | RELEASE | NEUROSCIENCES | MICE LACKING | OmniBank (R) | METABOLISM | VESICULAR MONOAMINE TRANSPORTER-2 | MITOCHONDRIAL COMPLEX-I | MOUSE MODEL | NEURONS | RAT-BRAIN | EXPRESSION | Oxidative Stress - physiology | Amino Acid Transport Systems, Acidic - metabolism | Mitochondrial Diseases - metabolism | Dopamine - genetics | Amino Acid Transport Systems, Acidic - deficiency | Male | Hereditary Central Nervous System Demyelinating Diseases - physiopathology | Motor Skills Disorders - genetics | Mice, 129 Strain | Substantia Nigra - metabolism | Corpus Striatum - cytology | Corpus Striatum - metabolism | Substantia Nigra - cytology | Mitochondrial Membrane Transport Proteins - genetics | Dopamine - deficiency | Exploratory Behavior - physiology | Psychomotor Disorders - metabolism | Psychomotor Disorders - genetics | Mitochondrial Membrane Transport Proteins - deficiency | Antiporters - genetics | Malates - metabolism | Female | Neural Pathways - physiopathology | Psychomotor Disorders - physiopathology | Dopamine - metabolism | Hereditary Central Nervous System Demyelinating Diseases - genetics | Antiporters - deficiency | Emotions - physiology | Mitochondrial Diseases - genetics | Mitochondrial Membrane Transport Proteins - metabolism | Mice, Inbred C57BL | Antiporters - metabolism | Hereditary Central Nervous System Demyelinating Diseases - metabolism | Mice, Knockout | Pregnancy | Motor Skills Disorders - metabolism | Animals | Neural Pathways - cytology | Amino Acid Transport Systems, Acidic - genetics | Neural Pathways - metabolism | Aspartic Acid - metabolism | Mice | Aspartic Acid - physiology | Mitochondrial Diseases - physiopathology | Tyrosine | Phenols | Aspartate | Neurochemistry | Mitochondria | Dopamine | Brain | Reactive oxygen species | Hyperreactivity | Brain stem | Hyperactivity | Neurons | Substantia nigra | Cortex | Amino acids | Metabolism | Cytosol | Vesicular amine transporter | Amine oxidase (flavin-containing) | NADH | Neostriatum | Anxiety | Index Medicus
Journal Article