X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (264) 264
humans (170) 170
animals (129) 129
creatine (129) 129
male (127) 127
glycine - analogs & derivatives (124) 124
glycine (104) 104
metabolism (97) 97
female (84) 84
arginine (82) 82
biochemistry & molecular biology (76) 76
glycine amidinotransferase (68) 68
rats (64) 64
brain (60) 60
guanidinoacetate (60) 60
physiological aspects (56) 56
glycine - metabolism (55) 55
amidinotransferases - metabolism (53) 53
inborn error (53) 53
creatine - metabolism (51) 51
glycine - blood (47) 47
amino acids (44) 44
adult (43) 43
analysis (42) 42
arginine-glycine amidinotransferase (41) 41
genetics & heredity (41) 41
amidinotransferases - genetics (40) 40
biosynthesis (40) 40
child (40) 40
creatine - blood (40) 40
glycine - urine (40) 40
biochemistry, general (39) 39
enzymes (37) 37
guanidinoacetate methyltransferase deficiency (36) 36
child, preschool (34) 34
creatine - deficiency (33) 33
metabolites (33) 33
mice (33) 33
life sciences (32) 32
arginine - metabolism (31) 31
guanidinoacetate n-methyltransferase (30) 30
plasma (29) 29
urine (29) 29
endocrinology & metabolism (28) 28
transferases (28) 28
creatinine (27) 27
dietary supplements (27) 27
guanidinoacetic acid (27) 27
neurosciences (27) 27
creatine - urine (26) 26
middle aged (26) 26
analytical chemistry (25) 25
life sciences, general (25) 25
neurobiology (25) 25
biochemical engineering (24) 24
brain - metabolism (24) 24
guanidinoacetate n-methyltransferase - deficiency (24) 24
guanidinoacetate n-methyltransferase - metabolism (24) 24
magnetic resonance spectroscopy (24) 24
mass spectrometry (24) 24
proteomics (24) 24
supplementation (24) 24
infant (23) 23
nutrition & dietetics (23) 23
agat (22) 22
amidinotransferases - deficiency (22) 22
creatine - biosynthesis (22) 22
diagnosis (22) 22
homocysteine (22) 22
kidney - enzymology (22) 22
research (22) 22
adolescent (21) 21
kidney - metabolism (21) 21
l-arginine (21) 21
mutation (21) 21
rats, sprague-dawley (21) 21
in-vivo (20) 20
liver (20) 20
medicine, research & experimental (20) 20
physiology (20) 20
proteins (20) 20
young adult (20) 20
methyltransferase deficiency (19) 19
aged (18) 18
amidinotransferase (18) 18
creatine - administration & dosage (18) 18
creatine - therapeutic use (18) 18
diet (18) 18
expression (18) 18
guanidinoacetate n-methyltransferase - genetics (18) 18
acid (17) 17
gamt (17) 17
kidney (17) 17
creatinine - urine (16) 16
kinetics (16) 16
medical laboratory technology (16) 16
membrane transport proteins - genetics (16) 16
pediatrics (16) 16
creatinine - blood (15) 15
energy metabolism (15) 15
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (309) 309
Japanese (6) 6
German (2) 2
Polish (2) 2
French (1) 1
Portuguese (1) 1
Russian (1) 1
Spanish (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 2001, Volume 69, Issue 5, pp. 1127 - 1133
Journal Article
FEBS Journal, ISSN 1742-464X, 09/2010, Volume 277, Issue 18, pp. 3844 - 3860
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 12/2015, Volume 116, Issue 4, pp. 252 - 259
Arginine:glycine aminotransferase (AGAT) ( ) deficiency is an autosomal recessive inborn error of creative synthesis. We performed an international survey... 
GATM | Cerebral creatine deficiency | Intellectual disability | Myopathy | MEDICINE, RESEARCH & EXPERIMENTAL | INBORN ERROR | METABOLISM | HOMOARGININE | ARGININE/GLYCINE AMIDINOTRANSFERASE | DISEASE | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | CREATINE DEFICIENCY | BRAIN | Glycine - analogs & derivatives | Developmental Disabilities - drug therapy | Speech Disorders - drug therapy | Amino Acid Metabolism, Inborn Errors - physiopathology | Glycine - urine | Humans | Child, Preschool | Amidinotransferases - genetics | Male | Developmental Disabilities - genetics | Intellectual Disability - genetics | Amino Acid Metabolism, Inborn Errors - diagnosis | Young Adult | Amino Acid Metabolism, Inborn Errors - genetics | Muscular Diseases - physiopathology | Muscular Diseases - drug therapy | Glycine - deficiency | Creatine - deficiency | Female | Amidinotransferases - chemistry | Child | Developmental Disabilities - diagnosis | Speech Disorders - diagnosis | Protein Structure, Tertiary | Developmental Disabilities - physiopathology | Glycine - blood | Amidinotransferases - deficiency | Gene Expression | Magnetic Resonance Spectroscopy | Protein Structure, Secondary | Speech Disorders - genetics | Models, Molecular | Treatment Outcome | Genes, Recessive | Sequence Analysis, DNA | Speech Disorders - physiopathology | Intellectual Disability - drug therapy | Intellectual Disability - physiopathology | Muscular Diseases - diagnosis | Intellectual Disability - diagnosis | Adolescent | Creatine - therapeutic use | Muscular Diseases - genetics | Mutation | Amino Acid Metabolism, Inborn Errors - drug therapy | Arginine | Glycine | Index Medicus
Journal Article
Journal Article
Journal Article
Journal Article
Bulletin of Siberian Medicine, ISSN 1682-0363, 2018, Volume 17, Issue 1, pp. 7 - 14
L-homoarginine (hArg) is a non-coding amino acid, the blood level reduction of which is associated with an increased risk of stroke and heart attack. In humans... 
Guanidinoacetic acid | Arginase | Creatine | Homoarginine | Arginine: glycine amidinotransferase | homoarginine | creatine | arginase | guanidinoacetic acid | arginine:glycine amidinotransferase
Journal Article
MicrobiologyOpen, ISSN 2045-8827, 06/2013, Volume 2, Issue 3, pp. 447 - 458
Journal Article
FEBS Open Bio, ISSN 2211-5463, 06/2016, Volume 6, Issue 6, pp. 603 - 609
Phaseolotoxins ( PHT s), which are produced by Pseudomonas , belong to a family of phosphoramidate natural products. Two nonproteinogenic amino acid... 
homoarginine | phaseolotoxin | amidinotransferase | biosynthesis | Biosynthesis | Amidinotransferase | Phaseolotoxin | Homoarginine | MECHANISM | L-ARGININEGLYCINE AMIDINOTRANSFERASE | CRYSTAL-STRUCTURE | TOXIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | ORNITHINE | ARGININE/GLYCINE AMIDINOTRANSFERASE | SYRINGAE PV. PHASEOLICOLA | CLUSTER
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 07/2013, Volume 109, Issue 3, pp. 260 - 268
Cerebral creatine deficiency syndromes (CCDS) are a group of inborn errors of creatine metabolism that involve and for creatine biosynthesis disorders and for... 
Creatine transporter defect | AGAT (Arginine:Glycine amidinotransferase) deficiency | GAMT (Guanidinoacetate Methyltransferase) deficiency | Cerebral creatine deficiency syndrome | GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY | MISSENSE VARIANTS | MEDICINE, RESEARCH & EXPERIMENTAL | GLYCINE AMIDINOTRANSFERASE DEFICIENCY | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSPORTER GENE SLC6A8 | INBORN ERROR | GAMT DEFICIENCY | ENZYME ASSAY | LINKED MENTAL-RETARDATION | METABOLISM | AGAT DEFICIENCY | GENETICS & HEREDITY | Humans | Movement Disorders - diagnosis | Amidinotransferases - genetics | Male | Intellectual Disability - metabolism | Amino Acid Metabolism, Inborn Errors - genetics | Membrane Transport Proteins - genetics | Amidinotransferases - blood | Amidinotransferases - chemistry | Brain Diseases, Metabolic, Inborn - genetics | Creatine - genetics | Models, Molecular | Plasma Membrane Neurotransmitter Transport Proteins - metabolism | Guanidinoacetate N-Methyltransferase - metabolism | Amidinotransferases - metabolism | Plasma Membrane Neurotransmitter Transport Proteins - genetics | Phenotype | Protein Conformation | Movement Disorders - genetics | Mutation | Developmental Disabilities - metabolism | Guanidinoacetate N-Methyltransferase - genetics | Developmental Disabilities - genetics | Language Development Disorders - metabolism | Brain Diseases, Metabolic, Inborn - diagnosis | Intellectual Disability - genetics | Amino Acid Metabolism, Inborn Errors - diagnosis | Amino Acid Metabolism, Inborn Errors - metabolism | Mental Retardation, X-Linked - genetics | Language Development Disorders - diagnosis | Mental Retardation, X-Linked - diagnosis | Creatine - metabolism | Creatine - deficiency | Female | Developmental Disabilities - diagnosis | Guanidinoacetate N-Methyltransferase - blood | Speech Disorders - diagnosis | Plasma Membrane Neurotransmitter Transport Proteins - deficiency | Speech Disorders - metabolism | Amidinotransferases - deficiency | Brain Diseases, Metabolic, Inborn - metabolism | Language Development Disorders - genetics | Speech Disorders - genetics | Creatinine - urine | Syndrome | Movement Disorders - metabolism | Guanidinoacetate N-Methyltransferase - deficiency | Intellectual Disability - diagnosis | Movement Disorders - congenital | Mental Retardation, X-Linked - metabolism | Physiological aspects | Enzymes | Metabolites | Creatine | Index Medicus
Journal Article
Amino Acids, ISSN 0939-4451, 8/2016, Volume 48, Issue 8, pp. 2025 - 2039
Skeletal muscles require energy either at constant low (e.g., standing and posture) or immediate high rates (e.g., exercise). To fulfill these requirements,... 
Biochemistry, general | Alanine | Neurobiology | Pyruvate | Glucose | Creatine | Skeletal muscle | Life Sciences | Analytical Chemistry | Life Sciences, general | Biochemical Engineering | Proteomics | Arginine:glycine amidinotransferase (AGAT) | HOMEOSTASIS | PGC-1-ALPHA | BIOCHEMISTRY & MOLECULAR BIOLOGY | KINASE | EXPENDITURE | SKELETAL-MUSCLE | AMIDINOTRANSFERASE | GLUCONEOGENESIS | MAGNETIC-RESONANCE | Arginine: glycine amidinotransferase (AGAT) | AMPK | ENERGY-METABOLISM | Developmental Disabilities - metabolism | Transcriptome | Adipose Tissue, White - metabolism | Amidinotransferases - genetics | Muscle, Skeletal - metabolism | Developmental Disabilities - genetics | Phosphocreatine - genetics | Obesity - genetics | Intellectual Disability - genetics | Intellectual Disability - metabolism | Speech Disorders - pathology | Amino Acid Metabolism, Inborn Errors - metabolism | Developmental Disabilities - pathology | Amino Acid Metabolism, Inborn Errors - genetics | Amino Acid Metabolism, Inborn Errors - pathology | Adipose Tissue, White - pathology | Speech Disorders - metabolism | Amidinotransferases - deficiency | Obesity - chemically induced | Intellectual Disability - pathology | Oxidative Phosphorylation | Speech Disorders - genetics | Metabolome | Amidinotransferases - metabolism | Mice, Knockout | Obesity - metabolism | Obesity - pathology | Animals | Mice | Phosphocreatine - metabolism | Muscle, Skeletal - pathology | Index Medicus
Journal Article