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index medicus (379) 379
humans (320) 320
male (155) 155
argininosuccinate synthase - deficiency (153) 153
female (147) 147
argininosuccinate synthetase (141) 141
animals (138) 138
argininosuccinate synthase - genetics (122) 122
argininosuccinate synthase - metabolism (111) 111
citrulline - blood (94) 94
arginine (92) 92
infant, newborn (68) 68
adult (67) 67
genetics & heredity (65) 65
urea - metabolism (59) 59
enzymes (58) 58
infant (57) 57
argininosuccinic aciduria (55) 55
mice (55) 55
liver - enzymology (54) 54
arginine - metabolism (53) 53
metabolism (53) 53
ammonia - blood (52) 52
citrullinemia (51) 51
biochemistry & molecular biology (50) 50
urea (47) 47
urea cycle (47) 47
citrulline (46) 46
mutation (46) 46
oncology (46) 46
argininosuccinate lyase - metabolism (45) 45
cancer (45) 45
medicine, research & experimental (43) 43
ornithine carbamoyltransferase deficiency disease (42) 42
ligases (41) 41
citrullinemia - genetics (40) 40
amino acids (39) 39
child, preschool (39) 39
citrulline - metabolism (39) 39
nitric oxide (38) 38
child (37) 37
expression (37) 37
physiological aspects (37) 37
rats (37) 37
liver (36) 36
carbamoyl-phosphate synthase - deficiency (35) 35
deficiency (35) 35
hyperammonemia (35) 35
middle aged (35) 35
argininosuccinate lyase (34) 34
deprivation (34) 34
research (34) 34
analysis (33) 33
argininosuccinate lyase - genetics (33) 33
cell biology (33) 33
abridged index medicus (32) 32
genetic aspects (32) 32
mutations (31) 31
arginase (30) 30
nitric-oxide synthase (30) 30
arginine deiminase (29) 29
article (29) 29
health aspects (29) 29
pregnancy (29) 29
cell line, tumor (28) 28
in-vivo (28) 28
proteins (28) 28
adolescent (27) 27
citrullinemia - diagnosis (27) 27
ligases - deficiency (27) 27
pediatrics (27) 27
gene expression (26) 26
argininosuccinate synthase (25) 25
cells, cultured (25) 25
disease models, animal (25) 25
arginase - metabolism (24) 24
endocrinology & metabolism (23) 23
genes (23) 23
liver - metabolism (23) 23
multidisciplinary sciences (23) 23
melanoma (22) 22
molecular sequence data (22) 22
phenotype (22) 22
amino acid metabolism, inborn errors - enzymology (21) 21
amino acid metabolism, inborn errors - genetics (21) 21
amino acid sequence (21) 21
arginine - blood (21) 21
arginine - deficiency (21) 21
base sequence (21) 21
gene (21) 21
hyperargininemia (21) 21
l-arginine (21) 21
messenger-rna (21) 21
nitric-oxide (21) 21
urea cycle disorders (21) 21
aged (20) 20
care and treatment (20) 20
classical citrullinemia (20) 20
hepatocellular-carcinoma (20) 20
hydrolases - pharmacology (20) 20
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Stem Cell Research and Therapy, ISSN 1757-6512, 07/2017, Volume 8, Issue 1, pp. 176 - 176
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Nature, ISSN 0028-0836, 11/2015, Volume 527, Issue 7578, pp. 379 - 383
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