X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (31868) 31868
Publication (4928) 4928
Book Review (637) 637
Book / eBook (457) 457
Book Chapter (384) 384
Newsletter (122) 122
Conference Proceeding (81) 81
Dissertation (23) 23
Newspaper Article (19) 19
Magazine Article (12) 12
Reference (8) 8
Data Set (5) 5
Paper (4) 4
Government Document (2) 2
Trade Publication Article (2) 2
Presentation (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (16790) 16790
animals (16057) 16057
humans (14416) 14416
mice (7277) 7277
biochemistry & molecular biology (7015) 7015
cell biology (6981) 6981
proteins (6177) 6177
male (5842) 5842
female (4490) 4490
physiological aspects (4185) 4185
mutation (3750) 3750
research (3504) 3504
rats (3442) 3442
neurosciences (3355) 3355
membrane proteins - metabolism (3254) 3254
analysis (3238) 3238
article (3127) 3127
expression (3000) 3000
cell membrane - metabolism (2905) 2905
research article (2844) 2844
membrane proteins - genetics (2834) 2834
mice, knockout (2770) 2770
gene expression (2751) 2751
multidisciplinary sciences (2688) 2688
mitochondria (2532) 2532
physiology (2532) 2532
oxidative stress (2461) 2461
metabolism (2415) 2415
plasma-membrane (2408) 2408
plant sciences (2332) 2332
membrane proteins (2331) 2331
signal transduction (2329) 2329
genetic aspects (2317) 2317
medicine (2305) 2305
apoptosis (2245) 2245
cells (2240) 2240
molecular sequence data (2218) 2218
cells, cultured (2195) 2195
life sciences (2166) 2166
membranes (2107) 2107
biological transport (2056) 2056
lipids (2056) 2056
biology (2043) 2043
protein (2008) 2008
mice, inbred c57bl (1991) 1991
protein transport (1991) 1991
rodents (1957) 1957
science (1949) 1949
amino acid sequence (1935) 1935
biochemistry (1925) 1925
cell line (1885) 1885
mitochondria - metabolism (1846) 1846
genes (1818) 1818
homeostasis (1807) 1807
transport (1785) 1785
membrane (1754) 1754
microbiology (1702) 1702
gene (1698) 1698
biophysics (1684) 1684
enzymes (1662) 1662
membrane transport proteins - genetics (1651) 1651
protein binding (1582) 1582
membrane transport proteins - metabolism (1578) 1578
immunology (1556) 1556
pharmacology & pharmacy (1486) 1486
models, biological (1481) 1481
phosphorylation (1463) 1463
genetics & heredity (1449) 1449
saccharomyces-cerevisiae (1446) 1446
health aspects (1431) 1431
adult (1429) 1429
brain (1414) 1414
cell membranes (1407) 1407
phenotype (1397) 1397
carrier proteins - metabolism (1363) 1363
plants (1361) 1361
endocrinology & metabolism (1347) 1347
identification (1334) 1334
disease models, animal (1320) 1320
gene-expression (1271) 1271
activation (1208) 1208
biochemistry, general (1186) 1186
molecular biology (1172) 1172
endoplasmic-reticulum (1169) 1169
calcium - metabolism (1156) 1156
neurons (1145) 1145
genetics (1131) 1131
kinases (1127) 1127
biosynthesis (1125) 1125
localization (1123) 1123
carrier proteins - genetics (1108) 1108
permeability (1108) 1108
mitochondrial dna (1104) 1104
in-vivo (1081) 1081
cancer (1080) 1080
medicine, research & experimental (1076) 1076
middle aged (1060) 1060
calcium (1059) 1059
disease (1052) 1052
rna, messenger - metabolism (1038) 1038
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (314) 314
UofT at Mississauga - Stacks (49) 49
UTL at Downsview - May be requested (37) 37
Earth Sciences (Noranda) - Stacks (31) 31
Engineering & Comp. Sci. - Stacks (16) 16
UofT at Scarborough - Stacks (16) 16
Collection Dvlpm't (Acquisitions) - Vendor file (13) 13
Collection Dvlpm't (Acquisitions) - Closed Orders (11) 11
Online Resources - Online (10) 10
Chemistry (A D Allen) - Stacks (6) 6
Physics - Stacks (3) 3
Engineering & Comp. Sci. - Reference (2) 2
Trinity College (John W Graham) - Stacks (2) 2
Trinity College (John W Graham) - Storage (2) 2
Collection Dvlpm't (Acquisitions) - Cancelled Order (1) 1
Dentistry (Harry R Abbott) - Stacks (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Gerstein Science - Missing (1) 1
Humber River Regional Hospital - Finch Stacks (1) 1
Physics - Missing (1) 1
Toronto East General Hospital - Stacks (1) 1
UofT at Mississauga - Reference (1) 1
UofT at Scarborough - May be requested in 6-10 wks (1) 1
UofT at Scarborough - Not Returned (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (32514) 32514
Japanese (42) 42
Spanish (29) 29
Chinese (28) 28
French (23) 23
Russian (17) 17
German (16) 16
Czech (5) 5
Portuguese (5) 5
Hungarian (4) 4
Polish (3) 3
Italian (2) 2
Ukrainian (2) 2
Bulgarian (1) 1
Dutch (1) 1
Korean (1) 1
Ndonga (1) 1
Norwegian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Cell Metabolism, ISSN 1550-4131, 06/2013, Volume 17, Issue 6, pp. 976 - 987
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 12/2015, Volume 97, Issue 6, pp. 894 - 903
Journal Article
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 4/2008, Volume 31, Issue 2, pp. 230 - 239
Creatine deficiency syndromes, either due to AGAT, GAMT or SLC6A8 deficiencies, lead to a complete absence, or a very strong decrease, of creatine within the... 
Biochemistry, general | Human Genetics | Pediatrics | Internal Medicine | Medicine & Public Health | Metabolic Diseases | GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY | LINKED MENTAL-RETARDATION | ARGININE RESTRICTION | ENERGY HOMEOSTASIS | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | IN-SITU HYBRIDIZATION | MAGNETIC-RESONANCE | CLINICAL CHARACTERISTICS | RAT-BRAIN | TRANSPORTER GENE SLC6A8 | INBORN ERROR | Glycine - analogs & derivatives | Glycine - metabolism | Prognosis | Guanidinoacetate N-Methyltransferase - genetics | Humans | Brain - enzymology | Amidinotransferases - genetics | Developmental Disabilities - genetics | Intellectual Disability - genetics | Membrane Transport Proteins - deficiency | Amino Acid Metabolism, Inborn Errors - genetics | Developmental Disabilities - enzymology | Membrane Transport Proteins - genetics | Movement Disorders - enzymology | Intellectual Disability - enzymology | Creatine - deficiency | Amidinotransferases - deficiency | Genetic Predisposition to Disease | Language Development Disorders - genetics | Speech Disorders - genetics | Language Development Disorders - enzymology | Phenotype | Animals | Guanidinoacetate N-Methyltransferase - deficiency | Movement Disorders - congenital | Speech Disorders - enzymology | Movement Disorders - genetics | Amino Acid Metabolism, Inborn Errors - enzymology | Creatine | Central nervous system
Journal Article
Biochimie, ISSN 0300-9084, 12/2015, Volume 119, pp. 146 - 165
Creatine is physiologically provided equally by diet and by endogenous synthesis from arginine and glycine with successive involvements of arginine glycine... 
GAMT | CRTR | SLC6A8 | AGAT | AMP activated protein kinase | Creatine | Secondary creatine disorders | GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY | OXIDATIVE STRESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | OXYGEN SPECIES GENERATION | UREA CYCLE DISORDERS | MAGNETIC-RESONANCE-SPECTROSCOPY | RAT-KIDNEY TRANSAMIDINASE | LINKED MENTAL-RETARDATION | ACUTE MYOCARDIAL-INFARCTION | TERM-FOLLOW-UP | ARGININE-GLYCINE AMIDINOTRANSFERASE | Amino Acid Transport Systems, Basic - genetics | Humans | Nerve Tissue Proteins - deficiency | Movement Disorders - diagnosis | Amidinotransferases - genetics | Intellectual Disability - metabolism | Biological Transport, Active | Gyrate Atrophy - enzymology | Amino Acid Metabolism, Inborn Errors - genetics | Intellectual Disability - enzymology | Brain Diseases, Metabolic, Inborn - genetics | Hyperammonemia - diagnosis | Hyperammonemia - genetics | Creatine - genetics | Urea Cycle Disorders, Inborn - metabolism | Creatine - biosynthesis | Gyrate Atrophy - genetics | Plasma Membrane Neurotransmitter Transport Proteins - metabolism | Guanidinoacetate N-Methyltransferase - metabolism | Amidinotransferases - metabolism | Plasma Membrane Neurotransmitter Transport Proteins - genetics | Language Development Disorders - enzymology | Urea Cycle Disorders, Inborn - diagnosis | Energy Metabolism | Urea Cycle Disorders, Inborn - enzymology | Movement Disorders - genetics | Mutation | Ornithine - deficiency | Amino Acid Transport Systems, Basic - metabolism | Amino Acid Metabolism, Inborn Errors - enzymology | S-Adenosylmethionine - metabolism | AMP-Activated Protein Kinases - metabolism | Hyperammonemia - metabolism | Developmental Disabilities - metabolism | Guanidinoacetate N-Methyltransferase - genetics | Ornithine - genetics | Developmental Disabilities - genetics | Language Development Disorders - metabolism | Brain Diseases, Metabolic, Inborn - enzymology | 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 | Mental Retardation, X-Linked - enzymology | Developmental Disabilities - enzymology | Language Development Disorders - diagnosis | Mental Retardation, X-Linked - diagnosis | Movement Disorders - enzymology | Creatine - metabolism | Hyperammonemia - enzymology | Creatine - deficiency | Gyrate Atrophy - diagnosis | Developmental Disabilities - diagnosis | Speech Disorders - diagnosis | Plasma Membrane Neurotransmitter Transport Proteins - deficiency | Speech Disorders - metabolism | Amidinotransferases - deficiency | Brain Diseases, Metabolic, Inborn - metabolism | Language Development Disorders - genetics | Ornithine - metabolism | Gyrate Atrophy - metabolism | Prenatal Diagnosis | Speech Disorders - genetics | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Amino Acid Transport Systems, Basic - deficiency | Movement Disorders - metabolism | Animals | Urea Cycle Disorders, Inborn - genetics | Guanidinoacetate N-Methyltransferase - deficiency | Intellectual Disability - diagnosis | Movement Disorders - congenital | Speech Disorders - enzymology | Methylation | Mental Retardation, X-Linked - metabolism | Antioxidants | Phosphates | Algorithms | Animal behavior | Physiological aspects | GABA | Glycine | Phosphotransferases | Medical research | Medicine, Experimental | Protein kinases | Life Sciences
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2009, Volume 41, Issue 2, pp. 234 - 239
Vitamin B(12) (cobalamin) is essential in animals for metabolism of branched chain amino acids and odd chain fatty acids, and for remethylation of homocysteine... 
Vitamin B 12 Deficiency - etiology | Transcobalamins - genetics | Humans | Male | Methylmalonic Acid - metabolism | Proteins - isolation & purification | Tissue Distribution | Membrane Transport Proteins - deficiency | Membrane Transport Proteins - genetics | Transcobalamins - isolation & purification | Female | Membrane Transport Proteins - metabolism | Vitamin B 12 Deficiency - metabolism | Child | Methylmalonic Acid - urine | Chromosome Deletion | Lysosome-Associated Membrane Glycoproteins - metabolism | Nucleocytoplasmic Transport Proteins - physiology | Chromosome Mapping | Chromosomes, Human, Pair 6 | Nucleocytoplasmic Transport Proteins - genetics | Polymorphism, Genetic | Proteins - genetics | Nucleocytoplasmic Transport Proteins - metabolism | Proteins - metabolism | Transcobalamins - metabolism | Vitamin B 12 Deficiency - genetics | Hyperhomocysteinemia - genetics | HeLa Cells | Hyperhomocysteinemia - complications | Vitamin B 12 - metabolism | Medical research | Heart surgery | Genes | Vitamin B | Genetics | Medical screening | Chromosomes | Nucleocytoplasmic Transport Proteins | Biochemistry, Molecular Biology | Vitamin B 12 Deficiency | Proteins | Life Sciences | Membrane Transport Proteins | Transcobalamins | Vitamin B 12 | Hyperhomocysteinemia | Methylmalonic Acid | Lysosome-Associated Membrane Glycoproteins | Hela Cells
Journal Article
Science, ISSN 0036-8075, 10/2006, Volume 314, Issue 5797, pp. 308 - 312
Journal Article
Cell Death and Differentiation, ISSN 1350-9047, 12/2017, Volume 24, Issue 12, pp. 2127 - 2138
Journal Article