X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (54976) 54976
Newspaper Article (2299) 2299
Book Chapter (623) 623
Book / eBook (243) 243
Newsletter (136) 136
Magazine Article (99) 99
Dissertation (91) 91
Web Resource (67) 67
Government Document (58) 58
Book Review (47) 47
Reference (31) 31
Trade Publication Article (21) 21
Publication (19) 19
Conference Proceeding (12) 12
Journal / eJournal (3) 3
Paper (3) 3
Streaming Video (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (34691) 34691
metabolic syndrome (24180) 24180
male (22101) 22101
female (20863) 20863
obesity (16496) 16496
animals (13477) 13477
risk factors (12923) 12923
adult (11907) 11907
metabolic disorders (11859) 11859
diabetes (11687) 11687
middle aged (11622) 11622
endocrinology & metabolism (10670) 10670
insulin resistance (10327) 10327
insulin-resistance (9088) 9088
research (8501) 8501
metabolism (8117) 8117
medicine (7717) 7717
metabolic diseases (7514) 7514
research article (7025) 7025
aged (6741) 6741
mice (6596) 6596
multidisciplinary sciences (6564) 6564
insulin (6490) 6490
analysis (6480) 6480
glucose (6479) 6479
body mass index (6299) 6299
medicine & public health (6197) 6197
inflammation (6144) 6144
health aspects (5984) 5984
nutritional and metabolic diseases (5877) 5877
physiological aspects (5854) 5854
diabetes mellitus (5663) 5663
internal medicine (5506) 5506
prevalence (5489) 5489
hypertension (5408) 5408
studies (5397) 5397
science (5390) 5390
risk (5260) 5260
type 2 diabetes (5200) 5200
genetic aspects (5177) 5177
lipids (5047) 5047
proteins (5003) 5003
disease (4953) 4953
diet (4916) 4916
cholesterol (4845) 4845
gene expression (4832) 4832
cardiovascular disease (4629) 4629
adolescent (4593) 4593
genetics & heredity (4443) 4443
endocrinology (4244) 4244
rodents (4173) 4173
nutrition & dietetics (4077) 4077
oxidative stress (4071) 4071
biochemistry & molecular biology (4032) 4032
child (4009) 4009
physiology (3924) 3924
blood pressure (3781) 3781
cardiovascular diseases (3683) 3683
pediatrics (3668) 3668
genetics (3655) 3655
liver (3624) 3624
association (3576) 3576
mutation (3504) 3504
medical research (3488) 3488
cardiovascular-disease (3451) 3451
expression (3383) 3383
genes (3366) 3366
body weight (3342) 3342
care and treatment (3335) 3335
mortality (3322) 3322
children (3305) 3305
atherosclerosis (3290) 3290
young adult (3266) 3266
medicine, research & experimental (3265) 3265
cell biology (3209) 3209
population (3197) 3197
nutrition (3187) 3187
cross-sectional studies (3146) 3146
epidemiology (3116) 3116
diagnosis (3057) 3057
rats (3040) 3040
review (2970) 2970
biology (2954) 2954
medicine and health sciences (2875) 2875
fatty acids (2857) 2857
risk-factors (2857) 2857
homeostasis (2852) 2852
human genetics (2850) 2850
biochemistry (2803) 2803
adipose-tissue (2798) 2798
triglycerides (2779) 2779
patients (2755) 2755
biology and life sciences (2726) 2726
phenotype (2725) 2725
enzymes (2621) 2621
age (2584) 2584
adipose tissue (2554) 2554
cancer (2510) 2510
body-mass index (2504) 2504
case-control studies (2498) 2498
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (54) 54
Online Resources - Online (23) 23
Collection Dvlpm't (Acquisitions) - Vendor file (15) 15
Collection Dvlpm't (Acquisitions) - Closed Orders (5) 5
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (4) 4
Gerstein Science - Periodical Stacks (3) 3
Gerstein Science - Bindery (2) 2
St. Michael's Hospital - Stacks (2) 2
Baycrest Hospital - Stacks (1) 1
Gerstein Science - Searching (1) 1
Holland Bloorview Kids Rehabilitation - Stacks (1) 1
Holland Bloorview Kids Rehabilitation - Sunnybrook Stacks (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Scarborough Hospital - General (1) 1
Scarborough Hospital - Online (1) 1
UTL at Downsview - May be requested (1) 1
UofT at Mississauga - Stacks (1) 1
West Park Healthcare Centre - Stacks (1) 1
Women's College Hospital - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (58149) 58149
Japanese (193) 193
French (183) 183
Portuguese (173) 173
German (149) 149
Spanish (136) 136
Russian (102) 102
Chinese (56) 56
Italian (45) 45
Polish (45) 45
Turkish (24) 24
Korean (20) 20
Czech (19) 19
Norwegian (19) 19
Hungarian (14) 14
Persian (10) 10
Arabic (8) 8
Danish (8) 8
Swedish (8) 8
Dutch (6) 6
Lithuanian (4) 4
Ukrainian (4) 4
Slovak (2) 2
Slovenian (2) 2
Breton (1) 1
Bulgarian (1) 1
Croatian (1) 1
Finnish (1) 1
Icelandic (1) 1
Romanian (1) 1
Serbian (1) 1
Urdu (1) 1
Welsh (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
PLoS genetics, ISSN 1553-7404, 2010, Volume 6, Issue 3, p. e1000874
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 brain, as measured by magnetic resonance spectroscopy... 
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
Human genetics, ISSN 1432-1203, 2015, Volume 135, Issue 2, pp. 209 - 222
Journal Article
Neuroscience, ISSN 0306-4522, 2007, Volume 145, Issue 4, pp. 1388 - 1396
Journal Article
Journal Article
Human genetics, ISSN 1432-1203, 2018, Volume 138, Issue 8-9, pp. 1051 - 1069
Journal Article
Journal Article