X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (165) 165
Publication (23) 23
Book / eBook (9) 9
Book Chapter (9) 9
Dissertation (6) 6
Book Review (4) 4
Newspaper Article (3) 3
Conference Proceeding (2) 2
Journal / eJournal (1) 1
Patent (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (104) 104
humans (83) 83
female (52) 52
male (44) 44
middle aged (31) 31
aged (26) 26
animals (25) 25
adult (21) 21
research (17) 17
analysis (16) 16
genetics & heredity (14) 14
oncology (14) 14
cell biology (13) 13
article (12) 12
adolescent (11) 11
genetic aspects (11) 11
genotype (11) 11
multidisciplinary sciences (11) 11
patients (11) 11
biochemistry & molecular biology (10) 10
gene expression (10) 10
genes (10) 10
genomes (10) 10
mice (10) 10
proteins (10) 10
retrospective studies (10) 10
surgery (10) 10
treatment outcome (10) 10
cancer (9) 9
genetics (9) 9
health aspects (9) 9
medicine (9) 9
medicine, general & internal (9) 9
population (9) 9
child, preschool (8) 8
identification (8) 8
mutation (8) 8
obstetrics & gynecology (8) 8
phenotype (8) 8
prospective studies (8) 8
asia (7) 7
biotechnology & applied microbiology (7) 7
child (7) 7
dermatology (7) 7
follow-up studies (7) 7
genomics (7) 7
risk (7) 7
studies (7) 7
women (7) 7
young adult (7) 7
abridged index medicus (6) 6
aged, 80 and over (6) 6
amino acid sequence (6) 6
care and treatment (6) 6
children (6) 6
gene expression profiling (6) 6
in-vitro (6) 6
infant (6) 6
medicine & public health (6) 6
models, molecular (6) 6
molecular sequence data (6) 6
mortality (6) 6
outcomes (6) 6
pelvic organ prolapse - surgery (6) 6
physiological aspects (6) 6
polymorphism, single nucleotide (6) 6
protein (6) 6
protein binding (6) 6
public health (6) 6
association (5) 5
cell differentiation (5) 5
complications (5) 5
dilated cardiomyopathy (5) 5
gene expression regulation (5) 5
gene-expression (5) 5
genetic predisposition to disease (5) 5
life sciences (5) 5
molecular biology (5) 5
neurosciences (5) 5
prevalence (5) 5
quality of life (5) 5
rats (5) 5
research article (5) 5
science (5) 5
singapore - epidemiology (5) 5
stress (5) 5
transplantation (5) 5
abstracts (4) 4
asian continental ancestry group - genetics (4) 4
base sequence (4) 4
binding sites (4) 4
biochemistry (4) 4
biology (4) 4
brain (4) 4
cell & tissue engineering (4) 4
cell line (4) 4
cells, cultured (4) 4
clinical neurology (4) 4
crystal structure (4) 4
crystallography, x-ray (4) 4
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (4) 4
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
UofT at Scarborough - Stacks (2) 2
Art - Library use only (1) 1
Indust. Rel's & Hum. Resources (Newman) - Library use only (1) 1
Innis College - Stacks (1) 1
Knox College (Caven) - Stacks (1) 1
Music - Stacks (1) 1
Regis College - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
UTL at Downsview - May be requested (1) 1
UofT Schools - Stacks (1) 1
UofT at Mississauga - Oversize (1) 1
UofT at Mississauga - Stacks (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
Victoria University Emmanuel College - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature, ISSN 0028-0836, 07/2015, Volume 523, Issue 7562, pp. 561 - 567
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 07/2017, Volume 62, Issue 7, pp. 711 - 715
Marfan syndrome is an autosomal dominant disorder affecting mainly the skeletal, ocular and cardiovascular systems. Most cases are caused by mutations in the... 
ELEMENTS | INSERTION | HUMAN-DISEASE | FIBRILLIN | MARFAN-SYNDROME | GENETICS & HEREDITY | PHENOTYPE | MUTATIONS | SVA | TGFBR2 | FAMILY | Microarray Analysis | Base Sequence | Humans | Child, Preschool | Exons - genetics | Male | Fibrillin-1 - genetics | Sinus of Valsalva - abnormalities | Child | Dilatation, Pathologic | Sequence Deletion - genetics
Journal Article
Science, ISSN 0036-8075, 1/2012, Volume 335, Issue 6064, pp. 85 - 88
Journal Article
Carcinogenesis, ISSN 0143-3334, 2015, Volume 36, Issue 7, pp. 757 - 768
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2013, Volume 8, Issue 9, pp. e74359 - e74359
Journal Article
Cell Research, ISSN 1001-0602, 03/2015, Volume 25, Issue 3, pp. 398 - 398
Journal Article
Nature (London), ISSN 0028-0836, 07/2015, Volume 523, Issue 7562
G-protein-coupled receptors (GPCRs) signal primarily through G proteins or arrestins. Arrestin binding to GPCRs blocks G protein interaction and redirects... 
X-ray crystallography | INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY | G protein-coupled receptors | BASIC BIOLOGICAL SCIENCES
Journal Article
Cell research, ISSN 1001-0602, 03/2015, Volume 25, Issue 3, pp. 398 - 398
Journal Article