X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (434703) 434703
Publication (48614) 48614
Newsletter (29198) 29198
Newspaper Article (4207) 4207
Conference Proceeding (4172) 4172
Book Chapter (3254) 3254
Book Review (2513) 2513
Dissertation (977) 977
Magazine Article (325) 325
Government Document (312) 312
Web Resource (205) 205
Book / eBook (187) 187
Reference (166) 166
Data Set (159) 159
Paper (101) 101
Trade Publication Article (62) 62
Journal / eJournal (59) 59
Streaming Video (19) 19
Presentation (8) 8
Archival Material (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (246155) 246155
index medicus (161985) 161985
female (142431) 142431
male (133712) 133712
polymorphism (115957) 115957
genetic aspects (97294) 97294
polymorphism, genetic (92483) 92483
genotype (88483) 88483
middle aged (80872) 80872
adult (80381) 80381
polymorphism, single nucleotide (76969) 76969
research (71052) 71052
genetics & heredity (70228) 70228
animals (65371) 65371
genes (61358) 61358
alleles (57554) 57554
aged (52349) 52349
genetic polymorphisms (52201) 52201
risk factors (51453) 51453
analysis (51411) 51411
genetic predisposition to disease (47749) 47749
single nucleotide polymorphisms (47632) 47632
genetic research (47212) 47212
genetics (45707) 45707
gene frequency (41673) 41673
polymerase chain reaction (41660) 41660
association (39210) 39210
case-control studies (38057) 38057
biochemistry & molecular biology (37590) 37590
mutation (37473) 37473
polymorphism, restriction fragment length (35696) 35696
polymorphisms (35225) 35225
molecular sequence data (33697) 33697
base sequence (32908) 32908
risk (32707) 32707
expression (31347) 31347
genetic variation (31118) 31118
genomics (29366) 29366
haplotypes (28723) 28723
dna (28341) 28341
phenotype (28156) 28156
gene (27536) 27536
oncology (26815) 26815
cancer (26568) 26568
adolescent (26321) 26321
research article (25760) 25760
population (25753) 25753
polymorphism, single nucleotide - genetics (25323) 25323
single-nucleotide polymorphism (24294) 24294
genomes (23351) 23351
health aspects (23092) 23092
immunology (22987) 22987
susceptibility (22815) 22815
disease (22452) 22452
identification (22223) 22223
physiological aspects (21255) 21255
article (20772) 20772
gene expression (20430) 20430
child (20266) 20266
gene polymorphism (19354) 19354
genetic markers (19315) 19315
medicine (19236) 19236
pharmacology & pharmacy (19226) 19226
phylogeny (18883) 18883
sequence analysis, dna (18406) 18406
neurosciences (18065) 18065
studies (17958) 17958
biotechnology & applied microbiology (17816) 17816
life sciences (17724) 17724
young adult (17721) 17721
aged, 80 and over (17531) 17531
multidisciplinary sciences (17307) 17307
microbiology (17080) 17080
evolution (16917) 16917
genetic diversity (16896) 16896
linkage disequilibrium (16655) 16655
polymorphism, genetic - genetics (16358) 16358
proteins (16128) 16128
population genetics (16123) 16123
mice (15826) 15826
cell biology (15501) 15501
medical research (15467) 15467
chromosome mapping (15415) 15415
genome-wide association (15402) 15402
evolutionary biology (14800) 14800
deoxyribonucleic acid--dna (14653) 14653
single nucleotide polymorphism (14433) 14433
genetic association studies (14197) 14197
biology (14125) 14125
chromosomes (14063) 14063
plant sciences (14061) 14061
mutations (13429) 13429
epidemiology (13167) 13167
asian continental ancestry group - genetics (13071) 13071
psychiatry (13063) 13063
genome-wide association study (12847) 12847
genotype & phenotype (12454) 12454
science (12398) 12398
pedigree (12391) 12391
genetic predisposition to disease - genetics (12047) 12047
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (76) 76
Online Resources - Online (51) 51
UofT at Mississauga - Stacks (16) 16
Collection Dvlpm't (Acquisitions) - Vendor file (11) 11
Earth Sciences (Noranda) - Stacks (10) 10
UTL at Downsview - May be requested (8) 8
Royal Ontario Museum - Stacks (7) 7
UofT at Scarborough - Stacks (7) 7
Robarts - Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Closed Orders (4) 4
Royal Ontario Museum - Periodical Stacks (4) 4
University Archives - Archives (2) 2
Earth Sciences (Noranda) - Missing (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Gerstein Science - Theses (1) 1
Mathematical Sciences - Stacks (1) 1
Scarborough Hospital - Online (1) 1
UofT at Scarborough - Withdrawn (1) 1
Victoria University E.J. Pratt - Oversize (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (464296) 464296
Russian (3641) 3641
French (1270) 1270
Polish (1154) 1154
Spanish (1080) 1080
German (966) 966
Czech (265) 265
Portuguese (263) 263
Hungarian (236) 236
Persian (228) 228
Turkish (162) 162
Italian (101) 101
Slovak (100) 100
Ukrainian (97) 97
Croatian (69) 69
Swedish (48) 48
Dutch (41) 41
Bulgarian (39) 39
Lithuanian (31) 31
Slovenian (29) 29
Finnish (28) 28
Danish (25) 25
Hebrew (19) 19
Serbian (19) 19
Japanese (17) 17
Norwegian (15) 15
Arabic (14) 14
Chinese (12) 12
Romanian (11) 11
Indonesian (6) 6
Korean (5) 5
Belarusian (4) 4
Bosnian (3) 3
Welsh (3) 3
Catalan (2) 2
Icelandic (2) 2
Azerbaijani (1) 1
Georgian (1) 1
Latvian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Molecular Biology Reports, ISSN 0301-4851, 5/2014, Volume 41, Issue 5, pp. 2859 - 2864
The most important feature of abdominal aortic aneurysm (AAA) pathogenesis is an enzymatic degradation of elastic lamellae and extracellular matrix proteins... 
Life Sciences | PAI - 1 −844 G/A polymorphism | Animal Biochemistry | Abdominal aortic aneurysm | t - PA −7351 C/T polymorphism | PAI - 1 −675 4G/5G polymorphism | u - PA 1788 C/T polymorphism | Animal Anatomy / Morphology / Histology | RFLP | PAI -1 -844 G/A polymorphism | t-PA -7351 C/T polymorphism | PAI-1 -675 4G/5G polymorphism | u-PA 1788 C/T polymorphism | t-PA-7351 C/T polymorphism | MYOCARDIAL-INFARCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | PAI-1-844 G/A polymorphism | PLASMINOGEN-ACTIVATOR INHIBITOR-1 | ENHANCER POLYMORPHISM | FIBRINOLYTIC SYSTEM | PAI-1-675 4G/5G polymorphism | MATRIX METALLOPROTEINASES | 4G/5G POLYMORPHISM | ISCHEMIC-STROKE | ASSOCIATION | SINGLE-NUCLEOTIDE POLYMORPHISMS | CORONARY-ARTERY-DISEASE | Gene Frequency | Humans | Middle Aged | Genotype | Male | Aortic Aneurysm, Abdominal - genetics | Urokinase-Type Plasminogen Activator - genetics | Tissue Plasminogen Activator - genetics | Case-Control Studies | INDEL Mutation | Polymorphism, Genetic | Alleles | Adult | Female | Aged | Polymorphism, Single Nucleotide | Plasminogen Activator Inhibitor 1 - genetics | Fibrin | Enzymes | Care and treatment | Tissue plasminogen activator | Analysis | Genes | Genetic research | Genetic aspects | Abdominal aneurysm | Genetic polymorphisms | Aneurysms | Genotype & phenotype | Risk factors | Veins & arteries | Polymorphism | PAI-1 −675 4G | u-PA 1788 C | T polymorphism | A polymorphism | PAI-1 −844 G | t-PA −7351 C | 5G polymorphism
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2014, Volume 9, Issue 9, p. e109222
Journal Article
2003, Methods in molecular biology, ISBN 9780896039681, Volume 212., xi, 269
Single nucleotide polymorphisms (SNPs) have become the markers of choice in elucidating the relationship between DNA sequence variation and susceptibility to... 
Chromosome polymorphism | Genetic markers | Variabilité génétique | Marqueurs génétiques | Polymorphisme chromosomique | Variation | Human genetics | Laboratory manuals | Human Genetics | Biomedicine
Book
Journal Article
PLoS One, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, p. e31230
Background: Behcet's disease is known as a recurrent, multisystem inflammation and immune-related disease. Protein tyrosine phosphatase non-receptor 22... 
RHEUMATOID-ARTHRITIS | IL10 | JAPANESE POPULATION | MULTIDISCIPLINARY SCIENCES | IL23R-IL12RB2 | TYROSINE-PHOSPHATASE PTPN22 | AUTOIMMUNE-DISEASE | GENE POLYMORPHISMS | VARIANT | GENOME-WIDE ASSOCIATION | SILK ROAD | Genetic Predisposition to Disease | Eye Diseases - ethnology | Gene Frequency | Humans | Middle Aged | Protein Tyrosine Phosphatase, Non-Receptor Type 22 - genetics | Genotype | Male | Case-Control Studies | Polymorphism, Genetic | Behcet Syndrome - ethnology | Eye Diseases - genetics | Immune System | Polymorphism, Restriction Fragment Length | China | Adolescent | Polymerase Chain Reaction | Adult | Female | Aged | Behcet Syndrome - genetics | Tyrosine | Medical research | Phosphatases | Analysis | Genes | Medicine, Experimental | Disease susceptibility | Genetic aspects | Single nucleotide polymorphisms | T cells | Behcet's syndrome | Haplotypes | Multiple sclerosis | Populations | Laboratories | Pathogenesis | Lymphocytes T | Single-nucleotide polymorphism | Kinases | Phosphatase | Proteins | Lymphocytes | Rheumatology | Inflammation | Regression analysis | Disease control | Patients | Minority & ethnic groups | Crohns disease | Polymerase chain reaction | Hospitals | Restriction fragment length polymorphism | Gene frequency | Rheumatoid arthritis | Diabetes | Autoimmune diseases | Health risk assessment | Protein-tyrosine-phosphatase | Polymorphism
Journal Article
Molecular and Cellular Biochemistry, ISSN 0300-8177, 1/2011, Volume 347, Issue 1, pp. 201 - 208
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, p. e0177160
Journal Article