X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (49465) 49465
Publication (6972) 6972
Newspaper Article (2647) 2647
Newsletter (991) 991
Book Review (553) 553
Book Chapter (518) 518
Conference Proceeding (105) 105
Web Resource (86) 86
Book / eBook (77) 77
Magazine Article (71) 71
Reference (57) 57
Report (57) 57
Dissertation (38) 38
Trade Publication Article (36) 36
Transcript (19) 19
Streaming Video (12) 12
Data Set (6) 6
Government Document (3) 3
Presentation (3) 3
Paper (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (32158) 32158
index medicus (25254) 25254
male (18475) 18475
animals (17408) 17408
female (17018) 17018
mutation (14518) 14518
genetics & heredity (13123) 13123
genes (11467) 11467
genetic aspects (9955) 9955
gene expression (9090) 9090
mice (8833) 8833
research (8220) 8220
gene (7762) 7762
genetics (6973) 6973
proteins (6652) 6652
adult (6386) 6386
biochemistry & molecular biology (6079) 6079
expression (5765) 5765
gene therapy (5656) 5656
phenotype (5533) 5533
analysis (5360) 5360
cell biology (5087) 5087
mutations (5042) 5042
child (5021) 5021
pedigree (4906) 4906
research article (4357) 4357
article (4029) 4029
adolescent (4003) 4003
neurosciences (3941) 3941
x chromosome (3935) 3935
genetic research (3910) 3910
molecular sequence data (3858) 3858
middle aged (3767) 3767
genomes (3737) 3737
multidisciplinary sciences (3581) 3581
child, preschool (3566) 3566
base sequence (3550) 3550
gene mutations (3535) 3535
genomics (3502) 3502
medicine (3479) 3479
disease (3469) 3469
physiological aspects (3392) 3392
health aspects (3327) 3327
cancer (3090) 3090
chromosomes (3071) 3071
medicine, research & experimental (3058) 3058
apoptosis (2966) 2966
biology (2859) 2859
deoxyribonucleic acid--dna (2853) 2853
identification (2843) 2843
oncology (2832) 2832
immunology (2730) 2730
dna (2703) 2703
genetic linkage (2687) 2687
protein (2640) 2640
infant (2613) 2613
gene-expression (2612) 2612
genotype (2545) 2545
polymerase chain reaction (2446) 2446
biotechnology & applied microbiology (2386) 2386
diagnosis (2364) 2364
dna mutational analysis (2356) 2356
science (2324) 2324
clinical neurology (2314) 2314
gene expression regulation (2306) 2306
amino acid sequence (2300) 2300
stem cells (2227) 2227
studies (2211) 2211
care and treatment (2207) 2207
pediatrics (2203) 2203
life sciences (2196) 2196
dna methylation (2190) 2190
risk factors (2122) 2122
medical research (2120) 2120
signal transduction (2082) 2082
rodents (2047) 2047
aged (2046) 2046
cells (2019) 2019
alleles (2002) 2002
patients (1993) 1993
hematology (1984) 1984
chromosome mapping (1919) 1919
molecular biology (1909) 1909
disease models, animal (1897) 1897
human genetics (1871) 1871
mutation - genetics (1870) 1870
evolution (1855) 1855
genetic disorders (1853) 1853
cell line (1826) 1826
family (1821) 1821
kinases (1810) 1810
mice, inbred c57bl (1769) 1769
transcription (1749) 1749
endocrinology & metabolism (1743) 1743
rna (1742) 1742
cells, cultured (1732) 1732
gene deletion (1715) 1715
review (1712) 1712
developmental biology (1692) 1692
genetic predisposition to disease (1687) 1687
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (36) 36
Online Resources - Online (6) 6
UofT at Mississauga - Stacks (6) 6
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (5) 5
Collection Dvlpm't (Acquisitions) - Vendor file (4) 4
Lakeridge Health Sciences - Oshawa (2) 2
St. Michael's College (John M. Kelly) - 2nd Floor (2) 2
St. Michael's Hospital - Stacks (2) 2
Trinity College (John W Graham) - Stacks (2) 2
UTL at Downsview - May be requested (2) 2
UofT at Scarborough - Stacks (2) 2
Baycrest Hospital - Stacks (1) 1
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Credit Valley Hospital - Stacks (1) 1
Dentistry (Harry R Abbott) - Withdrawn (1) 1
Earth Sciences (Noranda) - Stacks (1) 1
Trillium Health Centre - Stacks (1) 1
UofT Schools - Stacks (1) 1
UofT at Scarborough - Sunnybrook Stacks (1) 1
Victoria University Emmanuel College - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (53378) 53378
Japanese (256) 256
German (116) 116
French (104) 104
Chinese (84) 84
Russian (52) 52
Spanish (51) 51
Polish (12) 12
Korean (11) 11
Italian (10) 10
Dutch (9) 9
Portuguese (8) 8
Hungarian (6) 6
Turkish (4) 4
Arabic (3) 3
Danish (3) 3
Czech (2) 2
Norwegian (2) 2
Romanian (2) 2
Slovak (2) 2
Slovenian (2) 2
Swedish (2) 2
Persian (1) 1
Welsh (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature, ISSN 0028-0836, 09/2011, Volume 477, Issue 7363, pp. 211 - 215
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2010, Volume 5, Issue 1, p. e8870
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 131, Issue 6, pp. 1611 - 1623.e3
Background Mutations in signal transducer and activator of transcription (STAT) 1 cause a broad spectrum of disease, ranging from severe viral and bacterial... 
Allergy and Immunology | Signal transducer and activator of transcription 1 | regulatory T cell | immune dysregulation–polyendocrinopathy–enteropathy–X-linked | chronic mucocutaneous candidiasis | forkhead box protein 3 | aneurysms | immune dysregulation-polyendocrinopathy-enteropathy-X-linked | IMMUNOLOGY | DEFICIENCY | DISEASES | ALLERGY | REGULATORY T-CELLS | IPEX | EXPRESSION | IMMUNODEFICIENCY | T-Lymphocytes, Regulatory - metabolism | Polyendocrinopathies, Autoimmune - diagnosis | Humans | Transcriptional Activation | Interleukin-17 - immunology | Child, Preschool | Male | Intestinal Diseases - immunology | Lymphocyte Subsets - immunology | T-Lymphocytes, Regulatory - immunology | Lymphocyte Subsets - metabolism | STAT1 Transcription Factor - metabolism | Genes, Dominant | Th17 Cells - metabolism | Interleukins - immunology | Female | Genetic Diseases, X-Linked - genetics | Polyendocrinopathies, Autoimmune - genetics | Phosphorylation - drug effects | Child | Intestinal Diseases - genetics | Immunophenotyping | DNA - metabolism | Forkhead Transcription Factors - genetics | STAT1 Transcription Factor - genetics | Genetic Diseases, X-Linked - diagnosis | Syndrome | Interferon-alpha - immunology | Polyendocrinopathies, Autoimmune - immunology | Genetic Diseases, X-Linked - immunology | Intestinal Diseases - diagnosis | Autoantibodies - immunology | Phenotype | Adolescent | Th17 Cells - immunology | Mutation | Cell Line, Transformed | Interferon-gamma - pharmacology | Autoimmunity | Medical colleges | Invisibility | Molecular genetics | Mycoses | Aneurysms | Genetic aspects | Children | Health aspects
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2013, Volume 369, Issue 16, pp. 1529 - 1536
Journal Article
by Zhou, Q and Wang, X and Yu, Z and Wu, X and Chen, X and Li, J and Zhu, Z and Liu, B and Su, L
Oncogene, ISSN 0950-9232, 03/2017, Volume 36, Issue 13, pp. 1873 - 1886
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 10/2014, Volume 371, Issue 15, pp. 1407 - 1417
Journal Article
Human Mutation, ISSN 1059-7794, 12/2015, Volume 36, Issue 12, pp. 1176 - 1187
Journal Article
Cell, ISSN 0092-8674, 02/2018, Volume 172, Issue 5, pp. 897 - 909.e21
X-linked Dystonia-Parkinsonism (XDP) is a Mendelian neurodegenerative disease that is endemic to the Philippines and is associated with a founder haplotype. We... 
DYT3 | XDP | dystonia | transcriptome assembly | retrotransposon | Parkinson’s disease | genome assembly | intron retention | SVA | TAF1 | Parkinson's disease | II ELONGATION RATE | STEM-CELLS | HUMAN-DISEASE | RNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | INTRON RETENTION | GENE-EXPRESSION | INTERFERENCE | SEQUENCING DATA | VARIATION DISCOVERY | CELL BIOLOGY | TATA-Binding Protein Associated Factors - metabolism | Humans | Histone Acetyltransferases - genetics | Nerve Degeneration - genetics | Male | Genetic Loci | Transcription Factor TFIID - metabolism | RNA, Messenger - metabolism | Transcription Factor TFIID - genetics | Haplotypes - genetics | Short Interspersed Nucleotide Elements | Base Sequence | Histone Acetyltransferases - metabolism | Minisatellite Repeats - genetics | Female | Genetic Diseases, X-Linked - genetics | Neurons - metabolism | Alu Elements - genetics | Induced Pluripotent Stem Cells - metabolism | Dystonic Disorders - genetics | Introns - genetics | Alternative Splicing - genetics | RNA, Messenger - genetics | Transcriptome - genetics | TATA-Binding Protein Associated Factors - genetics | CRISPR-Cas Systems - genetics | Nerve Degeneration - pathology | Family | High-Throughput Nucleotide Sequencing | Models, Genetic | Genome, Human | Neural Stem Cells - metabolism | Cohort Studies | Nervous system diseases | Analysis | Genomics | Genetic research | Genetic aspects | Dystonia
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2012, Volume 7, Issue 1, pp. 51 - 51
Journal Article
Journal Article