X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (14939) 14939
Publication (2194) 2194
Book / eBook (1205) 1205
Dissertation (693) 693
Book Review (292) 292
Newsletter (219) 219
Book Chapter (199) 199
Newspaper Article (44) 44
Conference Proceeding (32) 32
Magazine Article (21) 21
Trade Publication Article (5) 5
Data Set (4) 4
Web Resource (4) 4
Government Document (2) 2
Paper (2) 2
Presentation (2) 2
Reference (2) 2
Streaming Video (2) 2
Patent (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (11328) 11328
index medicus (8352) 8352
male (6187) 6187
female (5490) 5490
animals (5030) 5030
mutation (4216) 4216
genetic aspects (3927) 3927
genetics (3803) 3803
research (3104) 3104
mice (3053) 3053
genetics & heredity (3022) 3022
adult (2714) 2714
medicine (2111) 2111
child (2034) 2034
research article (1956) 1956
proteins (1951) 1951
gene expression (1925) 1925
genes (1893) 1893
phenotype (1832) 1832
middle aged (1669) 1669
pedigree (1633) 1633
adolescent (1626) 1626
health aspects (1548) 1548
expression (1544) 1544
neurosciences (1489) 1489
multidisciplinary sciences (1478) 1478
mutations (1474) 1474
pathology (1467) 1467
biochemistry & molecular biology (1464) 1464
gene (1438) 1438
cell biology (1434) 1434
disease (1407) 1407
physiological aspects (1407) 1407
article (1387) 1387
child, preschool (1381) 1381
disease models, animal (1299) 1299
diagnosis (1260) 1260
analysis (1259) 1259
science (1232) 1232
biology (1197) 1197
medicine, research & experimental (1162) 1162
care and treatment (1109) 1109
apoptosis (1098) 1098
clinical neurology (1079) 1079
cancer (1077) 1077
infant (1066) 1066
risk factors (1019) 1019
oncology (1003) 1003
immunology (974) 974
aged (956) 956
molecular biology (948) 948
genomes (921) 921
gene mutations (914) 914
rodents (910) 910
review (905) 905
pediatrics (901) 901
genomics (831) 831
development and progression (798) 798
genetic disorders (796) 796
x chromosome (790) 790
studies (760) 760
genetic linkage (757) 757
mice, knockout (755) 755
medical research (752) 752
patients (750) 750
genotype (739) 739
mice, inbred c57bl (738) 738
deoxyribonucleic acid--dna (731) 731
signal transduction (728) 728
dna mutational analysis (713) 713
base sequence (699) 699
mutation - genetics (697) 697
protein (688) 688
infant, newborn (682) 682
genetic predisposition to disease (672) 672
molecular sequence data (667) 667
young adult (662) 662
ophthalmology (645) 645
identification (639) 639
kinases (623) 623
genetic diseases, x-linked - genetics (608) 608
biochemistry (606) 606
gene therapy (606) 606
neurology (606) 606
dna (604) 604
human genetics (600) 600
cells (597) 597
cell line, tumor (593) 593
life sciences (580) 580
syndrome (572) 572
magnetic resonance imaging (567) 567
immunohistochemistry (564) 564
stem cells (554) 554
usage (554) 554
brain - pathology (546) 546
chromosomes (541) 541
genetic research (534) 534
brain (532) 532
diseases (532) 532
cells, cultured (531) 531
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (859) 859
UofT at Mississauga - Stacks (128) 128
UTL at Downsview - May be requested (126) 126
UofT at Scarborough - Stacks (73) 73
Collection Dvlpm't (Acquisitions) - Closed Orders (64) 64
Collection Dvlpm't (Acquisitions) - Vendor file (62) 62
Online Resources - Online (46) 46
Robarts - Stacks (43) 43
St. Michael's College (John M. Kelly) - 2nd Floor (36) 36
Trinity College (John W Graham) - Stacks (17) 17
Earth Sciences (Noranda) - Stacks (15) 15
Law (Bora Laskin) - Stacks (15) 15
St. Augustine's Seminary - Stacks (14) 14
Victoria University E.J. Pratt - Stacks (14) 14
Holland Bloorview Kids Rehabilitation - Stacks (12) 12
OISE - Stacks (12) 12
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (12) 12
Royal Ontario Museum - Stacks (11) 11
Engineering & Comp. Sci. - Stacks (9) 9
Regis College - Stacks (8) 8
Gerstein Science - Reference (7) 7
Lakeridge Health Sciences - Oshawa (7) 7
New College (Ivey) - Stacks (6) 6
Scarborough Hospital - General (6) 6
Gerstein Science - Circulation Desk (5) 5
Gerstein Science - Missing (5) 5
Providence Healthcare - Stacks (5) 5
UofT at Scarborough - Withdrawn (5) 5
Media Commons - Microtexts (4) 4
St. Michael's Hospital - Stacks (4) 4
Victoria University Emmanuel College - Stacks (4) 4
Dentistry (Harry R Abbott) - Withdrawn (3) 3
Knox College (Caven) - Stacks (3) 3
Mt Sinai Hospital - Pathology (3) 3
Scarborough Hospital - Birchmount (3) 3
UofT at Mississauga - Reference (3) 3
UofT at Scarborough - May be requested in 6-10 wks (3) 3
Credit Valley Hospital - Stacks (2) 2
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (2) 2
Dentistry (Harry R Abbott) - Stacks (2) 2
Gerstein Science - Course Reserves (2) 2
Holland Bloorview Kids Rehabilitation - Reference (2) 2
Humber River Regional Hospital - Finch Stacks (2) 2
Institute for Christian Studies - Stacks (2) 2
Providence Healthcare - Reference (2) 2
St. Augustine's Seminary - Reference (2) 2
Toronto East General Hospital - Stacks (2) 2
Trinity College (John W Graham) - Reference (2) 2
Chemistry (A D Allen) - Reference (1) 1
Collection Dvlpm't (Acquisitions) - Cancelled Order (1) 1
Collection Dvlpm't (Acquisitions) - Online (1) 1
Collection Dvlpm't (Acquisitions) - Stacks (1) 1
Credit Valley Hospital - Missing (1) 1
Earth Sciences (Noranda) - Missing (1) 1
Engineering & Comp. Sci. - Reference (1) 1
Gerstein Science - Closed Orders (1) 1
Gerstein Science - Not Returned (1) 1
Gerstein Science - Searching (1) 1
Holland Bloorview Kids Rehabilitation - Sunnybrook Stacks (1) 1
Humber River Regional Hospital - Church Stacks (1) 1
Law (Bora Laskin) - Reserve desk (1) 1
Markham Stouffville Hospital - Stacks (1) 1
New College (Ivey) - Withdrawn (1) 1
OISE - May be requested in 6-10 wks (1) 1
OISE - Missing (1) 1
Providence Healthcare - Reserve desk (1) 1
Regis College - Reference (1) 1
St Josephs Health Centre - Stacks (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
St. Michael's College (John M. Kelly) - Reference (1) 1
St. Michael's Hospital - Circulation Desk (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
Toronto East General Hospital - Chaplain Dept. (1) 1
Trinity College (John W Graham) - Storage (1) 1
UofT at Mississauga - Closed Orders (1) 1
UofT at Mississauga - Not Returned (1) 1
UofT at Mississauga - Not returned (1) 1
UofT at Scarborough - Sunnybrook Stacks (1) 1
Victoria University E.J. Pratt - Reference (1) 1
Victoria University Emmanuel College - Reference (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 (16917) 16917
French (93) 93
Spanish (90) 90
German (59) 59
Russian (53) 53
Japanese (37) 37
Chinese (22) 22
Italian (22) 22
Portuguese (16) 16
Hungarian (10) 10
Turkish (9) 9
Czech (7) 7
Dutch (6) 6
Polish (6) 6
Arabic (4) 4
Swedish (4) 4
Korean (2) 2
Romanian (2) 2
Bulgarian (1) 1
Catalan (1) 1
Croatian (1) 1
Danish (1) 1
Norwegian (1) 1
Serbian (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, p. 14279
Journal Article
Current Opinion in Pediatrics, ISSN 1040-8703, 12/2013, Volume 25, Issue 6, pp. 708 - 714
Purpose of reviewTo summarize recent progress in our understanding of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-related... 
ITCH | autoimmunity | STAT1 | T regulatory cells | STAT5 | CD25 | FOXP3 | tolerance | TGF-BETA | GROWTH-HORMONE INSENSITIVITY | STAT5B MUTATION | CHRONIC MUCOCUTANEOUS CANDIDIASIS | CUTTING EDGE | INTESTINAL INFLAMMATION | ALPHA-CHAIN | TRANSCRIPTION FACTOR FOXP3 | REGULATORY T-CELLS | PEDIATRICS | SCURFY MOUSE MUTANT | Forkhead Transcription Factors - immunology | Immunologic Deficiency Syndromes - pathology | Humans | STAT5 Transcription Factor - immunology | Autoimmunity - genetics | Diabetes Mellitus, Type 1 - congenital | Male | Intestinal Diseases - immunology | Diarrhea - pathology | T-Lymphocytes, Regulatory - immunology | STAT5 Transcription Factor - genetics | Ubiquitin-Protein Ligases - immunology | Interleukin-2 Receptor alpha Subunit - genetics | Autoimmunity - immunology | Diarrhea - immunology | Female | Genetic Diseases, X-Linked - genetics | Polyendocrinopathies, Autoimmune - genetics | Immunologic Deficiency Syndromes - immunology | Interleukin-2 Receptor alpha Subunit - immunology | Genetic Predisposition to Disease | Intestinal Diseases - genetics | Repressor Proteins - genetics | Polyendocrinopathies, Autoimmune - pathology | Forkhead Transcription Factors - genetics | Mutation - genetics | Polyendocrinopathies, Autoimmune - immunology | Genetic Diseases, X-Linked - immunology | Immune System Diseases - congenital | Autoantibodies - immunology | Diarrhea - genetics | Repressor Proteins - immunology | Genetic Diseases, X-Linked - pathology | Immunologic Deficiency Syndromes - genetics | Ubiquitin-Protein Ligases - genetics | Intestinal Diseases - pathology | Tolerance
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 134, Issue 5, pp. 1131 - 1141.e9
Journal Article
Veterinary Pathology, ISSN 0300-9858, 7/2016, Volume 53, Issue 4, pp. 803 - 812
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 8/2010, Volume 107, Issue 33, pp. 14697 - 14702
Mutations in the MTM1 gene encoding myotubularin cause X-linked myotubular myopathy (XLMTM), a well-defined subtype of human centronuclear myopathy. Seven male... 
Animal models | Necklaces | Phosphatases | Muscular diseases | Canines | Dogs | Muscles | Biopsies | Genetic mutation | Skeletal muscle | Congenital myopathy | Animal model | Canine myopathy | Myotubularin | Necklace fibers | myotubularin | CENTRONUCLEAR MYOPATHY | MULTIDISCIPLINARY SCIENCES | MUSCULAR-DYSTROPHY | PHENOTYPE | HOMOLOG | canine myopathy | necklace fibers | FAMILY | PHOSPHATASE MYOTUBULARIN | MUSCLE-FIBERS | DOGS | LIPID PHOSPHATASE | animal model | SURVIVORS | congenital myopathy | Haplotypes | Humans | Cercopithecus aethiops | Molecular Sequence Data | Male | Muscle, Skeletal - metabolism | Myopathies, Structural, Congenital - genetics | Myopathies, Structural, Congenital - veterinary | Green Fluorescent Proteins - genetics | Dog Diseases - pathology | Base Sequence | Protein Tyrosine Phosphatases, Non-Receptor - genetics | Female | Genetic Diseases, X-Linked - genetics | Fluorescent Antibody Technique, Indirect | Amino Acid Sequence | Green Fluorescent Proteins - metabolism | Muscle, Skeletal - ultrastructure | Dog Diseases - genetics | Genotype | Microscopy, Electron | Mice, Knockout | Sequence Homology, Amino Acid | Animals | Pedigree | Protein Tyrosine Phosphatases, Non-Receptor - metabolism | Myopathies, Structural, Congenital - pathology | Genetic Diseases, X-Linked - pathology | Mice | Muscle, Skeletal - pathology | Mutation | COS Cells | Muscle diseases | Genetic aspects | Gene mutations | Properties | Identification and classification | Microtubules | MTM1 gene | Myotubes | Exons | Fetuses | X chromosome | proteasomes | Tubules | Data processing | Nuclei | Atrophy | Mitochondria | Biopsy | Protein folding | Age | Myopathy | Life Sciences | Genetics | Biological Sciences
Journal Article
Journal Article
Journal Article