X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (10059) 10059
Publication (1542) 1542
Book Chapter (125) 125
Book Review (100) 100
Conference Proceeding (28) 28
Dissertation (15) 15
Book / eBook (9) 9
Government Document (8) 8
Web Resource (3) 3
Data Set (2) 2
Magazine Article (1) 1
Paper (1) 1
Presentation (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (6507) 6507
index medicus (4871) 4871
germline mutations (4822) 4822
female (4081) 4081
mutation (3340) 3340
male (3231) 3231
oncology (2922) 2922
genetics & heredity (2371) 2371
adult (2215) 2215
genetic aspects (2085) 2085
animals (2073) 2073
middle aged (2071) 2071
cancer (1995) 1995
germline (1576) 1576
genetic predisposition to disease (1419) 1419
germline mutation (1367) 1367
aged (1355) 1355
research (1324) 1324
germ-line mutation (1293) 1293
gene (1261) 1261
genes (1124) 1124
gene mutations (1117) 1117
biochemistry & molecular biology (1026) 1026
phenotype (1021) 1021
genetics (1019) 1019
pedigree (1016) 1016
risk factors (987) 987
risk (980) 980
cell biology (979) 979
breast cancer (969) 969
tumors (944) 944
breast neoplasms - genetics (926) 926
article (876) 876
dna mutational analysis (861) 861
analysis (852) 852
expression (802) 802
mice (726) 726
adolescent (700) 700
genetic testing (681) 681
child (662) 662
ovarian-cancer (661) 661
breast-cancer (655) 655
base sequence (624) 624
proteins (624) 624
health aspects (606) 606
pathology (599) 599
genotype (596) 596
molecular sequence data (596) 596
families (594) 594
endocrinology & metabolism (578) 578
diagnosis (573) 573
genetic research (565) 565
microsatellite instability (565) 565
mutations (558) 558
identification (556) 556
brca1 (550) 550
colorectal cancer (547) 547
gene expression (536) 536
ovarian cancer (532) 532
ovarian neoplasms - genetics (523) 523
aged, 80 and over (521) 521
mutation - genetics (508) 508
polymerase chain reaction (503) 503
tumor-suppressor gene (496) 496
genomics (488) 488
carcinoma (485) 485
prognosis (485) 485
surgery (485) 485
immunohistochemistry (483) 483
genes, brca1 (480) 480
dna (469) 469
research article (464) 464
protein (463) 463
young adult (463) 463
prevalence (460) 460
brca2 (457) 457
deoxyribonucleic acid--dna (456) 456
alleles (450) 450
multidisciplinary sciences (440) 440
women (429) 429
colorectal neoplasms, hereditary nonpolyposis - genetics (424) 424
medicine & public health (422) 422
drosophila (418) 418
developmental biology (417) 417
child, preschool (415) 415
nonpolyposis colorectal-cancer (404) 404
genomes (401) 401
somatic mutations (398) 398
heterozygote (396) 396
susceptibility (391) 391
genes, brca2 (387) 387
care and treatment (379) 379
signal transduction (374) 374
disease (373) 373
epidemiology (371) 371
dna-binding proteins - genetics (358) 358
biology (356) 356
genetic counseling (356) 356
physiological aspects (356) 356
genetic screening (353) 353
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Earth Sciences (Noranda) - Stacks (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Gerstein Science - Stacks (1) 1
Law (Bora Laskin) - Stacks (1) 1
Online Resources - Online (1) 1
Regis College - Stacks (1) 1
Robarts - Stacks (1) 1
St. Michael's College (John M. Kelly) - 3rd Floor (1) 1
Trinity College (John W Graham) - Stacks (1) 1
UTL at Downsview - May be requested (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (9907) 9907
German (87) 87
French (84) 84
Spanish (31) 31
Korean (14) 14
Russian (10) 10
Czech (7) 7
Chinese (6) 6
Hungarian (6) 6
Japanese (6) 6
Polish (5) 5
Portuguese (4) 4
Arabic (1) 1
Italian (1) 1
Persian (1) 1
Slovak (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Human Genetics, ISSN 0340-6717, 2/2016, Volume 135, Issue 2, pp. 209 - 222
Journal Article
Nature Medicine, ISSN 1078-8956, 12/2014, Volume 20, Issue 12, pp. 1410 - 1416
The protein cytotoxic T lymphocyte antigen-4 (CTLA-4) is an essential negative regulator of immune responses, and its loss causes fatal autoimmunity in mice.... 
PATHWAYS | MEDICINE, RESEARCH & EXPERIMENTAL | CLINICAL-PICTURE | HOMEOSTASIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CELL BIOLOGY | AUTOIMMUNITY | REGULATORY T-CELLS | GERMLINE MUTATIONS | MICE | BLOCKADE | IMMUNODEFICIENCY | ABATACEPT | Recurrence | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Purpura, Thrombocytopenic, Idiopathic - genetics | Exons | Immune System Diseases - genetics | Humans | Middle Aged | Male | Anemia, Hemolytic, Autoimmune - genetics | Mutation, Missense | Respiratory Tract Infections - genetics | T-Lymphocytes, Regulatory - immunology | Autoimmune Diseases - genetics | Young Adult | Purpura, Thrombocytopenic, Idiopathic - immunology | Adult | Female | Endocytosis - genetics | Polyendocrinopathies, Autoimmune - genetics | Child | Endocytosis - immunology | Granuloma - genetics | Autoimmune Diseases - immunology | CTLA-4 Antigen - genetics | B7-1 Antigen - metabolism | Codon, Nonsense | CTLA-4 Antigen - immunology | Syndrome | Polyendocrinopathies, Autoimmune - immunology | Lung Diseases, Interstitial - immunology | Animals | B-Lymphocytes - immunology | Lung Diseases, Interstitial - genetics | Pedigree | Anemia, Hemolytic, Autoimmune - immunology | Adolescent | Respiratory Tract Infections - immunology | Granuloma - immunology | Heterozygote | Mice | Antigens | Gene mutations | Physiological aspects | Genetic aspects | Immunologic diseases | Research | Risk factors | Proteins | Homeostasis | Cytotoxicity | Ligands | T cell receptors | Mutation | Immune system
Journal Article
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 12/2015, Volume 373, Issue 24, pp. 2336 - 2346
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 12/2007, Volume 44, Issue 12, pp. 763 - 771
Journal Article
Pathology, ISSN 0031-3025, 02/2013, Volume 45, Issue 2, pp. 116 - 126
BAP1 (BRCA1-Associated Protein 1) was initially identified as a protein that binds to BRCA1. BAP1 is a tumour suppressor that is believed to mediate its... 
pathology | familial cancer | uveal melanoma | skin | diagnosis | inherited tumour susceptibility | melanoma | 3p21 loss syndrome | atypical Spitz tumour | germline mutation | BAP1 | Pathology | Inherited tumour susceptibility | Melanoma | Uveal melanoma | Atypical Spitz tumour | Familial cancer | Germline mutation | Skin | Diagnosis | PLEURAL MESOTHELIOMA | DNA-DAMAGE RESPONSE | BRCA1-ASSOCIATED PROTEIN-1 | RENAL-CELL CARCINOMA | BREAST-CANCER | POLYCOMB GROUP PROTEINS | SPITZ NEVI | HISTONE DEACETYLASE INHIBITORS | MALIGNANT MESOTHELIOMA | MYELODYSPLASTIC SYNDROMES | Neoplasms - metabolism | Carcinoma, Neuroendocrine - diagnosis | Melanoma - diagnosis | Humans | Lung Neoplasms - metabolism | Meningioma - genetics | Neoplasms - diagnosis | Paraganglioma - diagnosis | Adenocarcinoma - metabolism | Neoplasms - genetics | DNA Mutational Analysis | Melanoma - genetics | Gene Deletion | Nevus, Epithelioid and Spindle Cell - genetics | Skin Neoplasms - diagnosis | Tumor Suppressor Proteins - genetics | Biomarkers, Tumor - metabolism | Adenocarcinoma - genetics | Uveal Neoplasms - metabolism | Carcinoma, Neuroendocrine - metabolism | Lung Neoplasms - genetics | Melanoma - metabolism | Uveal Neoplasms - genetics | Genetic Predisposition to Disease | Meningioma - metabolism | Paraganglioma - genetics | Carcinoma, Neuroendocrine - genetics | Mesothelioma - diagnosis | Mesothelioma - genetics | Nevus, Epithelioid and Spindle Cell - metabolism | Ubiquitin Thiolesterase - genetics | Skin Neoplasms - metabolism | Immunohistochemistry - methods | Nevus, Epithelioid and Spindle Cell - diagnosis | Adenocarcinoma - diagnosis | Mesothelioma - metabolism | Paraganglioma - metabolism | Skin Neoplasms - genetics | Uveal Neoplasms - diagnosis | Biomarkers, Tumor - genetics | Meningioma - diagnosis | Mutation | Lung Neoplasms - diagnosis
Journal Article
Journal Article
International Journal of Cancer, ISSN 0020-7136, 05/2017, Volume 140, Issue 9, pp. 2051 - 2059
Journal Article
Journal of the National Cancer Institute, ISSN 0027-8874, 06/2005, Volume 97, Issue 12, pp. 931 - 935
The Birt-Rogg-Dube (BHD) syndrome is an inherited genodermatosis characterized by a predisposition to hamartomatous skin lesions, pulmonary cysts, and renal...