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Nature genetics, ISSN 1061-4036, 11/2013, Volume 45, Issue 11, pp. 1361 - 1367
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Major Histocompatibility Complex - genetics | Humans | DNA-Binding Proteins - genetics | Transcription Factors, TFII - genetics | China | STAT4 Transcription Factor - genetics | Tumor Necrosis Factor alpha-Induced Protein 3 | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 7 - genetics | Nuclear Proteins - genetics | Intracellular Signaling Peptides and Proteins - genetics | Sjogren's Syndrome - genetics | Sjogren's syndrome | Chromosome mapping | Genetic susceptibility | Genetic aspects | Single nucleotide polymorphisms | Identification and classification | Methods | Testing | Confidence intervals | Disease | Pathogenesis | Quality control | Genomes | Autoimmune diseases | Gene expression | Logistics | Index Medicus
Journal Article
2016, Di 1 ban., Pinakesi, ISBN 9787552015119, 3 volumes (3100 pages)
Book
2015, Di 1 ban., ISBN 9787550622999, 2, 2, 5, 365 pages
Book
Journal of affective disorders, ISSN 0165-0327, 2016, Volume 207, pp. 422 - 428
Psychiatry | Neuroticism | Depression | Gender differences | Anxiety | Serotonin transporter | Tri-allelic 5-HTTLPR polymorphism | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Promoter Regions, Genetic | Humans | Middle Aged | Asian Continental Ancestry Group - genetics | Genotype | Male | Personality - genetics | Depression - genetics | Polymorphism, Genetic | Young Adult | Anxiety - genetics | Psychiatric Status Rating Scales | Serotonin Plasma Membrane Transport Proteins - genetics | China | Personality Inventory | Alleles | Adult | Anxiety Disorders - genetics | Female | Phenols | Genetic aspects | Serotonin | Depression, Mental | College graduates | Yuan (China) | Analysis | Index Medicus
Journal Article
2004, 3rd ed., ISBN 9787100039338, 624, 676
Book
Nucleic acids research, ISSN 0305-1048, 01/2020, Volume 48, Issue D1, pp. D971 - D976
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Genetics, Population | Ethnic Groups - genetics | China | Humans | Asian Continental Ancestry Group - genetics | Databases, Genetic | Software | Genome, Human | Genomics - methods | Software Design | Web Browser | Index Medicus | Database Issue
Journal Article
International journal of cancer, ISSN 0020-7136, 07/2018, Volume 143, Issue 1, pp. 184 - 189
TAM | breast cancer | SNP | CYP2D6 | survival | Life Sciences & Biomedicine | Oncology | Science & Technology | Cytochrome P-450 CYP2D6 - genetics | Humans | Middle Aged | Breast Neoplasms - drug therapy | Disease-Free Survival | Breast Neoplasms - genetics | Estrogen Antagonists - therapeutic use | Tamoxifen - therapeutic use | Pharmacogenomic Variants | Adult | Female | Aged | Polymorphism, Single Nucleotide | Chemotherapy, Adjuvant | Aromatase Inhibitors - therapeutic use | Precision Medicine | Medical research | Care and treatment | Genes | Cytochrome P-450 | Adjuvant treatment | Breast cancer | Tamoxifen | Cancer patients | Analysis | Medicine, Experimental | Genetic aspects | Single nucleotide polymorphisms | Health aspects | Cancer | Therapy | Cytochrome P450 | Endocrine therapy | Single-nucleotide polymorphism | Multivariate analysis | Cancer therapies | Patients | Survival | Subgroups | Medical prognosis | Aromatase | CYP2D6 protein | Genotypes | Index Medicus
Journal Article
British journal of ophthalmology, ISSN 0007-1161, 09/2018, Volume 102, Issue 9, pp. 1308 - 1314
INFLAMMATORY-BOWEL-DISEASE | IDENTIFIES 2 | VOGT-KOYANAGI-HARADA | CROHNS-DISEASE | IL23R-IL12RB2 | SUSCEPTIBILITY LOCI | GENE POLYMORPHISMS | POLYMORPHISMS CONFER RISK | GENOME-WIDE ASSOCIATION | INNATE IMMUNITY | Genetics | Inflammation | Immunology | Life Sciences & Biomedicine | Ophthalmology | Science & Technology | Eye Diseases - ethnology | Humans | Male | Receptor-Interacting Protein Serine-Threonine Kinase 2 - genetics | Incidence | Receptor-Interacting Protein Serine-Threonine Kinase 2 - metabolism | Behcet Syndrome - ethnology | Ethnic Groups | Oxygenases - metabolism | Adult | Female | Protein Tyrosine Phosphatase, Non-Receptor Type 1 - genetics | Retrospective Studies | Behcet Syndrome - metabolism | Carotenoids - genetics | Genetic Predisposition to Disease | Genetic Association Studies | CCAAT-Enhancer-Binding Protein-beta - genetics | Gene Frequency | Behcet Syndrome - complications | Eye Diseases - etiology | Genotype | China - epidemiology | CCAAT-Enhancer-Binding Protein-beta - metabolism | Proteins - genetics | Protein Tyrosine Phosphatase, Non-Receptor Type 1 - metabolism | Eye Diseases - genetics | Proteins - metabolism | Alleles | Carotenoids - metabolism | Polymorphism, Single Nucleotide | Oxygenases - genetics | Inflammatory bowel disease | Consortia | Psoriasis | Ulcers | Leprosy | Population | Genomes | Epidemiology | Meta-analysis | Index Medicus | Laboratory Science | 1506
Journal Article
Pediatric research, ISSN 0031-3998, 02/2019, Volume 85, Issue 3, pp. 378 - 383
Journal Article
Journal of the neurological sciences, ISSN 0022-510X, 2015, Volume 358, Issue 1, pp. 153 - 157
Neurology | Pathology | Mitofusin 2 | Early onset | Charcot–Maria–Tooth | Axonal neuropathy | Hereditary neuropathy | Charcot-Maria-Tooth | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Humans | Middle Aged | Child, Preschool | Genotype | Male | Neural Conduction - physiology | Median Nerve - pathology | Mitochondrial Proteins - genetics | Charcot-Marie-Tooth Disease - pathology | Charcot-Marie-Tooth Disease - genetics | Young Adult | Phenotype | Sural Nerve - physiopathology | Sural Nerve - pathology | GTP Phosphohydrolases - genetics | Median Nerve - physiopathology | Adolescent | Adult | Female | Charcot-Marie-Tooth Disease - physiopathology | Mutation | Child | Cohort Studies | Index Medicus
Journal Article