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Annals of oncology, ISSN 0923-7534, 2017, Volume 28, Issue 2, pp. 339 - 343
Blinded independent central review | VEGFR inhibitor | Crossover | Rank-preserving structural failure time (RPSFT) | Antiangiogenics | Life Sciences & Biomedicine | Oncology | Science & Technology | Cross-Sectional Studies | Double-Blind Method | Humans | Kaplan-Meier Estimate | Proportional Hazards Models | Survival Rate | Antineoplastic Agents - administration & dosage | Indoles - administration & dosage | Pancreatic Neoplasms - drug therapy | Disease-Free Survival | Sunitinib | Pyrroles - administration & dosage | Neuroendocrine Tumors - diagnostic imaging | Neuroendocrine Tumors - drug therapy | Pancreatic Neoplasms - diagnostic imaging | Index Medicus
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Frontiers in cellular neuroscience, ISSN 1662-5102, 10/2013, Volume 7, pp. 196 - 196
Node of Ranvier | Extracellular matrix | Axon-glial interactions | Neurological disease | Ion channel | Guillain-Barre syndrome | Demyelinating diseases | Excitability | Nervous system | Neuronal-glial interactions | Cell adhesion molecules | Cell adhesion & migration | Neurological diseases | Proteins | Axons | Demyelination | Sodium channels (voltage-gated) | Potassium channels (voltage-gated) | Ion channels | Localization | Nodes of Ranvier | Life Sciences | Biomolecules | Biochemistry, Molecular Biology | Neurological Disease | Extracellular Matrix | axon-glia interaction | ion channel | node of Ranvier
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Allergy (Copenhagen), ISSN 0105-4538, 02/2005, Volume 60, Issue 2, pp. 150 - 158
skin tests | immediate reaction | nonimmediate reaction | diagnosis | premedication | contrast media | Nonimmediate reaction | Diagnosis | Immediate reaction | Contrast media | Skin tests | Premedication | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Drug Hypersensitivity - etiology | Drug Hypersensitivity - prevention & control | Contrast Media - adverse effects | Prevalence | Drug Hypersensitivity - epidemiology | Humans | Risk Factors | Drug Hypersensitivity - diagnosis | Iodine Compounds - adverse effects | Drug Hypersensitivity - physiopathology | Index Medicus
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Remote sensing (Basel, Switzerland), ISSN 2072-4292, 02/2017, Volume 9, Issue 2, pp. 157 - 157
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Shoulder & elbow, ISSN 1758-5732, 10/2017, Volume 9, Issue 4, pp. 272 - 278
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Physical review letters, ISSN 0031-9007, 2012, Volume 109, Issue 7, p. 072301/1
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British journal of dermatology (1951), ISSN 0007-0963, 01/2017, Volume 176, Issue 1, pp. 204 - 208
Life Sciences & Biomedicine | Dermatology | Science & Technology | Receptor, Fibroblast Growth Factor, Type 3 - genetics | Humans | Mutation, Missense - genetics | Abortion, Induced | Pregnancy | Fetal Death | Skin Neoplasms - genetics | Nevus, Sebaceous of Jadassohn - genetics | Adult | Female | Mosaicism | Infant, Newborn | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Tyrosine | Skin diseases | Genetic aspects | Skin | Neonates | Fetuses | Acne | K-Ras protein | Missense mutation | Scalp | Protein-tyrosine kinase receptors | Mutation | Protein-tyrosine kinase | Fibroblast growth factor receptor 2 | Fibroblast growth factor receptors | Tumors | Cancer | Life Sciences | Human health and pathology
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1997, ISBN 2842790189, 441
Book
Physical review letters, ISSN 0031-9007, 2014, Volume 113, p. 232504
Journal Article
Clinical genetics, ISSN 0009-9163, 02/2017, Volume 91, Issue 2, pp. 333 - 338
scrotal agenesis | whole‐exome sequencing | MAB21L1 | intellectual disability | whole-exome sequencing | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Abnormalities, Multiple - pathology | Humans | Intellectual Disability - pathology | Male | Developmental Disabilities - genetics | Homeodomain Proteins - genetics | Intellectual Disability - genetics | Homozygote | Developmental Disabilities - pathology | Exome - genetics | Phenotype | Animals | Mice | Scrotum - pathology | Mutation | Child | Abnormalities, Multiple - genetics | Frameshift Mutation - genetics | Agenesis | Genetic aspects | Genetics | Reproductive system | Rodents | Index Medicus | Life Sciences | Human health and pathology
Journal Article
BMC medical education, ISSN 1472-6920, 01/2018, Volume 18, Issue 1, pp. 15 - 15
Training | Research | Education | Career mobility | Internship and residency | Neoplasms | Education & Educational Research | Education, Scientific Disciplines | Social Sciences | Medical Oncology | Specialization | Cross-Sectional Studies | Internship and Residency | Employment | Humans | Career Choice | Students, Medical - statistics & numerical data | Surveys and Questionnaires | France | Education, Medical, Graduate | Medical students | Psychological aspects | Career choice | Analysis | Oncology | Social aspects | Index Medicus
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Clinical genetics, ISSN 0009-9163, 12/2016, Volume 90, Issue 6, pp. 509 - 517
oral–facial–digital syndrome | exome sequencing | IFT57 | ciliopathy | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Male | Craniofacial Abnormalities - physiopathology | Ellis-Van Creveld Syndrome - genetics | Young Adult | Ciliopathies - genetics | Adult | Female | Thorax - physiopathology | Dwarfism - physiopathology | Neck - physiopathology | Craniofacial Abnormalities - genetics | Ear - physiopathology | Ellis-Van Creveld Syndrome - physiopathology | Ear - abnormalities | Orofaciodigital Syndromes - genetics | Neck - abnormalities | Genetic Heterogeneity | Dwarfism - genetics | Homozygote | Exome - genetics | Phenotype | Ciliopathies - physiopathology | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Consanguinity | High-Throughput Nucleotide Sequencing | Orofaciodigital Syndromes - physiopathology | Mutation | Thorax - abnormalities | Proteins | Dysplasia | Analysis | Genetic aspects | Nucleotide sequencing | Multiple abnormalities | DNA sequencing | Index Medicus | Life Sciences | Human health and pathology
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Clinical genetics, ISSN 0009-9163, 06/2016, Volume 89, Issue 6, pp. 700 - 707
ultra‐rare disorders | severe intellectual disability | clinical and genetic heterogeneity | epileptic encephalopathy | clinical whole‐exome sequencing | Clinical whole-exome sequencing | Epileptic encephalopathy | Clinical and genetic heterogeneity | Ultra-rare disorders | Severe intellectual disability | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease - genetics | Reproducibility of Results | Humans | Child, Preschool | Male | Neurodevelopmental Disorders - genetics | Diagnostic Tests, Routine - trends | Genetic Testing - methods | Epilepsy - diagnosis | Intellectual Disability - genetics | Young Adult | Exome - genetics | Diagnostic Tests, Routine - methods | Intellectual Disability - diagnosis | Sensitivity and Specificity | Adolescent | Adult | Epilepsy - genetics | Female | Polymorphism, Single Nucleotide | High-Throughput Nucleotide Sequencing - methods | Child | Cohort Studies | Neurodevelopmental Disorders - diagnosis | Molecular genetics | Medical tests | Genetic testing | Intellectual disabilities | Diagnostic tests | Neurological disorders | Index Medicus | Life Sciences | Human health and pathology
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