UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.
Search Articles
Redox biology, ISSN 2213-2317, 04/2017, Volume 11, pp. 375 - 383
Antioxidants | Oxidative stress | Nijmegen breakage syndrome (NBS) | Oxidative damage | Bloom syndrome (BS) | Ataxia-telangiectasia (A-T) | Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Bloom Syndrome - pathology | Nijmegen Breakage Syndrome - pathology | NADPH Oxidase 4 - genetics | Reactive Oxygen Species - metabolism | Signal Transduction | Humans | Nijmegen Breakage Syndrome - metabolism | Gene Expression Regulation | Oxidative Stress - genetics | Bloom Syndrome - metabolism | Ataxia Telangiectasia - metabolism | Mitochondria - metabolism | Bloom Syndrome - genetics | Mitochondria - pathology | Lipoproteins, LDL - genetics | Nijmegen Breakage Syndrome - genetics | NADPH Oxidase 4 - metabolism | Poly(ADP-ribose) Polymerases - metabolism | Poly(ADP-ribose) Polymerases - genetics | Ataxia Telangiectasia - pathology | DNA Repair | Ataxia Telangiectasia - genetics | Lipoproteins, LDL - metabolism | DNA Damage | Index Medicus
Journal Article
Nature communications, ISSN 2041-1723, 11/2019, Volume 10, Issue 1, pp. 5284 - 18
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - genetics | Nicotinamide-Nucleotide Adenylyltransferase - metabolism | Humans | Aging, Premature - genetics | Autophagy-Related Protein-1 Homolog - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Mitophagy | Drosophila melanogaster - genetics | Drosophila melanogaster - metabolism | Animals | Werner Syndrome Helicase - metabolism | Werner Syndrome - metabolism | Cation Transport Proteins - metabolism | Werner Syndrome - genetics | Nicotinamide-Nucleotide Adenylyltransferase - genetics | Cation Transport Proteins - genetics | Werner Syndrome Helicase - genetics | Mutation | Aging, Premature - metabolism | Autophagy-Related Protein-1 Homolog - genetics | Intracellular Signaling Peptides and Proteins - genetics | NAD - metabolism | Disease Models, Animal | Phenotypes | Transcription | Nucleotides | Metabolism | DNA helicase | NAD | Mitochondria | Molecular modelling | Depletion | Werner's syndrome | Life span | Stem cells | Aging | Fruit flies | Nicotinamide | Invertebrates | Deoxyribonucleic acid--DNA | Index Medicus
Journal Article
3.
Full Text
Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions
Ageing research reviews, ISSN 1568-1637, 2016, Volume 33, pp. 105 - 114
Neurology | Internal Medicine | Human | Werner syndrome | Progeroid syndrome | Genomic instability | Life Sciences & Biomedicine | Geriatrics & Gerontology | Science & Technology | Cell Biology | Werner Syndrome - metabolism | DNA Repair | Humans | Werner Syndrome - genetics | DNA Replication | Aging, Premature - genetics | Werner Syndrome Helicase - genetics | Mutation | Exodeoxyribonucleases | Aging, Premature - metabolism | Werner Syndrome - diagnosis | Werner Syndrome - physiopathology | Telomeres | Genetic transcription | Health aspects | Genomics | Genes | Index Medicus
Journal Article
Science (American Association for the Advancement of Science), ISSN 0036-8075, 6/2015, Volume 348, Issue 6239, pp. 1160 - 1163
Journal Article
The Lancet (British edition), ISSN 0140-6736, 08/2003, Volume 362, Issue 9382, pp. 440 - 445
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | Complex syndromes | Medical sciences | Medical genetics | Werner Syndrome - classification | Humans | RNA, Messenger - genetics | Werner Syndrome Helicase | Cells, Cultured | Exons - genetics | Male | Mutation - genetics | Reverse Transcriptase Polymerase Chain Reaction | Mutation, Missense - genetics | RecQ Helicases | DNA Mutational Analysis | Pedigree | Werner Syndrome - genetics | Adolescent | Lamin Type A - genetics | Fibroblasts | Female | Registries | Exodeoxyribonucleases | Nuclear Proteins - genetics | Child | DNA Helicases - genetics | Werner Syndrome - diagnosis | Physiological aspects | Genetic aspects | Genetic disorders | Diagnosis | Werner syndrome | Gene mutations | Medical disorders | Patients | Mutation | Laboratories | Exons | mRNA | Lamins | Nuclei | Muscular dystrophy | Gene sequencing | DNA helicase | Proteins | Osteoporosis | Missense mutation | Atherosclerosis | Age | Deoxyribonucleic acid--DNA | Phenotypes | Cloning | Insulin | Molecular chains | Heterozygosity | Polymerase chain reaction | Studies | Werner's syndrome | Morphology | Skin | Diabetes | Index Medicus | Abridged Index Medicus
Journal Article
Nature genetics, ISSN 1061-4036, 10/1998, Volume 20, Issue 2, pp. 114 - 116
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | DNA Helicases - metabolism | RecQ Helicases | Electrophoresis, Polyacrylamide Gel | Humans | Werner Syndrome - genetics | Werner Syndrome Helicase | Exodeoxyribonucleases - metabolism | DNA - metabolism | Exodeoxyribonuclease V | Werner Syndrome - enzymology | DNA Helicases - genetics | Index Medicus
Journal Article
Ageing research reviews, ISSN 1568-1637, 01/2017, Volume 33, pp. 36 - 51
Aging | BLM | Cancer susceptibility | Bloom's syndrome | RecQ helicases | Genomic instability | Life Sciences & Biomedicine | Geriatrics & Gerontology | Science & Technology | Cell Biology | Genomic Instability | Humans | DNA Replication | RecQ Helicases - genetics | Aging, Premature - genetics | Bloom Syndrome - genetics | Aging - genetics | Werner Syndrome - genetics | Werner Syndrome Helicase - genetics | Bloom Syndrome - diagnosis | Mutation | DNA Helicases - physiology | Werner Syndrome - diagnosis | DNA replication | Disease susceptibility | Genetic transcription | Comparative analysis | Genes | Genomics | Index Medicus | Bloom’s syndrome | cancer susceptibility | aging | genomic instability
Journal Article
Anais brasileiros de dermatología, ISSN 0365-0596, 2017, Volume 92, Issue 2, pp. 271 - 272
Leg ulcer | Werner syndrome | Scleroderma | Progeria | Localized | Life Sciences & Biomedicine | Dermatology | Science & Technology | Leg Ulcer - etiology | Diagnosis, Differential | Scleroderma, Localized | Humans | Adult | Male | Werner Syndrome - complications | Werner Syndrome - diagnosis | Scleroderma, localized | Syndrome in Question
Journal Article
2012, Advances in Experimental Medicine and Biology, ISBN 1461406528, Volume 724
LMNA Gene | Werner Syndrome | Progeroid Syndrome | LMNA Mutation | Sensory Peripheral Neuropathy | Werner Syndrome - etiology | Werner Syndrome - metabolism | Humans | Werner Syndrome - genetics | Aging, Premature - complications | Aging, Premature - genetics | Progeria - genetics | Progeria - metabolism | Aging, Premature - metabolism | Progeria - etiology
Book Chapter
Aging clinical and experimental research, ISSN 1594-0667, 3/2019, Volume 31, Issue 3, pp. 425 - 429