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Nature communications, 06/2018, Volume 9, Issue 1, p. 2280
Genetic Therapy | Ubiquitin-Specific Proteases - genetics | Fanconi Anemia Complementation Group D2 Protein - genetics | Fanconi Anemia - metabolism | Humans | DNA Repair - physiology | DNA Repair - genetics | Fanconi Anemia Complementation Group C Protein - genetics | Fanconi Anemia Complementation Group A Protein - genetics | Fanconi Anemia Complementation Group D2 Protein - deficiency | Fanconi Anemia Complementation Group A Protein - metabolism | Fanconi Anemia Complementation Group Proteins - metabolism | Ubiquitination | Fanconi Anemia Complementation Group G Protein - genetics | Ubiquitin-Specific Proteases - deficiency | Fanconi Anemia Complementation Group G Protein - deficiency | BRCA1 Protein - metabolism | Fanconi Anemia - genetics | Ubiquitin-Specific Proteases - metabolism | Chromosomal Instability | Rad51 Recombinase - metabolism | Cell Line | Fanconi Anemia Complementation Group Proteins - deficiency | Fanconi Anemia Complementation Group Proteins - genetics | Fanconi Anemia Complementation Group G Protein - metabolism | Gene Knockout Techniques | Fanconi Anemia Complementation Group C Protein - metabolism | Fanconi Anemia Complementation Group D2 Protein - metabolism | Fanconi Anemia Complementation Group A Protein - deficiency | CRISPR-Cas Systems | Fanconi Anemia Complementation Group C Protein - deficiency | Fanconi Anemia - therapy | DNA Damage | Histones - metabolism | Mutation
Journal Article
Nature communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1 - 14
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Phenotypes | Stability | Deactivation | BRCA1 protein | Anemia | Abnormalities | DNA damage | Genotoxicity | Health risks | Crosslinking | Breast cancer | Genomes | Inactivation | Fanconi syndrome | DNA repair | Screens | Genomic instability | FANCC protein | Bone cancer | Bone marrow | Repair | Deoxyribonucleic acid--DNA | Cancer | Index Medicus
Journal Article
Molecular cell, ISSN 1097-2765, 01/2017, Volume 65, Issue 2, pp. 247 - 259
core complex | RING E3 | Fanconi anemia | FANCD2 | deubiquitination | FANCB | enzyme mechanism | monoubiquitination | DNA repair | Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Fanconi Anemia Complementation Group D2 Protein - genetics | Fanconi Anemia - metabolism | Humans | Multiprotein Complexes | Protein Multimerization | Substrate Specificity | Fanconi Anemia Complementation Group A Protein - metabolism | DNA-Binding Proteins - metabolism | Fanconi Anemia Complementation Group Proteins - metabolism | Ubiquitination | Transfection | Time Factors | Fanconi Anemia - genetics | Ubiquitin-Specific Proteases - metabolism | Recombinant Proteins - metabolism | Cell Line | Fanconi Anemia Complementation Group Proteins - genetics | Nuclear Proteins - metabolism | Fanconi Anemia Complementation Group G Protein - metabolism | DNA - metabolism | Inhibitor of Differentiation Protein 2 - metabolism | DNA - genetics | Fanconi Anemia Complementation Group C Protein - metabolism | Fanconi Anemia Complementation Group D2 Protein - metabolism | Protein Binding | Fanconi Anemia Complementation Group L Protein - metabolism | Fanconi Anemia Complementation Group E Protein - metabolism | Ubiquitin | Chemotherapy | Ligases | Genomics | Research institutes | Cancer | Fanconi's anemia | Proteins | Medical research | Molecular genetics | Medicine, Experimental | Index Medicus
Journal Article
Trends in genetics, ISSN 0168-9525, 03/2018, Volume 34, Issue 3, pp. 171 - 183
replication | cancer | aging | Fanconi anemia | developmental defects | DNA damage response | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fanconi Anemia Complementation Group Proteins - metabolism | Fanconi Anemia - metabolism | DNA Repair | Humans | Fanconi Anemia Complementation Group Proteins - genetics | Fanconi Anemia - pathology | Fanconi Anemia - genetics | Models, Genetic | Signal Transduction - genetics | DNA Damage | Mutation | Index Medicus | Replication | Fanconi anemia (FA) | Developmental defects | and Aging | DNA damage response (DDR) | Cancer
Journal Article
Current biology, ISSN 0960-9822, 09/2017, Volume 27, Issue 18, pp. R986 - R988
Biochemistry & Molecular Biology | Biology | Life Sciences & Biomedicine - Other Topics | Life Sciences & Biomedicine | Science & Technology | Cell Biology | DNA Replication | Fanconi Anemia Complementation Group Proteins - metabolism | Metabolic Networks and Pathways | Fanconi Anemia - metabolism | DNA Repair | Humans | Fanconi's anemia | Index Medicus
Journal Article
Clinical genetics, ISSN 0009-9163, 07/2015, Volume 88, Issue 1, pp. 13 - 24
bone marrow failure | Fanconi anaemia | cancer | congenital abnormalities | Congenital abnormalities | Bone marrow failure | Cancer | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fanconi Anemia - complications | Neoplasms - etiology | Humans | Male | Gene-Environment Interaction | Congenital Abnormalities - diagnosis | Phenotype | Fanconi Anemia - diagnosis | Neoplasms - genetics | Adult | Female | Disease Management | Fanconi Anemia - genetics | Fanconi Anemia - therapy | Child | Molecular biology | Fanconi's anemia | Medical research | Genetic disorders | Mutation | Index Medicus
Journal Article
Biology of blood and marrow transplantation, ISSN 1083-8791, 2017, Volume 23, Issue 9, pp. 1422 - 1428
Hematology, Oncology and Palliative Medicine | Late effects | Dyskeratosis congenita | Pediatric allogeneic hematopoietic cell transplant | Fanconi anemia | Diamond Blackfan anemia | Inherited bone marrow failure syndromes | Transplantation | Immunology | Life Sciences & Biomedicine | Hematology | Science & Technology | Bone Marrow Diseases - diagnosis | Humans | Anemia, Diamond-Blackfan - immunology | Hemoglobinuria, Paroxysmal - pathology | Anemia, Diamond-Blackfan - mortality | Dyskeratosis Congenita - mortality | Anemia, Aplastic - therapy | Fanconi Anemia - mortality | Transplantation, Homologous | Hemoglobinuria, Paroxysmal - immunology | Anemia, Aplastic - diagnosis | Bone Marrow Diseases - therapy | Dyskeratosis Congenita - diagnosis | Dyskeratosis Congenita - therapy | Anemia, Diamond-Blackfan - therapy | Hemoglobinuria, Paroxysmal - diagnosis | Child | Anemia, Aplastic - pathology | Hematopoietic Stem Cell Transplantation | International Cooperation | Bone Marrow Diseases - pathology | Consensus Development Conferences as Topic | Anemia, Diamond-Blackfan - diagnosis | Consensus | Fanconi Anemia - diagnosis | Bone Marrow Diseases - immunology | Survival Analysis | Fanconi Anemia - immunology | Fanconi Anemia - therapy | Hemoglobinuria, Paroxysmal - therapy | Dyskeratosis Congenita - immunology | Anemia, Aplastic - immunology | Pediatrics | Conferences, meetings and seminars | Immunodeficiency | Bone marrow | Genetic aspects | Medical screening | Conferences and conventions | Hematopoietic stem cells | Fanconi's anemia | Medical research | Epidemiology | Diseases | Medicine, Experimental | Children | Index Medicus | dyskeratosis congenita | pediatric allogeneic hematopoietic cell transplant | late effects | inherited bone marrow failure syndromes
Journal Article
Seminars in hematology, ISSN 0037-1963, 2006, Volume 43, Issue 3, pp. 147 - 156
Life Sciences & Biomedicine | Hematology | Science & Technology | Fanconi Anemia Complementation Group Proteins - physiology | Fanconi Anemia - diagnosis | Models, Biological | Humans | Fanconi Anemia Complementation Group Proteins - genetics | Fanconi Anemia - genetics | Heat-Shock Proteins - physiology | Fanconi Anemia Complementation Group Proteins - chemistry | Genetic Heterogeneity | Fanconi Anemia - blood | Index Medicus
Journal Article