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Allergology international, ISSN 1323-8930, 2018, Volume 67, Issue 1, pp. 43 - 54
Journal Article
International journal of hematology, ISSN 0925-5710, 9/2019, Volume 110, Issue 3, pp. 364 - 369
Medicine & Public Health | Hematology | Stem cell transplantation (SCT) | Wiskott–Aldrich syndrome (WAS) | Cyclophosphamide (CY) | Oncology | Tacrolimus (Tac) | Chimerism | Life Sciences & Biomedicine | Science & Technology | Humans | Child, Preschool | Hematopoietic Stem Cell Transplantation | Infant | Male | Wiskott-Aldrich Syndrome - therapy | Allografts | Transplantation Chimera - blood | Adolescent | Adult | Female | Retrospective Studies | Wiskott-Aldrich Syndrome - blood | Child | Surveys | Wiskott-Aldrich syndrome | Medical colleges | Medical research | Care and treatment | Patient outcomes | Stem cells | Medicine, Experimental | Transplantation | Hematopoietic stem cells | Graft-versus-host reaction | Cyclosporins | Prophylaxis | Stem cell transplantation | Multivariate analysis | Risk analysis | Risk factors | Hemopoiesis | Cyclophosphamide | Tacrolimus | Conditioning | Index Medicus
Journal Article
Journal of allergy and clinical immunology, ISSN 0091-6749, 2016, Volume 139, Issue 6, pp. 1914 - 1922
Allergy and Immunology | TNFAIP3 (A20) | Autoimmune lymphoproliferative syndrome | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Humans | Cells, Cultured | NF-kappa B - immunology | Infant | Male | Haploinsufficiency | Tumor Necrosis Factor alpha-Induced Protein 3 - genetics | Phenotype | Autoimmune Lymphoproliferative Syndrome - genetics | Leukocytes, Mononuclear - immunology | Autoimmune Lymphoproliferative Syndrome - immunology | Germ-Line Mutation | Tumor Necrosis Factor alpha-Induced Protein 3 - immunology | Gene mutations | Developmental biology | Analysis | Genomics | Genetic research | Genetic aspects | Information management | Children | Health aspects | Diseases | Pediatrics | Fas antigen | Disease | Transcription | Genes | Science | Frameshift mutation | Genomes | Kinases | Gene sequencing | Proteins | Signal transduction | Alterations | Functional anatomy | Databases | Pathways | Lymphocytes | Immunoglobulins | Patients | Tumor necrosis factor | Mutation | Autoimmune diseases | Apoptosis | Index Medicus | Abridged Index Medicus
Journal Article
Journal of allergy and clinical immunology, ISSN 0091-6749, 2015, Volume 136, Issue 4, pp. 1018 - 1024
Allergy and Immunology | hyper-IgM syndrome | Cryptosporidium parvum | Cryptococcus neoformans | CD40 ligand | hematopoietic stem cell transplantation | primary immunodeficiency | Pneumocystis jirovecii | combined immunodeficiency | class-switch recombination | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Humans | Japan | Child, Preschool | Hematopoietic Stem Cell Transplantation | Infant | Male | Treatment Outcome | Mutation - genetics | Hyper-IgM Immunodeficiency Syndrome, Type 1 - mortality | Young Adult | CD40 Ligand - genetics | Adolescent | Survival Analysis | Adult | Female | Retrospective Studies | Hyper-IgM Immunodeficiency Syndrome, Type 1 - surgery | Child | Immunoglobulin Class Switching - genetics | Medical colleges | Transplantation | Hematopoietic stem cells | Stem cells | Bone marrow | Bacterial infections | Mutation | Transplants & implants | Mortality | Index Medicus | Abridged Index Medicus
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Abnormal hematopoiesis and autoimmunity in human subjects with germline IKZF1 mutations
Journal of allergy and clinical immunology, ISSN 0091-6749, 2016, Volume 140, Issue 1, pp. 223 - 231
Allergy and Immunology | Acute lymphoblastic leukemia | Ikaros | common lymphoid progenitor | dysgammaglobulinemia | nuclear localization | B-cell deficiency | IKZF1 | autoimmune disease | germline mutation | DNA binding | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Autoimmunity | Humans | Autoimmune Diseases - immunology | Hematopoiesis - genetics | Male | Hematologic Diseases - immunology | Autoimmune Diseases - genetics | Ikaros Transcription Factor - genetics | Young Adult | B-Lymphocytes - immunology | Ikaros Transcription Factor - immunology | Adolescent | Germ-Line Mutation | Hematologic Diseases - genetics | Lymphocyte Count | Adult | Female | T-Lymphocytes - immunology | Child | Medical colleges | Developmental biology | Analysis | Leukemia | Immunodeficiency | Genetic aspects | Pediatrics | Flow cytometry | Lymphopoiesis | Transcription factors | Ikaros protein | Pathogenesis | Genomes | Kinases | Immunoglobulin A | Vasculitis | Systemic lupus erythematosus | Hematopoiesis | Cell cycle | Bone marrow | Localization | Age | Deoxyribonucleic acid--DNA | Binding | Nucleotide sequence | Abnormalities | Patients | Hemopoiesis | Diseases | Thrombocytopenic purpura | Chronic conditions | Lymphocytes B | Plasmids | Purpura | Pancytopenia | Stem cells | Mutation | Autoimmune diseases | Index Medicus | Abridged Index Medicus
Journal Article
Journal of allergy and clinical immunology, ISSN 0091-6749, 2014, Volume 135, Issue 4, pp. 988 - 997.e6
Allergy and Immunology | Common variable immunodeficiency | immunologic reconstitution | survival | hematopoietic stem cell transplantation | immunoglobulin substitution/replacement | mortality | hypogammaglobulinemia | outcome | BONE-MARROW-TRANSPLANTATION | ACUTE GVHD | DISORDERS | CLASSIFICATION | SEVERE APLASTIC-ANEMIA | EUROPEAN GROUP | VERSUS-HOST-DISEASE | WORKING PARTY | Journal Article | B-CELL | Research Support, Non-U.S. Gov't | Multicenter Study | BLOOD | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Follow-Up Studies | Humans | Middle Aged | Graft Survival | Male | Treatment Outcome | Common Variable Immunodeficiency - complications | Cause of Death | Young Adult | Common Variable Immunodeficiency - mortality | Common Variable Immunodeficiency - therapy | Adolescent | Hematopoietic Stem Cell Transplantation - adverse effects | Adult | Female | Graft vs Host Disease - prevention & control | Retrospective Studies | Transplantation Conditioning | Child | Graft vs Host Disease - etiology | Hematopoietic Stem Cells | Complications and side effects | Hospitals | Mortality | Stem cells | Immunological deficiency syndromes | Transplantation | Hematopoietic stem cells | Cytomegalovirus | Life expectancy | Transplants & implants | Lung diseases | Liver | Values | Infections | Patients | Lymphoma | Variables | Cell growth | Software | Age | Index Medicus | Abridged Index Medicus
Journal Article
Pediatrics international, ISSN 1328-8067, 09/2019, Volume 61, Issue 9, pp. 929 - 931
Journal Article
International journal of hematology, ISSN 0925-5710, 4/2019, Volume 109, Issue 4, pp. 382 - 389
SIFD | Medicine & Public Health | Hematology | Oncology | B-cell deficiency | TRNT1 | Endoplasmic reticulum stress | Life Sciences & Biomedicine | Science & Technology | Enzymes | Developmental biology | Anemia | College graduates | Immunodeficiency | Transplantation | B cells | T cells | Cell differentiation | Hematopoietic stem cells | Case studies | Analysis | Bone marrow | Genetic aspects | Transfer RNA | Cataracts | Severe combined immunodeficiency | Syngeneic grafts | Cardiomyopathy | Retinitis pigmentosa | Pathogenesis | Bone marrow transplantation | Stem cell transplantation | Lymphocytes T | Sideroblastic anemia | Developmental stages | Lymphocytes | Chemical synthesis | Phenotypes | Biochemical analysis | CD19 antigen | tRNA | Fever | Hemopoiesis | Lymphocytes B | Stem cells | CD20 antigen | Retinitis | Mutation | Endoplasmic reticulum | Cellular stress response | Index Medicus
Journal Article
Journal of allergy and clinical immunology, ISSN 0091-6749, 04/2018, Volume 141, Issue 4, pp. 1485 - 1488.e11
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Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders
Journal of allergy and clinical immunology, ISSN 0091-6749, 2017, Volume 141, Issue 1, pp. 322 - 328.e10
Allergy and Immunology | hematopoietic stem cell transplantation | Ataxia-telangiectasia | DNA repair disorders | DNA ligase IV deficiency | Nijmegen breakage syndrome | Cernunnos-XLF deficiency | Allergy | Immunology | Life Sciences & Biomedicine | Science & Technology | Prognosis | Follow-Up Studies | Humans | Child, Preschool | Infant | Male | DNA Repair-Deficiency Disorders - diagnosis | DNA Breaks, Double-Stranded | Young Adult | DNA Repair-Deficiency Disorders - mortality | Hematopoietic Stem Cell Transplantation - adverse effects | Female | Child | Graft vs Host Disease - diagnosis | Graft vs Host Disease - etiology | Virus Diseases | Kaplan-Meier Estimate | Treatment Outcome | DNA Repair | Adolescent | Alleles | Hematopoietic Stem Cell Transplantation - methods | Mutation | DNA Repair-Deficiency Disorders - genetics | DNA Repair-Deficiency Disorders - therapy | Graft-versus-host reaction | Radiosensitivity | Transplants & implants | Syngeneic grafts | DNA damage | Disorders | Bone marrow transplantation | Transplantation | Infections | Malignancy | Kinases | DNA repair | Alkylation | Proteins | Consortia | Lymphocytes | Cell cycle | Bone marrow | Ataxia | Conditioning | Repair | Deoxyribonucleic acid--DNA | Antigens | Complications | Anemia | Mortality | Immunodeficiency | DNA ligase (ATP) | Radiation therapy | Double-strand break repair | Patients | Survival | Immunological tolerance | Hemopoiesis | Cyclophosphamide | Chemotherapy | Breakage | Stem cells | Ataxia telangiectasia | Index Medicus | Abridged Index Medicus
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