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Journal Article
Haematologica, ISSN 0390-6078, 09/2017, Volume 102, Issue 10, pp. 1691 - 1703
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2017, Volume 23, Issue 9, pp. 1422 - 1428
Abstract Patients with inherited bone marrow failure syndromes (IBMFS) such as Fanconi anemia (FA), dyskeratosis congenita (DC), and Diamond Blackfan anemia... 
Hematology, Oncology and Palliative Medicine | Late effects | Dyskeratosis congenita | Pediatric allogeneic hematopoietic cell transplant | Fanconi anemia | Diamond Blackfan anemia | Inherited bone marrow failure syndromes | LONG-TERM SURVIVORS | Pediatric allogeneic | 4 DECADES | NATIONAL-CANCER-INSTITUTE | IMMUNOLOGY | CHRONIC HEALTH CONDITIONS | BIALLELIC MUTATIONS | FANCONI-ANEMIA | TRANSPLANTATION | hematopoietic cell transplant | INSTITUTE/PEDIATRIC BLOOD | DYSKERATOSIS-CONGENITA | DIAMOND-BLACKFAN ANEMIA | HEMATOLOGY | APLASTIC-ANEMIA | 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 | Transplantation | Medical screening | Conferences and conventions | Hematopoietic stem cells | Fanconi's anemia | Medical research | Epidemiology | Diseases | Medicine, Experimental | Children | dyskeratosis congenita | pediatric allogeneic hematopoietic cell transplant | late effects | inherited bone marrow failure syndromes
Journal Article
American Journal of Hematology, ISSN 0361-8609, 08/2015, Volume 90, Issue 8, pp. 702 - 708
Immune function abnormalities have been reported in patients with Fanconi anemia (FA), dyskeratosis congenita (DC) and, rarely, in Shwachman–Diamond syndrome... 
RESPONSES | IN-VITRO | COLONY-STIMULATING FACTOR | FANCONI-ANEMIA PATIENTS | DYSKERATOSIS-CONGENITA | MONONUCLEAR-CELLS | VIRUS-LIKE PARTICLES | NECROSIS-FACTOR-ALPHA | HEMATOLOGY | APLASTIC-ANEMIA | IMMUNODEFICIENCY | Hemoglobinuria, Paroxysmal - congenital | Dyskeratosis Congenita - drug therapy | Humans | Lipomatosis - congenital | Child, Preschool | Male | Anemia, Aplastic | Exocrine Pancreatic Insufficiency - diagnosis | Adrenal Cortex Hormones - therapeutic use | Exocrine Pancreatic Insufficiency - immunology | Dyskeratosis Congenita - diagnosis | T-Lymphocytes - drug effects | Tumor Necrosis Factor-alpha - immunology | Fanconi Anemia - pathology | B-Lymphocytes - pathology | Anemia, Diamond-Blackfan - pathology | Hemoglobinuria, Paroxysmal - diagnosis | Child | Membrane Proteins - biosynthesis | B-Lymphocytes - immunology | Anemia, Diamond-Blackfan - drug therapy | Bone Marrow Diseases - immunology | Adolescent | Bone Marrow Diseases - congenital | Lipomatosis - diagnosis | T-Lymphocytes - immunology | Fanconi Anemia - immunology | Killer Cells, Natural - drug effects | Granulocyte Colony-Stimulating Factor - immunology | Tumor Necrosis Factor-alpha - biosynthesis | Bone Marrow Diseases - diagnosis | Anemia, Diamond-Blackfan - immunology | Infant | Killer Cells, Natural - pathology | Case-Control Studies | Hemoglobinuria, Paroxysmal - immunology | Bone Marrow Diseases - drug therapy | Phytohemagglutinins - pharmacology | Killer Cells, Natural - immunology | Adult | Female | T-Lymphocytes - pathology | Immunoglobulins - biosynthesis | Cytokines - immunology | Exocrine Pancreatic Insufficiency - drug therapy | Lipomatosis - drug therapy | Membrane Proteins - immunology | Anemia, Diamond-Blackfan - diagnosis | Lipomatosis - immunology | B-Lymphocytes - drug effects | Fanconi Anemia - diagnosis | Granulocyte Colony-Stimulating Factor - biosynthesis | Interferon-gamma - immunology | Hemoglobinuria, Paroxysmal - drug therapy | Dyskeratosis Congenita - pathology | Family | Aged | Primary Cell Culture | Fanconi Anemia - drug therapy | Dyskeratosis Congenita - immunology | Cytokines - biosynthesis | Exocrine Pancreatic Insufficiency - congenital | Interferon-gamma - biosynthesis | immune deficiency | cytokines | Inherited bone marrow failure syndromes
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2017, Volume 140, Issue 4, pp. 1112 - 1119
Background Myb-like, SWIRM, and MPN domains 1 (MYSM1) is a transcriptional regulator mediating histone deubiquitination. Its role in human immunity and... 
Allergy and Immunology | stem cells | hematopoiesis | rare disease | Immunodeficiency | transplantation | P53 PROTEIN | PHOSPHORYLATION | DOUBLE-STRAND BREAKS | IMMUNOLOGY | LYMPHOCYTE DIFFERENTIATION | REFERENCE VALUES | UV-RADIATION | ALLERGY | STEM-CELL MAINTENANCE | EPIGENETIC REGULATION | HISTONE H2A DEUBIQUITINASE | Genome-Wide Association Study | Humans | Cells, Cultured | Hematopoietic Stem Cell Transplantation | Genotype | DNA Damage - immunology | DNA Repair - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | DNA-Binding Proteins - metabolism | Transcription Factors - metabolism | Ubiquitination | Hematopoiesis | Pedigree | Bone Marrow Diseases - immunology | Developmental Disabilities - immunology | Consanguinity | p38 Mitogen-Activated Protein Kinases - metabolism | Histones - metabolism | Immunologic Deficiency Syndromes - immunology | Sequence Deletion - genetics | Monoclonal antibodies | Codon | Analysis | Genomics | Transplantation | B cells | Nucleotide sequencing | Hematopoietic stem cells | Risk factors | DNA sequencing | Cataracts | Reactive oxygen species | Phosphorylation | p38 Protein | Transplants & implants | Transcription | Nonsense mutation | DNA damage | Genotoxicity | Stem cell transplantation | Genomes | Cognition | Kinases | Homozygosity | Phosphatase | Immunity | Blood | Gene sequencing | Proteins | Penicillin | Bone marrow | Deoxyribonucleic acid--DNA | Siblings | Stresses | Cell survival | U.V. radiation | Anemia | Stop codon | Patients | Survival | Stress | Hemopoiesis | Studies | Ultraviolet radiation | Lymphocytes B | Biopsy | Stem cells | Epigenetics | Bone | Mutation | Aberration | Leukocytes (granulocytic) | Gene mapping | Apoptosis
Journal Article
Journal Article
Journal Article
世界胃肠病学杂志:英文版, ISSN 1007-9327, 2017, Volume 23, Issue 35, pp. 6540 - 6545
Journal Article
Hematology/Oncology Clinics of North America, ISSN 0889-8588, 08/2018, Volume 32, Issue 4, pp. 643 - 655
Journal Article
Diagnostic Pathology, ISSN 1746-1596, 10/2018, Volume 13, Issue 1, pp. 82 - 7
BackgroundIndolent T-cell proliferative disorder of the GIT is a rare and provisional entity in the revised WHO 2016 classification. The patients usually have... 
Aberrant CD20 expression | Indolent T-cell lymphoproliferative disorder | Gastrointestinal tract | DISEASE | LYMPHOMA | PATHOLOGY | INFILTRATION | FEATURES | Immunohistochemistry | Predictive Value of Tests | Diagnosis, Differential | Cell Proliferation | Prognosis | Humans | Middle Aged | Biomarkers - analysis | Endoscopy, Gastrointestinal | Male | Lymphoproliferative Disorders - immunology | Bone Marrow Diseases - pathology | Lymphoproliferative Disorders - pathology | Bone Marrow Diseases - genetics | Phenotype | Gastrointestinal Diseases - genetics | Time Factors | Biopsy | Bone Marrow Diseases - immunology | Gastrointestinal Diseases - pathology | T-Lymphocytes - immunology | Antigens, CD20 - analysis | T-Lymphocytes - pathology | Gastrointestinal Diseases - immunology | Case studies | Lymphoproliferative disorders | Gastrointestinal system | Bone marrow | Genetic aspects | Diagnosis | Research | Gene expression | Health aspects | Disease | CD8 antigen | Viruses | Lymphocytes T | Pax5 protein | Blood | T-cell receptor | Lymphocytes | Classification | Colon | CD43 antigen | Endoscopy | CD56 antigen | Stomach | RNA viruses | Immunoglobulins | Lymphoid cells | Medical treatment | Lamina propria | CD3 antigen | Ribonucleic acid--RNA | Patients | CD4 antigen | Pathology | Chemotherapy | Lymphocytes B | Ulcers | Gene rearrangement | Heavy chains | CD20 antigen | Lymphomas | Diagnostic systems | Cytoplasm | Recognition | CD7 antigen
Journal Article