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The Journal of Dermatology, ISSN 0385-2407, 11/2019, Volume 46, Issue 11, pp. 1019 - 1023
Prominent dermal infiltration by Langerhans cells (LC) is a rare finding in patients with Omenn syndrome (OS). Here, we report the case study of a 7‐month‐old... 
dermal Langerhans cells | autoimmunity | severe combined immunodeficiency | Omenn syndrome | IL2RG gene | Antigens | Flow cytometry | Dermis | Immunoglobulin E | Lymphocytes T | Transplantation | Hypogammaglobulinemia | Eosinophilia | Lymph nodes | Blood flow | Lymphadenopathy | Alopecia | Cord blood | Genetic analysis | Peripheral blood | Langerhans cells | Skin | Umbilical cord | Mutation | Cell migration
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 139, Issue 6, pp. 1914 - 1922
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 140, Issue 1, pp. 223 - 231
Background Ikaros, which is encoded by IKZF1 , is a transcriptional factor that play a critical role in hematopoiesis. Somatic IKZF1 alterations are known to... 
Allergy and Immunology | Acute lymphoblastic leukemia | Ikaros | common lymphoid progenitor | dysgammaglobulinemia | nuclear localization | B-cell deficiency | IKZF1 | autoimmune disease | germline mutation | DNA binding | SYSTEM | ZINC FINGERS | ACTIVATION | DEFECTS | STAGE | B-CELL DIFFERENTIATION | IMMUNOLOGY | ALLERGY | LEUKEMOGENESIS | LYMPHOBLASTIC-LEUKEMIA | 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
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2007, Volume 46, Issue 26, pp. 4922 - 4925
Journal Article
Internal Medicine, ISSN 0918-2918, 2019, Volume 58, Issue 2, pp. 213 - 216
Journal Article
The Journal of Dermatology, ISSN 0385-2407, 11/2019, Volume 46, Issue 11, pp. 1019 - 1023
Journal Article
Internal Medicine, ISSN 0918-2918, 2019
A diagnosis of hereditary angioedema is usually made with recurrent episodes of swelling of the subcutaneous tissue with a family history. We herein report a... 
C1-inhibitor | hereditary angioedema | hypocomplementemia | submucosal edema | acute abdomen
Journal Article
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2016, Volume 138, Issue 6, pp. 1672 - 1680.e10
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2006, Volume 45, Issue 33, pp. 5527 - 5529
Why not combine the two? The asymmetric direct aldol reaction of two different aldehydes was catalyzed by a combined proline–surfactant organic catalyst in the... 
organocatalysis | aldol reaction | surfactants | asymmetric synthesis | green chemistry | Aldol reaction | Green chemistry | Asymmetric synthesis | Surfactants | Organocatalysis | ORGANIC-REACTIONS | MEDIA | CHEMISTRY, MULTIDISCIPLINARY | CATALYSTS | WATER
Journal Article
Chemical Communications, ISSN 1359-7345, 2007, Issue 24, pp. 2524 - 2526
A small organic molecule, Pro-NH(2), catalyzing the enantioselective aldol reaction "in water" not merely "in the presence of water" with good... 
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 07/2017, Volume 37, Issue 5, pp. 486 - 495
Journal Article