Mutations of the WASP Gene in 10 Japanese Patients With Wiskott-Aldrich Syndrome and X-linked Thrombocytopenia
スポンサーリンク
概要
著者
-
Nonoyama Shigeaki
Department of Pediatrics, National Defense Medical College
-
OKAWA Hiroji
Departments of Pediatrics, School of Medicine, Tokyo Medical and Dental University
-
Okawa Hiroji
Department Of Pediatrics Tokyo Medical And Dental University
-
Morio Tomohiro
Department Of Pediatrics And Developmental Biology Tokyo Medical And Dental University Graduate Scho
-
Morio Tomohiro
Department Of Pediatrics Tokyo Medical And Dental University School Of Medicine
-
Morio Tomohiro
Department Of General Medicine School Of Medicine Tokyo Medical And Dental University
-
Morio Tomohiro
Department Of Pediatrics Tokyo Medical And Dental University
-
SHIMADZU Mitsunobu
Department of Cytogenetic Analysis, Mitsubishi Kagaku Bioclinical Laboratory Inc.
-
IMAI Kohsuke
Department of Pediatrics, National Defense Medical College
-
Nonoyama Shigeaki
Department Of Human Ontogeny And Childhood Development Tokyo Medical And Dental University School Of
-
Nonoyama Shigeaki
Department Of Pediatrics Tokyo Medical And Dental University
-
Shimadzu Mitsunobu
Department Of Genetics Mitsubishi Kagaku Bio-clinical Laboratories
-
ITOH Sukeyuki
Department of Pediatrics, Tokyo Medical and Dental University
-
OCHS Hans
Department of Pediatrics, University of Washington
-
YATA Junichi
Department of Pediatrics, Tokyo Medical and Dental University
-
Imai Kohsuke
Department Of Pediatrics National Defense Medical College
-
Yata J
Department Of Pediatrics Tokyo Medical And Dental University
-
Itoh Sukeyuki
Department Of Pediatrics Tokyo Medical And Dental University
-
Ochs Hans
Department Of Pediatrics University Of Washington
-
Imai Kohsuke
National Defense Medical Coll. Saitama Jpn
-
YATA JUNICHI
Department of Pediatrics, School of Medicine, Tokyo Medical and Dental University
関連論文
- Fetal and Neonatal Development of Ca2+ Transients and Functional Sarcoplasmic Reticulum in Beating Mouse Hearts
- Induction of CD40 in Promyelocytic HL60 Cells Cultured with Retinoic Acid and/or Various Cytokines
- Successful treatment of chronic granulomatous disease with fludarabine-based reduced-intensity conditioning and unrelated bone marrow transplantation
- Clnical and biological aspects of acute lymphoblastic leukemia in 62 infants : Retrospective analysis of the Tokyo Children's Cancer Study Group
- Omenn Syndrome-Review of Several Phenotypes of Omenn Syndrome and RAG1/RAG2 Mutations in Japan
- Evans syndrome in a patient with Langerhans cell histiocytosis : possible pathogenesis of autoimmunity in LCH
- Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
- Coordinated Regulation of the Promoter and Enhancer Regions of Human CD23 Gene by Signal Through IL-4R and CD40, and the Role of Ku70/80 in the Enhancer Activity
- Phenotypic variations between affected siblings with ataxia-telangiectasia : ataxia-telangiectasia in Japan
- Recombinant adeno-associated virus-mediated gene transfer into human leukemia cell lines
- Qualitative and quantitative differences in the intensity of Fas-mediated intracellular signals determine life and death in T cells
- Automatic detection of immature platelets for decision making regarding platelet transfusion indications for pediatric patients
- Characterization of Epstein-Barr Virus (EBV)-Positive NK Cells Isolated from Hydroa Vacciniforme-Like Eruptions
- Induction of the high-affinity lgE receptor (FcεRI) on human mast cells by IL-4
- Qualitatively differential regulation of T cell activation and apoptosis by T cell receptor ζ chain ITAMs and their tyrosine residues
- Type Two Hyper-IgM Syndrome caused by Mutation in Activation-Induced Cytidine Deaminase
- Mutations of the WASP Gene in 10 Japanese Patients With Wiskott-Aldrich Syndrome and X-linked Thrombocytopenia
- Peripheral expansion of Vδ1-Jδ1/Jδ2^+ γδT cells and large granular lymphocytes in a patient with Wiskott-Aldrich syndrome
- TARC and MDC are produced by CD40 activated human B cells and are elevated in the sera of infantile atopic dermatitis patients
- Utility of Multiplex PCR in Detecting the Causative Pathogens for Pediatric Febrile Neutropenia
- Fatal degeneration of specialized cardiac muscle associated with chronic active Epstein-Barr virus infection
- Successful allogeneic hematopoietic stem cell transplantation for chronic granulomatous disease with inflammatory complications and severe infection
- Missense Mutations of the BMPR1B (ALK6) Gene in Childhood Idiopathic Pulmonary Arterial Hypertension
- Impaired cell adhesion, apoptosis, and signaling in WASP gene-disrupted Nalm-6 pre-B cells and recovery of cell adhesion using a transducible form of WASp
- Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis
- Fetal and Neonatal Development of Ca^ Transients and Functional Sarcoplasmic Reticulum in Beating Mouse Hearts
- Recurrent bacterial meningitis by three different pathogens in an isolated asplenic child
- Age and seasonal variations in the serum levels of 25-hydroxyvitamin D and 24,25-dihydroxyvitamin D in normal humans.
- The SCID mouse, a model for human diseases.
- Soluble ST2 and N-terminal pro-Brain Natriuretic Peptide Combination:– Useful Biomarker for Predicting Outcome of Childhood Pulmonary Arterial Hypertension –