about
Interaction of MCC2, a novel homologue of MCC tumor suppressor, with PDZ-domain Protein AIE-75Expression of AIE-75 PDZ-domain protein induces G2/M cell cycle arrest in human colorectal adenocarcinoma SW480 cellsDifference in target antigens between central tolerance and peripheral tolerance deficienciesRecurrence of juvenile dermatomyositis 8 years after remission.Pediatric Rheumatology Association of Japan recommendation for vaccination in pediatric rheumatic diseases.Autoantibodies to villin occur frequently in IPEX, a severe immune dysregulation, syndrome caused by mutation of FOXP3.Stroke During Norovirus Infection as the Initial Episode of Antiphospholipid Syndrome.A Post-Liver Transplant Girl With Recurrent Cramps in the Legs.Monocyte/macrophage-specific NADPH oxidase contributes to antimicrobial host defense in X-CGD.Chronic mucocutaneous candidiasis caused by a gain-of-function mutation in the STAT1 DNA-binding domain.Progression of palindromic rheumatism to juvenile idiopathic arthritis in a Japanese girl carrying heterozygous L110P-E148Q substitutions of MEFV gene.A heterozygous dominant-negative mutation in the coiled-coil domain of STAT1 is the cause of autosomal-dominant Mendelian susceptibility to mycobacterial diseases.Two novel gain-of-function mutations of STAT1 responsible for chronic mucocutaneous candidiasis disease: impaired production of IL-17A and IL-22, and the presence of anti-IL-17F autoantibody.Determination of the deletion breakpoints in two patients with contiguous gene syndrome encompassing CYBB gene.Rapid progression to pulmonary arterial hypertension crisis associated with mixed connective tissue disease in an 11-year-old girl.Elevation of serum IgE level and peripheral eosinophil count during T lymphocyte-directed gene therapy for ADA deficiency: implication of Tc2-like cells after gene transduction procedure.Difficulty in the diagnosis of bone and joint pain associated with pediatric acute leukemia; comparison with juvenile idiopathic arthritis.Tacrolimus in combination with methotrexate and corticosteroid for the treatment of child-onset anti-signal recognition particle antibody-positive necrotizing myopathy.Rapidly progressive and fatal neurocutaneous melanosis presenting as recurrent headacheComplications of childhood Sjögren syndromeExtremely high serum level of IgE during immunosuppressive therapy: paradoxical effect of cyclosporine A and tacrolimusA 75-kD autoantigen recognized by sera from patients with X-linked autoimmune enteropathy associated with nephropathyDevelopment of germinoma during the treatment of systemic-onset juvenile idiopathic arthritis with infliximabAnti-melanoma differentiation-associated gene 5 antibody is a diagnostic and predictive marker for interstitial lung diseases associated with juvenile dermatomyositisDisease specificity of anti-tryptophan hydroxylase-1 and anti-AIE-75 autoantibodies in APECED and IPEX syndromeFusarium falciforme infection in a patient with chronic granulomatous disease: Unique long-term course of epidural abscessEvaluation of systemic activity of pediatric primary Sjögren's syndrome by EULAR Sjögren's syndrome disease activity index (ESSDAI)Myositis-specific autoantibodies in Japanese patients with juvenile idiopathic inflammatory myopathiesClinical practice guidance for juvenile dermatomyositis (JDM) 2018-Update
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description
researcher ORCID ID=0000-0003-4956-4010
@en
name
I Kobayashi
@en
I Kobayashi
@nl
type
label
I Kobayashi
@en
I Kobayashi
@nl
prefLabel
I Kobayashi
@en
I Kobayashi
@nl
P106
P31
P496
0000-0003-4956-4010