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「"Kono M "[Author]」の検索結果

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Ectopic RASGRP2 (CalDAG-GEFI) expression in rheumatoid synovium contributes to the development of destructive arthritis.

Morphological and optical properties of human immature platelet-enriched population produced in immunodeficient mice.

SLAMF1 engagement inhibits T cell-B cell interaction and diminishes IL-6 production and plasmablast differentiation in systemic lupus erythematosus.

Correlation between the malignancy and prognosis of oral squamous cell carcinoma in the maximum standardized uptake value.

[A CASE OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE COMPLICATED WITH HENOCH-SCHÖNLEIN PURPURA NEPHRITIS].

A 4-bp deletion promoter variant (rs984225803) is associated with mild OCA4 among Japanese patients.

CaMK4 compromises podocyte function in autoimmune and nonautoimmune kidney disease.

Eosinophilia and systemic symptoms with transient ageusia: a drug reaction caused by zonisamide.

The benefits of high-resolution, real-time colour-imaging of lymphatic flow for sentinel lymph node biopsy.

Clinical significance of myeloperoxidase-anti-neutrophil cytoplasmic antibody in idiopathic interstitial pneumonias.

Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C-terminus of KIT.

Analysis of genotype/phenotype correlations in Japanese patients with dyschromatosis symmetrica hereditaria.

Decreased expression of Serine/arginine-rich splicing factor 1 in T cells from patients with active systemic lupus erythematosus accounts for reduced expression of RasGRP1 and DNA methyltransferase 1.

Prognostic evaluation of serum ferritin in acute exacerbation of idiopathic pulmonary fibrosis.

Haemin-induced cell death in human monocytic cells is consistent with ferroptosis.

Sterol profiles are valuable biomarkers for phenotype expression of Conradi-Hünermann-Happle syndrome with EBP mutations.

Dyschromatosis symmetrica hereditaria with chilblains due to a novel two-amino-acid deletion in the double-stranded RNA binding domain of ADAR1.

Strong correlation between cancer progression and anti-transcription intermediary factor 1γ antibodies in dermatomyositis patients.

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