Nakajima Tohru | Division Of Pediatric Cardiology Osaka Medical Center And Research Institute For Maternal And Child

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著作論文

Impaired Insulin Secretion in Four Tangier Disease Patients with ABCA1 Mutations
Significance of measuring serum apolipoprotein (apo) B-48 concentrations in evaluating the metabolism of chylomicrons and chylomicron remnants
C-Reactive Protein-Mediated Low-Density Lipoprotein Uptake by Human Monocyte-Derived Macrophages : Implications in Atherogenesis
Serum Matrix Metalloproteinases (MMPs) Levels Are Diagnostic Markers of Active Phase in Patients with Takayasu Arteritis
Minocycline Has a Steroid-Sparing Effect in Treatment of Takayasu Arteritis
A Plasma Protein Abundantly Expressed in Visceral Fat, Visfatin Modulates Inflammatory Response in Human Monocyte-derived Macrophages
A girl with 1p36 deletion syndrome and congenital fiber type disproportion myopathy
Visceral Fat Accumulation Contributes to Insulin Resistance, Small-Sized Low-Density Lipoprotein, and Progression of Coronary Artery Disease in Middle-Aged Non-Obese Japanese Men
SIGNIGICANCE OF VISCERAL FAT ACCUMULATION TO THE DEVELOPMENT OF CORONARY ARTERY DISEASE(CAD)IN NON-OBESE MEN : VISCERAL FAT SYNDROME AS A NEW CLINICAL ENTITY
3. Role of Adipocytokines on the Pathogenesis of Atherosclerosis in Visceral Obesity
LIPOPROTElN METABOLISM IN HYPER-ALPHA-LIPOPROTEINEMIA WITH DEFICIENCY OF CHOLESTERYL ESTER TRANSFER PROTEIN : Arteriosclerosis : 53 Annual Scientific Meeting, Japanese Circulation Society
Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA) gene
Human calcitonin receptor-like receptor for adrenomedullin : genomic structure, eight single-nucleotide polymorphisms, and haplotype analysis
A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia
Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population
Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population
Screening of 336 single-nucleotide polymorphisms in 85 obesity-related genes revealed McKusick-Kaufman syndrome gene variants are associated with metabolic syndrome

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