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