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Department Of Cell Biology Institute Of Nephrology Niigata University Graduate School Of Medical And | 論文
- Treatment with chondroitinase ABC alleviates bleomycin-induced pulmonary fibrosis
- Identification of hydroxyapatite deposits in the smooth muscle cells and ganglion cells of autopsied small intestines
- Spironolactone in Combination with Cilazapril Ameliorates Proteinuria and Renal Interstitial Fibrosis in Rats with Anti-Thy-1 Irreversible Nephritis
- Blockade of interferon-γ-inducible protein-10 attenuates chronic experimental colitis by blocking cellular trafficking and protecting intestinal epithelial cells
- Progressive Glomerulonephritis with Increasing Proteinuria Induced by a Second Attack to the Mesangial Cell
- A Novel Rat Model with Podocyte Injury in Developing Stage Glomeruli
- Early Intervention in Reducing Dietary Protein Intake Ameliorates Irreversible Mesangioproliferative Glomerulonephritis in Rats
- Not the ED1^+ but the ED3^+ Macrophage Participates in the Pathogenesis of Irreversible Glomerular Changes
- De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome : unequal sister chromatid exchange during paternal gametogenesis
- Neutralization of CXCL10 accelerates liver regeneration in carbon tetrachloride-induced acute liver injury
- Improvement of nephrotic syndrome by intensive lipid-lowering therapy in a patient with lipoprotein glomerulopathy
- Slit diaphragm dysfunction in proteinuric states : identification of novel therapeutic targets for nephrotic syndrome
- Tolvaptan, a selective oral vasopressin V2 receptor antagonist, ameliorates podocyte injury in puromycin aminonucleoside nephrotic rats
- CD28 superagonist-induced regulatory T cell expansion ameliorates mesangioproliferative glomerulonephritis in rats
- Molecular diagnosis and clinical onset of Charcot-Marie-Tooth disease in Japan
- Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms : 211G>A (G71R) mutation becomes a risk factor under inadequate feeding
- A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy