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Kidney International, ISSN 0085-2538, 12/2017, Volume 92, Issue 6, pp. 1419 - 1432
Journal Article
PLoS ONE, ISSN 1932-6203, 06/2014, Volume 9, Issue 6, p. e100777
Inhibition of sodium glucose cotransporter 2 (SGLT2) has been reported as a new therapeutic strategy for treating diabetes. However, the effect of SGLT2... 
OXIDATIVE STRESS | ACTIVATION | HYPERGLYCEMIA | SGLT2 INHIBITOR | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | RATS | COMPLICATIONS | MELLITUS | PANCREATIC-FUNCTION | RENAL INJURY | Inflammation - pathology | Oxidative Stress | Kidney Cortex - metabolism | Body Weight - drug effects | Diabetic Nephropathies - drug therapy | Male | Kidney Function Tests | Inflammation - metabolism | Kidney - metabolism | Glomerular Mesangium - metabolism | Glomerular Mesangium - drug effects | Homeostasis - drug effects | Kidney - physiopathology | Disease Models, Animal | Diabetic Nephropathies - pathology | Gene Expression | Glucosides - pharmacology | Kidney Tubules, Proximal - pathology | Kidney - drug effects | Macrophages - pathology | Diabetic Nephropathies - metabolism | Cells, Cultured | Diabetic Nephropathies - genetics | Kidney Cortex - pathology | Sodium-Glucose Transporter 2 - antagonists & inhibitors | Blood Glucose - drug effects | Glomerular Mesangium - pathology | Macrophages - metabolism | Animals | Insulin-Secreting Cells - drug effects | Kidney Tubules, Proximal - metabolism | Glucose - metabolism | Inflammation - genetics | Benzhydryl Compounds - pharmacology | Mice | Apoptosis | Oxidases | Type 2 diabetes | Blood sugar | Analysis | Body weight | Diabetic nephropathies | Hemoglobin | DNA polymerases | Gene expression | Health aspects | Oxidative stress | RNA-directed DNA polymerase | Syngeneic grafts | Homeostasis | Glucose | Macrophages | Blood | NAD(P)H oxidase | Biomedical materials | Hyperglycemia | Rodents | Biocompatibility | Blood pressure | Inhibition | Pancreas | Pharmaceutical sciences | Age | University graduates | Neurochemistry | Creatinine | Kidneys | Cytokines | Diabetes mellitus | Osteopontin | Inflammation | Dentistry | Metabolism | Medicine | Studies | Inhibitors | Nephropathy | Sodium | Monocyte chemoattractant protein | Fibrosis | Infiltration | Diabetes | Monocyte chemoattractant protein 1
Journal Article
Journal Article
The Journal of Pathology, ISSN 0022-3417, 04/2013, Volume 229, Issue 5, pp. 672 - 684
Mesangioproliferative glomerulonephritis is the most common nephritis worldwide. We examined the effects of low‐ and high‐dose telmisartan, an angiotensin II... 
IgA | chemokine | platelet‐derived growth factor receptor | telmisartan | nephropathy | fibrosis | mesangioproliferative glomerulonephritis | renin–angiotensin system | chemokine receptor | IgA nephropathy | platelet-derived growth factor receptor | renin-angiotensin system | reninangiotensin system | TUBULOINTERSTITIAL INJURY | PDGF-D | ANTAGONISM | PATHOLOGY | MESENCHYMAL TRANSITION | ONCOLOGY | NEPHRITIS | AMELIORATES PROTEINURIA | GROWTH-FACTOR | EXPRESSION | RENAL INTERSTITIAL FIBROSIS | Antihypertensive Agents - pharmacology | Humans | Hypertension - drug therapy | Male | Gene Expression Profiling | RNA, Messenger - metabolism | Angiotensin II Type 1 Receptor Blockers - pharmacology | Inflammation - metabolism | Benzimidazoles - administration & dosage | Nephrectomy | RNA Interference | Time Factors | Glomerular Mesangium - metabolism | Chemokine CCL20 - genetics | Glomerular Mesangium - drug effects | Glomerulonephritis, Membranoproliferative - metabolism | Angiotensin II Type 1 Receptor Blockers - administration & dosage | Cytoprotection | Disease Models, Animal | Glomerulonephritis, Membranoproliferative - pathology | Macrophages - pathology | Rats | Receptors, Platelet-Derived Growth Factor - genetics | Podocytes - pathology | Hypertension - metabolism | Proteinuria - physiopathology | Glomerulonephritis, Membranoproliferative - genetics | Macrophages - metabolism | Receptors, Platelet-Derived Growth Factor - metabolism | Fibrosis | Receptors, CCR6 - genetics | Benzoates - pharmacology | Benzimidazoles - pharmacology | Glomerular Mesangium - physiopathology | Mice | Rats, Wistar | Hydralazine - pharmacology | Antihypertensive Agents - administration & dosage | Isoantibodies | Glomerulonephritis, Membranoproliferative - drug therapy | Transfection | Hydrochlorothiazide - pharmacology | Inflammation - drug therapy | Receptors, CCR6 - metabolism | Blood Pressure - drug effects | Atenolol - pharmacology | Cell Line | Podocytes - metabolism | Cell Dedifferentiation - drug effects | Gene Expression Regulation | Proteinuria - metabolism | Hypertension - physiopathology | Benzoates - administration & dosage | Glomerular Mesangium - pathology | Animals | Proteinuria - drug therapy | Glomerulonephritis, Membranoproliferative - physiopathology | Podocytes - drug effects | Macrophages - drug effects | Receptors, Platelet-Derived Growth Factor - drug effects | Glomerulonephritis, Membranoproliferative - etiology | Inflammation - physiopathology | Blood Pressure | Benzimidazoles | Genomics | Podocytes | Cell Dedifferentiation | Chemokine CCL20 | Macrophages | Life Sciences | Angiotensin II Type 1 Receptor Blockers | Receptors, Platelet-Derived Growth Factor | Glomerulonephritis, Membranoproliferative | Antihypertensive Agents | Hypertension | Benzoates | Biochemistry, Molecular Biology | Glomerular Mesangium | Inflammation | Hydrochlorothiazide | Atenolol | Receptors, CCR6 | Hydralazine | RNA, Messenger | Proteinuria
Journal Article
American Journal of Pathology, The, ISSN 0002-9440, 2013, Volume 183, Issue 4, pp. 1269 - 1280
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 11/2010, Volume 78, Issue 9, pp. 905 - 919
We recently found a markedly lower prevalence of vascular complications, including kidney disease, in diabetic patients with Gilbert syndrome, a congenital... 
albuminuria | NADPH oxidase | diabetic nephropathy | oxidative stress | ACTIVATION | RATS | BETA | VASCULAR COMPLICATIONS | HEME OXYGENASE | UROLOGY & NEPHROLOGY | KIDNEY | EXPRESSION | SERUM BILIRUBIN | Diabetes Mellitus, Experimental - drug therapy | Diabetic Nephropathies - etiology | Humans | Transforming Growth Factor beta1 - metabolism | NADPH Oxidases - metabolism | Male | Biliverdine - pharmacology | Time Factors | Glomerular Mesangium - metabolism | Superoxides - metabolism | Glomerular Mesangium - drug effects | Hyperbilirubinemia, Hereditary - metabolism | Albuminuria - metabolism | Diabetes Mellitus, Experimental - complications | Diabetes Mellitus, Experimental - metabolism | Diabetic Nephropathies - prevention & control | Disease Models, Animal | Diabetic Nephropathies - pathology | Angiotensin II - metabolism | Endothelial Cells - metabolism | Diabetic Nephropathies - metabolism | Down-Regulation | Mice, Inbred C57BL | Cells, Cultured | Rats | Antioxidants - pharmacology | Hyperbilirubinemia, Hereditary - complications | NADPH Oxidase 4 | Albuminuria - prevention & control | Bilirubin - blood | Glomerular Mesangium - pathology | Animals | Rats, Gunn | Glucose - metabolism | Cell Proliferation - drug effects | Mice | Oxidative Stress - drug effects | Blood Glucose - metabolism | Endothelial Cells - drug effects
Journal Article
Journal Article