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PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 2, p. e54442
... Pollock 1 , Amanda Mather 1 Introduction Diabetic nephropathy is the leading cause of end stage kidney disease and its escalating incidence is a challenge to health... 
MATRIX | STIMULATION | MULTIDISCIPLINARY SCIENCES | DISEASE | HIGH GLUCOSE | GENE-EXPRESSION | PPAR-GAMMA AGONISTS | TRANSFORMING GROWTH FACTOR-BETA | Diabetes Mellitus - pathology | Epithelial Cells - metabolism | Gene Expression - drug effects | Diabetes Mellitus - genetics | Transcription Factor AP-1 - genetics | Epithelial Cells - drug effects | Humans | Diabetic Nephropathies - drug therapy | NF-kappa B - metabolism | Smad3 Protein - metabolism | Transcription Factor AP-1 - metabolism | Sodium-Glucose Transporter 1 - genetics | Smad3 Protein - genetics | Sodium-Glucose Transporter 1 - metabolism | Phosphorylation - drug effects | Interleukin-6 - metabolism | Transforming Growth Factor beta1 - pharmacology | Sodium-Glucose Transporter 2 - genetics | Collagen Type IV - metabolism | Sodium-Glucose Transporter 1 - antagonists & inhibitors | Promoter Regions, Genetic | Diabetic Nephropathies - pathology | Glucosides - pharmacology | Kidney Tubules, Proximal - pathology | Interleukin-6 - genetics | Sodium-Glucose Transporter 2 - metabolism | Diabetic Nephropathies - metabolism | Diabetes Mellitus - drug therapy | Diabetes Mellitus - metabolism | Toll-Like Receptor 4 - genetics | Diabetic Nephropathies - genetics | Epithelial Cells - pathology | Glucose - pharmacology | Toll-Like Receptor 4 - metabolism | Sodium-Glucose Transporter 2 - antagonists & inhibitors | Hypoglycemic Agents - pharmacology | NF-kappa B - genetics | Kidney Tubules, Proximal - metabolism | Collagen Type IV - genetics | Protein Binding | Benzhydryl Compounds - pharmacology | Kidney Tubules, Proximal - drug effects | Physiological aspects | Care and treatment | Genetic aspects | Research | Transforming growth factors | Diabetic nephropathies | Chromatin | Immunoprecipitation | Transforming growth factor-b | Interleukin | Clinical trials | Systematic review | Smad3 protein | Glucose | Kinases | Interleukin 6 | Proteins | Hyperglycemia | Rodents | Toll-like receptors | Collagen (type IV) | Hypoglycemic agents | Inhibition | Growth factors | Deoxyribonucleic acid--DNA | Immune system | Binding | Glucose transporter | Medical research | NF-κB protein | Diabetes mellitus | Markers | Activator protein 1 | Blocking | Reabsorption | Inflammation | Gene expression | Glucose transport | Medicine | High mobility group proteins | Hospitals | Inhibitors | Nephropathy | Sodium | Fibrosis | Kidney diseases | Diabetes | Transporter | Adenosine triphosphatase | Kidney transplantation | Deoxyribonucleic acid | DNA
Journal Article
Journal Article
Current medicinal chemistry, ISSN 0929-8673, 12/2010, Volume 17, Issue 34, pp. 4256 - 4269
Journal Article
Diabetes (New York, N.Y.), ISSN 1939-327X, 2016, Volume 65, Issue 3, pp. 755 - 767
Overcoming refractory massive proteinuria remains a clinical and research issue in diabetic nephropathy... 
MAINTENANCE | LYSOSOMES | NUMBER | MICROALBUMINURIA | INCREASE | ENDOCRINOLOGY & METABOLISM | TUBULE | MICE | DIFFERENTIATION | MTOR | REMISSION | Kidney - pathology | Microtubule-Associated Proteins - genetics | Diabetic Nephropathies - etiology | Humans | Middle Aged | Rats, Long-Evans | Male | Intracellular Signaling Peptides and Proteins - metabolism | Diabetes Mellitus, Type 2 - metabolism | Proteinuria - pathology | Autophagy | Young Adult | Kidney - metabolism | Lysosomes - metabolism | Diet, High-Fat | Adult | Female | Lysosomes - pathology | Diabetes Mellitus, Experimental - complications | Membrane Proteins - metabolism | Microfilament Proteins - metabolism | RNA-Binding Proteins - blood | Diabetes Mellitus, Experimental - metabolism | Diabetes Mellitus, Type 2 - complications | Intravital Microscopy | Proteinuria - etiology | Severity of Illness Index | Cell Line | Microscopy, Electron, Transmission | Diabetic Nephropathies - pathology | Microscopy, Electron, Scanning | Podocytes - metabolism | Diabetic Nephropathies - metabolism | Mice, Inbred C57BL | Proteinuria - metabolism | Rats | Mice, Transgenic | Blotting, Western | Mice, Knockout | Autophagy-Related Protein 7 | Animals | Autophagy-Related Protein 5 | Diabetes Mellitus, Experimental - pathology | Aged | Mice | Diabetes Mellitus, Type 2 - pathology | Apoptosis | Care and treatment | Diabetic nephropathies | Homeostasis | Influence | Dosage and administration | Research | Insulin | Proteinuria
Journal Article
American journal of physiology. Renal physiology, ISSN 1522-1466, 2015, Volume 308, Issue 9, pp. F993 - F1003
IL-1β-secreting nucleotide-binding oligomerization domain protein 3 (NLRP3) inflammasomes play a pivotal role in triggering innate immune responses in... 
Diabetic nephropathy | Uric acid | NLRP3 inflammasome | Macrophage | PHYSIOLOGY | INJURY | macrophage | CELL-PROLIFERATION | MECHANISMS | ALLOPURINOL | PATHOGENESIS | KIDNEY-FUNCTION | INFLAMMASOME | DISEASE | UROLOGY & NEPHROLOGY | uric acid | NF-KAPPA-B | diabetic nephropathy | URIC-ACID | Inflammasomes - metabolism | Diabetic Nephropathies - etiology | NLR Family, Pyrin Domain-Containing 3 Protein | Coculture Techniques | Diabetes Mellitus, Type 2 - genetics | Humans | Male | NF-kappa B - metabolism | Hyperuricemia - metabolism | Diabetes Mellitus, Type 2 - metabolism | Diabetic Nephropathies - immunology | Hyperuricemia - immunology | Inflammation - metabolism | Transfection | RNA Interference | Time Factors | Interleukin-1beta - metabolism | Diabetes Mellitus, Type 2 - immunology | HMGB1 Protein - metabolism | Inflammation Mediators - metabolism | Diabetic Nephropathies - prevention & control | Hyperuricemia - complications | Diabetes Mellitus, Type 2 - complications | Macrophages - immunology | Disease Models, Animal | Cell Line | Kidney Tubules, Proximal - immunology | Uric Acid - metabolism | Signal Transduction | Diabetic Nephropathies - metabolism | Diabetic Nephropathies - genetics | Inflammation - immunology | Inflammation - etiology | Disease Progression | Inflammasomes - genetics | Hyperuricemia - drug therapy | Carrier Proteins - genetics | Rats, Inbred OLETF | Macrophages - metabolism | Animals | Carrier Proteins - metabolism | Chemokine CXCL12 - metabolism | Kidney Tubules, Proximal - metabolism | Gout Suppressants - pharmacology | Macrophages - drug effects | Kidney Tubules, Proximal - drug effects | Receptors, Cytoplasmic and Nuclear - metabolism | Type 2 diabetes | Cellular proteins | Kidneys | Immune response | Physiological aspects | Genetic aspects | Properties | Injuries
Journal Article
Journal Article
Journal of cellular and molecular medicine, ISSN 1582-1838, 2017, Volume 21, Issue 11, pp. 2732 - 2747
...)‐induced diabetic nephropathy, and dynamically regulated in cultured mouse podocytes stimulated with high glucose, which showed a trend from rise to decline... 
MALAT1 | β‐catenin | high glucose | diabetic nephropathy | SRSF1 | podocyte | β-catenin | beta-catenin | MEDICINE, RESEARCH & EXPERIMENTAL | APOPTOSIS | RETAINED NONCODING RNA | PROLIFERATION | MESENCHYMAL TRANSITION | CELL BIOLOGY | GLOMERULAR SLIT DIAPHRAGM | ROLES | DYSFUNCTION | WNT | SPLICING FACTOR | RNA, Small Interfering - genetics | Diabetes Mellitus, Experimental - genetics | Male | Serine-Arginine Splicing Factors - metabolism | Serine-Arginine Splicing Factors - genetics | Glucose - toxicity | Diabetes Mellitus, Experimental - chemically induced | Diabetes Mellitus, Experimental - metabolism | Wnt Signaling Pathway | Promoter Regions, Genetic | Diabetic Nephropathies - pathology | Podocytes - metabolism | Diabetic Nephropathies - metabolism | Mice, Inbred C57BL | Diabetic Nephropathies - chemically induced | Gene Expression Regulation | Diabetic Nephropathies - genetics | RNA, Long Noncoding - genetics | Podocytes - pathology | beta Catenin - metabolism | beta Catenin - genetics | Protein Transport | Serine-Arginine Splicing Factors - antagonists & inhibitors | Feedback, Physiological | Animals | Podocytes - drug effects | beta Catenin - antagonists & inhibitors | Diabetes Mellitus, Experimental - pathology | Protein Binding | Mice | Streptozocin - toxicity | RNA, Long Noncoding - antagonists & inhibitors | RNA, Long Noncoding - metabolism | Cell Line, Transformed | RNA, Small Interfering - metabolism | Original
Journal Article