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PLoS ONE, ISSN 1932-6203, 01/2014, Volume 9, Issue 1, pp. e87936 - e87936
The growing incidence of chronic kidney disease remains a global health problem. Obesity is a major risk factor for type-2 diabetes and renal impairment.... 
CHRONIC HEART-FAILURE | TISSUE INFLAMMATION | ATRIAL-NATRIURETIC-PEPTIDE | WAIST CIRCUMFERENCE | GLUCOSE-METABOLISM | MULTIDISCIPLINARY SCIENCES | IN-VIVO | ENHANCES INSULIN SENSITIVITY | FACTOR-KAPPA-B | CHRONIC KIDNEY-DISEASE | HYPERTENSIVE-RATS | Tumor Necrosis Factor-alpha - metabolism | Atrial Natriuretic Factor - metabolism | Endothelin-1 - metabolism | Diabetic Nephropathies - metabolism | Rats | Male | Dinoprost - metabolism | Interleukins - metabolism | Hemin - metabolism | Rats, Zucker | Inflammation - metabolism | Kidney - metabolism | Macrophages - metabolism | Animals | Diabetic Nephropathies - physiopathology | Chemokine CCL3 - metabolism | Adiposity - physiology | Dinoprost - analogs & derivatives | Blood Glucose - metabolism | Heme Oxygenase (Decyclizing) - metabolism | Extracellular Matrix Proteins - metabolism | Kidney - physiopathology | Inflammation - physiopathology | Type 2 diabetes | Adipose tissues | Fibronectins | Obesity | Endothelin | Cytokines | Diabetic nephropathies | Macrophages | Risk factors | Glucose metabolism | Chronic kidney failure | Collagen | Heme | Natriuretic peptides | Adipose tissue | Syngeneic grafts | Selectivity | Adipocytes | Fibronectin | Proteins | Genotype & phenotype | Cyclic GMP | Fibroblasts | Physiology | Carbon monoxide | Public health | Pulmonary arteries | Endothelin 1 | Tumor necrosis factor-α | Metabolism | Gene expression | Studies | Oxygenase | Hemin | Nephropathy | Fibrosis | Interleukin 10 | Infiltration | Renal function | Paracrine signalling | Adiponectin | Interleukin 6 | Rodents | Diaphragm (anatomy) | Extracellular matrix | Tumor necrosis factor-TNF | Lesions | Inducers | Creatinine | Hypertension | Excretion | Kidneys | Diabetes mellitus | Markers | Health risks | Inflammation | Morbidity | Scaffolding | Insulin resistance | Diaphragm | Diabetes | Proteinuria | Index Medicus
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2011, Volume 6, Issue 12, pp. e28710 - e28710
Actin dynamics has emerged at the forefront of podocyte biology. Slit diaphragm junctional adhesion protein Nephrin is necessary for development of the... 
NEPHROTIC-SYNDROME | CANCER-CELL-MIGRATION | ACTIN-PEDESTAL FORMATION | TYROSINE PHOSPHORYLATION | 5'-INOSITOL PHOSPHATASE | GLOMERULAR PROTEIN | ESCHERICHIA-COLI | BIOLOGY | PHOSPHOINOSITIDE 3-KINASE | ADAPTER PROTEIN | KIDNEY SLIT DIAPHRAGM | Phosphorylation | Phosphatidylinositol Phosphates - metabolism | Humans | Actins - metabolism | Inositol Polyphosphate 5-Phosphatases | Gene Knockdown Techniques | Phosphotyrosine - metabolism | Multiprotein Complexes - metabolism | Cell Membrane - metabolism | Membrane Proteins - metabolism | Microfilament Proteins - metabolism | Contractile Proteins - metabolism | Podocytes - metabolism | Signal Transduction | Oncogene Proteins - metabolism | Protamines - metabolism | Podocytes - pathology | p21-Activated Kinases - metabolism | Filamins | src Homology Domains | Animals | Carrier Proteins - metabolism | Pseudopodia - metabolism | Models, Biological | Protein Binding | Mice | Adaptor Proteins, Signal Transducing - metabolism | Phosphatidylinositol-3,4,5-Trisphosphate 5-Phosphatases | Phosphoric Monoester Hydrolases - metabolism | RNA, Small Interfering - metabolism | Polymerization | Fc receptors | Inositol | Phosphatases | Muscle proteins | Actin | Cell culture | GTP-binding protein | Nephrology | Leukocyte migration | Activation | Kinases | Phosphatase | Myo-Inositol-1 (or 4)-monophosphatase | Medical schools | Cell adhesion & migration | Proteins | Cell activation | Cell growth | Epidermal growth factor | Dynamics | Fibroblasts | Diaphragm (anatomy) | Inositol polyphosphate 5-phosphatase | Trends | p21-activated kinase | Cell division | Crosslinking | Pseudopodia | Breast cancer | Clustering | Adhesion | Dynamic tests | CD16 antigen | Morphology | Cytoskeleton | Ligands | Mutation | Diaphragm | Cell migration | Index Medicus
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 0363-6127, 02/2011, Volume 300, Issue 2, pp. F549 - F560
Babayeva S, Zilber Y, Torban E. Planar cell polarity pathway regulates actin rearrangement, cell shape, motility, and nephrin distribution in podocytes. Am J... 
Polarized cells | Podocyte cytoskeleton | PHYSIOLOGY | EMBRYONIC-DEVELOPMENT | SLIT DIAPHRAGM | NEURAL-TUBE DEFECTS | SUBCELLULAR-LOCALIZATION | polarized cells | CONVERGENT EXTENSION | ASYMMETRIC LOCALIZATION | SIGNALING PATHWAY | UROLOGY & NEPHROLOGY | NEPHROTIC SYNDROME | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | VERTEBRATE GASTRULATION | podocyte cytoskeleton | Kidney - physiology | Wnt Proteins - pharmacology | Neural Tube Defects - physiopathology | Humans | Actins - metabolism | Microfilament Proteins - physiology | Intracellular Signaling Peptides and Proteins - metabolism | Wnt-5a Protein | Phosphoproteins - metabolism | Wnt Proteins - metabolism | Cell Movement - physiology | Kidney - metabolism | Membrane Proteins - physiology | Kidney Glomerulus - metabolism | Cytoskeletal Proteins - metabolism | Membrane Proteins - metabolism | Microfilament Proteins - metabolism | Phosphoproteins - physiology | Dishevelled Proteins | Kidney Glomerulus - cytology | Carrier Proteins - physiology | Proto-Oncogene Proteins - metabolism | Proto-Oncogene Proteins - pharmacology | Cell Line | Kidney Diseases, Cystic - physiopathology | Proteins - physiology | Nerve Tissue Proteins - physiology | Podocytes - metabolism | Podocytes - pathology | rho GTP-Binding Proteins - physiology | Nerve Tissue Proteins - metabolism | Adaptor Proteins, Signal Transducing - physiology | Animals | Carrier Proteins - metabolism | Guanylate Kinases | Proteins - metabolism | rho GTP-Binding Proteins - metabolism | Proto-Oncogene Proteins - physiology | Cytoskeleton - metabolism | Cell Polarity - physiology | Mice | Wnt Proteins - physiology | Adaptor Proteins, Signal Transducing - metabolism | Cell Shape - physiology | Intracellular Signaling Peptides and Proteins - physiology | Proteins | Filters | Kidneys | Rodents | Cell division | Cytoskeleton | Mutation | Ribonucleic acid--RNA | Index Medicus
Journal Article
Journal Article
Journal of Applied Physiology, ISSN 8750-7587, 08/2013, Volume 115, Issue 4, pp. 529 - 538
Long periods of skeletal muscle disuse result in muscle fiber atrophy, and mitochondrial production of reactive oxygen species (ROS) appears to be a required... 
Disuse atrophy | Oxidative stress | Mitochondrial signaling | SPORT SCIENCES | PHYSIOLOGY | ATROPHY | PGC-1-ALPHA | SOLEUS MUSCLE | KAPPA-B | AUTOPHAGY | DISUSE | INDUCED DIAPHRAGM WEAKNESS | MESSENGER-RNA | disuse atrophy | DYSFUNCTION | mitochondrial signaling | oxidative stress | Calpain - metabolism | Reactive Oxygen Species - metabolism | Peptide Hydrolases - genetics | Caspase 3 - metabolism | Immobilization | Muscle, Skeletal - metabolism | Muscle Fibers, Skeletal - drug effects | Muscle Fibers, Skeletal - metabolism | Calpain - genetics | Proteolysis - drug effects | Mitochondria - genetics | Muscle, Skeletal - drug effects | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Caspase 3 - genetics | Female | Muscular Atrophy - prevention & control | Peptide Hydrolases - metabolism | Biomarkers - metabolism | Muscular Atrophy - metabolism | Ubiquitin-Protein Ligases - metabolism | Rats | Muscular Atrophy - genetics | Mitochondria - metabolism | Signal Transduction - genetics | Antioxidants - pharmacology | Mitochondria - drug effects | Transcription Factors - genetics | Down-Regulation - drug effects | Muscular Atrophy - drug therapy | Rats, Sprague-Dawley | Down-Regulation - genetics | Proteasome Endopeptidase Complex - genetics | Transcription Factors - metabolism | Animals | Signal Transduction - drug effects | Proteasome Endopeptidase Complex - metabolism | Ubiquitin-Protein Ligases - genetics | Proteins | Antioxidants | Biomarkers | Musculoskeletal system | Molecules | Oxygen | Index Medicus
Journal Article
Science, ISSN 0036-8075, 6/2005, Volume 308, Issue 5729, pp. 1801 - 1804
Focal and segmental glomerulosclerosis (FSGS) is a kidney disorder of unknown etiology, and up to 20% of patients on dialysis have been diagnosed with it. Here... 
Receptors | Kidneys | Messenger RNA | Focal segmental glomerulosclerosis | Calcium | HEK293 cells | Cell lines | Reports | Kidney cells | Kidney diseases | Genetic mutation | INSERTION | PROTEIN | SLIT DIAPHRAGM | NEPHRIN | MULTIDISCIPLINARY SCIENCES | GENETIC-HETEROGENEITY | PODOCIN | NEPHROTIC SYNDROME | EXPRESSION | ALPHA-ACTININ-4 | GLOMERULAR-DISEASE | Haplotypes | Uridine Triphosphate - metabolism | Calcium Channels - metabolism | Calcium - metabolism | Exons | Glomerulosclerosis, Focal Segmental - genetics | Humans | Male | Mutation, Missense | Sodium - metabolism | Kidney - metabolism | Receptor, Angiotensin, Type 1 - genetics | Transfection | Kidney Glomerulus - metabolism | Female | Cell Membrane - metabolism | GTP-Binding Protein alpha Subunits, Gq-G11 - metabolism | Kidney Tubules - metabolism | Calcium Channels - genetics | Calcium Signaling | Cell Line | Angiotensin II - pharmacology | TRPC6 Cation Channel | Angiotensin II - metabolism | TRPC Cation Channels | Uridine Triphosphate - pharmacology | Chromosomes, Human, Pair 11 - genetics | Sequence Analysis, DNA | Carbachol - pharmacology | Patch-Clamp Techniques | Pedigree | Calcium Channels - chemistry | Receptor, Angiotensin, Type 1 - metabolism | Amino Acid Substitution | Glomerulonephritis | Case studies | Research | Analysis | Heredity | Mutation | Chromosomes | Genes | Index Medicus
Journal Article
Biology of Blood and Marrow Transplantation, ISSN 1083-8791, 2013, Volume 19, Issue 4, pp. 538 - 546
Abstract Mesenchymal stem cells (MSC) attenuate albuminuria and preserve normal renal histology in diabetic mice. However, the effects of MSC on glomerular... 
Hematology, Oncology and Palliative Medicine | Diabetic nephropathy | Cell therapy | Podocyte injury | Bone morphogenetic protein-7 | Mesenchymal stem cells | Proteinuria | SLIT DIAPHRAGM | ACUTE-RENAL-FAILURE | MECHANISMS | IMMUNOLOGY | ALLOXAN | TRANSPLANTATION | REPAIR | KIDNEY INJURY | HIGH GLUCOSE | MICE | DIFFERENTIATION | STROMAL CELLS | HEMATOLOGY | Green Fluorescent Proteins | Kidney - pathology | Streptozocin | Bone Morphogenetic Protein 7 - genetics | Male | Intracellular Signaling Peptides and Proteins - metabolism | Vascular Endothelial Growth Factor A - metabolism | Proteinuria - pathology | Vascular Endothelial Growth Factor A - genetics | Diabetes Mellitus, Experimental - therapy | Proteinuria - prevention & control | Proteinuria - chemically induced | Kidney - metabolism | Mesenchymal Stromal Cells - cytology | Diabetes Mellitus, Experimental - chemically induced | Membrane Proteins - metabolism | Diabetes Mellitus, Experimental - metabolism | Diabetic Nephropathies - prevention & control | Intracellular Signaling Peptides and Proteins - genetics | Genes, Reporter | Biomarkers - metabolism | Diabetic Nephropathies - pathology | Gene Expression | Podocytes - metabolism | Membrane Proteins - genetics | Diabetic Nephropathies - metabolism | Diabetic Nephropathies - chemically induced | Mesenchymal Stromal Cells - metabolism | Proteinuria - metabolism | Rats | Podocytes - pathology | Rats, Sprague-Dawley | Animals | Bone Morphogenetic Protein 7 - metabolism | Diabetes Mellitus, Experimental - pathology | Mice | Blood Glucose - metabolism | Mesenchymal Stem Cell Transplantation | Glucose metabolism | Endothelial growth factors | Type 1 diabetes | Blood sugar | Stem cells | Diabetic nephropathies | Fluorescence | Index Medicus
Journal Article
Journal Article
Critical Care Medicine, ISSN 0090-3493, 07/2011, Volume 39, Issue 7, pp. 1749 - 1759
BACKGROUND:Mechanical ventilation is a life-saving intervention used to provide adequate pulmonary ventilation in patients suffering from respiratory failure.... 
atrophy | antioxidant | redox signaling | respiratory muscles | oxidative stress | weaning | REQUIREMENTS | ACTIVATION | ARRANGEMENT | CONTRACTILE DYSFUNCTION | REPERFUSION INJURY | HYDROPEROXIDE | RAT DIAPHRAGM | SKELETAL-MUSCLE MITOCHONDRIA | CRITICAL CARE MEDICINE | Calpain - metabolism | Diaphragm - drug effects | Mitochondria, Muscle - metabolism | Oxidative Stress - physiology | Actins - metabolism | Caspase 3 - metabolism | Diaphragm - ultrastructure | Muscle Fibers, Skeletal - drug effects | Tripartite Motif Proteins | Muscular Atrophy - physiopathology | Respiration, Artificial - adverse effects | Muscle Fibers, Skeletal - ultrastructure | Muscle Proteins - metabolism | Mitochondria, Muscle - physiology | Female | Muscular Atrophy - prevention & control | Diaphragm - metabolism | Muscle Weakness - prevention & control | Muscular Atrophy - etiology | Muscle Fibers, Skeletal - physiology | Diaphragm - physiopathology | Muscle Weakness - etiology | Ubiquitin-Protein Ligases - metabolism | Rats | SKP Cullin F-Box Protein Ligases - metabolism | Rats, Sprague-Dawley | Hydrogen Peroxide - metabolism | Animals | Muscle Contraction - drug effects | Muscle Contraction - physiology | Mitochondria, Muscle - drug effects | Muscle Weakness - physiopathology | Oxidative Stress - drug effects | Oligopeptides - pharmacology | Index Medicus | Abridged Index Medicus
Journal Article
Development (Cambridge), ISSN 0950-1991, 10/2017, Volume 144, Issue 19, pp. 3547 - 3561
Hoxa5 is essential for development of several organs and tissues. In the respiratory system, loss of Hoxa5 function causes neonatal death due to respiratory... 
Respiratory system development | Diaphragm | Mouse | Trachea | Lung | Hoxa5 | DEFECTS | PHRENIC-NERVE | LUNG DEVELOPMENT | DEVELOPMENTAL BIOLOGY | SKELETAL-MUSCLE | MUTANT MICE | TRACHEAL CARTILAGE | DIAPHRAGMATIC-HERNIAS | COLLAGEN GENE | CELL-FUNCTION | MOUSE LUNG | Homeodomain Proteins - metabolism | Male | Trachea - metabolism | Diaphragm - ultrastructure | Muscle Fibers, Skeletal - metabolism | Phosphoproteins - metabolism | Cell Differentiation - genetics | Organ Specificity - genetics | Muscle Development | Gene Expression Regulation, Developmental | Gene Deletion | Female | Diaphragm - innervation | Diaphragm - metabolism | Respiratory System - embryology | Animals, Newborn | SOX9 Transcription Factor - metabolism | Cartilage - embryology | Mesoderm - embryology | Genotype | Signal Transduction - genetics | Phosphoproteins - genetics | Cartilage - metabolism | Trachea - embryology | Homeodomain Proteins - genetics | Motor Neurons - metabolism | Animals | Models, Biological | Respiratory System - metabolism | Survival Analysis | Mesoderm - metabolism | Respiratory Mucosa - metabolism | Body Patterning - genetics | Crosses, Genetic | Hypoplasia | Neonates | Motor neurons | Mesenchyme | Epithelial cells | Innervation | Central nervous system | Lethality | Conditional mutant | Epithelium | Respiratory system | Morphogenesis | Respiratory tract | Gene targeting | Clonal deletion | Rodents | Respiration | Index Medicus
Journal Article