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Nature, ISSN 0028-0836, 09/2011, Volume 477, Issue 7362, pp. 54 - 62
Journal Article
Kidney International, ISSN 0085-2538, 08/2012, Volume 82, Issue 4, pp. 454 - 464
Dense deposit disease and glomerulonephritis with isolated C3 deposits are glomerulopathies characterized by deposits of C3 within or along the glomerular... 
complement | glomerulonephritis | clinical immunology | membranoproliferative glomerulonephritis (MPGN) | LONG-TERM | HEMOLYTIC-UREMIC SYNDROME | MESANGIOCAPILLARY GLOMERULONEPHRITIS | GLOMERULONEPHRITIS TYPE-II | MACULAR DEGENERATION | FACTOR-H DEFICIENCY | GLOMERULAR-FILTRATION-RATE | UROLOGY & NEPHROLOGY | MUTATIONS | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | MEMBRANE COFACTOR PROTEIN | Humans | Child, Preschool | Male | Complement System Proteins - metabolism | Young Adult | Time Factors | DNA Mutational Analysis | Renal Insufficiency - immunology | Child | Glomerulonephritis, Membranoproliferative - pathology | Genetic Predisposition to Disease | Risk Assessment | Complement C3 - metabolism | Gene Frequency | Risk Factors | Glomerulonephritis - genetics | Glomerulonephritis - immunology | Glomerulonephritis - mortality | Biomarkers - blood | Kidney Glomerulus - pathology | Disease Progression | Glomerulonephritis, Membranoproliferative - genetics | Glomerulonephritis, Membranoproliferative - immunology | Phenotype | Complement Factor H - metabolism | Glomerulonephritis, Membranoproliferative - mortality | Glomerulonephritis - pathology | Adolescent | Age of Onset | Membrane Cofactor Protein - genetics | Kidney Glomerulus - immunology | Mutation | Complement Factor I - metabolism | Haplotypes | Complement C3 Nephritic Factor - genetics | Glomerulonephritis - therapy | Infant | Case-Control Studies | Adult | Complement System Proteins - genetics | Female | Membrane Cofactor Protein - metabolism | Complement Pathway, Alternative - genetics | France | Renal Insufficiency - genetics | Kaplan-Meier Estimate | Complement Factor I - genetics | Treatment Outcome | Chi-Square Distribution | Glomerulonephritis, Membranoproliferative - therapy | Biopsy | Complement C3 Nephritic Factor - metabolism | Complement Factor H - genetics | Index Medicus
Journal Article
Journal Article
Kidney International, ISSN 0085-2538, 11/2013, Volume 84, Issue 5, pp. 920 - 930
Podocytes are highly specialized epithelial cells with complex actin cytoskeletal architecture crucial for maintenance of the glomerular filtration barrier.... 
glomerular filtration barrier | glomerular disease | cytoskeleton | transgenic mouse | podocyte | NEPHRIN | PROTEINURIA | DIRECT TARGET | CELL BIOLOGY | NEURONAL DEVELOPMENT | ACTIN REORGANIZATION | DISEASE | UROLOGY & NEPHROLOGY | KIDNEY PODOCYTES | FOCAL SEGMENTAL GLOMERULOSCLEROSIS | Renal Insufficiency - enzymology | Phosphorylation | Podocytes - enzymology | rac1 GTP-Binding Protein - deficiency | Desoxycorticosterone Acetate | Male | cdc42 GTP-Binding Protein - metabolism | Acute Kidney Injury - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Mice, 129 Strain | Renal Insufficiency - etiology | Actin Depolymerizing Factors - metabolism | Nephrectomy | Time Factors | Cell Shape | Hypertension - chemically induced | Acute Kidney Injury - chemically induced | Albuminuria - metabolism | Membrane Proteins - metabolism | Hypertension - enzymology | Hypertension - genetics | Neuropeptides - genetics | Disease Models, Animal | Protamines | Neuropeptides - deficiency | Renal Insufficiency - genetics | Signal Transduction | Acute Kidney Injury - pathology | Mice, Inbred C57BL | Genotype | Neuropeptides - metabolism | Podocytes - pathology | Acute Kidney Injury - enzymology | Mice, Knockout | Phenotype | Animals | Renal Insufficiency - pathology | cdc42 GTP-Binding Protein - genetics | Mice | rac1 GTP-Binding Protein - metabolism | cdc42 GTP-Binding Protein - deficiency | rac1 GTP-Binding Protein - genetics | Index Medicus
Journal Article
The Journal of Physiology, ISSN 0022-3751, 06/2009, Volume 587, Issue 11, pp. 2635 - 2646
Journal Article
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 12/2012, Volume 122, Issue 12, pp. 4401 - 4411
Journal Article
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 12/2015, Volume 290, Issue 51, pp. 30280 - 30290
Journal Article
International Journal of Hematology, ISSN 0925-5710, 3/2016, Volume 103, Issue 3, pp. 283 - 291
Journal Article
British Journal of Haematology, ISSN 0007-1048, 08/2017, Volume 178, Issue 4, pp. 629 - 639
Micro‐albuminuria and glomerular hyperfiltration are primary indicators of renal dysfunctions in Sickle Cell Disease ( SCD ), with more severe manifestations... 
albuminuria | APOL | glomerular filtration rate | HMOX | sickle cell disease | HMOX1 | APOL1 | HEMOGLOBIN | RISK-FACTORS | VARIANTS | ALPHA-THALASSEMIA | PREVALENCE | CHILDREN | GLOMERULAR-FILTRATION-RATE | MICROALBUMINURIA | CHRONIC KIDNEY-DISEASE | HEMATOLOGY | PROGRESSION | Albuminuria - epidemiology | Lipoproteins, HDL - genetics | Prospective Studies |