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Scientific reports, ISSN 2045-2322, 01/2020, Volume 10, Issue 1, pp. 1500 - 11
The polycystin-1 (PC1), polycystin-2 (PC2) and fibrocystin proteins, the respective products of the PKD1, PKD2 and PKHD1 genes, are abundant in urinary... 
Urine | Proteins | Post-translation | Membrane vesicles | Proteolysis
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2014, Volume 9, Issue 5, p. e97326
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 07/2011, Volume 26, Issue 7, pp. 1425 - 1436
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2014, Volume 9, Issue 9, p. e107006
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 10/2018, Volume 29, Issue 10, pp. 2482 - 2492
Background: The major form of autosomal dominant polycystic kidney disease is caused by heterozygous mutations in PKD1, the gene that encodes polycystin-1... 
KIDNEY-DISEASE | TRIPLEX DNA | PROTEIN | kidney disease | EXTRACELLULAR DOMAIN | IDENTIFICATION | genetic renal disease | GENE | polycystic kidney disease | CYST FORMATION | SEQUENCE | UROLOGY & NEPHROLOGY | MUTATIONS | EXPRESSION | Basic Research
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 0363-6127, 2015, Volume 309, Issue 9, pp. F764 - F769
Nephrogenic systemic fibrosis (NSF) is a devastating condition associated with gadolinium (Gd3+)-based contrast agents (GBCAs) in patients with kidney disease.... 
Osteopontin | MEPE | Sclerostin | Chronic kidney disease | DMP1 | Nephrogenic system fibrosis | FGF23 | PHEX | chronic kidney disease | PHYSIOLOGY | osteopontin | MOTIF | sclerostin | HYPOPHOSPHATEMIA | METABOLISM | MINERALIZATION | RENALLY IMPAIRED RATS | UROLOGY & NEPHROLOGY | UPDATE | BONE | nephrogenic system fibrosis | HYP | Kidney - pathology | Glycoproteins - metabolism | Familial Hypophosphatemic Rickets - metabolism | Male | Peptide Fragments - pharmacology | Nephrogenic Fibrosing Dermopathy - metabolism | Phosphoproteins - metabolism | X-Ray Microtomography | Organometallic Compounds | Familial Hypophosphatemic Rickets - genetics | Kidney - metabolism | Nephrogenic Fibrosing Dermopathy - prevention & control | Kidney - diagnostic imaging | PHEX Phosphate Regulating Neutral Endopeptidase - pharmacology | Protein Interaction Domains and Motifs | Familial Hypophosphatemic Rickets - complications | Extracellular Matrix Proteins - metabolism | Cytoprotection | Disease Models, Animal | PHEX Phosphate Regulating Neutral Endopeptidase - metabolism | Peptide Fragments - metabolism | Signal Transduction | Drug Stability | Mice, Inbred C57BL | Nephrogenic Fibrosing Dermopathy - chemically induced | Nephrogenic Fibrosing Dermopathy - genetics | Meglumine - analogs & derivatives | Magnetic Resonance Imaging | Animals | Contrast Media | Protein Binding | Nephrogenic Fibrosing Dermopathy - diagnosis | Gadolinium DTPA | Development and progression | Care and treatment | Research | Patient outcomes | Risk factors | Fibrosis | Index Medicus
Journal Article
Blood, ISSN 0006-4971, 11/2013, Volume 122, Issue 21, pp. 925 - 925
Abstract Decades of research has established that the most effective treatment for sickle cell disease (SCD) and Cooley’s anemia is increased fetal hemoglobin... 
Journal Article
Blood, ISSN 0006-4971, 11/2011, Volume 118, Issue 21, pp. 353 - 353
Abstract Abstract 353 Sickle cell disease (SCD) impacts one of 400 African-Americans born each year. Augmentation of fetal hemoglobin (HbF) levels is widely... 
Journal Article
Blood Cells, Molecules and Diseases, ISSN 1079-9796, 03/2007, Volume 38, Issue 2, pp. 170 - 171
Journal Article
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