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animals (140) 140
sodium-phosphate cotransporter proteins (87) 87
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sodium-phosphate cotransporter proteins, type ii (19) 19
biological transport (18) 18
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rats, sprague-dawley (17) 17
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rna, messenger - metabolism (13) 13
symporters - metabolism (13) 13
biochemistry & molecular biology (12) 12
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rats, wistar (12) 12
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brush-border membrane (11) 11
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inorganic-phosphate (11) 11
kidney cortex - metabolism (11) 11
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nephrology (11) 11
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sodium (11) 11
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cell biology (10) 10
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phosphates - antagonists & inhibitors (10) 10
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sodium-phosphate cotransporter proteins - antagonists & inhibitors (10) 10
sodium-phosphate cotransporter proteins, type iia - genetics (10) 10
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endocrinology & metabolism (9) 9
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vascular calcification (8) 8
xenopus laevis (8) 8
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Toxicology and Applied Pharmacology, ISSN 0041-008X, 2008, Volume 232, Issue 1, pp. 125 - 134
Inorganic arsenate (As ) is a common contaminant of underground water. Following oral exposure, it is assumed that As is distributed and crosses cell membranes... 
Brush-border membrane vesicles | Arsenic | PiT-1 | Toxicokinetics | Phosphonoformate | Arsenate | Intestine | PiT-2 | NaPi-IIb | NaPi-IIa | NaPi-IIc | Xenopus laevis oocyte | Na/Pi cotransporter | Vascular smooth muscle cells | Phosphate transport | TRIVALENT | PIT 1 | INORGANIC-PHOSPHATE TRANSPORT | SMALL-INTESTINE | METHYLARSONOUS ACID | ARSENITE | MONOMETHYLARSONOUS ACID | I-COTRANSPORTER | PHARMACOLOGY & PHARMACY | TOXICOLOGY | VESICLES | URINARY-EXCRETION | GLUTATHIONE | Intestinal Mucosa - metabolism | Sodium-Phosphate Cotransporter Proteins, Type IIb - genetics | Arsenates - metabolism | Arsenates - toxicity | Sodium-Phosphate Cotransporter Proteins, Type IIb - antagonists & inhibitors | Sodium-Phosphate Cotransporter Proteins, Type IIb - metabolism | Oocytes | Sodium-Phosphate Cotransporter Proteins, Type IIa - metabolism | Dose-Response Relationship, Drug | Sodium-Phosphate Cotransporter Proteins, Type IIc - metabolism | Cloning, Molecular | Cell Membrane - metabolism | Sodium-Phosphate Cotransporter Proteins - metabolism | Myocytes, Smooth Muscle - metabolism | Sodium-Phosphate Cotransporter Proteins - genetics | Xenopus laevis | Cells, Cultured | Rats | Water Pollutants, Chemical - metabolism | Animals | Water Pollutants, Chemical - toxicity | Kidney Tubules, Proximal - metabolism | Sodium-Phosphate Cotransporter Proteins - antagonists & inhibitors | Sodium-Phosphate Cotransporter Proteins, Type III - metabolism | Intestine, Small - metabolism | Kinetics | Phosphates | Oxides | Cell membranes | Index Medicus | ARSENATES | FRESH WATER | RATS | INTESTINES | MEMBRANE TRANSPORT | 60 APPLIED LIFE SCIENCES | SODIUM PHOSPHATES | KIDNEYS | ARSENIC | SPECTROSCOPY | CELL MEMBRANES | URINE | OOCYTES | BILE | BLOOD
Journal Article
Journal of Cellular Physiology, ISSN 0021-9541, 04/2008, Volume 215, Issue 1, pp. 47 - 54
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2017, Volume 12, Issue 5, p. e0178219
Natural antisense transcripts (NATs) are complementary to protein coding genes and potentially regulate their expression. Despite widespread occurrence of NATs... 
SUPPRESSOR | DOUBLE-STRANDED-RNA | DEFECTS | PROTEIN | NONCODING RNAS | INJECTION | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | INTERFERENCE | SODIUM-PHOSPHATE COTRANSPORTER | IDENTIFICATION | RNA, Complementary - metabolism | Sodium-Phosphate Cotransporter Proteins, Type IIb - genetics | Zebrafish Proteins - metabolism | Cerebellum - metabolism | Zebrafish Proteins - antagonists & inhibitors | Embryo, Nonmammalian - metabolism | Embryonic Development - genetics | Sodium-Phosphate Cotransporter Proteins, Type IIb - antagonists & inhibitors | Sodium-Phosphate Cotransporter Proteins, Type IIb - metabolism | Zebrafish - genetics | DEAD-box RNA Helicases - genetics | Morpholinos - metabolism | Animals | In Situ Hybridization | DEAD-box RNA Helicases - antagonists & inhibitors | RNA Interference | Gene Expression Regulation, Developmental | Zebrafish - metabolism | Cerebellum - growth & development | Zebrafish Proteins - genetics | DEAD-box RNA Helicases - metabolism | RNA, Small Interfering - metabolism | Embryonic development | Eukaryotes | RNA | Zebra fish | Genetic aspects | Models | Research | Antisense DNA | Cerebellum | Brain | Regulations | Regulators | Hybrids | Spermatogenesis | Genomics | Fission | Proteins | Genotype & phenotype | Developmental stages | Coding | Fertility | Physiology | Masking | Deoxyribonucleic acid--DNA | Complementarity | Developmental biology | Double-stranded RNA | Interference | Zebrafish | Injection | Gene expression | Mammals | Embryos | Embryonic growth stage | Gene silencing | Sodium | Gene loci | Aberration | Codons | Binding sites | Kidney transplantation | Phosphates | Chromatin | Accessibility | Gene regulation | Homeostasis | Genomes | Biology | Tissues | Defects | Embryogenesis | Biological effects | Intestine | DNA methylation | Kidneys | Fertilization | Telencephalon | Antisense RNA | Radioactive half-life | Ribonucleic acid--RNA | Vertebrates | Hedgehog protein | MicroRNAs | Regulatory mechanisms (biology) | Methylation | Molecular biology | Deoxyribonucleic acid | Ribonucleic acid | DNA
Journal Article
Journal Article
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 08/2007, Volume 293, Issue 2, pp. 606 - 620
Journal Article
Oncotarget, ISSN 1949-2553, 03/2016, Volume 7, Issue 12, pp. 14569 - 14585
Journal Article
PLoS ONE, ISSN 1932-6203, 01/2013, Volume 8, Issue 1, p. e53393
The regulation of phosphate (Pi) handling is crucial during calcification of the aortic valve. Gene profiling of Pi transporters revealed that VIC culture... 
PHOSPHATE | SIGNAL | TRIAL | OSTEOPONTIN | STENOSIS | MULTIDISCIPLINARY SCIENCES | VASCULAR CALCIFICATION | MUSCLE-CELL CALCIFICATION | Calcinosis - genetics | RNA, Small Interfering - genetics | Gene Expression - drug effects | Heart Valve Diseases - pathology | Apoptosis - drug effects | Humans | Middle Aged | Aortic Valve - drug effects | Male | Membrane Potential, Mitochondrial - drug effects | Proto-Oncogene Proteins c-akt - genetics | Aortic Valve - pathology | Heart Defects, Congenital - genetics | Sodium-Phosphate Cotransporter Proteins, Type III - genetics | Aged, 80 and over | Female | Calcinosis - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Phosphates - pharmacology | Endothelial Cells - metabolism | Cytochromes c - metabolism | Cells, Cultured | Heart Defects, Congenital - pathology | Mitochondria - metabolism | Mitochondria - drug effects | Aortic Valve - metabolism | Phosphates - metabolism | Signal Transduction - drug effects | Heart Valve Diseases - metabolism | Heart Valve Diseases - genetics | Aged | Heart Defects, Congenital - metabolism | Sodium-Phosphate Cotransporter Proteins, Type III - metabolism | Calcinosis - pathology | Endothelial Cells - pathology | Sodium-Phosphate Cotransporter Proteins, Type III - antagonists & inhibitors | Endothelial Cells - drug effects | Phosphates | Heart valve diseases | Care and treatment | Research | Gene expression | Cytochrome | Calcification (ectopic) | Heart | Disease | Transcription | Valves | Lipids | Smooth muscle | AKT protein | Kinases | Tissues | Cytosol | Experiments | Pit1 protein | Mitochondria | Control | Mineralization | Surgery | Aorta | Membrane potential | Rheumatic heart disease | Culture | AKT1 protein | siRNA | Cytochrome c | Calcification | Control valves | Aortic valve | Transporter | Apoptosis
Journal Article
Drug Metabolism and Pharmacokinetics, ISSN 1347-4367, 2006, Volume 21, Issue 3, pp. 217 - 221
Journal Article