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Kidney International, ISSN 0085-2538, 05/2018, Volume 93, Issue 5, pp. 1073 - 1085
Circulating inorganic phosphate exhibits a remarkable daily oscillation based on food intake. In humans and rodents, the daily oscillation in response to food... 
NAD | phosphate | daily oscillation | Npt2c | Nampt | Npt2a | CIRCADIAN-RHYTHM | SERUM PHOSPHATE | CARDIOVASCULAR-DISEASE | HEMODIALYSIS-PATIENTS | ADENINE-DINUCLEOTIDE | UROLOGY & NEPHROLOGY | PARATHYROID-HORMONE | DIETARY PHOSPHATE | DIURNAL-VARIATION | CHRONIC KIDNEY-DISEASE | STAGE RENAL-DISEASE | Biomarkers - urine | Liver - enzymology | Sodium-Phosphate Cotransporter Proteins, Type IIb - genetics | Kidney - enzymology | Male | Mice, 129 Strain | Nicotinamide Phosphoribosyltransferase - antagonists & inhibitors | Sodium-Phosphate Cotransporter Proteins, Type IIb - metabolism | Sodium-Phosphate Cotransporter Proteins, Type IIa - metabolism | Nicotinamide Phosphoribosyltransferase - metabolism | Time Factors | Sodium-Phosphate Cotransporter Proteins, Type IIc - genetics | Sodium-Phosphate Cotransporter Proteins, Type IIc - metabolism | Phosphates - urine | Phosphates - blood | Female | Cytokines - genetics | NAD - metabolism | Cytokines - metabolism | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Biomarkers - blood | Nicotinamide Phosphoribosyltransferase - deficiency | Circadian Rhythm | Sodium-Phosphate Cotransporter Proteins, Type IIc - deficiency | Renal Elimination | Sodium-Phosphate Cotransporter Proteins, Type IIa - genetics | Nicotinamide Phosphoribosyltransferase - genetics | Animals | Sodium-Phosphate Cotransporter Proteins, Type IIb - deficiency | Sodium-Phosphate Cotransporter Proteins, Type IIa - deficiency | Cytokines - deficiency | Cytokines - antagonists & inhibitors | Intestines - enzymology | NADPH | Plasma | Renal function | Homeostasis | Proteins | Sodium phosphate | Clonal deletion | Intestine | Phosphate | Rodents | Light | Phosphoribosyltransferase | Intestinal absorption | Food | Excretion | Kidneys | Mortality | Reabsorption | Metabolism | Sodium | Hepatocytes | Food intake | Nicotinamide phosphoribosyltransferase | Nicotinamide | Kidney diseases
Journal Article
Kidney International, ISSN 0085-2538, 11/2006, Volume 70, Issue 9, pp. 1548 - 1559
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 1931-857X, 09/2009, Volume 297, Issue 3, pp. 671 - 678
Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a rare autosomal recessively inherited disorder, characterized by hypophosphatemia, short... 
Hereditary hypophosphatemic rickets | Bone mineralization | SLC34A3 | HOMEOSTASIS | PHYSIOLOGY | TRANSPORTER | ALKALINE-PHOSPHATASE | hereditary hypophosphatemic rickets | bone mineralization | I COTRANSPORTER | HYPERCALCIURIA | LEADS | UROLOGY & NEPHROLOGY | MUTATIONS | REABSORPTION | Bone and Bones - pathology | Familial Hypophosphatemic Rickets - metabolism | Homeostasis | Hypercalciuria - pathology | Male | Sodium-Phosphate Cotransporter Proteins, Type IIa - metabolism | Familial Hypophosphatemic Rickets - genetics | Familial Hypophosphatemic Rickets - prevention & control | Sodium-Phosphate Cotransporter Proteins, Type IIc - genetics | Sodium-Phosphate Cotransporter Proteins, Type IIc - metabolism | Bone and Bones - metabolism | Phosphates - urine | Phosphorus, Dietary - administration & dosage | Aging | Familial Hypophosphatemic Rickets - pathology | Phosphates - blood | Female | Hypercalciuria - genetics | Kidney Tubules - metabolism | Calcification, Physiologic - genetics | Mice, Inbred C57BL | Genotype | Kidney Calculi - metabolism | Sodium-Phosphate Cotransporter Proteins, Type IIc - deficiency | Mice, Knockout | Sodium-Phosphate Cotransporter Proteins, Type IIa - genetics | Phenotype | Phosphates - metabolism | Animals | Microvilli - metabolism | Hypercalciuria - metabolism | Sodium-Phosphate Cotransporter Proteins, Type IIa - deficiency | Mice
Journal Article
Journal Article
Journal Article
American Journal of Physiology - Renal Physiology, ISSN 1931-857X, 08/2009, Volume 297, Issue 2, pp. 350 - 361
Journal Article
Journal Article
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 11/2009, Volume 94, Issue 11, pp. 4433 - 4438
Context: Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a metabolic disorder due to homozygous loss-of-function mutations in the SLC34A3... 
OSTEOMALACIA | HOMEOSTASIS | METABOLISM | FIBROBLAST-GROWTH-FACTOR-23 | MEN | ENDOCRINOLOGY & METABOLISM | BONE HISTOMORPHOMETRY |