LE WE PMID CA
NPT2c7820NPT2c

1 alpha hydroxylase

Bartter s syndrome

Calbindin D9k

CASR

Claudin2

CLC Kb

ClC5

Curcumin

CYP24A1 1 25 hydroxyvitamin d3 24 hydroxylase

Dent s syndrome

Docosahexaenoic acid

Fatty acids (Omega3)

Fatty acids (Omega6)

FGF23

Hypercalciuric nephrolithiasis with hypophosphatemia

Hypocalciemic hypercalciuria autosomal dominant

Hypomagnesemia with hypercalciuria familiar

Hypophophatemic rickets with hypercalciuria

Kidney (Malformation)

Klotho

Lithocholic acid

LRP5 LDL Receptor Related Protein5 Arrow

Nephrocalcinosis

Npt2a

NPT2c

Osteocalcin

Osteopontin

Paracellin1

PHEX

RANKL

Receptor (RXR)

Receptor (Vitamin D)

Runx2

Transporter (Sodium and phosphate)

TRPV5

TRPV6

Vitamin D

Vitamin D3 (Calcitriol)

2009  
1
Genetic causes of hypercalciuric nephrolithiasis.
[18446382] Pediatr Nephrol 24(12): 2321-32 (2009)
2009  
2
Type IIc sodium-dependent phosphate transporter regulates calcium metabolism.
[19056871] J Am Soc Nephrol 20(1): 104-13 (2009)
2012  
3
Molecular Mechanisms of Vitamin D Action.
[22782502] Calcif Tissue Int (): (2012)
2007  
4
Vitamin D receptor: key roles in bone mineral pathophysiology, molecular mechanism of action, and novel nutritional ligands.
[18290715] J Bone Miner Res 22 Suppl 2(): V2-10 (2007)
2007  
5
1,25-Dihydroxyvitamin D3/VDR-mediated induction of FGF23 as well as transcriptional control of other bone anabolic and catabolic genes that orchestrate the regulation of phosphate and calcium mineral metabolism.
[17293108] J Steroid Biochem Mol Biol 103(3-5): 381-8 (2007)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.



  • NPT2c

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