Functional characterization of two naturally occurring mutations in the human sodium-phosphate cotransporter type IIa.
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Genetic disorders of phosphate regulationAutosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile HypercalcemiaRecent advances in the renal-skeletal-gut axis that controls phosphate homeostasisThe population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus.The changing face of hypophosphatemic disorders in the FGF-23 eraExome sequencing identifies a novel homozygous mutation in the phosphate transporter SLC34A1 in hypophosphatemia and nephrocalcinosisDeciphering PiT transport kinetics and substrate specificity using electrophysiology and flux measurements.Nephrolithiasis-associated bone disease: pathogenesis and treatment options.A missense mutation in the sodium phosphate co-transporter Slc34a1 impairs phosphate homeostasis.Insights from genetic disorders of phosphate homeostasisGenetic causes of hypercalciuric nephrolithiasis.Familial tumoral calcinosis and the role of O-glycosylation in the maintenance of phosphate homeostasis.Disorders of phosphate homeostasis and tissue mineralisation.FGF23 and syndromes of abnormal renal phosphate handlingPhosphate homeostasis and the renal-gastrointestinal axis.The SLC34 family of sodium-dependent phosphate transporters.Genetic diseases of renal phosphate handling.Regulation of renal phosphate handling: inter-organ communication in health and disease.Tubular and genetic disorders associated with kidney stones.Loss of function of NaPiIIa causes nephrocalcinosis and possibly kidney insufficiency.Chronic Hyperphosphatemia and Vascular Calcification Are Reduced by Stable Delivery of Soluble Klotho.Renal phosphate handling and inherited disorders of phosphate reabsorption: an update.Voltage- and substrate-dependent interactions between sites in putative re-entrant domains of a Na(+)-coupled phosphate cotransporter.Substrate interactions in the human type IIa sodium-phosphate cotransporter (NaPi-IIa).
P2860
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P2860
Functional characterization of two naturally occurring mutations in the human sodium-phosphate cotransporter type IIa.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
Functional characterization of ...... sphate cotransporter type IIa.
@en
type
label
Functional characterization of ...... sphate cotransporter type IIa.
@en
prefLabel
Functional characterization of ...... sphate cotransporter type IIa.
@en
P2093
P2860
P1476
Functional characterization of ...... osphate cotransporter type IIa
@en
P2093
Heini Murer
Jürg Biber
Leila V Virkki
Nati Hernando
P2860
P304
P356
10.1359/JBMR.2003.18.12.2135
P577
2003-12-01T00:00:00Z