Impaired urinary osteopontin excretion in Npt2a-/- mice.

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Response of Npt2a knockout mice to dietary calcium and phosphorus.Intraperitoneal pyrophosphate treatment reduces renal calcifications in Npt2a null mice.

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P2860

Impaired urinary osteopontin excretion in Npt2a-/- mice.

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http://www.wikidata.org/entity/Q40482983

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

@zh-cn

2016年学术文章

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2016年学术文章

@zh-my

2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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Impaired urinary osteopontin excretion in Npt2a-/- mice.

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type

Item

label

Impaired urinary osteopontin excretion in Npt2a-/- mice.

@en

prefLabel

Impaired urinary osteopontin excretion in Npt2a-/- mice.

@en

P1476

Impaired urinary osteopontin excretion in Npt2a-/- mice.

@en

P2093

Chuanlong Zhu

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Clemens Bergwitz

http://www.w3.org/2001/XMLSchema#string

Daniel Caballero

http://www.w3.org/2001/XMLSchema#string

Julian Ponsetto

http://www.w3.org/2001/XMLSchema#string

Yuwen Li

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P2860

SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis

Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.

Idiopathic calcium nephrolithiasis: a review of pathogenic mechanisms in the light of genetic studies

ENPP1-Fc prevents mortality and vascular calcifications in rodent model of generalized arterial calcification of infancy

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia

Proteolytic processing of osteopontin by PHEX and accumulation of osteopontin fragments in Hyp mouse bone, the murine model of X-linked hypophosphatemia

Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.

A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.

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scholarly article

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10.1152/AJPRENAL.00367.2016

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312

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2016-10-26T00:00:00Z

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27784695

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Impaired urinary osteopontin excretion in Npt2a-/- mice.

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P2860

P2860

Impaired urinary osteopontin excretion in Npt2a-/- mice.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932