(Q46274827)

21 December 2017

title

Npt2a and Npt2c in mice play distinct and synergistic roles in inorganic phosphate metabolism and skeletal development (English)

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21 December 2017

author name string

Hiroko Segawa

1

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21 December 2017

Akemi Onitsuka

2

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21 December 2017

Junya Furutani

3

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21 December 2017

Ichiro Kaneko

4

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21 December 2017

Fumito Aranami

5

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21 December 2017

Natsuki Matsumoto

6

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21 December 2017

Yuka Tomoe

7

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21 December 2017

Masashi Kuwahata

8

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21 December 2017

Mikiko Ito

9

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21 December 2017

Mitsuru Matsumoto

10

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21 December 2017

Minqi Li

11

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21 December 2017

Norio Amizuka

12

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21 December 2017

Ken-ichi Miyamoto

13

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21 December 2017

publication date

1 July 2009

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21 December 2017

American Journal of Physiology - Renal Physiology

published in

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21 December 2017

volume

297

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21 December 2017

issue

3

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21 December 2017

page(s)

F671-8

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21 December 2017

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

cites work

1 reference

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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

21 January 2018

1 reference

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Regulation of phosphate transport in proximal tubules.

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Renal calcification in mice homozygous for the disrupted type IIa Na/Pi cotransporter gene Npt2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Osteomalacia in hereditary hypophosphatemic rickets with hypercalciuria: a correlative clinical-histomorphometric study

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Role of the vitamin D receptor in FGF23 action on phosphate metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Administration of oral charcoal adsorbent (AST-120) suppresses low-turnover bone progression in uraemic rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIc

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

New aspect of renal phosphate reabsorption: the type IIc sodium-dependent phosphate transporter.

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Hypophosphatemia leads to rickets by impairing caspase-mediated apoptosis of hypertrophic chondrocytes

21 January 2018

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21 January 2018

1 reference

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The roles of Na/Pi-II transporters in phosphate metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Effect of hydrolysis-resistant FGF23-R179Q on dietary phosphate regulation of the renal type-II Na/Pi transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Type IIc sodium-dependent phosphate transporter regulates calcium metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Regulation of phosphorus homeostasis by the type iia na/phosphate cotransporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Differential effects of Npt2a gene ablation and X-linked Hyp mutation on renal expression of Npt2c

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

A new kindred with hereditary hypophosphatemic rickets with hypercalciuria: implications for correct diagnosis and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Hereditary hypophosphatemic rickets with hypercalciuria: a study for the phosphate transporter gene type IIc and osteoblastic function

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

Ubiquitin ligase Smurf1 controls osteoblast activity and bone homeostasis by targeting MEKK2 for degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00156.2009

10.1152/AJPRENAL.00156.2009

21 January 2018

Identifiers

DOI

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21 December 2017

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21 December 2017