Role of the putative PKC phosphorylation sites of the type IIc sodium-dependent phosphate transporter in parathyroid hormone regulation-Reference-Cited by-同舟云学术

Role of the putative PKC phosphorylation sites of the type IIc sodium-dependent phosphate transporter in parathyroid hormone regulation

Published:2019-03-21 Issue:7 Volume:23 Page:898-907
ISSN:1342-1751
Container-title:Clinical and Experimental Nephrology
language:en
Short-container-title:Clin Exp Nephrol

Author:

Fujii Toru,Segawa Hiroko^ORCID,Hanazaki Ai,Nishiguchi Shiori,Minoshima Sakura,Ohi Akiko,Tominaga Rieko,Sasaki Sumire,Tanifuji Kazuya,Koike Megumi,Arima Yuki,Shiozaki Yuji,Kaneko Ichiro,Ito Mikiko,Tatsumi Sawako,Miyamoto Ken-ichi

Funder

Ministry of Education, Culture, Sports, Science, and Technology of Japan

The Salt Science Research Foundation

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Nephrology,Physiology

Link

http://link.springer.com/content/pdf/10.1007/s10157-019-01725-6.pdf

Reference37 articles.

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3. Beck L, Karaplis AC, Amizuka N, Hewson AS, Ozawa H, Tenenhouse HS. Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalities. Proc Natl Acad Sci USA. 1998;95(9):5372–7.

4. Bergwitz C, Roslin NM, Tieder M, Loredo-Osti JC, Bastepe M, Abu-Zahra H, et al. 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. Am J Hum Genet. 2006;78(2):179–92.

5. Lorenz-Depiereux B, Benet-Pages A, Eckstein G, Tenenbaum-Rakover Y, Wagenstaller J, Tiosano D, et al. Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3. Am J Hum Genet. 2006;78(2):193–201.

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