(Q34707645)

4 August 2017

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

1 reference

hereditary hypophosphatemic rickets with hypercalciuria

4 August 2017

0 references

author name string

Takehisa Yamamoto

1

1 reference

4 August 2017

Toshimi Michigami

2

1 reference

4 August 2017

Fumito Aranami

3

1 reference

4 August 2017

Hiroko Segawa

4

1 reference

4 August 2017

Kousei Yoh

5

1 reference

4 August 2017

Shigeo Nakajima

6

1 reference

4 August 2017

Ken-ichi Miyamoto

7

1 reference

4 August 2017

Keiichi Ozono

8

1 reference

4 August 2017

language of work or name

1 reference

25 October 2007

1 reference

Journal of Bone and Mineral Metabolism

4 August 2017

1 reference

4 August 2017

25

1 reference

4 August 2017

6

1 reference

4 August 2017

407-413

1 reference

https://scigraph.springernature.com/pub.10.1007/s00774-007-0776-6

4 August 2017

0 references

cites work

Abnormal response of osteoblasts from Hyp mice to 1,25-dihydroxyvitamin D3

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00774-007-0776-6

In vivo osteogenic activity of isolated human bone cells

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Bone Response to Phosphate Salts, Ergocalciferol, and Calcitriol in Hypophosphatemic Vitamin D-Resistant Rickets

1 reference

12 December 2020

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

1 reference

12 December 2020

Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter

1 reference

12 December 2020

Hereditary hypophosphatemic rickets with hypercalciuria

1 reference

12 December 2020

The role of fibroblast growth factor 23 for hypophosphatemia and abnormal regulation of vitamin D metabolism in patients with McCune-Albright syndrome

1 reference

12 December 2020

Phosphate transport by osteoblasts from X-linked hypophosphatemic mice.

1 reference

12 December 2020

Defective bone formation by transplanted Hyp mouse bone cells into normal mice

1 reference

12 December 2020

Mutations in CLCN5 chloride channel in Japanese patients with low molecular weight proteinuria

1 reference

12 December 2020

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

1 reference

12 December 2020

Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia

1 reference

12 December 2020

Some observations on bone mineral in a case of vitamin D resistant rickets

1 reference

12 December 2020

Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene.

1 reference

12 December 2020

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

1 reference

12 December 2020

Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria

1 reference

12 December 2020

Tumor-induced osteomalacia--unveiling a new hormone

1 reference

12 December 2020

A single case of hypophosphatemic rickets with hypercalciuria.

1 reference

12 December 2020

Phosphate regulates the stability of skeletal alkaline phosphatase activity in human osteosarcoma (SaOS-2) cells without equivalent effects on the level of skeletal alkaline phosphatase immunoreactive protein

1 reference

12 December 2020

Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00774-007-0776-6

Identifiers

DOI

1 reference

4 August 2017

1 reference