Results
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6381.
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6382.
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Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3. [electronic resource] by
- Lorenz-Depiereux, Bettina
- Benet-Pages, Anna
- Eckstein, Gertrud
- Tenenbaum-Rakover, Yardena
- Wagenstaller, Janine
- Tiosano, Dov
- Gershoni-Baruch, Ruth
- Albers, Norbert
- Lichtner, Peter
- Schnabel, Dirk
- Hochberg, Ze'ev
- Strom, Tim M
Producer: 20071106
In:
American journal of human genetics vol. 78
Availability: No items available.
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6383.
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FGF-23 transgenic mice demonstrate hypophosphatemic rickets with reduced expression of sodium phosphate cotransporter type IIa. [electronic resource] by
- Shimada, Takashi
- Urakawa, Itaru
- Yamazaki, Yuji
- Hasegawa, Hisashi
- Hino, Rieko
- Yoneya, Takashi
- Takeuchi, Yasuhiro
- Fujita, Toshiro
- Fukumoto, Seiji
- Yamashita, Takeyoshi
Producer: 20040305
In:
Biochemical and biophysical research communications vol. 314
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6384.
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6385.
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Pharmacological inhibition of fibroblast growth factor (FGF) receptor signaling ameliorates FGF23-mediated hypophosphatemic rickets. [electronic resource] by
- Wöhrle, Simon
- Henninger, Christine
- Bonny, Olivier
- Thuery, Anne
- Beluch, Noemie
- Hynes, Nancy E
- Guagnano, Vito
- Sellers, William R
- Hofmann, Francesco
- Kneissel, Michaela
- Graus Porta, Diana
Producer: 20160328
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 28
Availability: No items available.
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6386.
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Neonatal iron deficiency causes abnormal phosphate metabolism by elevating FGF23 in normal and ADHR mice. [electronic resource] by
- Clinkenbeard, Erica L
- Farrow, Emily G
- Summers, Lelia J
- Cass, Taryn A
- Roberts, Jessica L
- Bayt, Christine A
- Lahm, Tim
- Albrecht, Marjorie
- Allen, Matthew R
- Peacock, Munro
- White, Kenneth E
Producer: 20140904
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 29
Availability: No items available.
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6387.
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6388.
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6389.
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6390.
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6391.
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6392.
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Soluble klotho and autosomal dominant polycystic kidney disease. [electronic resource] by
- Pavik, Ivana
- Jaeger, Philippe
- Ebner, Lena
- Poster, Diane
- Krauer, Fabienne
- Kistler, Andreas D
- Rentsch, Katharina
- Andreisek, Gustav
- Wagner, Carsten A
- Devuyst, Olivier
- Wüthrich, Rudolf P
- Schmid, Christoph
- Serra, Andreas L
Producer: 20120612
In:
Clinical journal of the American Society of Nephrology : CJASN vol. 7
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6393.
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6394.
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6395.
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6396.
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6397.
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Novel mutations in the 1alpha-hydroxylase (P450c1) gene in three families with pseudovitamin D-deficiency rickets resulting in loss of functional enzyme activity in blood-derived macrophages. [electronic resource] by
- Smith, S J
- Rucka, A K
- Berry, J L
- Davies, M
- Mylchreest, S
- Paterson, C R
- Heath, D A
- Tassabehji, M
- Read, A P
- Mee, A P
- Mawer, E B
Producer: 19990615
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 14
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6398.
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6399.
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6400.
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