-
1
-
-
0000165617
-
Parathyroid hormone: Physiology, chemistry, biosynthesis, secretion, metabolism, and mode of action
-
DeGroot, L.J., ed. Philadelphia, PA: W.B. Saunders
-
Potts JT Bringhurst FR, Gardella TJ et al. Parathyroid hormone: physiology, chemistry, biosynthesis, secretion, metabolism, and mode of action. In: DeGroot LJ, ed. Endocrinology. Philadelphia, PA: W.B. Saunders, 1996 920 65.
-
(1996)
Endocrinology.
, pp. 920-65
-
-
Potts, J.T.1
Bringhurst, F.R.2
Gardella, T.J.3
-
2
-
-
35948956577
-
Parathyroid hormone and parathyroid hormone-related peptide in the regulation of calcium homeostasis and bone development
-
DeGroot, L., Jameson, J., eds. Philadelphia, PA: W.B. Saunders Company
-
Jüppner H, Gardella T, Brown E et al. Parathyroid hormone and parathyroid hormone-related peptide in the regulation of calcium homeostasis and bone development. In: DeGroot L, Jameson J, eds. Endocrinology, 5th edn. Philadelphia, PA: W.B. Saunders Company, 2005 1377 417.
-
(2005)
Endocrinology, 5th Edn.
, pp. 1377-417
-
-
Jüppner, H.1
Gardella, T.2
Brown, E.3
-
3
-
-
33846261191
-
Parathyroid hormone-dependent endocytosis of renal type IIc Na-Pi cotransporter
-
Segawa H, Yamanaka S, Onitsuka A et al. Parathyroid hormone-dependent endocytosis of renal type IIc Na-Pi cotransporter. Am J Physiol Renal Physiol 2007 292: F395 403.
-
(2007)
Am J Physiol Renal Physiol
, vol.292
-
-
Segawa, H.1
Yamanaka, S.2
Onitsuka, A.3
-
5
-
-
0002304218
-
Parathyroid Hormone and parathyroid hormone-related peptide in calcium homeostasis, bone metabolism, and bone development: The proteins, their genes, and receptors
-
Avioli, L., Krane, S., eds. New York: Academic Press
-
Potts JT Jüppner H. Parathyroid Hormone and parathyroid hormone-related peptide in calcium homeostasis, bone metabolism, and bone development: the proteins, their genes, and receptors. In: Avioli L, Krane S, eds. Metabolic Bone Disease. New York: Academic Press, 1997 51 94.
-
(1997)
Metabolic Bone Disease.
, pp. 51-94
-
-
Potts, J.T.1
Jüppner, H.2
-
6
-
-
0029160578
-
A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets
-
The HYP Consortium.
-
The HYP Consortium. A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. Nat Genet 1995 11: 130 6.
-
(1995)
Nat Genet
, vol.11
, pp. 130-6
-
-
-
7
-
-
0033763097
-
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF-23
-
The ADHR Consortium; White KE, Evans WE et al. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF-23. Nat Genet 2000 26: 345 8.
-
(2000)
Nat Genet
, vol.26
, pp. 345-8
-
-
Adhr Consortium, T.1
White, K.E.2
Evans, W.E.3
-
8
-
-
35948953864
-
A homozygous missense mutation S129P in FGF-23 causes tumoral calcinosis with hyperphosphatemia
-
Bergwitz C, Banerjee S, Abu-Zahra H, Miyauchi A, Jüppner H. A homozygous missense mutation S129P in FGF-23 causes tumoral calcinosis with hyperphosphatemia. J Bone Miner Res 2005 20: F444.
-
(2005)
J Bone Miner Res
, vol.20
-
-
Bergwitz, C.1
Banerjee, S.2
Abu-Zahra, H.3
Miyauchi, A.4
Jüppner, H.5
-
9
-
-
31544460435
-
Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium/phosphate cotransporter gene SLC34A3
-
Lorenz-Depiereux B, Benet-Pages A, Eckstein G et al. Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium/phosphate cotransporter gene SLC34A3. Am J Hum Genet 2006 78: 193 201.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 193-201
-
-
Lorenz-Depiereux, B.1
Benet-Pages, A.2
Eckstein, G.3
-
10
-
-
33750427897
-
DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis
-
2006
-
Lorenz-Depiereux B, Bastepe M, Benet-Pagès A et al. 2006 DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. Nat Genet 2006 38: 1248 50.
-
(2006)
Nat Genet
, vol.38
, pp. 1248-50
-
-
Lorenz-Depiereux, B.1
Bastepe, M.2
Benet-Pagès, A.3
-
11
-
-
2642546399
-
Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis
-
Topaz O, Shurman D, Bergman R et al. Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis. Nat Genet 2004 36: 579 81.
-
(2004)
Nat Genet
, vol.36
, pp. 579-81
-
-
Topaz, O.1
Shurman, D.2
Bergman, R.3
-
12
-
-
0037179681
-
Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter
-
Prié D, Huart V, Bakouh N et al. Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium-phosphate cotransporter. N Engl J Med 2002 347: 983 91.
-
(2002)
N Engl J Med
, vol.347
, pp. 983-91
-
-
Prié, D.1
Huart, V.2
Bakouh, N.3
-
13
-
-
31544481921
-
SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH) predict a key role for the sodium-phosphate co-transporter NaPi-IIc in maintaining phosphate homeostasis and skeletal function
-
Bergwitz C, Roslin N, Tieder M et al. SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria (HHRH) predict a key role for the sodium-phosphate co-transporter NaPi-IIc in maintaining phosphate homeostasis and skeletal function. Am J Hum Genet 2006 78: 179 92.
-
(2006)
Am J Hum Genet
, vol.78
, pp. 179-92
-
-
Bergwitz, C.1
Roslin, N.2
Tieder, M.3
-
14
-
-
34848871595
-
Homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis
-
Ichikawa S, Imel EA, Kreiter ML et al. Homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis. J Clin Invest 2007 117: 2684 91
-
(2007)
J Clin Invest
, vol.117
, pp. 2684-91
-
-
Ichikawa, S.1
Imel, E.A.2
Kreiter, M.L.3
-
15
-
-
33646578195
-
Regulation of fibroblast growth factor-23 signaling by Klotho
-
2007
-
Kurosu H, Ogawa Y, Miyoshi M et al. 2006 Regulation of fibroblast growth factor-23 signaling by Klotho. J Biol Chem 2007 281: 6120 3.
-
(2006)
J Biol Chem
, vol.281
, pp. 6120-3
-
-
Kurosu, H.1
Ogawa, Y.2
Miyoshi, M.3
-
16
-
-
33845631059
-
Klotho converts canonical FGF receptor into a specific receptor for FGF-23
-
Urakawa I, Yamazaki Y, Shimada T et al. Klotho converts canonical FGF receptor into a specific receptor for FGF-23. Nature 2006 444: 770 4.
-
(2006)
Nature
, vol.444
, pp. 770-4
-
-
Urakawa, I.1
Yamazaki, Y.2
Shimada, T.3
-
17
-
-
33750454816
-
Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism
-
Feng JQ, Ward LM, Liu S et al. Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism. Nat Genet 2006 38: 1310 15.
-
(2006)
Nat Genet
, vol.38
, pp. 1310-15
-
-
Feng, J.Q.1
Ward, L.M.2
Liu, S.3
-
18
-
-
10744226781
-
MEPE has the properties of an osteoblastic phosphatonin and minhibin
-
Rowe P, Kumagai Y, Gutierrez G et al. MEPE has the properties of an osteoblastic phosphatonin and minhibin. Bone 2004 34: 303 19.
-
(2004)
Bone
, vol.34
, pp. 303-19
-
-
Rowe, P.1
Kumagai, Y.2
Gutierrez, G.3
-
19
-
-
14044267649
-
Fibroblast growth factor 7: An inhibitor of phosphate transport derived from oncogenic osteomalacia-causing tumors
-
Carpenter T, Ellis B, Insogna K, Philbrick W, Sterpka J, Shimkets R. Fibroblast growth factor 7: an inhibitor of phosphate transport derived from oncogenic osteomalacia-causing tumors. J Clin Endocrinol Metab 2005 90: 1012 20.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 1012-20
-
-
Carpenter, T.1
Ellis, B.2
Insogna, K.3
Philbrick, W.4
Sterpka, J.5
Shimkets, R.6
-
20
-
-
29144490730
-
Secreted frizzled-related protein-4 reduces sodium-phosphate co-transporter abundance and activity in proximal tubule cells
-
Berndt T, Bielesz B, Craig T et al. Secreted frizzled-related protein-4 reduces sodium-phosphate co-transporter abundance and activity in proximal tubule cells. Pflugers Arch 2006 451: 579 87.
-
(2006)
Pflugers Arch
, vol.451
, pp. 579-87
-
-
Berndt, T.1
Bielesz, B.2
Craig, T.3
-
21
-
-
85047693146
-
Secreted frizzled-related protein 4 is a potent tumor-derived phosphaturic agent
-
Berndt T, Craig T, Bowe A et al. Secreted frizzled-related protein 4 is a potent tumor-derived phosphaturic agent. J Clin Invest 2003 112: 785 94.
-
(2003)
J Clin Invest
, vol.112
, pp. 785-94
-
-
Berndt, T.1
Craig, T.2
Bowe, A.3
-
22
-
-
0022002364
-
Hereditary hypophosphatemic rickets with hypercalciuria
-
Tieder M, Modai D, Samuel R et al. Hereditary hypophosphatemic rickets with hypercalciuria. N Engl J Med 1985 312: 611 17.
-
(1985)
N Engl J Med
, vol.312
, pp. 611-17
-
-
Tieder, M.1
Modai, D.2
Samuel, R.3
-
23
-
-
0023127407
-
"idiopathic" hypercalciuria and hereditary hypophosphatemic rickets. Two phenotypical expressions of a common genetic defect
-
Tieder M, Modai D, Shaked U et al. "Idiopathic" hypercalciuria and hereditary hypophosphatemic rickets. Two phenotypical expressions of a common genetic defect. N Engl J Med 1987 316: 125 9.
-
(1987)
N Engl J Med
, vol.316
, pp. 125-9
-
-
Tieder, M.1
Modai, D.2
Shaked, U.3
-
24
-
-
0037205468
-
Growth-related renal type II Na/Pi cotransporter
-
Segawa H, Kaneko I, Takahashi A et al. Growth-related renal type II Na/Pi cotransporter. J Biol Chem 2002 277: 19665 72.
-
(2002)
J Biol Chem
, vol.277
, pp. 19665-72
-
-
Segawa, H.1
Kaneko, I.2
Takahashi, A.3
-
25
-
-
33749558921
-
Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria
-
Ichikawa S, Sorenson AH, Imel EA, Friedman NE, Gertner JM, Econs MJ. Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria. J Clin Endocrinol Metab 2006 91: 4022 7.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 4022-7
-
-
Ichikawa, S.1
Sorenson, A.H.2
Imel, E.A.3
Friedman, N.E.4
Gertner, J.M.5
Econs, M.J.6
-
26
-
-
35948955837
-
Hypophosphatemic rickets with hyper calciuria due to mutation in SLC34A3/NaPi-llc can be masked by vitamin D deficiency and can be associated with renal calcifications
-
in press).
-
Kremke B, Bergwitz C, Ahrens W et al. Hypophosphatemic rickets with hyper calciuria due to mutation in SLC34A3/NaPi-llc can be masked by vitamin D deficiency and can be associated with renal calcifications. Eur J Endocrinol (in press).
-
Eur J Endocrinol
-
-
Kremke, B.1
Bergwitz, C.2
Ahrens, W.3
-
27
-
-
0344442745
-
Functional characterization of two naturally occurring mutations in the human sodium-phosphate cotransporter type IIa
-
Virkki L, Forster I, Hernando N, Biber J, Murer H. Functional characterization of two naturally occurring mutations in the human sodium-phosphate cotransporter type IIa. J Bone Miner Res 2003 18: 2135 41.
-
(2003)
J Bone Miner Res
, vol.18
, pp. 2135-41
-
-
Virkki, L.1
Forster, I.2
Hernando, N.3
Biber, J.4
Murer, H.5
-
28
-
-
0031035615
-
Autosomal dominant hypophosphatemic rickets/osteomalacia: Clinical characterization of a novel renal phosphate-wasting disorder
-
Econs M, McEnery P. Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder. J Clin Endocrinol Metab 1997 82: 674 81.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 674-81
-
-
Econs, M.1
McEnery, P.2
-
29
-
-
0031452349
-
Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13
-
Econs M, McEnery P, Lennon F, Speer M. Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13. J Clin Invest 1997 100: 2653 7.
-
(1997)
J Clin Invest
, vol.100
, pp. 2653-7
-
-
Econs, M.1
McEnery, P.2
Lennon, F.3
Speer, M.4
-
30
-
-
0035186837
-
Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23
-
White K, Carn G, Lorenz-Depiereux B, Benet-Pages A, Strom T, Econs M. Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23. Kidney Int 2001 60: 2079 86.
-
(2001)
Kidney Int
, vol.60
, pp. 2079-86
-
-
White, K.1
Carn, G.2
Lorenz-Depiereux, B.3
Benet-Pages, A.4
Strom, T.5
Econs, M.6
-
31
-
-
33646529865
-
The roles of specific genes implicated as circulating factors involved in normal and disordered phosphate homeostasis: Frp-4, MEPE, and FGF-23
-
White K, Larsson T, Econs M. The roles of specific genes implicated as circulating factors involved in normal and disordered phosphate homeostasis: Frp-4, MEPE, and FGF-23. Endocr Rev 2006 27: 221 41.
-
(2006)
Endocr Rev
, vol.27
, pp. 221-41
-
-
White, K.1
Larsson, T.2
Econs, M.3
-
32
-
-
14344279878
-
Cloning and characterization of FGF-23 as a causative factor of tumor-induced osteomalacia
-
2001
-
Shimada T, Mizutani S, Muto T et al. 2001 Cloning and characterization of FGF-23 as a causative factor of tumor-induced osteomalacia. Proc Natl Acad Sci USA 2001 98: 6500 5.
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 6500-5
-
-
Shimada, T.1
Mizutani, S.2
Muto, T.3
-
33
-
-
17744395066
-
The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting
-
White K, Jonsson K, Carn G et al. The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting. J Clin Endocrinol Metab 2001 86: 497 500.
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 497-500
-
-
White, K.1
Jonsson, K.2
Carn, G.3
-
34
-
-
18744371012
-
Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia
-
Yamazaki Y, Okazaki R, Shibata M et al. Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia. J Clin Endocrinol Metab 2002 87: 4957 60.
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 4957-60
-
-
Yamazaki, Y.1
Okazaki, R.2
Shibata, M.3
-
35
-
-
20244368616
-
Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia
-
Jonsson K, Zahradnik R, Larsson T et al. Fibroblast growth factor 23 in oncogenic osteomalacia and X-linked hypophosphatemia. N Engl J Med 2003 348: 1656 62.
-
(2003)
N Engl J Med
, vol.348
, pp. 1656-62
-
-
Jonsson, K.1
Zahradnik, R.2
Larsson, T.3
-
36
-
-
33744956771
-
Sensitivity of Fibroblast Growth Factor 23 measurements in tumor-induced osteomalacia
-
Imel E, Peacock M, Pitukcheewanont P et al. Sensitivity of Fibroblast Growth Factor 23 measurements in tumor-induced osteomalacia. J Clin Endocrinol Metab 2006 91: 2055 61.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 2055-61
-
-
Imel, E.1
Peacock, M.2
Pitukcheewanont, P.3
-
37
-
-
0344945402
-
Circulating concentration of FGF-23 increases as renalfunction declines in patients with chronic kidney disease, but does not change in response to variation in phosphate intake in healthy volunteers
-
Larsson T, Nisbeth U, Ljunggren O, Jüppner H, Jonsson K. Circulating concentration of FGF-23 increases as renalfunction declines in patients with chronic kidney disease, but does not change in response to variation in phosphate intake in healthy volunteers. Kidney Int 2003 64: 2272 9.
-
(2003)
Kidney Int
, vol.64
, pp. 2272-9
-
-
Larsson, T.1
Nisbeth, U.2
Ljunggren, O.3
Jüppner, H.4
Jonsson, K.5
-
38
-
-
2342481131
-
FGF-23 in patients with end-stage renal disease on hemodialysis
-
Imanishi Y, Inaba M, Nakatsuka K et al. FGF-23 in patients with end-stage renal disease on hemodialysis. Kidney Int 2004 65: 1943 6.
-
(2004)
Kidney Int
, vol.65
, pp. 1943-6
-
-
Imanishi, Y.1
Inaba, M.2
Nakatsuka, K.3
-
39
-
-
27744545673
-
Fibroblast growth factor-23 mitigates hyperphosphatemia but accentuates calcitriol deficiency in chronic kidney disease: New insight into secondary hyperparathyroidism
-
Gutierrez O, Isakova T, Rhee E et al. Fibroblast growth factor-23 mitigates hyperphosphatemia but accentuates calcitriol deficiency in chronic kidney disease: new insight into secondary hyperparathyroidism. J Am Soc Nephrol 2005 16: 2205 15.
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 2205-15
-
-
Gutierrez, O.1
Isakova, T.2
Rhee, E.3
-
40
-
-
31544450766
-
Effect of manipulating serum phosphorus with phosphate binder on circulating PTH and FGF-23 in renal failure rats
-
Nagano N, Miyata S, Abe M, Kobayashi N, Wakita S, Yamashita T, Wada M. Effect of manipulating serum phosphorus with phosphate binder on circulating PTH and FGF-23 in renal failure rats. Kidney Int 2006 69: 531 7.
-
(2006)
Kidney Int
, vol.69
, pp. 531-7
-
-
Nagano, N.1
Miyata, S.2
Abe, M.3
Kobayashi, N.4
Wakita, S.5
Yamashita, T.6
Wada, M.7
-
41
-
-
35948944177
-
Regulation of bone remodeling and mineralization by FGF-23 and PTH
-
TH-F CO88
-
Wesseling K, Jüppner H, Jimenez W et al. Regulation of bone remodeling and mineralization by FGF-23 and PTH. J Am Soc Nephrol 2006 17: TH-F CO88 (abstract).
-
(2006)
J Am Soc Nephrol
, vol.17
-
-
Wesseling, K.1
Jüppner, H.2
Jimenez, W.3
-
42
-
-
0141525564
-
Serum FGF-23 levels in normal and disordered phosphorus homeostasis
-
Weber T, Liu S, Indridason O, Quarles L Serum FGF-23 levels in normal and disordered phosphorus homeostasis. J Bone Miner Res 2003 18: 1227 34.
-
(2003)
J Bone Miner Res
, vol.18
, pp. 1227-34
-
-
Weber, T.1
Liu, S.2
Indridason, O.3
Quarles, L.4
-
43
-
-
26944499850
-
Role of matrix extracellular phosphoglycoprotein in the pathogenesis of X-linked hypophosphatemia
-
Liu S, Brown T, Zhou J et al. Role of matrix extracellular phosphoglycoprotein in the pathogenesis of X-linked hypophosphatemia. J Am Soc Nephrol 2005 16: 1645 53.
-
(2005)
J Am Soc Nephrol
, vol.16
, pp. 1645-53
-
-
Liu, S.1
Brown, T.2
Zhou, J.3
-
44
-
-
9644303231
-
Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice
-
Sitara D, Razzaque MS, Hesse M et al. Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice. Matrix Biol 2004 23: 421 32.
-
(2004)
Matrix Biol
, vol.23
, pp. 421-32
-
-
Sitara, D.1
Razzaque, M.S.2
Hesse, M.3
-
45
-
-
33745850756
-
Pathogenic role of FGF-23 in Hyp mice
-
Liu S, Zhou J, Tang W, Jiang X, Rowe DW, Quarles LD. Pathogenic role of FGF-23 in Hyp mice. Am J Physiol Endocrinol Metab 2006 291: E38 49.
-
(2006)
Am J Physiol Endocrinol Metab
, vol.291
-
-
Liu, S.1
Zhou, J.2
Tang, W.3
Jiang, X.4
Rowe, D.W.5
Quarles, L.D.6
-
46
-
-
33746406756
-
Regulation of C-terminal and intact FGF-23 by dietary phosphate in men and women
-
Burnett S, Gunawardene S, Bringhurst F, Jüppner H, Lee H, Finkelstein J. Regulation of C-terminal and intact FGF-23 by dietary phosphate in men and women. J Bone Miner Res 2006 21: 1187 96.
-
(2006)
J Bone Miner Res
, vol.21
, pp. 1187-96
-
-
Burnett, S.1
Gunawardene, S.2
Bringhurst, F.3
Jüppner, H.4
Lee, H.5
Finkelstein, J.6
-
47
-
-
27844501565
-
Dietary and serum phosphorus regulate fibroblast growth factor 23 expression and 1,25-dihydroxyvitamin D metabolism in mice
-
Perwad F, Azam N, Zhang M, Yamashita T, Tenenhouse H, Portale A. Dietary and serum phosphorus regulate fibroblast growth factor 23 expression and 1,25-dihydroxyvitamin D metabolism in mice. Endocrinology 2005 146: 5358 64.
-
(2005)
Endocrinology
, vol.146
, pp. 5358-64
-
-
Perwad, F.1
Azam, N.2
Zhang, M.3
Yamashita, T.4
Tenenhouse, H.5
Portale, A.6
-
48
-
-
28444486604
-
1alpha,25-Dihydroxyvitamin D3 upregulates FGF-23 gene expression in bone: The final link in a renal-gastrointestinal-skeletal axis that controls phosphate transport
-
Kolek O, Hines E, Jones M et al. 1alpha,25-Dihydroxyvitamin D3 upregulates FGF-23 gene expression in bone: the final link in a renal-gastrointestinal-skeletal axis that controls phosphate transport. Am J Physiol Gastrointest Liver Physiol 2005 289: G1036 42.
-
(2005)
Am J Physiol Gastrointest Liver Physiol
, vol.289
-
-
Kolek, O.1
Hines, E.2
Jones, M.3
-
49
-
-
19944430581
-
Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation
-
White KE, Cabral JM, Davis SI et al. Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation. Am J Hum Genet 2005 76: 361 7.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 361-7
-
-
White, K.E.1
Cabral, J.M.2
Davis, S.I.3
-
50
-
-
33644869881
-
Extended mutational analyses of FGFR1 in osteoglophonic dysplasia
-
Farrow E, Davis S, Mooney S et al. Extended mutational analyses of FGFR1 in osteoglophonic dysplasia. Am J Med Genet 2006 140: 537 9.
-
(2006)
Am J Med Genet
, vol.140
, pp. 537-9
-
-
Farrow, E.1
Davis, S.2
Mooney, S.3
-
51
-
-
35948978015
-
A Lebanese Family with Osteosclerosis and Hypophosphatemia
-
Bastepe M, Shlossberg H, Murdock H, Jüppner H, Rittmaster R. A Lebanese Family with Osteosclerosis and Hypophosphatemia. J Bone Miner Res 1999 14: S558.
-
(1999)
J Bone Miner Res
, vol.14
-
-
Bastepe, M.1
Shlossberg, H.2
Murdock, H.3
Jüppner, H.4
Rittmaster, R.5
-
52
-
-
20044383563
-
Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype
-
Ye L, Mishina Y, Chen D et al. Dmp1-deficient mice display severe defects in cartilage formation responsible for a chondrodysplasia-like phenotype. J Biol Chem 2005 280: 6197 203.
-
(2005)
J Biol Chem
, vol.280
, pp. 6197-203
-
-
Ye, L.1
Mishina, Y.2
Chen, D.3
-
53
-
-
35948952710
-
MEPE is overexpressed in osteocytes of the DMP1 (Dentin Matrix Protein 1) null mouse, contributing to the hypophosphatemia and osteomalacia
-
Harris S, Gluhak-Heinrich J, Harris M et al. MEPE is overexpressed in osteocytes of the DMP1 (Dentin Matrix Protein 1) null mouse, contributing to the hypophosphatemia and osteomalacia. J Bone Miner Res 2005 20: SA462.
-
(2005)
J Bone Miner Res
, vol.20
-
-
Harris, S.1
Gluhak-Heinrich, J.2
Harris, M.3
-
54
-
-
28144464147
-
DMP1 depletion decreases bone mineralization in vivo: An FTIR imaging analysis
-
Epub 2005.
-
Ling Y, Rios HF, Myers ER, Lu Y, Feng JQ, Boskey AL. DMP1 depletion decreases bone mineralization in vivo: an FTIR imaging analysis. J Bone Miner Res 2005 Dec 20(12): 2169 77. Epub 2005.
-
(2005)
J Bone Miner Res
, vol.2012
, pp. 2169-77
-
-
Ling, Y.1
Rios, H.F.2
Myers, E.R.3
Lu, Y.4
Feng, J.Q.5
Boskey, A.L.6
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