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1 f 25(OH) vitamin D, parathyroid hormone, and fibroblast growth factor 23.
2 roid hormone, 1,25-dihydroxyvitamin D(3), or fibroblast growth factor 23.
3 of reduced parathyroid hormone and increased fibroblast growth factor 23.
4 l power to identify novel genetic traits for fibroblast growth factor 23.
5 pression of the phosphate-regulating hormone fibroblast growth factor 23.
6 calcemia, changes in parathyroid hormone, or fibroblast growth factor 23.
7 creases in alkaline phosphatase activity and fibroblast growth factor-23.
8 phosphate excretion, parathyroid hormone, or fibroblast growth factor-23.
10 ed osteomalacia involves tumor expression of fibroblast growth factor 23, a hormone that inhibits pro
11 ), and recent findings suggest that blocking fibroblast growth factor 23 actions may be the most effe
12 aline phosphatase, higher circulating intact fibroblast growth factor 23 and decreased bone formation
13 nd Ip6k2 reduced the plasma concentration of fibroblast growth factor 23 and increased bone resorptio
14 te, specifically the secretion and action of fibroblast growth factor 23 and parathyroid hormone.
15 e blood of cKO mice had an elevated level of fibroblast growth factor 23 and reduced level of phospho
17 ors of osteocytic secreted proteins, such as fibroblast growth factor 23 and sclerostin, have been us
18 thelial cells blocked the effects of PTH and fibroblast growth factor 23 and stabilized the NPT2A-NHE
19 baseline (1990-1992) serum levels of intact fibroblast growth factor-23 and incident ESRD in 13,448
20 related to mineral metabolism/calcification (fibroblast growth factor-23 and OPG [osteoprotegerin]),
21 ke protein 1), CTSL1 (cathepsin L1), FGF-23 (fibroblast growth factor 23), and MMP-12 (matrix metallo
22 d 24,25-dihydroxyvitamin D, decreased intact fibroblast growth factor 23, and elevated inorganic phos
23 tubular reabsorption of phosphate (TRP (%)), fibroblast growth factor 23, and intact parathyroid horm
24 otif chemokine ligand, CD5, interleukin 12B, fibroblast growth factor-23, and monocyte chemoattractan
26 ect the elevated plasma levels of osteocytic fibroblast growth factor 23 but decreased the elevated l
27 st growth factor 23 (iFGF23) into C-terminal fibroblast growth factor 23 (cFGF23), elevated levels of
30 artery disease, diabetes, dialysis vintage, fibroblast growth factor-23 concentration, and age, wher
35 vel circulating phosphaturic factors such as fibroblast growth factor 23 (FGF-23) and PHEX are respon
39 conducted to clarify the role of klotho and fibroblast growth factor 23 (FGF-23) in human arterial r
43 gh level of the phosphate-regulating hormone fibroblast growth factor 23 (FGF-23) is associated with
44 roid hormone (PTH), 1,25(OH)2D3 (1,25D), and fibroblast growth factor 23 (FGF-23) maintains mineral h
45 hate, calcium, parathyroid hormone (PTH) and fibroblast growth factor 23 (FGF-23) were studied up to
47 bulin and mucin domain containing 4 (TIMD4), fibroblast growth factor 23 (FGF-23), growth differentia
49 kidney disease (CKD) by increased levels of fibroblast growth factor-23 (FGF-23) and parathyroid hor
50 ge-dependent phenotype correlated with serum fibroblast growth factor-23 (FGF-23) and phosphorus leve
51 trations of the phosphate-regulating hormone fibroblast growth factor-23 (FGF-23) are elevated in pat
58 ently, several phosphaturic peptides such as fibroblast growth factor-23 (FGF-23), secreted frizzled
59 hrough cross-talk between RAAS and vitamin D-fibroblast growth factor-23 (FGF-23)-Klotho pathways.
61 by parathyroid hormone (PTH), suppression by fibroblast growth factor 23 (FGF23) and 1,25-dihydroxyvi
62 ip between repeated measures of vitamin D or fibroblast growth factor 23 (FGF23) and infectious and c
63 Klotho acts as transmembrane co-receptor for fibroblast growth factor 23 (FGF23) and is a key regulat
64 morphological, and biochemical phenotypes of fibroblast growth factor 23 (Fgf23) and klotho ablated m
66 e demonstrate systemic and direct effects of Fibroblast growth factor 23 (FGF23) and Klotho, which no
67 mone (PTH), the vitamin D system, vitamin K, fibroblast growth factor 23 (FGF23) and phosphatase enzy
69 (3) elicited the expected increase of plasma fibroblast growth factor 23 (FGF23) and reduction of par
70 sphatemic states arising from high levels of fibroblast growth factor 23 (FGF23) are also associated
76 s of the parathyroid hormone (PTH)-vitamin D-fibroblast growth factor 23 (FGF23) axis, creatinine, an
77 DHR) is unique among the disorders involving Fibroblast growth factor 23 (FGF23) because individuals
78 genetic analysis or measurement of levels of fibroblast growth factor 23 (FGF23) before treatment.
79 c inflammation and elevations in the hormone fibroblast growth factor 23 (FGF23) contribute to cardia
81 etabolic regulators, including elevations of fibroblast growth factor 23 (FGF23) directly contribute
85 asma levels of the osteocyte-derived hormone fibroblast growth factor 23 (FGF23) have emerged as a po
86 tency, which antagonize excessive actions of fibroblast growth factor 23 (FGF23) in hereditary hypoph
89 fibroblast growth factor receptor (FGFR) and fibroblast growth factor 23 (FGF23) indicates that its b
90 f adults with the phosphaturic human hormone fibroblast growth factor 23 (FGF23) induces tubule expre
98 The regulation of the phosphaturic factor fibroblast growth factor 23 (FGF23) is not well understo
101 l phosphate-wasting associated with elevated fibroblast growth factor 23 (FGF23) levels and normocalc
102 iations between elevated serum phosphate and fibroblast growth factor 23 (FGF23) levels and risks of
111 assay, B-type natriuretic peptide (BNP) and fibroblast growth factor 23 (FGF23) were recently identi
112 signaling complexes of the endocrine hormone fibroblast growth factor 23 (FGF23) with fibroblast grow
113 sylation of the phosphate-regulating hormone fibroblast growth factor 23 (FGF23) within osteocytes of
114 lcium, phosphate, parathyroid hormone (PTH), fibroblast growth factor 23 (FGF23), 25-hydroxyvitamin D
117 eocyte-derived, phosphate-regulating hormone fibroblast growth factor 23 (FGF23), a risk factor for p
118 cation: elevated circulating 1,25D, 25D, and fibroblast growth factor 23 (FGF23), activation of vitam
119 iprocal manner by parathyroid hormone (PTH), fibroblast growth factor 23 (FGF23), and 1,25(OH)(2)D(3)
120 e is regulated by parathyroid hormone (PTH), fibroblast growth factor 23 (FGF23), and 1,25(OH)(2)D(3)
121 ,25(OH)2D3 (1,25D), parathyroid hormone, and fibroblast growth factor 23 (FGF23), and their interacti
122 perphosphatemia is associated with increased fibroblast growth factor 23 (FGF23), arterial calcificat
123 egulator of the phosphate-regulating hormone fibroblast growth factor 23 (FGF23), because humans with
125 a, and osteopenia, with elevated circulating fibroblast growth factor 23 (FGF23), calcitriol (1,25-D(
126 atus, and tested for mediation by C-terminal fibroblast growth factor 23 (FGF23), hemoglobin and para
127 cterised by elevated serum concentrations of fibroblast growth factor 23 (FGF23), hypophosphataemia,
128 on evolving concepts regarding the roles of fibroblast growth factor 23 (FGF23), inflammation and sy
129 ar bone osteocytes in Hyp mice overexpressed fibroblast growth factor 23 (Fgf23), its expression in m
130 nd related hormones, parathyroid hormone and fibroblast growth factor 23 (FGF23), on cardiac remodeli
131 1), the calcium-sensing receptor (CASR), and fibroblast growth factor 23 (FGF23), proteins that contr
132 form of inherited rickets featuring elevated fibroblast growth factor 23 (FGF23), reduced 1,25-dihydr
134 h concentrations of circulating phosphatonin fibroblast growth factor 23 (FGF23), which causes renal
135 sis of the bone-derived phosphaturic hormone fibroblast growth factor 23 (FGF23), which results in re
137 unique basal and parathyroid hormone (PTH)-, fibroblast growth factor 23 (FGF23)-, and 1,25(OH)2D3-me
142 n (mKL) and recognized as the coreceptor for fibroblast growth factor-23 (FGF23) and a circulating so
143 ercent tubular reabsorption of phosphate and fibroblast growth factor-23 (FGF23) at all CKD stages, a
149 low serum vitamin D levels, increased serum fibroblast growth factor-23 (Fgf23), and osteomalacia.
150 ated longitudinal changes in serum levels of fibroblast growth factor-23 (FGF23), parathyroid hormone
151 ny of which are similar to those observed in fibroblast growth factor-23 (FGF23)-deficient mice.
155 sm (including abnormalities in phosphate and fibroblast growth factor 23 [FGF23]) contribute to adver
156 ading triggers physiologic release of FGF23 (fibroblast growth factor-23) from the bone to maintain p
157 other bone health markers, including intact fibroblast growth factor-23 (iFGF-23), intact parathyroi
158 D promotes production and cleavage of intact fibroblast growth factor 23 (iFGF23) into C-terminal fib
159 reted proteins parathyroid hormone (PTH) and fibroblast growth factor 23 inhibited Pi uptake by induc
162 imed to assess the effect of paricalcitol on fibroblast growth factor-23/KLOTHO axis in renal transpl
163 rminal pro-B-type natriuretic peptide level, fibroblast growth factor 23 level, estimated glomerular
164 Phosphate binder therapy restored plasma fibroblast growth factor 23 levels but had no effect on
167 ad range of kidney function, higher baseline fibroblast growth factor-23 levels were associated with
168 rus levels, circulating phosphaturic hormone fibroblast growth factor-23 levels, and heart mass.
170 diator of pathologic cardiac remodeling, and fibroblast growth factor-23 may contribute to cardiac re
171 ency anemia, but certain formulations induce fibroblast growth factor 23-mediated hypophosphatemia.
173 ion did not affect serum calcium, phosphate, fibroblast growth factor-23, or alkaline phosphatase lev
174 r KTx: the aortic calcification index (ACI), fibroblast growth factor 23, osteoprotegerin (OPG), fetu
175 ns of certain molecules, such as phosphates, fibroblast growth factor 23, parathyroid hormone, sclero
176 d markers of mineral metabolism, the highest fibroblast growth factor-23 quintile (>54.6 pg/ml) compa
177 s, acts as an essential co-receptor with the fibroblast growth factor 23 receptor complex to regulate
178 rathyroid hormone and phosphatonins, such as fibroblast growth factor 23, regulate the activity of th
180 ake stimulates parathyroid hormone (PTH) and fibroblast growth factor-23 secretion, increasing phosph
181 ighted the effect of phosphate depletion and fibroblast growth factor-23 suppression on the developme
183 pass renal clearance of parathyroid hormone, fibroblast growth factor 23, vitamin D metabolites, and
187 sphorus, calcitriol, parathyroid hormone, or fibroblast growth factor-23 were not consistently associ
188 s regulated by parathyroid hormone (PTH) and fibroblast growth factor 23, which requires Na(+)/H(+) e
189 ced intact parathyroid hormone and increased fibroblast growth factor-23, with a trend to increase in