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1 calcemia, changes in parathyroid hormone, or fibroblast growth factor 23.
2 f 25(OH) vitamin D, parathyroid hormone, and fibroblast growth factor 23.
3 roid hormone, 1,25-dihydroxyvitamin D(3), or fibroblast growth factor 23.
4 phosphate excretion, parathyroid hormone, or fibroblast growth factor-23.
6 ed osteomalacia involves tumor expression of fibroblast growth factor 23, a hormone that inhibits pro
8 e blood of cKO mice had an elevated level of fibroblast growth factor 23 and reduced level of phospho
9 baseline (1990-1992) serum levels of intact fibroblast growth factor-23 and incident ESRD in 13,448
10 d 24,25-dihydroxyvitamin D, decreased intact fibroblast growth factor 23, and elevated inorganic phos
11 ect the elevated plasma levels of osteocytic fibroblast growth factor 23 but decreased the elevated l
12 st growth factor 23 (iFGF23) into C-terminal fibroblast growth factor 23 (cFGF23), elevated levels of
15 artery disease, diabetes, dialysis vintage, fibroblast growth factor-23 concentration, and age, wher
20 vel circulating phosphaturic factors such as fibroblast growth factor 23 (FGF-23) and PHEX are respon
27 gh level of the phosphate-regulating hormone fibroblast growth factor 23 (FGF-23) is associated with
28 roid hormone (PTH), 1,25(OH)2D3 (1,25D), and fibroblast growth factor 23 (FGF-23) maintains mineral h
31 kidney disease (CKD) by increased levels of fibroblast growth factor-23 (FGF-23) and parathyroid hor
32 ge-dependent phenotype correlated with serum fibroblast growth factor-23 (FGF-23) and phosphorus leve
33 trations of the phosphate-regulating hormone fibroblast growth factor-23 (FGF-23) are elevated in pat
40 ently, several phosphaturic peptides such as fibroblast growth factor-23 (FGF-23), secreted frizzled
41 hrough cross-talk between RAAS and vitamin D-fibroblast growth factor-23 (FGF-23)-Klotho pathways.
43 ip between repeated measures of vitamin D or fibroblast growth factor 23 (FGF23) and infectious and c
44 morphological, and biochemical phenotypes of fibroblast growth factor 23 (Fgf23) and klotho ablated m
46 sphatemic states arising from high levels of fibroblast growth factor 23 (FGF23) are also associated
50 s of the parathyroid hormone (PTH)-vitamin D-fibroblast growth factor 23 (FGF23) axis, creatinine, an
51 DHR) is unique among the disorders involving Fibroblast growth factor 23 (FGF23) because individuals
54 asma levels of the osteocyte-derived hormone fibroblast growth factor 23 (FGF23) have emerged as a po
59 The regulation of the phosphaturic factor fibroblast growth factor 23 (FGF23) is not well understo
61 l phosphate-wasting associated with elevated fibroblast growth factor 23 (FGF23) levels and normocalc
62 iations between elevated serum phosphate and fibroblast growth factor 23 (FGF23) levels and risks of
65 ,25(OH)2D3 (1,25D), parathyroid hormone, and fibroblast growth factor 23 (FGF23), and their interacti
66 egulator of the phosphate-regulating hormone fibroblast growth factor 23 (FGF23), because humans with
68 nd related hormones, parathyroid hormone and fibroblast growth factor 23 (FGF23), on cardiac remodeli
69 1), the calcium-sensing receptor (CASR), and fibroblast growth factor 23 (FGF23), proteins that contr
71 unique basal and parathyroid hormone (PTH)-, fibroblast growth factor 23 (FGF23)-, and 1,25(OH)2D3-me
72 n (mKL) and recognized as the coreceptor for fibroblast growth factor-23 (FGF23) and a circulating so
75 low serum vitamin D levels, increased serum fibroblast growth factor-23 (Fgf23), and osteomalacia.
76 ated longitudinal changes in serum levels of fibroblast growth factor-23 (FGF23), parathyroid hormone
81 D promotes production and cleavage of intact fibroblast growth factor 23 (iFGF23) into C-terminal fib
83 imed to assess the effect of paricalcitol on fibroblast growth factor-23/KLOTHO axis in renal transpl
84 rminal pro-B-type natriuretic peptide level, fibroblast growth factor 23 level, estimated glomerular
87 ad range of kidney function, higher baseline fibroblast growth factor-23 levels were associated with
90 diator of pathologic cardiac remodeling, and fibroblast growth factor-23 may contribute to cardiac re
92 ion did not affect serum calcium, phosphate, fibroblast growth factor-23, or alkaline phosphatase lev
93 r KTx: the aortic calcification index (ACI), fibroblast growth factor 23, osteoprotegerin (OPG), fetu
94 ns of certain molecules, such as phosphates, fibroblast growth factor 23, parathyroid hormone, sclero
95 d markers of mineral metabolism, the highest fibroblast growth factor-23 quintile (>54.6 pg/ml) compa
97 ake stimulates parathyroid hormone (PTH) and fibroblast growth factor-23 secretion, increasing phosph
98 ighted the effect of phosphate depletion and fibroblast growth factor-23 suppression on the developme
100 pass renal clearance of parathyroid hormone, fibroblast growth factor 23, vitamin D metabolites, and
103 sphorus, calcitriol, parathyroid hormone, or fibroblast growth factor-23 were not consistently associ
104 ced intact parathyroid hormone and increased fibroblast growth factor-23, with a trend to increase in
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