コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 llular LBPs such as serum albumin and plasma retinol binding protein.
2 yx in a manner similar to retinol binding in retinol-binding protein.
3 ne tetramer of TTR can bind two molecules of retinol-binding protein.
4 bundant substrate: retinol bound to cellular retinol-binding protein.
5 Here we show that mouse and human SAAs are retinol binding proteins.
6 it upon ligand binding by mammalian cellular retinol-binding proteins.
7 hibitor families, as well as fatty acid- and retinol-binding proteins.
9 orage, and metabolism of retinoids, cellular retinol-binding protein 1 (CRBP1) is essential for traff
11 in, and desmin, and negatively with cellular retinol-binding protein 1 and matrix metalloproteinase 2
12 on, retinol-related genes such as CRABP2 and retinol-binding protein 1 were overexpressed in WT, and
13 eased markers of dedifferentiation, cellular retinol-binding protein 1, and matrix metalloproteinase
16 uced by immunization with interphotoreceptor retinol-binding protein 1177-1191 peptide were treated b
18 are located near the transthyretin (TTR) and retinol binding protein 4 (RBP4) genes which encode majo
20 lective increase in plasma and intra-adipose retinol binding protein 4 (RBP4) that preceded obesity.
21 sed in the vascular endothelial cells, while retinol binding protein 4 (rbp4) was expressed in the yo
22 L-HDLs showed a reduced content of lipocalin retinol binding protein 4 and apolipoprotein M and in th
25 investigate the mechanisms by which elevated retinol-binding protein 4 (RBP4) causes insulin resistan
28 onsiderable evidence that both retinoids and retinol-binding protein 4 (RBP4) contribute to the devel
36 bition of the retinol-induced interaction of retinol-binding protein 4 (RBP4) with transthyretin (TTR
37 onizing the retinol-dependent interaction of retinol-binding protein 4 (RBP4) with transthyretin in t
42 adipocytokines (interleukin-6, adiponectin, retinol-binding protein 4) or soluble intercellular adhe
43 variate analysis) determinant of circulating retinol-binding protein 4, a reliable proxy for retinol
44 e show, using DNA arrays, that expression of retinol binding protein-4 (RBP4) is elevated in adipose
45 s of TNF-alpha, IL-6, adiponectin, resistin, retinol binding protein-4, or intraabdominal fat volume.
46 high-molecular-weight adiponectin, resistin, retinol binding protein-4, or intraabdominal obesity, su
49 our serum proteins-carcinoembryonic antigen, retinol binding protein, alpha1-antitrypsin, and squamou
50 the fatty acid binding proteins and cellular retinol binding protein also are down-regulated in the a
53 usly quantifying iron (ferritin), vitamin A (retinol-binding protein), and inflammation (C-reactive p
58 m constitutive hepatic proteins (prealbumin, retinol-binding protein, and transferrin) increased with
59 enases (RoDH), which recognize holo-cellular retinol-binding protein as substrate, had been cloned, e
60 ions with both unbound and CRBP(I) (cellular retinol-binding protein)-bound retinal, but apo-CRBP(I)
62 Km of approximately 0.7 microM, and cellular retinol-binding protein-bound retinal, with a Km of appr
63 esponse tests work on the principle that apo-retinol-binding protein builds up in the liver as liver
64 y using high-pressure liquid chromatography, retinol-binding protein by using ELISA, and alanine amin
66 and serum amyloid-A and an increase in serum retinol-binding protein compared with placebo (p < .05).
71 toward retinoids in the presence of cellular retinol-binding protein (CRBP) type I or cellular retina
72 e lipid-binding protein (KLBP), the cellular retinol-binding protein (CRBP), and the cellular retinoi
73 ic-acid-binding protein (CRABP) and cellular retinol-binding protein (CRBP), as well as their relatio
74 RA biosynthesis pathway consists of cellular retinol-binding protein (Crbp), retinol dehydrogenase (D
80 ow that Rald is present in rodent fat, binds retinol-binding proteins (CRBP1, RBP4), inhibits adipoge
81 ol), and proximal renal tubular dysfunction (retinol-binding protein/creatinine ratio >2.93mug/mmol a
84 ein II (CRBP II) is a member of the cellular retinol-binding protein family, which is expressed prima
86 tamin A is transported in the blood bound to retinol-binding protein (holo-RBP), and its target cells
88 ding serum retinol binding protein, cellular retinol binding protein I and cellular retinol binding p
90 cyl chloromethyl ketone (AcDCMK) or cellular retinol-binding protein I (CRBP) diminished the generati
93 e structure and dynamics of rat apo-cellular retinol binding protein II (apo-CRBP II) in solution has
94 protein cavity, we redesigned human cellular retinol binding protein II (hCRBPII) to fully encapsulat
95 cid increases the mRNA level of the cellular retinol binding protein II and the rate of retinol uptak
96 lular retinol binding protein I and cellular retinol binding protein II have been disrupted by homolo
97 inol-binding protein I (CRBP I) and cellular retinol-binding protein II (CRBP II) are closely homolog
100 e and backbone dynamics of rat holo cellular retinol-binding protein II (holo-CRBP II) in solution ha
101 fter CM-RE uptake, the levels of retinol and retinol-binding protein in serum, and retinoid levels in
102 mechanism for the uptake of retinol bound to retinol-binding protein in the small intestine of suckli
104 s (ferritin, serum transferrin receptor, and retinol binding protein) in settings of prevalent inflam
105 d missense mutations in RBP4, encoding serum retinol binding protein, in three families with eye malf
106 is transported to and taken up by the eye by retinol-binding protein-independent and retinoic acid-re
107 the ability of M-TTR to form a complex with retinol binding protein, indicate that M-TTR forms a ter
108 me oxygenase-1 (HO-1) and interphotoreceptor retinol binding protein (IRBP) were determined 1 to 2 da
111 5 ng/mL or 32 pmol/L), vitamin A deficiency (retinol-binding protein <14.7 mug/mL or 0.70 mumol/L) an
113 luded height for age at 10 weeks, vitamin D, retinol binding protein, maternal education, household i
114 le transferrin receptor or vitamin A status (retinol-binding protein or retinol)] and >/=1 biomarker
115 ons as the high-affinity receptor for plasma retinol binding protein (RBP) and mediates cellular upta
118 transports vitamin A from its blood carrier retinol binding protein (RBP) into cells, and it also fu
121 s transported in the blood as a complex with retinol binding protein (RBP), but the molecular mechani
124 ular-weight proteins beta2-microglobulin and retinol binding protein (RBP)], although other measures
126 reported previously that mice lacking plasma retinol-binding protein (RBP) are phenotypically normal
127 Binding of the natural ligands thyroxine or retinol-binding protein (RBP) by Ser52Pro variant TTR st
129 The molten globule state of human serum retinol-binding protein (RBP) has been postulated previo
131 ate uptake of retinol from its blood carrier retinol-binding protein (RBP) into cells and to function
136 s, respectively: serum retinol, 90% and 78%; retinol-binding protein (RBP), 40% and 91%; retinol/RBP
137 aditional RDR test, could be circumvented if retinol-binding protein (RBP), a more stable marker of V
138 oss of CMOI function studies in mice lacking retinol-binding protein (RBP), an established model of e
140 inol is transported around the body bound to retinol-binding protein (RBP), is transferred across the
151 molecule metabolically interacting with TTR [retinol-binding protein (RBP)], for possible association
152 on retinyl esters (CM-REs), retinol bound to retinol-binding protein (RBP-ROH), and total retinol wer
154 f mice with a pNO(2)Phe(43) mutant of murine retinol-binding protein (RBP4) also elicited a high tite
159 Our aim was to elucidate the role of the retinol-binding protein receptor STRA6, mediating cellul
160 ascade, suppressed CRBP-I/RARalpha (cellular retinol-binding protein/retinoic acid receptor alpha) ex
161 entify SAAs as a family of microbe-inducible retinol binding proteins, reveal a unique protein archit
162 media did not result from increased retinol-retinol-binding protein secretion but was dependent on t
163 least one retinoid binding protein (cellular retinol binding protein) serves as a retinoid concentrat
166 retinoid-binding protein (IRBP) or cellular retinol-binding protein, suggesting that peropsin plays
168 binding protein (CRBP)-III, an intracellular retinol-binding protein that is expressed solely in hear
169 nstitutive serum protein levels (prealbumin, retinol binding protein, transferrin) and decreased seru
170 riptionally up-regulated by RA, the cellular retinol binding protein type I (CRBPI) and the RA recept
172 by the enterocyte is complexed with cellular retinol-binding protein type 2 and the complex serves as
174 etinol oxidation in the presence of cellular retinol-binding protein type I (CRBPI) than human micros
176 esence of a 10-fold molar excess of cellular retinol-binding protein type I, which is believed to seq
177 9cRA)-inducible enhancer of the rat cellular retinol-binding protein type II gene (CRBP II) was shown
178 ulation (3-4-fold) in the level of cytosolic retinol-binding protein type III (CRBPIII) in adipose ti
181 -binding protein, type I (CrbpI), encoded by retinol-binding protein, type 1 (Rbp1), is a chaperone o
189 friendly approaches are hemoglobin (anemia), retinol-binding protein (vitamin A), and iron (transferr
191 toichiometry of three interacting molecules, retinol-binding protein, vitamin A, and L-thyroxine, not
195 reception in mice, animals mutated in plasma retinol binding protein were placed on a vitamin A-free
197 therefore represents a novel class of small retinol-binding protein, which appears to be confined to
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。