ライフサイエンスコーパス: lipocalin

1 ecule-1 and neutrophil gelatinase-associated lipocalin).

2 ecule-1 and neutrophil gelatinase-associated lipocalin.

3 the same protein, which was identified as a lipocalin.

4 , junb, and neutrophil gelatinase-associated lipocalin.

5 tact PCs in tears are native ligands of tear lipocalin.

6 activation neutrophil gelatinase-associated lipocalin.

7 in response to allergenic and nonallergenic lipocalins.

8 s from house dust mites and cockroaches, and lipocalins.

9 days were categorized as secreted, including lipocalins.

10 lar pocket is similar among human and animal lipocalins.

11 -based immunosensing technique for detecting lipocalin 1 (LCN1), a DR biomarker.

12 ge markers, neutrophil gelatinase-associated lipocalin 1, and interleukin 6 were also assessed.

13 e 3' clustering of rare codons, unlike human lipocalin-1 and 21 other widely expressed human tear gen

14 Mechanistically, LINC00305 interacted with lipocalin-1 interacting membrane receptor (LIMR), enhanc

15 g proteins-zinc-alpha2-glycoprotein (AZGP1), Lipocalin-1, Albumin, S100A7, S100A8 and S100A9-revealed

16 nferior for neutrophil gelatinase-associated lipocalin [14.7 mug/L (interquartile range 7.60-28.9) vs

17 Lipocalin 2 (LCN-2) is an innate immune protein that is

18 usly secretion of the iron chelating protein lipocalin 2 (LCN2) and protons, which acidify the urine.

19 We have recently characterized the role of lipocalin 2 (Lcn2) as a new adipose-derived cytokine in

20 Here, we identify lipocalin 2 (lcn2) as an inducible factor that is secret

21 ough molecular and genetic analyses in mice, lipocalin 2 (LCN2) as an osteoblast-enriched, secreted p

22 We identified lipocalin 2 (LCN2) as both a marker of deactivated macro

23 hils rely on the siderophore-binding protein lipocalin 2 (Lcn2) in a "tug-of-war" for iron.

24 Lipocalin 2 (LCN2) is a novel adipokine that negatively

25 The innate immune protein lipocalin 2 (Lcn2) is able to specifically bind Ent and

26 We have previously demonstrated that lipocalin 2 (LCN2) is an innate immunity protein that bi

27 how that a mutant form (K3Cys) of endogenous lipocalin 2 (LCN2) is filtered by the kidney but can byp

28 Lipocalin 2 (LCN2) regulates infection response and incr

29 Upregulation of S100A8, S100A9, and lipocalin 2 (LCN2) were confirmed by Western blots, and

30 at tNLGs mediate a potent CRISPR knockout of Lipocalin 2 (Lcn2), a known breast cancer oncogene, in h

31 Lipocalin 2 (Lcn2), a member of the lipocalin family, is

32 In this study, we report that lipocalin 2 (Lcn2), a recently characterized adipokine/c

33 d the potential of cerebrospinal fluid (CSF) lipocalin 2 (LCN2), a secreted glycoprotein that has bee

34 Lipocalin 2 (LCN2), a siderophore-binding protein, is in

35 ulating levels of the secreted glycoprotein, lipocalin 2 (Lcn2), an adipokine previously associated w

36 Lipocalin 2 (Lcn2), an innate immune protein, has emerge

37 s-including kidney injury molecule-1 (Kim1), lipocalin 2 (Lcn2), and keratin 8 (Krt8)-and of several

38 However, Ent is bound by the host protein lipocalin 2 (Lcn2), preventing bacterial reuptake of afe

39 oprotection markers, including COX-2 itself, lipocalin 2 (LCN2), tissue inhibitor of metalloproteinas

40 gainst K. pneumoniae, which was dependent on lipocalin 2 (LCN2).

41 Lipocalin 2 (Lcn2; 24p3; neutrophil gelatinase-associate

42 ine and secreting the bacteriostatic protein lipocalin 2 (LCN2; also known as NGAL).

43 Lipocalin 2 (Lcn2; siderocalin, 24p3) plays a central ro

44 Lipocalin 2 (Lpc-2) was the best protein biomarker of se

45 osterone system (RAAS) activation, and serum lipocalin 2 and biomarkers of inflammation and cardiac s

46 Lipocalin 2 is highly expressed in the lung where it exe

47 Lipocalin 2 levels increased with RAAS activation compar

48 Lipocalin 2 may be important in modulating aldosterone-i

49 Although lipocalin 2 production was observed to be Dectin-1 and I

50 Importantly, exogenous lipocalin 2 rescued viral exacerbation of S. aureus infe

51 8 signaling is required for the induction of lipocalin 2 secretion and iron sequestration in the sple

52 ory factors such as dietary iron and luminal lipocalin 2 should be taken into consideration for optim

53 During RAAS activation, lipocalin 2 was related to biomarkers of inflammation (t

54 that use catecholate-type siderophores, and lipocalin 2(-/-) mice are highly susceptible to infectio

55 rtened colons, and increased fecal levels of lipocalin 2), metabolic syndrome, and an inability to cl

56 ain Salmonella by promoting the induction of lipocalin 2, a host antimicrobial factor that inhibits b

57 s survival advantage is counter-regulated by lipocalin 2, a siderophore-binding host protein, which r

58 ated adipocytes-namely, coenzyme A synthase, lipocalin 2, and cortactin.

59 F9, IL-6, IL-19, CCL20, S100A7/A8/A9, DEFB4, lipocalin 2, and peptidase inhibitor 3 (p < 0.05), indic

60 We demonstrate that similar to lipocalin 2, Bet v 1 is capable of binding iron via cate

61 bial protein siderocalin (SCN; also known as lipocalin 2, neutrophil gelatinase-associated lipocalin/

62 vercome iron restriction by the host protein lipocalin 2, which counteracts some siderophores, is ess

63 observed to be Dectin-1 and IL-22 dependent, lipocalin 2-deficient mice did not demonstrate impaired

64 phimurium is unaffected by E. coli Nissle in lipocalin 2-deficient mice.

65 ounter-regulated by the presence of iron and lipocalin 2.

66 h a striking structural resemblance to human lipocalin 2.

67 8; CCL20/FCH, 8.36; PI3 [elafin]/FCH, 15.40; lipocalin 2/FCH, 6.94, human beta-defensin 2 [DEFB4A]/FC

68 helial-derived antimicrobial factors such as lipocalin-2 (LCN-2), a protein that specifically inhibit

69 n was associated with PAMP translocation and lipocalin-2 (LCN2) and chemokine (C-X-C motif) ligand 1

70 hin the CSF express the iron-binding protein lipocalin-2 (LCN2) and its receptor SCL22A17.

71 he antimicrobial siderophore-binding peptide Lipocalin-2 (Lcn2) are observed in inflammatory bowel di

72 and vehicle-treated DIO mice, we identified lipocalin-2 (Lcn2) as the gene most strongly upregulated

73 ich immunoassay (IA) was developed for human lipocalin-2 (LCN2) by functionalizing a KOH-treated poly

74 Lipocalin-2 (LCN2) emerged as a relevant adipokine invol

75 Unexpectedly, the lipocalin-2 (Lcn2) gene, which encodes neutrophil gelati

76 Lipocalin-2 (Lcn2) is a biomarker for many inflammatory-

77 Lipocalin-2 (Lcn2) is an innate immune protein elevated

78 Lipocalin-2 (LCN2) is secreted from adipocytes, and its

79 thelicidin antimicrobial protein (Camp), and lipocalin-2 (Lcn2) mRNA expression giving rise to cells

80 Lipocalin-2 (LCN2) promotes malignant development in man

81 In the mouse, the osteoblast-derived hormone Lipocalin-2 (LCN2) suppresses food intake and acts as a

82 Lipocalin-2 (LCN2) was originally isolated from human ne

83 over 100 different cytokines, we found that Lipocalin-2 (LCN2) was the most substantially elevated p

84 SubAB induces expression of a novel form of Lipocalin-2 (LCN2), and describe its biological activity

85 levels of a specific inflammatory cytokine, lipocalin-2 (LCN2), were elevated in the plasmas of pati

86 regulated factors is the acute phase protein lipocalin-2 (LCN2).

87 docrine function of bone that is mediated by Lipocalin-2 (LCN2).

88 an overcome metal ion starvation mediated by lipocalin-2 and calprotectin via alternative pathways, I

89 ression of antimicrobial proteins, including lipocalin-2 and calprotectin, which sequester essential

90 l ADC decrease and elevated plasma levels of lipocalin-2 and microRNA-150, was associated with a fata

91 ed by the immobilization of rabbit polygonal lipocalin-2 antibody on gold nanoparticles attached on g

92 m of MMA-associated kidney disease, identify lipocalin-2 as a biomarker of increased oxidative stress

93 Finally, we identify lipocalin-2 as the key secreted factor downstream of Tcf

94 that STAT1 is required for IFNgamma-induced lipocalin-2 expression in murine adipocytes.

95 atic inflammation-related proteins including lipocalin-2 in db/db mice were attenuated by CR.

96 g others suppressor of cytokine signaling-3, lipocalin-2, and alpha1-antichymotrypsin.

97 ion of biomarkers, including K16, Ki67, CD3, lipocalin-2, CD11c, dendritic cell lysosome-associated m

98 Recently, the secreted protein 24p3 (lipocalin-2, neutrophil gelatinase-associated lipocalin

99 bial protein siderocalin (SCN; also known as lipocalin-2, neutrophil gelatinase-associated lipocalin,

100 ys identified numerous biomarkers, including lipocalin-2, which was then used to monitor the response

101 trophils from mice genetically deficient for lipocalin 24p3 (24p3(-/-)) are defective in many neutrop

102 Lipocalin 24p3 (24p3) is a neutrophil secondary granule

103 ng siderophore synthesis while up-regulating lipocalin 24p3 expression via TLR signaling.

104 However, a general role for the lipocalin 24p3 in the hematopoietic system has not been

105 cretes siderophore-binding proteins, such as lipocalin 24p3, which limit siderophore-mediated iron im

106 of urinary neutrophil gelatinase-associated lipocalin after the 2 infusions (P = 0.917).

107 The recently identified dog lipocalin allergen Can f 4 is an important respiratory a

108 an in vitro system we compared the effect of lipocalin allergens and nonallergenic homologues on huma

109 Sequence similarities between the lipocalin allergens Can f 6, Fel d 4 (cat) and Equ c 1 (

110 Accordingly, deficient loading of lipocalin allergens establishes their capacity to induce

111 induces IL-10 expression by DCs treated with lipocalin allergens, attenuating the T(H)2 bias and indu

112 gen Can f 6, a member of a distinct class of lipocalin allergens, has very similar properties to Fel

113 , hLCN1 and hLCN2, and most important animal lipocalin allergens, such as Can f 1, Can f 2 and Can f

114 as major facilitator family transporters and lipocalins, also reflect the evolution of xenobiotic ada

115 ntration of neutrophil gelatinase-associated lipocalin, an established AKI biomarker, and the associa

116 utility of neutrophil gelatinase-associated lipocalin and creatinine, alone and in combination, for

117 ty, and for neutrophil gelatinase-associated lipocalin and cystatin C, with poorer survival.

118 Neutrophil gelatinase-associated lipocalin and liver fatty acid-binding protein associati

119 ast-derived metabolic hormones (osteocalcin, lipocalin and sclerostin) and the clinical evidence that

120 Urinary neutrophil gelatinase-associated lipocalin and urinary kidney injury molecule 1 predicted

121 oth urinary neutrophil gelatinase-associated lipocalin and varying creatinine-based metrics of renal

122 ed transcripts with contigs with identity to lipocalins and acid tail proteins being the most represe

123 We examined whether lipocalins and FPR3 colocalize within the cells by using

124 lasma NGAL (neutrophil gelatinase-associated lipocalin) and NT-proBNP (N-terminal pro-B-type natriure

125 ecule-1 and neutrophil gelatinase-associated lipocalin, and doses>/=0.005 mg/kg induced the early res

126 n C (Scyc), neutrophil gelatinase-associated lipocalin, and interleukin-18 in predicting early graft

127 tor (CTGF), neutrophil gelatinase-associated lipocalin, and kidney injury molecule-1 (KIM-1).

128 Biomarkers, neutrophil gelatinase-associated lipocalin, and kidney injury molecule-1 were successfull

129 These included lysozyme, lactoferrin, tear lipocalin, and lacritin.

130 , histones, neutrophil gelatinase-associated lipocalin, and proteinase-3) were elevated in the blood

131 protein B1, neutrophil gelatinase-associated lipocalin, and S100B were higher in nonsurvivors than su

132 iostin, and neutrophil gelatinase-associated lipocalin; and a two-fold decrease in glycosylated clust

133 Thereby, lipocalins are able to transport a variety of biological

134 Levels of human lipocalins are elevated in nonallergic inflammation and

135 Among the latter especially lipocalins are multifaceted: they may have an immunomodu

136 the formyl peptide receptor 3 in allergy to lipocalins are outstanding examples of research into the

137 Serum neutrophil gelatinase-associated lipocalin at day 3 was lower in the NEVKP group (1267 +/

138 sits in a closed pocket at the centre of the lipocalin barrel.

139 We anticipate that lipocalin-based ON-switches have the potential to be bro

140 Only the tear lipocalin-bearing fractions showed phosphocholines (104

141 of urinary neutrophil gelatinase-associated lipocalin best predicted the primary outcome when measur

142 loop protruding from strands 5 and 6 of the lipocalin beta-barrel.

143 mitting FAPs has been created from bacterial lipocalin Blc (named DiBs).

144 Cathepsin S-digested allergenic lipocalins, but not digestion products of nonallergenic

145 c activity and cross-reactivity with the dog lipocalin Can f 1.

146 FPR3 and lipocalins colocalize in the same vesicles in DCs.

147 y inducing the release of a mosquito lipoxin/lipocalin complex.

148 show that this factor consists of a Lipoxin/Lipocalin complex.

149 ive patterns were observed between different lipocalin components.

150 ukin-6, and neutrophil gelatinase-associated lipocalin concentrations.

151 hough the intact phospholipids bound to tear lipocalin corresponded precisely in mass and relative si

152 ntin [OPN], neutrophil gelatinase-associated lipocalin, cystatin C, trefoil factor 3, tissue inhibito

153 Can f 6 is a new lipocalin dog allergen that cross-reacts with lipocalins

154 Differential expression of these I. ricinus lipocalins during feeding at distinct developmental stag

155 man retinol binding protein 4 (hRBP4) of the lipocalin family interacts with engineered hRBP4 binders

156 emonstrate the Plasmodium-tailored role of a lipocalin family member in hemozoin formation and unders

157 LCN13 is a lipocalin family member involved in glucose metabolism,

158 Apolipoprotein M (apoM), a lipocalin family member, preferentially associates with

159 Swim, a putative member of the Lipocalin family of extracellular transport proteins, bi

160 The C8gamma subunit, a member of the lipocalin family of proteins that bind and transport sma

161 expression of Evokin (a lipid carrier of the lipocalin family), and in their ability to convert arach

162 Apolipoprotein D (apoD), a member of the lipocalin family, is a 29-kDa secreted glycoprotein that

163 Lipocalin 2 (Lcn2), a member of the lipocalin family, is up-regulated in a variety of epithe

164 beta-Lactoglobulin (BLG) is a member of lipocalin family, proteins with ability to bind small hy

165 mmalian siderophore-binding protein from the lipocalin family, specifically binds lanthanide and acti

166 -pi interactions have been overlooked in the lipocalin family.

167 113 crystal and solution structures from the lipocalin family.

168 ions were uncovered in TL and throughout the lipocalin family.

169 d the prevalence of sensitization to the cat lipocalin Fel d 7 among 140 cat-sensitized Swedish patie

170 mucus, reveals a glycosylated protein with a lipocalin fold.

171 ng a 10-stranded beta-barrel with a modified lipocalin fold.

172 ures of Japanin, an 18 kDa immune-modulatory lipocalin from the Brown Ear Tick (Rhipicephalus appendi

173 ipocalin dog allergen that cross-reacts with lipocalins from horse and cat.

174 m molecules neutrophil gelatinase-associated lipocalin, galectin-3, and lipocalin-like prostaglandin

175 Contrary to previously identified tomato lipocalin gene DQ222981, SlVRSLip was not regulated by c

176 This lipocalin had no cross-reactivity with common and golden

177 TL, a prominent and promiscuous lipocalin, has a key role in lipid binding at the ocular

178 ructure, polymorphism and functions of these lipocalins have been well described in the western Europ

179 robust predictions showing these I. ricinus lipocalins have the potential to bind monoamines similar

180 or proteins neutrophil gelatinase-associated lipocalin, hemopexin, and transferrin were increased in

181 , including neutrophil gelatinase-associated lipocalin, high-mobility group protein B1, intracellular

182 r similarity analysis of human and mammalian lipocalins highlights their function in innate immunity

183 rposition modeling were compared among human lipocalins, hLCN1 and hLCN2, and most important animal l

184 ker levels (neutrophil gelatinase-associated lipocalin, IL-18, and kidney injury molecule-1 measured

185 biomarkers: neutrophil gelatinase-associated lipocalin, IL-18, kidney injury molecule-1 (KIM-1), live

186 eak urinary neutrophil gelatinase-associated lipocalin, IL-18, KIM-1, liver fatty acid binding protei

187 Beta-lactoglobulin (BLG) is a bovine lipocalin in milk with an innate defense function.

188 recipitation verified FODE complexed to tear lipocalin in tears.

189 FODE is bound to tear lipocalin in tears.

190 ced urinary neutrophil gelatinase-associated lipocalin in the first week posttransplant.

191 kers (e.g., neutrophil gelatinase-associated lipocalin) in this patient group.

192 Limb development membrane protein-1 (LMBR1)/lipocalin-interacting membrane receptor (LIMR)-type prot

193 Despite the fact that tear lipocalin is reduced in dry eye patients, FODE removal f

194 Multi-sensitization towards lipocalin, kallikrein and secretoglobin components is as

195 to other severe asthmatics positive to fewer lipocalin/kallikrein/secretoglobin components.

196 rleukin 18, neutrophil gelatinase-associated lipocalin, kidney injury molecule 1, and liver fatty aci

197 cystatin C, neutrophil gelatinase-associated lipocalin, kidney injury molecule-1, and IL-18 in 528 pa

198 jury (urine neutrophil gelatinase-associated lipocalin, kidney injury molecule-1, calbindin), followe

199 croalbumin, neutrophil gelatinase-associated lipocalin, kidney injury molecule-1, IL-18, and liver-ty

200 rs (urinary neutrophil gelatinase-associated lipocalin, kidney injury molecule-1, urinary liver-type

201 in (CLU), glycoproteins IIb/IIIa (ITGA2B/3), lipocalin (LCN2), lactoferrin (LTF), and the thrombopoet

202 chloroplastic lipocalin, now renamed plastid lipocalin (LCNP).

203 and plasma neutrophil gelatinase-associated lipocalin level higher than 150 ng/mL enrolled between A

204 enrollment neutrophil gelatinase-associated lipocalin level was independently associated with surviv

205 enrollment neutrophil gelatinase-associated lipocalin level was the greatest (c-statistic, 0.78 [95%

206 Serum neutrophil gelatinase-associated lipocalin levels are strongly predictive of survival-to-

207 SlVRSLip is the first lipocalin-like gene shown to be involved in resistance t

208 iopsy and assayed for the urinary biomarkers lipocalin-like prostaglandin D synthase (L-PGDS), alpha(

209 tinase-associated lipocalin, galectin-3, and lipocalin-like prostaglandin D2 synthase with an MRA.

210 e give structural evidence that Bet v 1 is a lipocalin-like protein with a striking structural resemb

211 a parasite species secrete and internalize a lipocalin-like protein, PV5, to control heme crystalliza

212 ted by TYLCV infection was a gene encoding a lipocalin-like protein.

213 NGAL/LCN2 (neutrophil gelatinase-associated lipocalin/lipocalin 2), a secreted glycoprotein that bin

214 initial and neutrophil gelatinase-associated lipocalin measured 3 hours after cardiopulmonary bypass

215 eas GFR and neutrophil gelatinase-associated lipocalin, monocyte chemoattractant protein-1, and tumor

216 n levels of neutrophil gelatinase-associated lipocalin, monocyte chemoattractant protein-1, and tumor

217 The lipocalin mouse 24p3 has been implicated in diverse phys

218 fication of neutrophil gelatinase-associated lipocalin mRNA.

219 Neutrophil gelatinase-associated lipocalin, myeloperoxidase, and intracellular ROS levels

220 dney Injury Neutrophil Gelatinase-Associated Lipocalin [N-GAL] Evaluation of Symptomatic Heart Failur

221 , including neutrophil gelatinase-associated lipocalin (NGAL) and podocalyxin, concomitant with upreg

222 (CysC) and neutrophil gelatinase-associated lipocalin (NGAL) can predict development of renal dysfun

223 MMP-9/neutrophil gelatinase-associated lipocalin (NGAL) complex is also significantly increased

224 osensor for neutrophil gelatinase-associated lipocalin (NGAL) detection has been developed.

225 ich encodes neutrophil gelatinase-associated lipocalin (NGAL) had the highest fold increase (~60).

226 Urinary neutrophil gelatinase-associated lipocalin (NGAL) has emerged an early marker protein, pr

227 tic role of neutrophil gelatinase-associated lipocalin (NGAL) in a large population of patients with

228 Neutrophil gelatinase-associated lipocalin (NGAL) is a diagnostic marker of intrinsic kid

229 Neutrophil gelatinase-associated lipocalin (NGAL) is a novel renal biomarker that may pre

230 Neutrophil gelatinase-associated lipocalin (NGAL) is an early marker of acute kidney inju

231 etection of neutrophil gelatinase-associated lipocalin (NGAL) is developed by the immobilization of r

232 ion between neutrophil gelatinase-associated lipocalin (NGAL) levels and cardiovascular and all-cause

233 Human neutrophil gelatinase associated lipocalin (NGAL) was found to be involved in 1alpha,25(O

234 el of urine neutrophil gelatinase-associated lipocalin (NGAL) was lower (P = 0.031) in the treated gr

235 MMP-9, and neutrophil gelatinase-associated lipocalin (NGAL) were found in diseased groups compared

236 biotin, and neutrophil gelatinase-associated lipocalin (NGAL) were the most robust markers but were n

237 ipocalin-2, neutrophil gelatinase-associated lipocalin (NGAL)), which is expressed in the distal neph

238 e of plasma neutrophil gelatinase-associated lipocalin (NGAL), a novel marker of renal tubular damage

239 asmin (CP), neutrophil gelatinase-associated lipocalin (NGAL), and monocyte chemotactic protein 1 (MC

240 biomarker, neutrophil gelatinase associated lipocalin (NGAL), combined with contemporary biomarkers

241 values for neutrophil gelatinase-associated lipocalin (NGAL), interleukin-18 (IL-18), kidney injury

242 d levels of neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1) and e

243 Urine neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1), IL-1

244 croalbumin, neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1), IL-1

245 , including neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1), live

246 in (IL)-18, neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1, serum creati

247 Urinary neutrophil gelatinase-associated lipocalin (NGAL), monomeric NGAL (mNGAL), interleukin-18

248 etection of neutrophil gelatinase-associated lipocalin (NGAL), which is a new diagnostic marker of ac

249 and termed neutrophil gelatinase-associated lipocalin (NGAL).

250 and plasma neutrophil gelatinase-associated lipocalin (NGAL); each measurement was on the day of AKI

251 The neutrophil gelatinase-associated lipocalin (NGAL, also known as LCN2) and its cellular re

252 [KIM-1] and neutrophil gelatinase-associated lipocalin [NGAL]) and oxidative stress (8-hydroxy-2'-deo

253 Lcn2; 24p3; neutrophil gelatinase-associated lipocalin [NGAL]) is an antimicrobial host defense facto

254 , KIM-1 and neutrophil gelatinase-associated lipocalin, NGAL), kidney growth, and glomerulosclerosis,

255 , suPAR and neutrophil gelatinase-associated lipocalin, NGAL.

256 ipocalin 2, neutrophil gelatinase-associated lipocalin/NGAL, or 24p3).

257 o more than three animal-derived components--lipocalin (nMus m 1, rEqu c 1, Fel d 4, rCan f 1, 2), ka

258 orophyllide a oxygenase or the chloroplastic lipocalin, now renamed plastid lipocalin (LCNP).

259 y for urine neutrophil gelatinase-associated lipocalin on the day after surgery.

260 rs and determine the molecules bound to tear lipocalin or other proteins.

261 ipocalin-2, neutrophil gelatinase-associated lipocalin, or 24p3) into the urinary tract.

262 GDS) siRNA and its inhibitor HQL-79, but not lipocalin PGDS (L-PGDS) siRNA and its inhibitor AT-56, s

263 mokine, and CCL26/eotaxin-3), T(H)17/T(H)22 (lipocalins, PI3/elafin, CCL20, S100A7/S100A8/S100A9, and

264 gamma2 were found to have elevated levels of Lipocalin prostaglandin D synthase (L-PGDS) expression i

265 In this study, we define a new role for lipocalin prostaglandin D synthase (L-PGDS) in the contr

266 The lipocalin protein family harbours allergens in mammalian

267 h levels of neutrophil gelatinase-associated lipocalin representing acute tubular injury (corrected R

268 itrogen and neutrophil gelatinase-associated lipocalin, respectively.

269 HL-HDLs showed a reduced content of lipocalin retinol binding protein 4 and apolipoprotein M

270 Tear lipocalin retrieves lipid rapidly from the human ocular

271 surface and to test the hypothesis that tear lipocalin retrieves lipids from the eyes of normal and d

272 num lycopersicum virus resistant/susceptible lipocalin (SlVRSLip).

273 employed in this study characterized unique lipocalins that play a role in tick blood-feeding and tr

274 es the three I. ricinus lipocalins with tick lipocalins that sequester monoamines, leukotrienes and f

275 transcriptome for specific, uncharacterized lipocalins: three were identified.

276 Temperature-induced lipocalins (TILs) play an essential role in the response

277 ons were tested experimentally in human tear lipocalin (TL).

278 IL)-18, and neutrophil gelatinase-associated lipocalin to predict PNF and DGF in 335 DCD kidneys pres

279 IL-18, and neutrophil gelatinase-associated lipocalin to predict viability of DCD kidneys varies fro

280 increase in neutrophil gelatinase-associated lipocalin to suggest tubular injury.

281 We hypothesize that binding of allergenic lipocalins to FPR3 might be a mechanism for induction of

282 milies (EF-hand, Tropomyosin, CAP, Profilin, Lipocalin, Trypsin-like serine protease, Cupin, BetV1, E

283 Renal vein neutrophil gelatinase-associated lipocalin, tumor necrosis factor-alpha, monocyte chemoat

284 secrete PGD2 in proinflammatory conditions, Lipocalin-type prostaglandin D synthase (L-PGDS) express

285 d rise in COX (cyclooxygenase)-2 and L-PGDS (lipocalin-type prostaglandin D synthase) expression, whi

286 We show in this paper that lipocalin-type prostaglandin D2 (PGD2) synthase (L-PGDS)

287 t retinaldehyde dehydrogenase 2 (RALDH2) and lipocalin-type prostaglandin D2 synthase (LPGDS), which,

288 The levels of WIHN, lipocalin-type prostaglandin D2 synthase (Ptgds), and it

289 Among these are lipocalins, ubiquitous barrel-shaped proteins that seque

290 her urinary neutrophil gelatinase-associated lipocalin (uNGAL) can accurately predict persistent AKI,

291 el of urine neutrophil gelatinase-associated lipocalin (uNGAL) for diagnosing AKI and its prognostic

292 rker (urine neutrophil gelatinase-associated lipocalin [uNGAL]), forming a composite biomarker for pr

293 0.05), and neutrophil gelatinase-associated lipocalin urine protein (55.6 +/- 21.3 mug/mL versus 2.7

294 Separation of tear lipocalin was confirmed by SDS tricine gradient PAGE.

295 Urinary neutrophil gelatinase-associated lipocalin was measured at baseline and again less than 1

296 but urinary neutrophil gelatinase-associated lipocalin was most useful (81% specificity, 68% sensitiv

297 Urine neutrophil gelatinase-associated lipocalin was the most sensitive marker among those stud

298 , and NGAL [neutrophil gelatinase-associated lipocalin]) were evaluated (N=105).

299 ing urinary neutrophil gelatinase-associated lipocalin with a novel creatinine-based metric, both ava

300 ng 803 sequences places the three I. ricinus lipocalins with tick lipocalins that sequester monoamine