ライフサイエンスコーパス: HA

1 HA and M2 are strongly coclustered in the plasma membran

2 HA degradation requires either ERManI enzymatic activity

3 HA digestion in wild type NSC cultures or in the SGZ ind

4 HA dose-dependently inhibited TLR2-induced TNF-alpha pro

5 HA is known to swell, fitting a linear elastic model wit

6 HA is synthesized by NSCs and increases in the SGZ with

7 HA polymers are rationally designed from relatively low-

8 HA was determined by a competition between the coating H

9 at residues 156, 158, 189, and 193 of MN/10 HA to those in BJ/92 switched the MN/10 antigenic phenot

10 Compared to nHA-LC, Ostim((R)) (35% HA content) showed less and smaller particle agglomerate

11 The nHA-LC (38% HA content) paste supported bone formation with a high d

12 We found that, when segment 4 (HA) of coinfecting parental viruses was modified, there

13 on The highly concentrated nHA-HC paste (48% HA content) formed oversized particle agglomerates which

14 ophilia A (AHA) and congenital hemophilia A (HA) are primarily directed to the A2 and C2 domains.

15 ixtures (200 mmol/L) high in either acetate (HA), propionate (HP), butyrate (HB) or placebo (PLA) wer

16 changing, for instance, the pKa of the acid HA versus the concentration or partial pressure of a rea

17 s using the common PCR inhibitor humic acid (HA) as a model.

18 nd Ag(+) in solution when adding humic acid (HA) to bacterial suspensions.

19 h is relatively enriched in hyaluronic acid (HA) and flexible.

20 ime-dependent deposition of hyaluronic acid (HA) and increased expression of markers for alternative

21 ing pathological amounts of hyaluronic acid (HA) or chondroitin sulfate (CS) did not directly increas

22 gional interactions between hyaluronic acid (HA), collagen and the spatial origins of mechanical stre

23 bolism and the signaling of hyaluronic acid (HA), the major component of the extracellular matrix (EC

24 on [D-dimer], and fibrosis (hyaluronic acid [HA]) were measured at baseline and through 96 weeks of A

25 id (SA), natural organic matter (humic acid, HA), and dissolved silicates.

26 Hyaluronan (hyaluronic acid; HA) instillation to the bladder has been used to treat K

27 particles loaded with hydroxycinnamic acids (HA-NCs) have diameter of 224-253nm, encapsulation effici

28 TOP-PCR adopts homogeneous "half adaptor" (HA), generated by annealing P oligo (carrying a phosphat

29 Additionally, HA and HC-HA/PTX3 inhibited migration but only HC-HA/PTX

30 ood supply to bile duct and lack of adequate HA flow is thought to be a risk factor for biliary compl

31 th its ability to induce homotypic adhesion (HA).

32 H3N2 strains, the acute Ab response against HA exhibited an inherent bias toward lambda L chain usag

33 othelial barrier-associated protein, altered HA production, and induced abnormal urothelial different

34 18 days of exposure to 3454 m high altitude (HA) without drug intervention (control, CONT) as well as

35 Anti-CD44 Ab and HA treatments reduced NF-kappaB translocation, IL-1beta

36 yos, HYAL2 and HA were readily detected, and HA levels decreased with age.

37 RP, TNF, sIL-6R, I-FABP, sCD14, D-dimer, and HA levels were elevated in acute HIV infection.

38 Conversely, CA, FA, and HA increased Pu sorption to goethite at pH 3, suggesting

39 t with this, in wild-type embryos, HYAL2 and HA were readily detected, and HA levels decreased with a

40 A single reassortant with the NP and HA gene segments from CIV-H3N2 was selected for characte

41 or (HR) expression were detected by qPCR and HA secretion by enzymatic immunoassay.

42 aman bands associated with the scaffolds and HA with the spatial offset depended on the depth at whic

43 lucidate the differences in trogocytosis and HA formation mediated by anti-CD20 mAbs RTX and GA101, a

44 antly increased accumulation of versican and HA, especially in the perivascular and peribronchial reg

45 Anti-HA antibodies bind to, but do not neutralize, the report

46 Anti-HA antibodies were cross-reactive against multiple subty

47 ricted, leukemia-associated minor H antigen, HA-1; (2) a CD8 coreceptor to promote function of the cl

48 A (HAAA) sections compared to normal aortae (HA).

49 Hepatocyte area (HA) and lobule radius (LR) were also measured.

50 e effect of lower measured hepatic arterial (HA) flow (<400 mL/min) on biliary complications and graf

51 that, in several mouse tumour models such as HA-expressing 4T1 mammary carcinoma cells, OVA-expressin

52 NSC proliferation, and CD44-null as well as HA-disrupted wild type NSCs demonstrate delayed neuronal

53 Surface-associated HA was required for eIF4E's oncogenic activities suggest

54 Specifically, HR was increased at HA from 64 +/- 10 to 74 +/- 12 beats min(-1) during the

55 Unexpectedly, the sympathoactivation at HA that was evidenced by increased circulating noradrena

56 ation of both Eley-Rideal (ER) and hot atom (HA) mechanisms when H impinges on adsorbed CO2, and we s

57 Given the strong correlation between HA neuron excitability and behavioral arousal, we invest

58 riable and no significant difference between HA and FA was found for major chemical groups, that is,

59 WTI and is promoted by a cross-talk between HA, CD73/adenosine signaling, and other profibrotic medi

60 rase domain of hemagglutinin (HA) and blocks HA-mediated membrane fusion.

61 tivity mediated by native TCR coexpressed by HA-1 TCR T cells.

62 the transient CD44 overexpression induced by HA.

63 f proinflammatory response in macrophages by HA was mediated by CD44.

64 the reduction in NF-kappaB translocation by HA.

65 and microcomputed tomography to characterize HA in mouse models of advanced breast cancer in relevant

66 rrets with viral vectors expressing chimeric HA, aimed at boosting Ab reactivity against the HA stem

67 ermined by a competition between the coating HA-Ag and the HRP labeled HA antibody (HRP-HA-Ab).

68 The T-11 COBRA HA vaccine elicited antibodies with HAI and neutralizati

69 ike particle (VLP) vaccines expressing COBRA HA proteins elicited antibodies with hemagglutination in

70 characterization of 17 prototype H3N2 COBRA HA proteins were screened in mice and ferrets for the el

71 The top leading COBRA HA candidates were tested against cocirculating variants

72 s with COBRA HA based viruses or using COBRA HA based vaccines to boost preexisting antibodies induce

73 ies induced by wild-type H1N1 viruses, COBRA HA antigens elicited sera with the broadest HAI reactivi

74 Overall, priming naive ferrets with COBRA HA based viruses or using COBRA HA based vaccines to boo

75 , while the stunting of fusion by deacylated HA acting in isolation may be balanced by other viral pr

76 Compared to wild-type HA, deacylated HA is correlated with released particles with flat envel

77 porphyrins in DMF as an example, decreasing [HA] 10-fold lowers etaeff by 59 mV and decreases the TOF

78 pegvorhyaluronidase alfa (PEGPH20) degrades HA, thereby increasing drug delivery.

79 RA technology was effectively used to design HA immunogens that elicited antibodies that neutralized

80 designed trimers can both capture and detect HA in a paper-based diagnostic format, neutralizes influ

81 rochemical immunosensor capable of detecting HA with high sensitivity and selectivity was developed.

82 hibitors, gefitinib or ibrutinib, diminishes HA formation and trogocytosis by GA101.

83 support for a model in which PEP87 disrupts HA function by displacing native interactions of the neu

84 by metastatic breast cancer feature distinct HA materials properties.

85 The dual drug HA conjugate can inhibit 4T1 tumor growth in vivo during

86 vo than free DOX and GEM and the single drug HA conjugates.

87 o increase bioaccessibility, we encapsulated HAs in lipid-core nanocapsules (NCs) based on a biodegra

88 Four conditions including and excluding HA + ROCK and its effect on early attachment rates and p

89 the elongated 260-loop increases the exposed HA surface and can contribute to antigenic variation in

90 For HA immunoreactivity, we documented both consistently and

91 This increased accumulation for HA-treated MSC yielded a substantial reduction in inflam

92 that demannosylation is a critical step for HA degradation.

93 clade classifications, an automated tool for HA subtype numbering conversion, linkouts to disease eve

94 mice were exposed to ozone or short-fragment HA (sHA), and AHR was assayed via flexiVent.

95 l contribution to biliary complications from HA thrombosis.

96 Furthermore, HA and NP have been shown to be concentrated in choleste

97 oblasts isolated from control mice generated HA-enriched cable structures in the ECM, providing a sub

98 We analyzed human H1 HA head and stalk domain sequences and found substantial

99 the conserved conformation as in H7 and H10 HAs.

100 Since avian-origin H15 HA viruses have been shown to cause enhanced disease in

101 Here, we show that the H15 HA has a high preference for avian receptor analogs by g

102 The extended 150-loop of the H15 HA retains the conserved conformation as in H7 and H10 H

103 can contribute to antigenic variation in H15 HAs.

104 overlaps with the pocket occupied by some H3 HA-specific inhibitors, indicating the high relevance of

105 nt formulations to broaden responses to H5N1 HA based antigens, and show that this broadening is func

106 T-cell epitopes and low immunogenicity of H7 HA remains unknown due to the lack of animal models repr

107 to recapitulate the low immunogenicity of H7 HA.

108 cantly improved the immunogenicity of the H7 HA in the humanized mouse model, leading to a greater th

109 ADCC-Abs titers directed against H7N9 HA or NA proteins.

110 m826 binds to H7N9 HA with subnanomolar affinity at acidic pH and 10-fold l

111 rystal structure of m826 complexed with H7N9 HA indicates that m826 binds an epitope that may be full

112 higher toward H7N9 NP, as compared with H7N9 HA or NA proteins, and correlated strongly with ADCC-Abs

113 Heavy chain-Hyaluronan/Pentraxin 3 (HC-HA/PTX3) is a complex purified from human amniotic membr

114 Additionally, HA and HC-HA/PTX3 inhibited migration but only HC-HA/PTX3 inhibite

115 Furthermore, HC-HA/PTX3 significantly reduced the extent of infiltration

116 onjunctival and subcutaneous injection of HC-HA/PTX3 preserved tear secretion and conjunctival goblet

117 Only HC-HA/PTX3 dose-dependently inhibited proliferation and EMT

118 d HC-HA/PTX3 inhibited migration but only HC-HA/PTX3 inhibited collagen gel contraction.

119 a mouse model of cGVHD to examine whether HC-HA/PTX3 could attenuate dry eye disease elicited by cGVH

120 HC/HA volume surgeons had a significantly lower rate of sur

121 performed by high cumulative/high annual (HC/HA) surgeons increased from 38.3% to 58.4% (P < 0.01) wi

122 Hemagglutinin (HA), a glycoprotein abundant on the virion surface, is i

123 roteins that bind influenza A hemagglutinin (HA) at its conserved receptor binding site.

124 and by ECL replacement with a hemagglutinin (HA) tag.

125 murine macrophages through a hemagglutinin (HA)-mediated mechanism.

126 predicted phenotypic effects, hemagglutinin (HA) clade classifications, an automated tool for HA subt

127 of the surface glycoproteins hemagglutinin (HA) and neuraminidase (NA) with the cell surface recepto

128 052, in combination with H5N1 hemagglutinin (HA) based antigens.

129 ntified T-cell epitopes in H7 hemagglutinin (HA) which potentially enhance regulatory T cell response

130 uished, based on variation in hemagglutinin (HA): B/Victoria/2/87-like (B/Vic) and B/Yamagata/16/88-l

131 tetanus toxoid and influenza hemagglutinin (HA) from H1N1 and newly emergent subtypes such as H5N1 a

132 Some proteins, like hemagglutinin (HA), NA, and M2, are integral membrane proteins.

133 vestigial esterase domain of hemagglutinin (HA) and blocks HA-mediated membrane fusion.

134 ely on the antigenic match of hemagglutinin (HA) for vaccine strain selection, and most vaccines rely

135 he influenza envelope protein hemagglutinin (HA), the low pH in the endosome triggers a transition fr

136 nfected cells and recombinant hemagglutinin (HA), neuraminidase (NA), and nucleoprotein (NP) proteins

137 s with relatively acid-stable hemagglutinin (HA) proteins are rendered incapable of pH-induced trigge

138 rotype 6 (Ad6) to express the hemagglutinin (HA) gene from influenza A/PR/8/34 virus.

139 usly acquire mutations in the hemagglutinin (HA) glycoprotein that abrogate binding of human antibodi

140 to influenza virus target the hemagglutinin (HA) glycoprotein, which is the major antigen on the surf

141 f the Ab response against the hemagglutinin (HA) protein elicited by influenza infection.

142 o acid at position 158 of the hemagglutinin (HA) protein substantially affected the systemic replicat

143 ntibody responses against the hemagglutinin (HA) surface glycoprotein; however, the diversity of HAs

144 Key mutations in the virus hemagglutinin (HA) protein or reassortment with other pandemic viruses

145 f RIV4 (45 mug of recombinant hemagglutinin [HA] per strain, 180 mug of protein per dose) versus stan

146 pe and mutant MN/10 or BJ/92 hemagglutinins (HAs) were constructed and probed for reactivity with fer

147 Histamine (HA) is a biogenic amine that can accumulate to high conc

148 uit is the posterior hypothalamic histamine (HA) system, implicated in supporting wakefulness and hig

149 Histaminergic (HA) neurons, found in the posterior hypothalamic tuberom

150 However, HA instillation ameliorated bladder hyperactivity, lesse

151 However, HA-enriched matrices increased production of vascular en

152 g HA-Ag and the HRP labeled HA antibody (HRP-HA-Ab).

153 Hyaluronan (HA) is a major component of this structure.

154 ma is characterized by excessive hyaluronan (HA) accumulation in the tumor microenvironment, elevatin

155 ceptor for the glycosaminoglycan hyaluronan (HA) demonstrate a number of neurological disturbances in

156 llular matrix (ECM), enriched in hyaluronan (HA) and its binding partner versican, which promotes mon

157 absence of a CD44-specific Ab or hyaluronan (HA).

158 CE STATEMENT We demonstrate that hyaluronan (HA) with different molecular weights produces opposing n

159 um- and phosphate-containing hydroxyapatite (HA) mineral within a collagenous matrix.

160 Nanocrystalline hydroxyapatite (HA) has good biocompatibility and the potential to suppo

161 Porous hydroxyapatite (HA) bone grafting material has been used to fill periodo

162 We found that IAV HA glycoproteins induce ER stress, resulting in HA degra

163 ed upon pH-induced conformational changes in HA.

164 leading to a greater than 4-fold increase in HA-binding IgG responses.

165 glycoproteins induce ER stress, resulting in HA degradation via ERAD and consequent inhibition of IAV

166 harbouring the same mutation (Ser301Phe) in HA that abolishes 46B8 binding to HA at low pH.

167 The T-cell product includes HA-1 TCR CD4(+) T cells to augment the persistence and f

168 and that primary tumors can further increase HA immaturity even before secondary tumor formation, mim

169 Increased HA levels and mesenchymal cells, but not vascular endoth

170 tabolism in Hyal2(-/-) mice causes increased HA, which may promote endothelial-to-mesenchymal transit

171 able HA content, we confirmed that increased HA leads to mechanically softer hydrogels, consistent wi

172 abnormalities were associated with increased HA, vimentin-positive cells, and fibrosis in Hyal2(-/-)

173 wn of these proteins substantially increases HA expression and IAV replication.

174 Individually, HA, NA, M1, M2, and NP were shown to self-associate in o

175 The importance of IL-10-induced HA synthesis for regenerative wound healing is demonstra

176 f chimeric VLPs (cVLPs) containing influenza HA and GPI-anchored CCL28 as antigen and mucosal adjuvan

177 nI, which play a critical role in initiating HA degradation.

178 Interestingly, HA-CS NPs differentially adsorbed two unique anti-inflam

179 n the case of humic acid, incorporation into HA aggregates.

180 etween the coating HA-Ag and the HRP labeled HA antibody (HRP-HA-Ab).

181 levels or engagement of CD44 by its ligand (HA) or a CD44-specific Ab reduced NF-kappaB translocatio

182 he dissolution of QDs, while with low light, HA alone did not change their dissolution.

183 With sufficient light, HA increased the dissolution of QDs, while with low ligh

184 ers, comprising bundles of small needle-like HA crystals, formed on etched surfaces that were cut per

185 on of large, randomly distributed plate-like HA crystals that were weakly attached, regardless of rod

186 Lower HA flows were associated with decreased graft survival (

187 regulates the expression of CD44, the major HA cell membrane receptor.

188 tumor cell dissemination contain less-mature HA (i.e., smaller, less-perfect, and less-oriented cryst

189 odel of localized breast cancer, metaphyseal HA nanocrystals were also smaller and less perfect than

190 ion of 2 amino acid mutations and a modified HA tag at the C terminus of PB1, which is sufficient to

191 to control membrane curvature and to modify HA's interaction with M1 protein, while the stunting of

192 e data demonstrate that disruption of normal HA catabolism in Hyal2(-/-) mice causes increased HA, wh

193 rmed by hyaluronic acid-coated chitosan NPs (HA-CS NPs).

194 tally relevant ligands (e.g., 10 mg L(-1) of HA or 100 muM of silicates).

195 th AHA (n = 115) and in 52%, 57%, and 81% of HA inhibitor patients (n = 63).

196 ns is preceded by intraislet accumulation of HA, a highly hygroscopic polymer.

197 nes of evidence suggest that the activity of HA neurons is important in the regulation of vigilance d

198 ed glycosylation site in antigenic site B of HA emerged, and these viruses remain prevalent today.

199 zymes that synthesize the building blocks of HA, UDP-Glucuronic acid and UDP-N-Acetyl-Glucosamine, as

200 used to compare the molecular composition of HA and FA.

201 dol stabilizes the prefusion conformation of HA that inhibits the large conformational rearrangements

202 The degree of HA varies between CLL patients and positively correlates

203 d both the electrophysiological diversity of HA neurons in brain slices and the effect of their acute

204 The effect of HA on HR depended on the type of autonomic inhibition (P

205 The effect of HA-coatings on murine MSC was functionally determined bo

206 rt because it facilitates rapid formation of HA-HC complexes.

207 th spatially-matched histochemical images of HA, collagen and vessel perfusion.

208 und healing is demonstrated by inhibition of HA synthesis in a murine wound model by administering 4-

209 umbelliferone, a small-molecule inhibitor of HA synthesis, reduced HA accumulation, diminished swelli

210 raditional vaccines induced robust levels of HA inhibition (HI) titers, but failed to protect against

211 r dose) versus standard-dose IIV4 (15 mug of HA per strain, 60 mug of protein per dose) to compare th

212 a fundamental stage in the precipitation of HA, with PHOSPHO1 being identified as the principal enzy

213 to the fluorescence and color properties of HA and that hydrogen peroxide might whiten HA-AAAs by ox

214 While the role of HA in malignancy is well-defined, the mechanisms driving

215 The 45 degrees rotation of HA providing full intensity modulation of transmitted th

216 t the acute, cell type-specific silencing of HA neurons during wakefulness is sufficient to not only

217 H3 numbering) in the major antigenic site of HA was reported to be responsible for the antigenic drif

218 , 165, or 166 in the major antigenic site of HA.

219 The major antigenic sites of HA are located in the globular head subdomain, which is

220 little is known about the optimal spacing of HA ligands, which ought to bridge binding sites within o

221 A crystal structure of HA with bound Fab6649 shows the conserved antibody footp

222 mL for grade 4 FLA (1 mL equals 1 syringe of HA filler).

223 This occurs despite the observed tendency of HA to inhibit colonization on bare glass surfaces when s

224 The total mean (SD) volume of HA used was 6.1 (3.1) mL for grade 2 FLA; 9.3 (4.2) mL f

225 face glycoprotein; however, the diversity of HAs across species and antigenic drift of circulating st

226 receptor-binding site and the stem region on HA is severely constrained by their functional roles in

227 strain selection, and most vaccines rely on HA inhibition titers to determine efficacy, despite the

228 ggesting that eIF4E potentiates an oncogenic HA program.

229 specific to the HA head and stalk, but only HA stalk-specific antibodies mediated ADCC efficiently a

230 on of hyaluronan-metabolizing enzymes and/or HA receptors in KIC.

231 t influence VLP shape, lipid composition, or HA lateral spacing, acylation significantly affected env

232 ngs did not exhibit increases in versican or HA in these regions and had strikingly reduced numbers o

233 l region contained smaller and less-oriented HA nanocrystals relative to ones that constitute the dia

234 ion that occurred in epidemic strains, other HA mutations can confer resistance to antibodies that re

235 solate with six gene segments (PB2, PB1, PA, HA, NA, and NS) sharing >99% sequence identity with thos

236 Here, we obtained two anti-A(H1N1)pdm09 HA monoclonal antibodies that failed to neutralize virus

237 s with bimodal listening experience (CI plus HA in contralateral ear) completed a questionnaire that

238 The majority of continuing bimodal (CI plus HA) participants reported adapting to using both devices

239 ound in the PRF (56.46% +/- 9.26%) and PRF + HA (63.39% +/- 16.52%) groups compared to controls (15.9

240 effectiveness of autologous PRF versus PRF + HA in treatment of IBDs in patients with chronic periodo

241 ity magnetic immunocapture to rapidly purify HA-tagged mitochondria from homogenized mammalian cells

242 12 (pdm2009); antibodies in CL6649 recognize HAs from the entire period.

243 Both enzymes cleaved recombinant HA from several strains of the H1 and/or H3 virus subtyp

244 Electrochemically reduced HA enhanced NO2-to-HONO conversion by a factor of 2 rela

245 ion by a factor of 2 relative to non-reduced HA.

246 -molecule inhibitor of HA synthesis, reduced HA accumulation, diminished swelling, and restored basal

247 Strikingly, eIF4E inhibition alone repressed HA levels as effectively as directly targeting HA with h

248 A combination of virus resistance, HA interaction, and molecular dynamics simulation studie

249 s diseases associated with oxidative stress, HAs can be exploited for attractive nutraceutical applic

250 levels as effectively as directly targeting HA with hyaluronidase.

251 to incorporate ts mutations and a C-terminal HA tag.

252 Gene Ontology analysis demonstrates that HA-CS NPs were the least immunogenic nanocarriers.

253 This work was based on the hypothesis that HA treatment altered the bladder urothelial layer and th

254 The results show that HA can be reliably detected at depths of 0-2.3 mm, which

255 The HA is composed of a globular head domain for receptor bi

256 appa-biased Ab response directed against the HA globular head and stem regions.

257 allenge, and antibodies directed against the HA head were the major contributor toward immune protect

258 aimed at boosting Ab reactivity against the HA stem region, also elicited an Igkappa-biased response

259 Using recombinant viruses, we identify the HA genomic segment as the mediator of cell death inhibit

260 h in the PB2 and NS1 proteins and two in the HA protein.

261 her, our results indicate that shifts in the HA receptor affinity are just an early adaptation step o

262 t viruses encoding amino acid changes in the HA stalk domain replicated well in vitro, and viruses in

263 Arbidol binds in a hydrophobic cavity in the HA trimer stem at the interface between two protomers.

264 position towards the N-terminus side of the HA PCS (P2 position) avoided hydrophobic residues, where

265 glycosylation at positions 158 to 160 of the HA protein and that this N-linked glycosylation enhanced

266 augment the persistence and function of the HA-1 TCR CD8(+) T cells and includes only memory T cells

267 9 safety switch to enable elimination of the HA-1 TCR T cells in case of toxicity; and (4) a CD34-CD2

268 an optokinetic zone spans a ZII+/- pair: the HA zones span the P5+/- and P7+/- ZII stripe pairs, wher

269 Moreover, our observations indicate that the HA prefusion structure (and perhaps the metastable state

270 These findings demonstrate that the HA protein stalk domain can undergo limited drift under

271 infection induced antibodies specific to the HA head and stalk, but only HA stalk-specific antibodies

272 The HAs of H15 viruses contain an insertion in the 150-loop

273 safety and efficacy and supports use of this HA filler for treatment of HIV-associated FLA with durab

274 approximately 40-fold more likely to bind to HA than nonrolling cells in shear flow.

275 301Phe) in HA that abolishes 46B8 binding to HA at low pH.

276 protein levels in HAAA sections compared to HA.

277 red cell product and tracking of transferred HA-1 TCR T cells.

278 binding sites within or across the trimeric HA molecules.

279 Tumor HA levels were measured retrospectively using a novel af

280 Among the four mutations detected, the two HA mutations were analyzed by generating recombinant vir

281 ating H3N2 strains compared to the wild-type HA antigens that were represented in commercial influenz

282 cted by antibodies elicited by the wild-type HA from viruses selected as the vaccine candidates.

283 panel than VLP vaccines expressing wild-type HA proteins.

284 Compared to wild-type HA, deacylated HA is correlated with released particles

285 In hydrogels with variable HA content, we confirmed that increased HA leads to mech

286 While viral HA acylation is crucial in virus replication, its physic

287 antibodies that recognize influenza A virus HA can be protective, but the mechanism is not completel

288 s of Arbidol in complex with influenza virus HA from pandemic 1968 H3N2 and recent 2013 H7N9 viruses.

289 While low molecular weight HA increases sensitivity to mechanical stimulation, high

290 echanical stimulation, high molecular weight HA reduces sensitization, attenuating inflammatory and n

291 patial offset depended on the depth at which HA was located.

292 While HA acylation did not influence VLP shape, lipid composit

293 f HA and that hydrogen peroxide might whiten HA-AAAs by oxidizing the benzene ring in AAAs.

294 rrets for the elicitation of antibodies with HA inhibition (HAI) activity against human seasonal H3N2

295 d acute lung injury and, in association with HA, generates an ECM that promotes leukocyte infiltratio

296 fluence within 10-15 days when cultured with HA + ROCK.

297 ly cocluster, but the association of M1 with HA or NA is dependent upon the means of expression.

298 .53 to 1.00; P = .049) and for patients with HA-high tumors (HR, 0.51; 95% CI, 0.26 to 1.00; P = .048

299 In patients with HA-high tumors (PAG v AG), the objective response rate w

300 s much HONO was formed when NO2 reacted with HA that was photoreduced by irradiation with UV-visible