ライフサイエンスコーパス: shedding of

1 netic analysis of paired specimens confirmed shedding of 2 distinct HSV-2 strains collected at differ

2 g of the mammalian Aurora B kinase, triggers shedding of a kinetochore protein, preventing microtubul

3 typic H5N1 virus was associated with reduced shedding of a pandemic H1N1 virus challenge, while vacci

4 how that genetic depletion of SUB2 abolishes shedding of a range of parasite proteins, identifying pr

5 ytes, resulting in significantly upregulated shedding of ADAM17 substrates, including EGF-family grow

6 d physicochemical modification of Ag NPs and shedding of Ag+, leading to an increased bioavailability

7 levels in all tissues and show virtually no shedding of all tested ADAM17 substrates, to clarify the

8 on of ErbB receptors through the proteolytic shedding of an ErbB ligand.

9 r of ADAM9, these results indicate increased shedding of angiotensin-converting enzyme in the alveola

10 and ADAM cleavage assays to demonstrate that shedding of at least 12 of these proteins are potentiall

11 B. bronchiseptica or B. pertussis inhibited shedding of B. bronchiseptica.

12 hanism of immune escape involving tumor cell shedding of B7-H6, a ligand for the activating receptor

13 ated recognition by metalloprotease-mediated shedding of B7-H6.

14 in the feed showed a progressive decline in shedding of bacteria, significantly lower immune respons

15 examined for evidence of diarrhea and fecal shedding of bacteria.

16 e biochemistry of epithelial bonding and the shedding of binding proteins on the sperm head.

17 No shedding of Bordetella pertussis was detected in systema

18 Ectodomain shedding of both human and mouse RAGE was dependent on A

19 Selective inhibition of ADAM17 prevented the shedding of both molecules.

20 llergen-induced miR-132-3p may contribute to shedding of bronchial epithelial cells.

21 undergo a process termed "uncoating," i.e., shedding of CA molecules from the conical lattice.

22 hanism studies showed that CgA inhibited the shedding of cancer cells in circulation from primary tum

23 Surgery induces increased shedding of cancer cells into the circulation, suppresse

24 dependent ATP release regulates this through shedding of CD21 and CD62L.

25 ein KIF2A, which subsequently alleviated the shedding of CD44 from DCs.

26 nd in vivo results point to a P2X7-dependent shedding of CD62L (with high levels in the serum), which

27 ctivity of CD39 and, therefore, abrogate the shedding of CD62L.

28 processes involving cleavage, processing, or shedding of cell adhesion molecules, growth factors, cyt

29 Studying the shedding of cell membrane-bound hTNF by Adam17, a known

30 Proteolytic shedding of cell surface proteins generates paracrine si

31 rize a novel viral strategy to influence the shedding of cell-surface molecules involved in immune re

32 e in extracellular matrix (ECM) turnover and shedding of cell-surface molecules.

33 This is due to decreased shedding of cell-surface N-cadherin by the ADAM family p

34 Respiratory symptoms and shedding of challenge virus were assessed.

35 In contrast, VEGFA induced shedding of charged GAGs.

36 t ADAM10 activity contributes to HDM-induced shedding of chemokines, including CCL20.

37 onensin, indicating that HDM induces surface shedding of chemokines.

38 asmic action of the retrograde IFT motor and shedding of ciliary ectosomes.

39 epredation in feedlots contributing to fecal shedding of ciprofloxacin-resistant E. coli, but a singl

40 ively associated with increased cattle fecal shedding of ciprofloxacin-resistant E. coli.

41 ributes and ADT-sensitivity, and reduces the shedding of circulating tumor cells in vivo with signifi

42 In support of our primary hypothesis, shedding of CMV DNA in semen was associated with increas

43 HIV DNA levels (p = 0.09) and more frequent shedding of CMV in seminal plasma (p = 0.002).

44 Increased PTC apoptosis allowed luminal shedding of cystine crystals and was partially compensat

45 ory signaling events by promoting ectodomain shedding of cytokine precursors and cytokine receptors.

46 Vaginal shedding of cytomegalovirus (CMV) DNA was determined lon

47 ive cholestyramine therapy reduced the fecal shedding of daptomycin-resistant E. faecium by up to 80-

48 binding induces ADAM10-dependent ectodomain shedding of DDR1.

49 cantly reduced the expression of heparanase, shedding of DeltaHS, and loss of occludin as detected by

50 embrane metalloprotease mediating ectodomain shedding of diverse membrane proteins, was recently sugg

51 ferentiation, whereas TIMP3 may modulate the shedding of DLK1, a regulator of adipogenesis.

52 Pretransplant urinary BKV shedding of donor and recipient is a risk for posttransp

53 Pretransplant urinary BKV shedding of donor or recipient was a significant risk fa

54 captures the complex dynamics, including the shedding of droplets.

55 Inhibiting ectodomain shedding of Dsg2 with the matrix metalloproteinase inhib

56 M16F-expressing cells then undergo extensive shedding of ectosomes.

57 functional relevance of iRhom2 in regulating shedding of EGF receptor (EGFR) ligands is established b

58 gulates oligodendrogenesis by modulating the shedding of EGFR ligands TGFalpha and HB-EGF and, conseq

59 rowth factor receptor (EGFR) activity and on shedding of EGFR ligands; exposure to 12% CO2 without ad

60 tion of PI(4,5)P2, a reaction needed for the shedding of endocytic factors from their membranes.

61 ase inhibitor studies show that constitutive shedding of endogenous DDR1 in breast cancer HCC1806 cel

62 Shedding of endogenous Tim-3 was found in primary human

63 ion of the endothelium leads to an increased shedding of endothelial cell microparticles (MP).

64 Cell adhesion was reversed by shedding of endothelial E-selectin, P-selectin, and alph

65 further induces activation of Rho kinase and shedding of endothelial microparticles carrying miR-503,

66 UA-induced shedding of endothelial TM may represent a novel mechani

67 The shedding of epithelial cell layers is usually effective

68 Programmed death and shedding of epithelial cells is a powerful defense mecha

69 The reduced shedding of essential postsynaptic cell adhesion protein

70 uction in oxygen coincides with an increased shedding of eukaryotic viruses in the oxycline, and a sh

71 rse astrophysical phenomena, for example the shedding of excess angular momentum from protostars by t

72 We demonstrate that flow-induced shedding of extracellular matrix from surface-attached b

73 han Coronin 1C-reexpressing cells due to the shedding of extracellular vesicles (EVs) containing MT1-

74 The generation and shedding of extracellular vesicles (EVs), including exos

75 ith PMA or N-ethyl-maleimide resulted in the shedding of FcgammaRIIIA/CD16A and CD62L, a specific sub

76 The shedding of FcgammaRIIIA/CD16A was at least partially AD

77 Finally, the shedding of FcgammaRIIIA/CD16A was restricted to activat

78 Moreover, the shedding of FcgammaRIIIA/CD16A was strongly correlated w

79 in host response to bacterial infection and shedding of foodborne pathogens, a systematic profiling

80 fferentially regulate synthesis, charge, and shedding of GAGs in GEnCs.

81 ors involves the synthesis and extracellular shedding of gangliosides, a class of biologically active

82 teases, heparanase, and hyaluronidase to the shedding of glycocalyx.

83 Ectodomain shedding of glycoprotein (GP) Ibalpha is thought to medi

84 Ligand-induced ectodomain shedding of glycoprotein VI (GPVI) is a metalloproteinas

85 Shedding of gp120, known to severely complicate structur

86 and ADAM17 can produce sgp130 by ectodomain shedding of gp130, even though this mechanism only accou

87 r was associated with macrothrombocytopenia, shedding of GPIbalpha, impaired platelet adhesion to von

88 tion of either of the ITAM receptors induces shedding of GPVI and proteolysis of the ITAM domain in F

89 egation but minimally affected shear-induced shedding of GPVI.

90 nce of GPVI ligand, was sufficient to induce shedding of GPVI.

91 al-regulated kinases (ERK1/2) pathway by the shedding of growth factors which triggers the formation

92 Prolonged, high-level IHS (ie, shedding of >5000 RNA copies/mL) was observed in 1 iART

93 nation is achieved is poorly understood, but shedding of guidance cues by metalloproteinases is emerg

94 ZIKV NS1 induced shedding of HA and HS and altered expression of CD44 and

95 a showed decreased expression and ectodomain shedding of HB-EGF and reduced incidence of cancer devel

96 oned medium on the expression and ectodomain shedding of HB-EGF by TNFalpha-converting enzyme/a disin

97 conditioning were associated with prolonged shedding of HCoV in HCT recipients.

98 mal models of sepsis or endotoxemia leads to shedding of heparan fragments from the endothelial glyco

99 y high glucose was associated with increased shedding of heparan sulfate (DeltaHS) and the tight junc

100 confirmed the superfusion results and caused shedding of heparan sulfate, pointing to disruption of t

101 Here, we describe extracellular shedding of HEPCAM at two alpha-sites through a disinteg

102 To investigate the role of genital shedding of herpesviruses in human immunodeficiency viru

103 Shedding of HHV in saliva was prospectively studied in p

104 The PCR assay demonstrated shedding of HHV-7, EBV, HHV-6, and CMV, listed by order

105 symptomatic STIs, is associated with seminal shedding of HIV in men receiving ART, conferring a poten

106 However, isolated shedding of HIV type 1 (HIV-1) in semen (IHS) can occur

107 es a potential mechanism for acquisition and shedding of HIV via chronic leukocyte recruitment to the

108 TV has been shown to increase vaginal shedding of HIV, which may influence HIV sexual and peri

109 cantly reduced the number of days of vaginal shedding of HSV-2 DNA compared with that for mock-immuni

110 7 for prevention of genital disease, vaginal shedding of HSV-2 DNA, and latent infection of dorsal ro

111 imals had little effect on recurrent vaginal shedding of HSV-2 DNA, despite significantly reducing ge

112 r, 5/8 animals in each group had subclinical shedding of HSV-2 DNA, on 15/168 days for the gC2/gD2 gr

113 inate recurrent lesions or recurrent vaginal shedding of HSV-2 DNA.

114 rrent genital lesions, and recurrent vaginal shedding of HSV-2 DNA; however, protection was incomplet

115 Pharmacological treatments revealed that shedding of hTfR1 by PC7 requires endocytosis into acidi

116 Here, ectodomain shedding of human and murine IL-23R was identified as an

117 Intermittent shedding of human immunodeficiency virus type 1 (HIV) in

118 tion of ICOS/ICOSL results in ADAM10-induced shedding of ICOSL on B cells and moderate ICOS internali

119 pport a role for metalloproteinase-dependent shedding of IgLON family members in regulating neurite o

120 dentify that platelet-inflammasome-dependent shedding of IL-1beta and caspase-1-carrying platelet EVs

121 Inflammasome activation and platelet shedding of IL-1beta-rich microparticles correlated with

122 Furthermore, IL-1beta induced shedding of IL-1R2 in vivo.

123 Shedding of IL-23R was induced by stimulation with the p

124 henocopying hyperactivation of ADAM-mediated shedding of IL-6R as single substrate.

125 ion in this model, it is not ADAM17-mediated shedding of IL-6R within the pouch that orchestrates thi

126 We report that during cystitis, shedding of infected bladder epithelial cells (BECs) was

127 spiratory viruses revealed that NS2 promotes shedding of infected epithelial cells, resulting in two

128 Shedding of infectious prions in saliva and urine is tho

129 Shedding of infectious SARS-CoV-2 was observed up to 70

130 RS-CoV-2-positive individuals as a proxy for shedding of infectious virus.

131 from COVID-19 does not necessarily indicate shedding of infective virions.

132 rane repair by regulating ESCRT III-mediated shedding of injured plasma membrane.

133 "positive" test results and reproduction and shedding of intact virus.

134 ve and inducible metalloproteinase-dependent shedding of integrin beta2 from mouse macrophages are de

135 es the ability of metalloproteinase-mediated shedding of integrin beta2 to promote macrophage efflux

136 tes, and that NMDAR activity is required for shedding of its ectodomain by metalloproteinases.

137 The shedding of its ectodomain from the cell surface is phys

138 Rapid shedding of Juno from the oolemma after fertilization su

139 toxicity and was able to selectively inhibit shedding of known ADAM10 substrates in several cell-base

140 phils showing signs of increased reactivity: shedding of l-selectin, CD11b upregulation, increased ox

141 uding enhancement of NADPH oxidase activity, shedding of l-selectin, or mobilization of CD11b.

142 cell to modulate the function and ectodomain shedding of l-selectin.

143 We use chronic shedding of Leptospira interrogans serovar Pomona in Cal

144 Proteolytic shedding of ligands for the NK group 2D (NKG2D) receptor

145 l tract, which resulted in a delayed vaginal shedding of live organisms, accelerated the chlamydial s

146 naling within B cells is blunted through the shedding of LMP1 via exosomes.

147 significantly slowed down after 10 h due to shedding of LRP-1 from the cell surface and formation of

148 s in TIMP-3 mRNA levels, but correlated with shedding of LRP1.

149 17) is a membrane-bound enzyme that mediates shedding of many membrane-bound molecules, thereby regul

150 Shedding of mcr-1 E. coli by small gull flocks followed

151 eveloped a new assay to quantitatively track shedding of membrane proteins from the surface of EVs.

152 metalloprotease 10 (ADAM10) is required for shedding of membrane proteins such as EGF, betacellulin,

153 creases soluble RANKL by reducing ectodomain shedding of membrane RANKL through downregulation of met

154 y amyloid fibrils is caused by the molecular shedding of membrane-active oligomers in a process that

155 ible step in many signalling pathways is the shedding of membrane-anchored proteins.

156 active ADAMs are responsible for ectodomain shedding of membrane-associated proteins.

157 rm of CD154 (sCD154), which results from the shedding of membrane-bound CD154, plays a key role in th

158 ugh inhibition of invadopodia maturation and shedding of membrane-derived microvesicles, the two key

159 ey to this process is the protease-mediated "shedding" of membrane-tethered ligands, which then activ

160 ntify the proteolytic enzyme responsible for shedding of meprin A, we generated stable HEK cell lines

161 istate 13-acetate-, and ionomycin-stimulated shedding of meprin beta and meprin A in the medium of bo

162 ponsible for the constitutive and stimulated shedding of meprin beta and meprin A.

163 -acetate and ionomycin stimulated ectodomain shedding of meprin beta and meprin A.

164 verexpression of ADAM10 resulted in enhanced shedding of meprin beta from both transfectants.

165 This induces ectodomain shedding of metalloprotease-sensitive cell surface prote

166 ubicin and melphalan) selectively affect the shedding of MIC molecules that are sensitive to proteoly

167 Shedding of microbial extracellular vesicles constitutes

168 SEM images show distinct shedding of microvilli-like features upon treatment with

169 Patients with sepsis also displayed reduced shedding of monocyte tumor necrosis factor receptors upo

170 thin the lipid bilayer, an event preceded by shedding of most of the substrate's ectodomain by alpha-

171 indings support a role for MT3-MMP-dependent shedding of NgR1 in regulating excitatory synapse develo

172 In contrast, shedding of non-expiratory micron-scale particulates fro

173 ses is attenuated, and they have an enhanced shedding of noninfectious particles and are incapable of

174 (human Y422) is shown to be associated with shedding of NUP62 from the nuclear pore complex (NPC) an

175 n presentation, modulation of apoptosis, and shedding of obsolete protein.

176 maged, and its degradation is accompanied by shedding of one or more glycocalyx components into the b

177 Stimulated shedding of other ADAM17 substrates, such as TGFalpha, i

178 c strains from adhesion to NETs involved the shedding of outer membrane vesicles (OMVs) that outcompe

179 embly of the actin cytoskeleton, followed by shedding of plasma membrane microvesicles, disassembly a

180 schemic cerebral circulation indicated local shedding of platelet CD84.

181 Any fecal shedding of poliovirus type 1 was 8.8, 9.1, and 13.5% in

182 This approach enabled us to discriminate the shedding of prions in saliva and the detection of prions

183 nt to CWD biology from our analyses: (i) the shedding of prions in saliva increases with time postino

184 f chronic wasting disease (CWD) results from shedding of prions produced at high titers in the periph

185 genicity through tissue factor upregulation, shedding of procoagulant MPs, endothelial nitric oxide s

186 to P4, and was associated with a progressive shedding of procoagulant MPs.

187 We propose that shedding of PrP(c) could be a potential target for thera

188 in the CNS of HIV-infected people, increase shedding of PrP(c) from human astrocytes by increasing t

189 These results indicate that by promoting the shedding of PrP(C) in human neurons, ADAM10 activation p

190 Here we observed that ectodomain shedding of RAGE is critical for its role in regulating

191 ution to the bedding reservoir compared with shedding of resistant bacteria in faeces.

192 Circadian shedding of retinal photoreceptor cell discs with subseq

193 Vaccinees exhibited significantly reduced shedding of RhCMV in saliva and urine following RhCMV ch

194 onuclear cells exposed to RhCMV antigens and shedding of RhCMV in saliva.

195 Shedding of RotaTeq vaccine strains in 7 of 13 infants w

196 corded, and nasal secretions were tested for shedding of RV-A16 ribonucleic acid.

197 oglobulin G titers were associated with less shedding of S. Typhi (P < .0001).

198 lture, and asymptomatic bacteremia and stool shedding of S. Typhi was also observed.

199 Shedding of S. Typhi was more common than S. Paratyphi.

200 did not receive mOPV2, as assessed by faecal shedding of Sabin 2 by reverse transcriptase quantitativ

201 However, faecal shedding of Sabin 2 in household contacts was increased

202 Faecal shedding of Sabin 2 in infants who did not receive the m

203 Shedding of Salmonella Typhi or Paratyphi in the stool o

204 of ERM by siRNA blocked the P2X7R-dependent shedding of sAPPalpha.

205 rical results predict the previously unknown shedding of satellite droplets during the destabilizatio

206 TNF-alpha-induced MMP9-mediated shedding of SDC4 is likely to contribute to the endothel

207 herapeutic anti-EGFR antibodies also inhibit shedding of sEGFR, thus implicating the cell surface pre

208 Shedding of sEphrin-B2 promotes fibroblast chemotaxis an

209 d yet ADAM17 is unable to support stimulated shedding of several of its substrates, including heparin

210 e we show that activity-dependent ectodomain shedding of signal regulatory protein-alpha (SIRPalpha)

211 samples from 37 participants, we found that shedding of sIL-6R from neutrophils was greater in carri

212 Thus, ectodomain shedding of SIRPalpha is an activity-dependent trans-syn

213 In addition, shedding of SNAP-Tac into the medium was greatly influen

214 ALL, TRC105 alone was ineffective due to the shedding of soluble CD105.

215 Shedding of soluble DLK1 (sDLK1) by pre-adipocytes was i

216 critical role in phagocytosis), resulting in shedding of soluble-Mer (sMER) and loss of MERTK functio

217 , is crucial for the rapid activation of the shedding of some, but not all substrates of ADAM17.

218 gulation of Tyro3 and Mer mRNA and increased shedding of sTyro3 and sMer.

219 ain proteases responsible for the ectodomain shedding of surface proteins.

220 In this study, we demonstrate that the shedding of syndecan-1 by MMP-3 and MMP-7 supports viral

221 However, secreted MMP-7 participated in the shedding of Syndecan-4 from the surface of B-lymphocytes

222 of MMP-7 which in turn is important for the shedding of Syndecan-4 in response to infectious stimuli

223 lux of chemokines through the regulation and shedding of syndecans.

224 for development of therapeutics that prevent shedding of T. gondii parasites.

225 Inhibiting ectodomain shedding of TbetaRIII increased TGF-beta responsiveness

226 ction is also critically dependent on normal shedding of terminally differentiated keratinocytes, a p

227 mic domain of ADAM17 show reduced stimulated shedding of the ADAM10 substrate betacellulin, whereas t

228 levated CO2 also inhibited stretch-activated shedding of the ADAM17 substrate TNFR1 from airway epith

229 tacellulin, whereas the ionomycin-stimulated shedding of the ADAM17 substrates CD62-L and TGFalpha is

230 ic stellate cells exhibited iRhom2-dependent shedding of the ADAM17 substrates TNFR1 and TNFR2.

231 regulating extracellular matrix turnover and shedding of the adipogenic regulator DLK1, but that in a

232 s concomitantly with disease progression and shedding of the bacteria in feces.

233 Despite shedding of the bacteria, the remnant matrix remains int

234 Sprouting angiogenesis is regulated by shedding of the C-type lectin family 14, member A (CLEC1

235 brane, which in turn results in cleavage and shedding of the damaged part of the cell membrane.

236 Proteolytic shedding of the ectodomain is thought to redirect activa

237 Regulated shedding of the ectodomain of cell membrane proteins by

238 Imatinib stimulated shedding of the EGFR ligand heparin-binding EGF-like gro

239 poietic cells, supported TACE maturation and shedding of the EGFR ligand TGF-alpha in Rhbdf2-deficien

240 evidence of a mechanism involving ectodomain shedding of the EGFR ligands amphiregulin (AREG) and TGF

241 dent manner, leading to increased ectodomain shedding of the epidermal growth factor (EGF) receptor (

242 We show that shedding of the extracellular domain of activated leukoc

243 It was reported that exercise promotes the shedding of the extracellular domain of Fndc5, generatin

244 Many vertebrates replace teeth through shedding of the functional tooth.

245 elial-to-mesenchymal transition (EndoMT) and shedding of the glycocalyx are early changes of endothel

246 Degradation and shedding of the glycocalyx by enzymes, such as hyaluroni

247 We hypothesized that marked shedding of the glycocalyx core protein, syndecan-1, occ

248 addition of mim6 to 10-1074 did not promote shedding of the gp120 subunit of Env.

249 mechanisms, including but not limited to: 1) shedding of the HER2 extracellular domain, 2) steric hin

250 naceous substrates provided by mucus and the shedding of the intestinal epithelium.

251 Chemically induced shedding of the lectin-like domain of TBM resulted in si

252 Antibody-induced shedding of the major surface protein circumsporozoite p

253 this article, we describe that an increased shedding of the NKG2D ligand MICA is observed postinfect

254 in and metalloproteinase) protease-dependent shedding of the Notch ligand Delta-like 1 (Dll1), leadin

255 her by increasing ADAM17-mediated ectodomain shedding of the Notch receptor or by modification of spe

256 The shedding of the old exoskeleton that occurs in insects a

257 An early event is the shedding of the outermost fibrous corona layer of the ki

258 ated platelets and endothelial cells induces shedding of the P-selectin ectodomain into the circulati

259 tment of neutrophils to the nasal cavity, or shedding of the pathogen.

260 e I was activated through the acid-triggered shedding of the polymeric shell of the NCa, resulting in

261 s present on syndecan core proteins suppress shedding of the proteoglycan.

262 es in an "inside-out" fashion the ectodomain shedding of the receptor.

263 CV30 also induces shedding of the S1 subunit, indicating an additional mec

264 TSPN6 also inhibits the shedding of the SDC4 ectodomain, mimicking the effects o

265 s undesired premature drug release until the shedding of the shell, which accelerates the cleavage of

266 NMDA receptor activation rapidly triggers shedding of the signalling-competent NRG2 extracellular

267 cretase complex is preceded and regulated by shedding of the substrate's ectodomain by alpha- or beta

268 atosis characterized by lifelong, continuous shedding of the upper epidermis.

269 adverse events, immune responses, and faecal shedding of the vaccine virus for 28 days.

270 aluate the persistence, biodistribution, and shedding of the vector following subretinal delivery.

271 proteases of the ADAM family, leading to the shedding of their ectodomains.

272 ion as cell surface receptors, or mainly via shedding of their secreted ectodomains, such as neurotro

273 eased hyaluronidase activity, suggesting the shedding of these components.

274 Shedding of these micelles into the aqueous solution res

275 After shedding of this ectodomain, CTF-eta is further processe

276 susceptibility gene for ccRCC and ectodomain shedding of this molecule may be a predictive biomarker

277 PMA-induced shedding of Tim-3 was abrogated by deletion of amino aci

278 idue within the intracellular domain rescues shedding of Tim-3.

279 protection of hepatocytes involves the rapid shedding of TNF receptor 1 to limit TNFalpha signaling.

280 ng TNF-converting enzyme-mediated ectodomain shedding of TNF type I receptor (TNFR1), the membrane-bo

281 TNF-alpha convertase (TACE), which controls shedding of TNF-alpha and its biological activity in viv

282 complexes, stimulated iRHOM2/TACE-dependent shedding of TNF-alpha in mouse and human cells.

283 role for iRhom2 in promoting ADAM17-mediated shedding of TNFRs in hepatic stellate cells, which reduc

284 Ectodomain shedding of transmembrane precursor proteins generates n

285 Ectodomain shedding of tumor necrosis factor receptor 1 (TNFR1) pro

286 altered by sepsis and may result in reduced shedding of tumor necrosis factor receptors.

287 ng ALCAM in tumor-bearing mice revealed that shedding of tumor, but not host-derived ALCAM is elevate

288 betaFurKO cells show impaired cleavage or shedding of vacuolar-type ATPase (V-ATPase) subunits Ac4

289 Of importance, shedding of VEGF-165 from the cell surface together with

290 Increased shedding of VEGFR2 (via inhibition of constitutive endoc

291 Shedding of VEGFR2 produces an N-terminal soluble fragme

292 or Rab5, increases dramatically the cleavage/shedding of VEGFR2.

293 t the utility of analyzing sewage to monitor shedding of viral pathogens and the high viral diversity

294 The shedding of viral RNA from sputum outlasted the end of s

295 l cells at the neuro-epithelial junction and shedding of virus at the epithelial surface.

296 nital HSV-2 infection that recapitulates the shedding of virus experienced by humans.

297 emination or replication and does not induce shedding of virus with stool.

298 and mouse plasma, indicating that ectodomain shedding of VLDLR occurs endogenously.

299 Shedding of VPAC2 from the ciliary surface results in te

300 morbidity and mortality but did not prevent shedding of West African challenge viruses.