ライフサイエンスコーパス: homotypic

1 aments consist entirely of a single isoform (homotypic).

2 N1)pdm09 recipients, the PPAb titers against homotypic A(H1N1)pdm09 vaccine were similar to those aga

3 lls is associated with its ability to induce homotypic adhesion (HA).

4 These isoforms differentially regulate HLMC homotypic adhesion and survival.

5 CD74 on MCL cells by the HexAbs resulted in homotypic adhesion and triggered intracellular changes t

6 Ninjurin1 is a homotypic adhesion molecule that contributes to leukocyt

7 These include VE-cadherin, a homotypic adhesion molecule that regulates endothelial b

8 o aggregation are not fully accounted for by homotypic adhesion, and that further factors influence t

9 sible for its unique properties of increased homotypic adhesion, apoptosis resistance and budding.

10 R cells show negligible cell-cell homotypic adhesion, as well as non-specific cell-substra

11 Although VE-cadherin induces EC homotypic adhesion, N-cadherin function in ECs remains l

12 of leukocyte migration that is initiated by homotypic adhesive interactions between platelets, leadi

13 The functional significance of these homotypic aggregates in regulating T cell function remai

14 human neutrophils causes rapid (</= 30 min) homotypic aggregation and NET release by a mechanism tha

15 We identify a role for ERK in homotypic aggregation and NET release.

16 undergo a rapid, ECM-dependent mechanism of homotypic aggregation and NETosis in response to C. albi

17 s hyphae and fibronectin, with VLA3 inducing homotypic aggregation and VLA5 regulating NETosis.

18 Neither homotypic aggregation nor NETosis occurs when human neut

19 In addition, CD44 silencing promoted homotypic aggregation of LS147T cells, a phenotype that

20 activated state permits NETosis but prevents homotypic aggregation.

21 McTNs) that facilitate cell reattachment and homotypic aggregation.

22 eterotypic enhancers are stronger than their homotypic analogs and favor specific transcription facto

23 ignaling mechanism for pseudokinases whereby homotypic and heterotypic association is used to assembl

24 targeting sequence, and participates in both homotypic and heterotypic associations with itself and L

25 sting complex EphA4 signaling involving both homotypic and heterotypic cell-cell interactions.

26 ace and programed cell-cell adhesion between homotypic and heterotypic cells via sequence-specific DN

27 ble, with rates of disorders and patterns of homotypic and heterotypic continuity similar to those ob

28 ared etiologies and mechanisms, predict both homotypic and heterotypic continuity.

29 tudy investigates the role of T cells during homotypic and heterotypic DENV reinfection.

30 ted by the ability of Hax-1 proteins to form homotypic and heterotypic dimers with binding affinities

31 Macropinosomes mature through homotypic and heterotypic fusion with endosomes and ulti

32 series to describe the gating properties of homotypic and heterotypic GJ channels.

33 These motifs can facilitate homotypic and heterotypic interactions between TM helice

34 A (NTD and CTD, respectively) engage in both homotypic and heterotypic interactions to create the cap

35 s share highly conserved C-termini mediating homotypic and heterotypic interactions within and betwee

36 e distribution of these breast cell lines in homotypic and heterotypic invasion assays.

37 However, the association between homotypic and heterotypic NAb titers and protection agai

38 ional intercellular communication in several homotypic and heterotypic populations by visualizing the

39 y testing cognate TFRE activities in varying homotypic and heterotypic promoter architectures.

40 ls are an important statistical correlate of homotypic and heterotypic response and may limit severit

41 and RV5 exert similar effectiveness against homotypic and heterotypic rotavirus strains.

42 Intercellular small RNA transfer can be both homotypic and heterotypic.

43 expressing different Cx isoforms and forming homotypic and/or heterotypic GJ channels.

44 Our results suggest that higher order homotypic and/or heterotypic interactions within distinc

45 We found that the most abundant homotypic arrangement for p75(NTR) is a trimer and that

46 Homotypic association of SgK269 and SgK223 was also demo

47 nnexin A2 reduces both vesicle formation and homotypic Atg16L vesicle fusion.

48 The diversity of homotypic BcR contacts leading to cell-autonomous signal

49 Further, we found that IgSF9 mediated homotypic binding and cell aggregation, but failed to in

50 Homotypic binding of rVN was also seen.

51 equently observed, the mechanistic basis for homotypic binding site synergy is poorly understood.

52 These homotypic binding sites often exhibit synergy, whereby t

53 activated N-methyl-d-aspartate receptors in homotypic, but not heterotypic, MSNs.

54 interaction and recruits procaspase-1 via a homotypic caspase recruitment domain interaction.

55 uggesting that adhesion could be mediated by homotypic CdiA-CdiA interactions.

56 functions as a retention factor, increasing homotypic cell adhesion and limiting tumor spreading to

57 3, 4B4, and AIIB2 by their ability to induce homotypic cell aggregation.

58 Homotypic cell fusion occurs in several cell types inclu

59 Homotypic cell sorting observed after ectopic cell surfa

60 We model homotypic cell-cell adhesion and heterotypic cell-baseme

61 Bdl induces homotypic cell-cell adhesion in vitro and mediates neuri

62 N-cadherin is a homotypic cell-cell adhesion receptor commonly overexpre

63 cell death initiated by actomyosin-dependent homotypic cell-in-cell invasion that can be observed in

64 Therefore, our data uncover the existence of homotypic cell-to-cell communication among mobile innate

65 The latter include seven types of homotypic chains as well as mixed ubiquitin chains.

66 While structural characterization of homotypic chains has been well elucidated, less is known

67 TFs, helping to explain the observation that homotypic chains of binding sites express at low levels.

68 d the expression driven by CREs comprised of homotypic chains of KLF4 binding sites.

69 Collective activation and homotypic clustering drove cytokine sharing and acted as

70 act as direct drivers of gene expression in homotypic clusters of binding sites, independent of spac

71 ltiple copies of single mRNAs organize into 'homotypic clusters' that occupy defined positions within

72 following cargo binding to the neighboring, homotypic coiled-coil region.

73 absence of coupling for these mutants in the homotypic configuration could be explained by shifts in

74 KIT mutations, reveals that the strength of homotypic contacts and the cooperativity in the action o

75 ative interactions mediated by multiple weak homotypic contacts between receptor molecules are respon

76 At homotypic contacts, junctional N-cadherin bonds downregu

77 There was significant homotypic continuity from age 3 to age 6 for anxiety, at

78 uture occurrences of both the same disorder (homotypic continuity) and other disorders (heterotypic c

79 nd not an artifact of failure to control for homotypic continuity.

80 region of the BicD structure with classical, homotypic core packing.

81 el mechanism for electrical rectification in homotypic Cx36 GJs.

82 gardless of the specific type of GJ channel (homotypic Cx43 and Cx45, and heterotypic Cx43/Cx45 and C

83 ermore, these mutations induced formation of homotypic DC clusters, which represent close correlates

84 Homotypic death domain (DD)-DD interactions are importan

85 tment and activation in several complexes by homotypic death domain-fold interactions.

86 rate phages that are either closely related (homotypic defence) or unrelated (heterotypic defence) to

87 Four patients with homotypic DENV reinfections were identified and confirme

88 ibe the first set of virologically confirmed homotypic DENV reinfections.

89 ally forms heterodimers with Dpp rather than homotypic dimers, providing a possible explanation for t

90 We recently reported that a trans-dimer, homotypic disulfide bond involving Cys367 in keratin 14

91 have evolved means to preferentially take up homotypic DNA containing short and genus-specific sequen

92 cadherin recapitulated this outcome, whereas homotypic E-cadherin engagement promoted apoptotic signa

93 r attachment protein receptors [SNAREs]) and homotypic endoplasmic reticulum (ER) fusion (Sey1p) for

94 with an inert interface and during fusion of homotypic epithelial layers.

95 demonstrate that Sey1p, like ATLs, mediates homotypic ER fusion.

96 al change of the cytosolic domain to achieve homotypic ER membrane fusion.

97 um (ER) network is dynamically maintained by homotypic (ER-ER) fusion.

98 d activation, underlying the requirement for homotypic F and HN interactions in viral entry.

99 Cells were recombined and cultured as either homotypic [(F(C))(E(C)) and (F(N))(E(N))] or heterotypic

100 n GSC enabled perivascular migration through homotypic forward signalling.

101 lysosome depends on the GTPase Rab7 and the homotypic fusion and protein sorting (HOPS) complex, but

102 ein and subunit of the Vps-C complexes HOPS (homotypic fusion and protein sorting) and CORVET (class

103 We find that the tethering complex HOPS (homotypic fusion and protein sorting); the small GTPases

104 We show that the homotypic fusion and protein-sorting/class C vacuole pro

105 ations in the vacuolar tether complex, HOPS (HOmotypic fusion and vacuolar Protein Sorting complex).

106 -to-lysosomal trafficking, controlled by the homotypic fusion and vacuole protein sorting (HOPS) comp

107 The multisubunit tethering homotypic fusion and vacuole protein sorting (HOPS) comp

108 lian homolog of yeast VPS41, a member of the homotypic fusion and vacuole protein sorting (HOPS) comp

109 vacuole/lysosome, they are integrated by the homotypic fusion and vacuole protein sorting (HOPS) comp

110 Homotypic fusion and vacuole protein sorting (HOPS) is a

111 The multisubunit homotypic fusion and vacuole protein sorting (HOPS) memb

112 The conserved vacuolar/lysosomal homotypic fusion and vacuole protein sorting (HOPS) teth

113 lysosome fusion in a manner dependent on the homotypic fusion and vacuole protein sorting (HOPS) teth

114 Qc-SNARE Vam7p is a binding partner for the homotypic fusion and vacuole protein sorting complex (a

115 The large tethering complex, homotypic fusion and vacuole protein sorting complex (HO

116 amily GTPase Ypt7p and its effector complex, homotypic fusion and vacuole protein sorting complex (HO

117 nd that this permeabilization is enhanced by homotypic fusion and vacuole protein sorting complex (HO

118 phate (PI3P) and the tethering complex HOPS (homotypic fusion and vacuole protein sorting complex), w

119 The hexameric vacuolar HOPS (homotypic fusion and vacuole protein sorting) complex in

120 C core vacuole/endosome tethering) and HOPS (homotypic fusion and vacuole protein sorting) tethering

121 e Vps34p, and Vps39p, a subunit of the HOPS (homotypic fusion and vacuole protein sorting) tethering

122 etrameric adaptor protein complex) and HOPS (homotypic fusion and vacuole protein sorting)-tethering

123 r lipids, and the Rab-effector complex HOPS (homotypic fusion and vacuole protein sorting).

124 ctures of Vps33, the SM subunit of the yeast homotypic fusion and vacuole protein-sorting (HOPS) comp

125 omes via an interaction with the class C Vps/homotypic fusion and vacuole protein-sorting (HOPS) comp

126 mutations disrupting all six members of the homotypic fusion and vacuole protein-sorting (HOPS) mult

127 Mitochondrial integrity relies on homotypic fusion between adjacent outer membranes, which

128 it, rotary proton pump whose precise role in homotypic fusion is controversial.

129 ER homotypic fusion is driven by the large GTPase atlastin.

130 nhibit SNARE-mediated fusion and promote the homotypic fusion of Chlamydia inclusions.

131 n RAB families and is essential for in vitro homotypic fusion of early endosomes.

132 The homotypic fusion of endoplasmic reticulum (ER) membranes

133 The homotypic fusion of endoplasmic reticulum membranes is c

134 coding the atlastin-1 GTPase, which mediates homotypic fusion of ER tubules to form the polygonal ER

135 usion from lysosomal fusion and inducing the homotypic fusion of inclusions.

136 RabS(Rab7) mediates homotypic fusion of late endosomes/vacuoles in a homotyp

137 wo distinct processes: microtubule-dependent homotypic fusion of mLDs and expansion of individual mLD

138 Vacuole generation involved the homotypic fusion of Munc13-4(+)/Rab7(+) SGs, followed by

139 1 that implicates the SNARE protein VTI11 in homotypic fusion of protein storage and lytic vacuoles.

140 autophagosomal machinery to CCVs for optimal homotypic fusion of the Coxiella-containing compartments

141 endent membrane fusion pathway in vitro, the homotypic fusion of yeast vacuoles (lysosomes).

142 Like other intracellular fusion events, the homotypic fusion of yeast vacuoles requires a Rab GTPase

143 The homotypic fusion of yeast vacuoles requires the Rab-fami

144 These enlarged endosomes are the result of homotypic fusion promoted by Rab20 expression.

145 Vacuole homotypic fusion requires a group of regulatory lipids t

146 tures from the plasma membrane, and in their homotypic fusion to form phagophore structures.

147 lar compound events (i.e. granule-to-granule homotypic fusion) was severely reduced in the absence of

148 typic fusion of late endosomes/vacuoles in a homotypic fusion- and vacuole protein sorting/Vps41-depe

149 gi network (TGN) to endosome traffic and TGN homotypic fusion.

150 nus of the SaHV-1 gD PFD that contributes to homotypic fusion.

151 trograde transport (clustering) before their homotypic fusion.

152 CC transporters in the regulation of vacuole homotypic fusion.

153 me/prevacuolar compartment (PVC) and for TGN homotypic fusion.

154 and thus prime mammalian COPII vesicles for homotypic fusion.

155 or Arl8 (Arf-like GTPase 8) and its effector homotypic fusion/vacuole protein sorting complex (HOPS)

156 axon terminals form two independent sets of homotypic gap junctions, a feature which might be import

157 uggest that an essential interaction between homotypic gD and gH/gL occurs during both HSV-1 and SaHV

158 rom mice cultured on astrocyte islands with "homotypic" glutamatergic or GABAergic pairs and autaptic

159 While protection against homotypic H5 virus is primarily mediated by virus-neutra

160 hocytic activation molecule (SLAM) family of homotypic haematopoietic cell-specific receptors, we det

161 ads to acute illness and results in lifelong homotypic immunity, but individuals remain susceptible t

162 leads to acute illness followed by lifelong homotypic immunity, but susceptibility to infection by t

163 ence consistent with the expected impacts of homotypic immunity, heterotypic immunity, and immune enh

164 m VE-cadherin results in loss of VE-cadherin homotypic interaction and AJ disassembly; however, the s

165 amiana, we define multiple sites of N domain homotypic interaction and infer that it forms a parallel

166 -1), we previously demonstrated a functional homotypic interaction between gD and gH/gL.

167 The model also predicts an unfavorable homotypic interaction between TFs, helping to explain th

168 o suppress TNF-induced necrosis, and its RIP homotypic interaction motif (RHIM) domain was required t

169 ix (Z-form) and receptor-interacting protein homotypic interaction motif (RHIM) domains for protein h

170 nifested this function by binding to the RIP homotypic interaction motif (RHIM) domains of TRIF and R

171 Here we show that the RIP homotypic interaction motif (RHIM) in RIPK1 prevents the

172 However, an intact RIP homotypic interaction motif (RHIM) is essential.

173 ell death pathway requires an N-terminal RIP homotypic interaction motif (RHIM) within R1, acting in

174 ain a motif with some resemblance to the RIP Homotypic Interaction Motif (RHIM), a domain found in ma

175 ase (RIP) 3 (also called RIPK3) mediates RIP homotypic interaction motif (RHIM)-dependent programmed

176 t apoptosis together with competitors of RIP homotypic interaction motif (RHIM)-dependent signal tran

177 activates programmed necrosis through a RIP homotypic interaction motif-dependent association of TRI

178 partners-RIP1, DAI, or TRIF-via a common RIP homotypic interaction motif.

179 t contain receptor-interacting protein (RIP) homotypic interaction motifs (RHIM) play a key role in c

180 Here, we report that the RIP homotypic interaction motifs (RHIMs) of RIP1 and RIP3 me

181 , located in the SEFIR domain, abolished the homotypic interaction of ACT1 with IL-17 receptors, with

182 t biological relevance for the W187-mediated homotypic interaction of NS1.

183 To examine the homotypic interaction site on gD, we evaluated the funct

184 To map this homotypic interaction site on gH/gL, we generated HSV-1/

185 The NS4A TM domain exhibited a strong homotypic interaction that was comparable in affinity to

186 separate alpha121 and alpha345 networks by a homotypic interaction through their trimeric noncollagen

187 Here we document self-association (homotypic interaction) of the NP of the prototypic arena

188 rt a model in which WRM-1, which can undergo homotypic interaction, binds LIT-1 and thereby generates

189 To map the site of this homotypic interaction, we created a series of gD chimera

190 To define the gH and gL requirements for homotypic interaction, we evaluated the function of a pa

191 gation through transmembrane domain-mediated homotypic interaction.

192 cts with gH also was required for functional homotypic interaction.

193 connect with prospective glomeruli based on homotypic interactions among neurons expressing the same

194 l tether between the two organelles, forming homotypic interactions and heterocomplexes with its homo

195 smic domain of atlastin acts as a tether and homotypic interactions are timed by GTP binding and hydr

196 previously observed to mediate nectin/nectin homotypic interactions as well as TIGIT/necl-5 recogniti

197 ns initiate intracellular signalling through homotypic interactions between epitopes that are specifi

198 Controlling both homotypic interactions between iHeps and heterotypic int

199 The phenotypes indicate that these promote homotypic interactions between melanophores and xanthoph

200 double-positive thymocytes that provide key homotypic interactions between signaling lymphocyte acti

201 Homotypic interactions between the costimulatory molecul

202 we show that this interaction competes with homotypic interactions between the N termini of differen

203 as adherens junction protein, which through homotypic interactions contributes to the maintenance of

204 overlap with an epitope in D4 that mediates homotypic interactions essential for KIT activation.

205 The energetically unfavorable homotypic interactions in D4-7 may be required for re-or

206 -angle scattering data provided evidence for homotypic interactions in D4-7.

207 ogether, our data show that ligand-dependent homotypic interactions in D5 and D7 are essential for VE

208 X-ray scattering data is consistent with the homotypic interactions in D5 and D7.

209 for VEGFR dimerization and activation, with homotypic interactions in D5.

210 Interestingly, the homotypic interactions in the membrane proximal Ig-like

211 These homotypic interactions in turn promote binding of the in

212 e effector caspase-1, which interact through homotypic interactions of caspase recruitment domains (C

213 Moreover, these analyses revealed reversible homotypic interactions of NT5B at low pH and in high cal

214 We have further characterized homotypic interactions of TcpB using hydrogen/deuterium

215 AJs are formed by calcium-dependent homotypic interactions of the ectodomains of single memb

216 high structural similarity among them, only homotypic interactions participate in complex formation,

217 a transition in the stiffness of E-cadherin homotypic interactions regulates actin and membrane dyna

218 n to enhance binding to host cells, B domain homotypic interactions support cell accumulation and bio

219 ns between pre-amyloid oligomers prevent the homotypic interactions that would lead to mature amyloid

220 ct mediated by receptor biasing toward ErbB3 homotypic interactions uncommonly formed by native neure

221 d neuronal development, ALCAM undergoes both homotypic interactions with other ALCAM molecules and he

222 nimal region in Dab2 that modulates platelet homotypic interactions, all of which provide the foundat

223 1 is the only SYP protein that is capable of homotypic interactions, and is able to interact with bot

224 Our results indicate that Cox15 exhibits homotypic interactions, forming highly stable complexes

225 urface involved in the death effector domain homotypic interactions.

226 interaction motif (RHIM) domains for protein homotypic interactions.

227 pre-nucleation events are dominated by Abeta homotypic interactions.

228 The structures reveal similar homotypic interactions: the GRASP domain forms a dimer i

229 JAM-B as the major ligand for JAM-C, whereas homotypic JAM-C interactions remained at background leve

230 e 2 exceeded chance levels (P < .05) for all homotypic (median tetrachoric correlation of rho = 0.54

231 nhancer that is synergistically activated by homotypic MEF2 binding sites.

232 eport that autophagosome maturation requires homotypic membrane fusion catalyzed by SNARE proteins.

233 he dynamin superfamily, is known to catalyse homotypic membrane fusion in the smooth endoplasmic reti

234 Homotypic membrane fusion of the endoplasmic reticulum (

235 network of tubules and sheets that requires homotypic membrane fusion to be maintained.

236 es nucleotide hydrolysis to the catalysis of homotypic membrane fusion to form a branched endoplasmic

237 The formation of the ER requires homotypic membrane fusion, which is mediated by a family

238 Homotypic membrane tethering by the Golgi reassembly and

239 protein (GRASP) proteins are Golgi-localized homotypic membrane tethers that organize Golgi stacks in

240 ss greater efficacy in fusion as compared to homotypic MFN1 or MFN2 complexes.

241 tes mitochondrial fusion exclusively through homotypic MFN2 trans complexes.

242 omotion of axon outgrowth, consistent with a homotypic mode of action.

243 ecific associations for both heterotypic and homotypic motif-pairs with particular haematopoietic cel

244 regulated myeloma cell adhesion, increasing homotypic myeloma cell adhesion while decreasing myeloma

245 ure, nonlinear spatial summation, and strong homotypic neighbor electrical coupling.

246 rate a role for NKG2D-ligand interaction via homotypic NK cell contact in NK cell effector function.

247 o, that innate immune NK cells can engage in homotypic NK-to-NK cell interactions for optimal surviva

248 atorial complexity of eight linkage types in homotypic (one chain type per polymer) and heterotypic (

249 the issue of whether the PLAD mediates only homotypic or also heterotypic interactions remained inco

250 Homotypic or entotic cell-in-cell invasion is an integri

251 Mice were sequentially infected with homotypic or heterotypic DENV serotypes, and T cell subs

252 ccurs upon engagement with their ligands via homotypic or heterotypic interactions.

253 ct structural motifs participating in either homotypic or heterotypic interactions.

254 protected against reinfection with either a homotypic or heterotypic serotype 2 weeks later.

255 - and heterotypic combinations, but only the homotypic pairs were able to trans-complement.

256 We classified strains as homotypic, partly heterotypic, and fully heterotypic bas

257 Homotypic priming induced a robust neutralizing antibody

258 olfactory bulb mitral cells is an emergent, homotypic property of local networks and sensory informa

259 the dimerization domain is consistent with a homotypic protein-protein interaction.

260 tions that are created through extracellular homotypic protein-protein interactions between cadherin

261 t replicate by recruitment and conversion of homotypic proteins into growing protein aggregates.

262 ASC interacts with NLRP3 via a homotypic PYD interaction and recruits procaspase-1 via

263 s form at inflammasomes and that PYD/DED and homotypic PYD interaction modes are similar.

264 PYD- and CARD-containing adapter ASC through homotypic PYD interactions.

265 g a caspase recruitment domain (ASC) through homotypic PYD-PYD interactions and the assembly of an in

266 ocesses, indicating that both connexins form homotypic rather than heterotypic or heteromeric gap jun

267 EGF and a NRG moiety, can potentially drive homotypic receptor interactions and diminish formation o

268 cell membrane regions and ligand-independent homotypic receptor preassembly, thereby preventing sTNF-

269 is thought to result in lifelong immunity to homotypic reinfection (ie, reinfection with the same ser

270 for protection against heterotypic, but not homotypic, reinfection.

271 Homotypic reinfections with DENV-1, DENV-2, and DENV-3 o

272 ored following 5 consecutive days of chronic homotypic restraint stress (CHS), via up-regulating hypo

273 st the A(H1N1)pdm09 vaccine than against the homotypic seasonal A(H1N1) vaccine.

274 phosphomimetic mutant of SNAP23 can mediate homotypic SG fusion in triggered cells.

275 idence is provided for SNAP23 involvement in homotypic SG fusion that occurs in the activated cells.

276 cles in controlling SNAP23 SNARE function in homotypic SG fusion.

277 for both heterotypic SG-plasma membrane and homotypic SG-SG fusion.

278 iases while accounting for the phenomenon of homotypic site clustering commonly observed in developme

279 ed immunity was strongest against completely homotypic strains and weakest against fully heterotypic

280 ne effectiveness, comparing effectiveness of homotypic strains with fully or partly heterotypic strai

281 effectiveness was 94% (95% CI 80-98) against homotypic strains, 71% (39-86) against partly heterotypi

282 accine effectiveness was 83% (78-87) against homotypic strains, 82% (70-89) against single-antigen va

283 ultiple stress-evoked responses to the same (homotypic) stressor experienced repeatedly.

284 trocyte subpopulations selectively regulated homotypic synapses through metabotropic glutamate recept

285 While homotypic TIR domain interactions mediate receptor activ

286 arization drives the transition of S105 from homotypic to heterotypic oligomeric interactions.

287 Our results show that APLP1 forms homotypic trans complexes at cell-cell contacts.

288 derm adhesion through a mechanism other than homotypic trans interactions between the two cell groups

289 t endosomal maturation is essential, whereas homotypic vacuolar fusion is not.

290 rocess, we studied fragment formation during homotypic vacuolar lysosome membrane fusion in Saccharom

291 ical presence of the V-ATPase, that promotes homotypic vacuole fusion in yeast.

292 Studies of homotypic vacuole-vacuole fusion in the yeast Saccharomy

293 y that can provide long-term immunity to the homotypic virus and can provide short-term immunity (onl

294 rovide lifelong humoral immunity against the homotypic virus strain.

295 otyped vesicular stomatitis virus results in homotypic virus-cell fusion.

296 ld increase in blockade response against the homotypic VLP by day 8 postchallenge.

297 todomain assembled ligand independently in a homotypic way.

298 over, the adhesive property occurred in both homotypic with Cx50 expressed in both pairing cells and

299 ecific subtypes pattern mosaics by mediating homotypic (within-subtype) short-range repulsive interac

300 In vitro reconstitution of homotypic yeast vacuole fusion from purified components