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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     Vascular endothelial (VE)-cadherin forms homotypic adherens junctions (AJs) in the endothelium, w
4 lls is associated with its ability to induce homotypic adhesion (HA).
5  These isoforms differentially regulate HLMC homotypic adhesion and survival.
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  of leukocyte migration that is initiated by homotypic adhesive interactions between platelets, leadi
11         The functional significance of these homotypic aggregates in regulating T cell function remai
12  human neutrophils causes rapid (</= 30 min) homotypic aggregation and NET release by a mechanism tha
13                We identify a role for ERK in homotypic aggregation and NET release.
14  undergo a rapid, ECM-dependent mechanism of homotypic aggregation and NETosis in response to C. albi
15 s hyphae and fibronectin, with VLA3 inducing homotypic aggregation and VLA5 regulating NETosis.
16                                      Neither homotypic aggregation nor NETosis occurs when human neut
17 McTNs) that facilitate cell reattachment and homotypic aggregation.
18 IP factor (HBZ), in Jurkat T cells increases homotypic aggregation.
19 activated state permits NETosis but prevents homotypic aggregation.
20 of recombinant Ub precursors to give various homotypic and even branched Ub probes at multi-milligram
21 ignaling mechanism for pseudokinases whereby homotypic and heterotypic association is used to assembl
22 targeting sequence, and participates in both homotypic and heterotypic associations with itself and L
23 sting complex EphA4 signaling involving both homotypic and heterotypic cell-cell interactions.
24 ace and programed cell-cell adhesion between homotypic and heterotypic cells via sequence-specific DN
25 GK domain assembly that influence subsequent homotypic and heterotypic complex formation.
26 ared etiologies and mechanisms, predict both homotypic and heterotypic continuity.
27 tudy investigates the role of T cells during homotypic and heterotypic DENV reinfection.
28 ted by the ability of Hax-1 proteins to form homotypic and heterotypic dimers with binding affinities
29                Macropinosomes mature through homotypic and heterotypic fusion with endosomes and ulti
30  both steady-state and kinetic properties of homotypic and heterotypic GJ channels composed of these
31                  These motifs can facilitate homotypic and heterotypic interactions between TM helice
32 These studies yield a set of rules regarding homotypic and heterotypic interactions that are likely t
33 A (NTD and CTD, respectively) engage in both homotypic and heterotypic interactions to create the cap
34 s share highly conserved C-termini mediating homotypic and heterotypic interactions within and betwee
35 e distribution of these breast cell lines in homotypic and heterotypic invasion assays.
36             However, the association between homotypic and heterotypic NAb titers and protection agai
37 ional intercellular communication in several homotypic and heterotypic populations by visualizing the
38 y testing cognate TFRE activities in varying homotypic and heterotypic promoter architectures.
39 , NS1-CDN vaccinations conferred significant homotypic and heterotypic protection from DENV2-induced
40  and RV5 exert similar effectiveness against homotypic and heterotypic rotavirus strains.
41            Importantly, niclosamide affected homotypic and heterotypic signaling critical to intercel
42        Our results suggest that higher order homotypic and/or heterotypic interactions within distinc
43 connectivity was found both between similar (homotypic) and different (heterotypic) types of cells, w
44              We found that the most abundant homotypic arrangement for p75(NTR) is a trimer and that
45 ncompassing the same set of RBDs as separate homotypic arrays.
46  that the ability of mRNAs to self-sort into homotypic assemblies is an inherent property of an messe
47                                              Homotypic association of SgK269 and SgK223 was also demo
48 nnexin A2 reduces both vesicle formation and homotypic Atg16L vesicle fusion.
49  While the SSPE F required the presence of a homotypic attachment protein, MeV H, in order to fuse, M
50 terotypic interaction being favored over the homotypic Axin DIX interaction.
51                             The diversity of homotypic BcR contacts leading to cell-autonomous signal
52 eles, only IGLV3-21*01 facilitates effective homotypic BCR-BCR interaction that results in autonomous
53        Further, we found that IgSF9 mediated homotypic binding and cell aggregation, but failed to in
54                                              Homotypic binding of rVN was also seen.
55 equently observed, the mechanistic basis for homotypic binding site synergy is poorly understood.
56                                        These homotypic binding sites often exhibit synergy, whereby t
57 cell surface receptor that identifies kin by homotypic binding, and in so doing exchanges outer membr
58  activated N-methyl-d-aspartate receptors in homotypic, but not heterotypic, MSNs.
59 uggesting that adhesion could be mediated by homotypic CdiA-CdiA interactions.
60  functions as a retention factor, increasing homotypic cell adhesion and limiting tumor spreading to
61 3, 4B4, and AIIB2 by their ability to induce homotypic cell aggregation.
62                                     We model homotypic cell-cell adhesion and heterotypic cell-baseme
63                                  Bdl induces homotypic cell-cell adhesion in vitro and mediates neuri
64 reased cell-substrate adhesion and decreased homotypic cell-cell adhesion strength.
65 cell death initiated by actomyosin-dependent homotypic cell-in-cell invasion that can be observed in
66 Therefore, our data uncover the existence of homotypic cell-to-cell communication among mobile innate
67            The latter include seven types of homotypic chains as well as mixed ubiquitin chains.
68         While structural characterization of homotypic chains has been well elucidated, less is known
69 TFs, helping to explain the observation that homotypic chains of binding sites express at low levels.
70 d the expression driven by CREs comprised of homotypic chains of KLF4 binding sites.
71 S attenuated the immune response to a second homotypic challenge.
72 timulated DSG3-CAART IFN-gamma secretion and homotypic clustering, consistent with an activated pheno
73  act as direct drivers of gene expression in homotypic clusters of binding sites, independent of spac
74 ltiple copies of single mRNAs organize into 'homotypic clusters' that occupy defined positions within
75 ranules) are composed of RNA, in the form of homotypic clusters, and proteins required for germline d
76 ctor binding site (TFBS) patterns, including homotypic clusters, heterotypic clusters, and enhanceoso
77 ed from the same gene assemble into discrete homotypic clusters.
78  following cargo binding to the neighboring, homotypic coiled-coil region.
79 n1 and Mfn2 and abolishes fusion activity of homotypic complexes.
80  KIT mutations, reveals that the strength of homotypic contacts and the cooperativity in the action o
81 ative interactions mediated by multiple weak homotypic contacts between receptor molecules are respon
82                                           At homotypic contacts, junctional N-cadherin bonds downregu
83 uture occurrences of both the same disorder (homotypic continuity) and other disorders (heterotypic c
84 nd not an artifact of failure to control for homotypic continuity.
85 region of the BicD structure with classical, homotypic core packing.
86                                Akin to their homotypic counterparts, branched chains elicit a wide ar
87 ct of the heavily studied coding benefits of homotypic coupling to heterotypic coupling across parall
88 el mechanism for electrical rectification in homotypic Cx36 GJs.
89 gardless of the specific type of GJ channel (homotypic Cx43 and Cx45, and heterotypic Cx43/Cx45 and C
90 ermore, these mutations induced formation of homotypic DC clusters, which represent close correlates
91                                              Homotypic death domain (DD)-DD interactions are importan
92 rate phages that are either closely related (homotypic defence) or unrelated (heterotypic defence) to
93                           Four patients with homotypic DENV reinfections were identified and confirme
94 ibe the first set of virologically confirmed homotypic DENV reinfections.
95 ally forms heterodimers with Dpp rather than homotypic dimers, providing a possible explanation for t
96     We recently reported that a trans-dimer, homotypic disulfide bond involving Cys367 in keratin 14
97 have evolved means to preferentially take up homotypic DNA containing short and genus-specific sequen
98 ents and fluid properties of heterotypic and homotypic droplets.
99 cadherin recapitulated this outcome, whereas homotypic E-cadherin engagement promoted apoptotic signa
100 s in spatial chromatin conformation based on homotypic enhancer association, resulting in cooperative
101 with an inert interface and during fusion of homotypic epithelial layers.
102 um (ER) network is dynamically maintained by homotypic (ER-ER) fusion.
103 further highlight the potential relevance of homotypic Fab:Fab interactions in targeting oligomeric c
104 engages a composite epitope and an extensive homotypic Fab:Fab interface.
105                        We further identify a homotypic FnIII-2-FnIII-2 interaction in mediating the d
106 ety with polarized fluorescent light elicits homotypic Forster resonance energy transfer (homo-FRET),
107 n GSC enabled perivascular migration through homotypic forward signalling.
108  lysosome depends on the GTPase Rab7 and the homotypic fusion and protein sorting (HOPS) complex, but
109  vacuole/endosome tethering (CORVET) and the homotypic fusion and protein sorting (HOPS) complexes, w
110 d Vps41, independent of their known roles in homotypic fusion and protein sorting (HOPS)-mediated ves
111     We find that the tethering complex HOPS (homotypic fusion and protein sorting); the small GTPases
112 ntify VPS39-a gene encoding a subunit of the homotypic fusion and protein-sorting (HOPS) complex-as a
113                             We show that the homotypic fusion and protein-sorting/class C vacuole pro
114 vacuole/lysosome, they are integrated by the homotypic fusion and vacuole protein sorting (HOPS) comp
115 -to-lysosomal trafficking, controlled by the homotypic fusion and vacuole protein sorting (HOPS) comp
116                   The multisubunit tethering homotypic fusion and vacuole protein sorting (HOPS) comp
117 lian homolog of yeast VPS41, a member of the homotypic fusion and vacuole protein sorting (HOPS) comp
118               VPS16 encodes a subunit of the homotypic fusion and vacuole protein sorting (HOPS) comp
119 , a component of the endolysosomal tethering homotypic fusion and vacuole protein sorting (HOPS) comp
120                                              Homotypic fusion and vacuole protein sorting (HOPS) is a
121                             The multisubunit homotypic fusion and vacuole protein sorting (HOPS) memb
122 lysosome fusion in a manner dependent on the homotypic fusion and vacuole protein sorting (HOPS) teth
123 (SNAREs), that catalyze membrane fusion, and homotypic fusion and vacuole protein sorting (HOPS), tha
124                 The large tethering complex, homotypic fusion and vacuole protein sorting complex (HO
125 phate (PI3P) and the tethering complex HOPS (homotypic fusion and vacuole protein sorting complex), w
126                 The hexameric vacuolar HOPS (homotypic fusion and vacuole protein sorting) complex in
127 he yeast vacuolar tethering/SM complex HOPS (homotypic fusion and vacuole protein sorting) increases
128 C core vacuole/endosome tethering) and HOPS (homotypic fusion and vacuole protein sorting) tethering
129 m yeast vacuoles including SNAREs, the HOPS (homotypic fusion and vacuole protein sorting) tethering
130 r lipids, and the Rab-effector complex HOPS (homotypic fusion and vacuole protein sorting).
131 ctures of Vps33, the SM subunit of the yeast homotypic fusion and vacuole protein-sorting (HOPS) comp
132            Mitochondrial integrity relies on homotypic fusion between adjacent outer membranes, which
133 it, rotary proton pump whose precise role in homotypic fusion is controversial.
134 nhibit SNARE-mediated fusion and promote the homotypic fusion of Chlamydia inclusions.
135 n RAB families and is essential for in vitro homotypic fusion of early endosomes.
136 VE3 (RHD3) is an atlastin GTPase involved in homotypic fusion of endoplasmic reticulum (ER) tubules i
137                                          The homotypic fusion of endoplasmic reticulum membranes is c
138 coding the atlastin-1 GTPase, which mediates homotypic fusion of ER tubules to form the polygonal ER
139 eatment, a process that is paralleled by the homotypic fusion of granules and their heterotypic fusio
140 ces Chlamydia pathogenicity by promoting the homotypic fusion of inclusions and shares structural and
141 usion from lysosomal fusion and inducing the homotypic fusion of inclusions.
142              Vacuole generation involved the homotypic fusion of Munc13-4(+)/Rab7(+) SGs, followed by
143 1 that implicates the SNARE protein VTI11 in homotypic fusion of protein storage and lytic vacuoles.
144 autophagosomal machinery to CCVs for optimal homotypic fusion of the Coxiella-containing compartments
145 endent membrane fusion pathway in vitro, the homotypic fusion of yeast vacuoles (lysosomes).
146  Like other intracellular fusion events, the homotypic fusion of yeast vacuoles requires a Rab GTPase
147   These enlarged endosomes are the result of homotypic fusion promoted by Rab20 expression.
148 tures from the plasma membrane, and in their homotypic fusion to form phagophore structures.
149 lar compound events (i.e. granule-to-granule homotypic fusion) was severely reduced in the absence of
150  and thus prime mammalian COPII vesicles for homotypic fusion.
151 nus of the SaHV-1 gD PFD that contributes to homotypic fusion.
152 trograde transport (clustering) before their homotypic fusion.
153 ipids throughout the stages of yeast vacuole homotypic fusion.
154 me/prevacuolar compartment (PVC) and for TGN homotypic fusion.
155 gi network (TGN) to endosome traffic and TGN homotypic fusion.
156 or Arl8 (Arf-like GTPase 8) and its effector homotypic fusion/vacuole protein sorting complex (HOPS)
157  axon terminals form two independent sets of homotypic gap junctions, a feature which might be import
158 uggest that an essential interaction between homotypic gD and gH/gL occurs during both HSV-1 and SaHV
159 rom mice cultured on astrocyte islands with "homotypic" glutamatergic or GABAergic pairs and autaptic
160                     While protection against homotypic H5 virus is primarily mediated by virus-neutra
161 hocytic activation molecule (SLAM) family of homotypic haematopoietic cell-specific receptors, we det
162 ads to acute illness and results in lifelong homotypic immunity, but individuals remain susceptible t
163  leads to acute illness followed by lifelong homotypic immunity, but susceptibility to infection by t
164  virus 1 (HSV1) UL39-encoded ICP6 blocks RIP homotypic interacting motif (RHIM) signal transduction,
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 F, the four mammalian proteins harboring RIP homotypic interaction motif (RHIM) domains, are key comp
172                    Here we show that the RIP homotypic interaction motif (RHIM) in RIPK1 prevents the
173                       However, an intact RIP homotypic interaction motif (RHIM) is essential.
174 ell death pathway requires an N-terminal RIP homotypic interaction motif (RHIM) within R1, acting in
175 ain a motif with some resemblance to the RIP Homotypic Interaction Motif (RHIM), a domain found in ma
176     RIPK1 deficiency, or mutation of its RIP homotypic interaction motif (RHIM), triggers ZBP1-depend
177                Caspase-6 facilitated the RIP homotypic interaction motif (RHIM)-dependent binding of
178 t apoptosis together with competitors of RIP homotypic interaction motif (RHIM)-dependent signal tran
179 perinatal lethality in mice in which the RIP homotypic interaction motif domain of RIPK1 has been mut
180  activates programmed necrosis through a RIP homotypic interaction motif-dependent association of TRI
181 partners-RIP1, DAI, or TRIF-via a common RIP homotypic interaction motif.
182  to RHIM [receptor-interacting protein (RIP) homotypic interaction motif], an amyloid motif regulatin
183 t contain receptor-interacting protein (RIP) homotypic interaction motifs (RHIM) play a key role in c
184 , located in the SEFIR domain, abolished the homotypic interaction of ACT1 with IL-17 receptors, with
185                               To examine the homotypic interaction site on gD, we evaluated the funct
186                                  To map this homotypic interaction site on gH/gL, we generated HSV-1/
187        The NS4A TM domain exhibited a strong homotypic interaction that was comparable in affinity to
188 separate alpha121 and alpha345 networks by a homotypic interaction through their trimeric noncollagen
189 rt a model in which WRM-1, which can undergo homotypic interaction, binds LIT-1 and thereby generates
190                      To map the site of this homotypic interaction, we created a series of gD chimera
191     To define the gH and gL requirements for homotypic interaction, we evaluated the function of a pa
192 gation through transmembrane domain-mediated homotypic interaction.
193 cts with gH also was required for functional homotypic interaction.
194  connect with prospective glomeruli based on homotypic interactions among neurons expressing the same
195 l tether between the two organelles, forming homotypic interactions and heterocomplexes with its homo
196 smic domain of atlastin acts as a tether and homotypic interactions are timed by GTP binding and hydr
197 previously observed to mediate nectin/nectin homotypic interactions as well as TIGIT/necl-5 recogniti
198 ns initiate intracellular signalling through homotypic interactions between epitopes that are specifi
199                             Controlling both homotypic interactions between iHeps and heterotypic int
200   The phenotypes indicate that these promote homotypic interactions between melanophores and xanthoph
201  double-positive thymocytes that provide key homotypic interactions between signaling lymphocyte acti
202 kably strong adhesion forces by establishing homotypic interactions between single cells, leading to
203                                              Homotypic interactions between the costimulatory molecul
204  we show that this interaction competes with homotypic interactions between the N termini of differen
205       TraA is fluid on the cell surface, and homotypic interactions between TraA from juxtaposed cell
206  overlap with an epitope in D4 that mediates homotypic interactions essential for KIT activation.
207 X-ray scattering data is consistent with the homotypic interactions in D5 and D7.
208  for VEGFR dimerization and activation, with homotypic interactions in D5.
209                           Interestingly, the homotypic interactions in the membrane proximal Ig-like
210  that tau filament ends engage in a range of homotypic interactions involving monomers, oligomers, an
211       Biomolecular interactions-particularly homotypic interactions mediated by self-associating intr
212            Functional analyses revealed that homotypic interactions occur for all Ag43 classes but si
213 e effector caspase-1, which interact through homotypic interactions of caspase recruitment domains (C
214 Moreover, these analyses revealed reversible homotypic interactions of NT5B at low pH and in high cal
215                We have further characterized homotypic interactions of TcpB using hydrogen/deuterium
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 chanism whereby UnDOx enables the controlled homotypic interactions within the distal titin spring to
223     Our results indicate that Cox15 exhibits homotypic interactions, forming highly stable complexes
224 interaction motif (RHIM) domains for protein homotypic interactions.
225 pre-nucleation events are dominated by Abeta homotypic interactions.
226 induces structural ordering of PbCSP through homotypic interactions.
227                The structures reveal similar homotypic interactions: the GRASP domain forms a dimer i
228 JAM-B as the major ligand for JAM-C, whereas homotypic JAM-C interactions remained at background leve
229  Rho GTPase-activating protein, Gap21/23, to homotypic junctions.
230 LLPS de novo as well as prevent formation of homotypic liquid droplets.
231 e 2 exceeded chance levels (P < .05) for all homotypic (median tetrachoric correlation of rho = 0.54
232 nhancer that is synergistically activated by homotypic MEF2 binding sites.
233 ar clamp that is essential for IncA-mediated homotypic membrane fusion during infection.
234 he dynamin superfamily, is known to catalyse homotypic membrane fusion in the smooth endoplasmic reti
235                                              Homotypic membrane fusion of the endoplasmic reticulum (
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 omotion of axon outgrowth, consistent with a homotypic mode of action.
241 ecific associations for both heterotypic and homotypic motif-pairs with particular haematopoietic cel
242 ure, nonlinear spatial summation, and strong homotypic neighbor electrical coupling.
243 e VGluT3 cells and the distribution of their homotypic neighbors.
244  relation to the spatial positioning of such homotypic neighbors; rather, this cell type modulates th
245 rate a role for NKG2D-ligand interaction via homotypic NK cell contact in NK cell effector function.
246 o, that innate immune NK cells can engage in homotypic NK-to-NK cell interactions for optimal surviva
247 atorial complexity of eight linkage types in homotypic (one chain type per polymer) and heterotypic (
248  the issue of whether the PLAD mediates only homotypic or also heterotypic interactions remained inco
249                                              Homotypic or entotic cell-in-cell invasion is an integri
250         Mice were sequentially infected with homotypic or heterotypic DENV serotypes, and T cell subs
251 ccurs upon engagement with their ligands via homotypic or heterotypic interactions.
252 ct structural motifs participating in either homotypic or heterotypic interactions.
253  protected against reinfection with either a homotypic or heterotypic serotype 2 weeks later.
254                     We classified strains as homotypic, partly heterotypic, and fully heterotypic bas
255 EDWI-3 degrades numerous neoblast mRNAs in a homotypic ping-pong cycle, it is also guided to another
256 le of intercellular instructed-assembly from homotypic precursors, this work illustrates a new approa
257 adherin 11, and protocadherin 19) results in homotypic preference ex vivo and patterning robustness i
258                                              Homotypic priming induced a robust neutralizing antibody
259 iple mechanisms, including interference with homotypic protein interactions and the selection of the
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 s form at inflammasomes and that PYD/DED and homotypic PYD interaction modes are similar.
263 PYD- and CARD-containing adapter ASC through homotypic PYD interactions.
264 g a caspase recruitment domain (ASC) through homotypic PYD-PYD interactions and the assembly of an in
265 ocesses, indicating that both connexins form homotypic rather than heterotypic or heteromeric gap jun
266                                  SLAMF6 is a homotypic receptor of the Ig-superfamily whose exact rol
267 is thought to result in lifelong immunity to homotypic reinfection (ie, reinfection with the same ser
268  for protection against heterotypic, but not homotypic, reinfection.
269                                              Homotypic reinfections with DENV-1, DENV-2, and DENV-3 o
270 ling has been reported to occur only between homotypic retinal ganglion cells, in line with the conce
271 e propensity for heterotypic peptide-RNA and homotypic RNA LLPS, which results in a switch between co
272  phosphomimetic mutant of SNAP23 can mediate homotypic SG fusion in triggered cells.
273 idence is provided for SNAP23 involvement in homotypic SG fusion that occurs in the activated cells.
274 cles in controlling SNAP23 SNARE function in homotypic SG fusion.
275  for both heterotypic SG-plasma membrane and homotypic SG-SG fusion.
276 itment of distant T cells through long-range homotypic signalling, in part mediated via the diffusion
277 iases while accounting for the phenomenon of homotypic site clustering commonly observed in developme
278                          Here we encapsulate homotypic spinal cord neural stem cells (scNSCs) in an a
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 f pubertal immune challenge in response to a homotypic stressor later in life in CD-1 mice.
284 uated immune response following a subsequent homotypic stressor.
285 ultiple stress-evoked responses to the same (homotypic) stressor experienced repeatedly.
286 trocyte subpopulations selectively regulated homotypic synapses through metabotropic glutamate recept
287  of deMs due to their dominant employment of homotypic TF binding site (TFBS) clusters, as opposed to
288                   These findings thus reveal homotypic tiling of LTMR subtype axonal projections in h
289 arization drives the transition of S105 from homotypic to heterotypic oligomeric interactions.
290 al projections also exhibit a fine degree of homotypic topographic adjacency.
291            Our results show that APLP1 forms homotypic trans complexes at cell-cell contacts.
292 rocess, we studied fragment formation during homotypic vacuolar lysosome membrane fusion in Saccharom
293 ical presence of the V-ATPase, that promotes homotypic vacuole fusion in yeast.
294  added dioctanoyl (C8) PI(3,5)P(2) abolishes homotypic vacuole fusion.
295                                   Studies of homotypic vacuole-vacuole fusion in the yeast Saccharomy
296 otyped vesicular stomatitis virus results in homotypic virus-cell fusion.
297 ld increase in blockade response against the homotypic VLP by day 8 postchallenge.
298 todomain assembled ligand independently in a homotypic way.
299 over, the adhesive property occurred in both homotypic with Cx50 expressed in both pairing cells and
300                   In vitro reconstitution of homotypic yeast vacuole fusion from purified components

 
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