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1 LAT into MCs due to retargeting of LAT to an intracellular compartment.
2 gets certain isoforms of the protein to this intracellular compartment.
3 ins label both the Golgi and also an unknown intracellular compartment.
4 tilin shedding at the cell surface and in an intracellular compartment.
5 in, resulted in accumulation of KCa2.3 in an intracellular compartment.
6 erroportin was retained abnormally within an intracellular compartment.
7  store, suggesting that Mg was trapped in an intracellular compartment.
8 d localization of the protein product to the intracellular compartment.
9  and glutathione redox potential within each intracellular compartment.
10 synthesized when this bacterium is within an intracellular compartment.
11 e hypothesis that T2R sorting occurs from an intracellular compartment.
12  to malaria DNA by targeting it to a TLR9(+) intracellular compartment.
13 nfection, prior to relocation to a different intracellular compartment.
14 in increases delivery of enterobactin to the intracellular compartment.
15  subcellular localization in an unidentified intracellular compartment.
16 alized both at the plasma membrane and in an intracellular compartment.
17 s to be pH dependent, requiring an acidified intracellular compartment.
18 n of the GH.GHR complex both proceed from an intracellular compartment.
19 t cell types studied, MYOC is limited to the intracellular compartment.
20 ion of the deficient enzyme into its natural intracellular compartment.
21 phosphate removed during hemodialysis is the intracellular compartment.
22  hypothesis that signaling may occur from an intracellular compartment.
23 ponse following exposure of viral DNA to the intracellular compartment.
24 genous human wild-type SOD1 (HuWtSOD1) in an intracellular compartment.
25 ted in rapid transport of CD244 to an acidic intracellular compartment.
26 n also function as a second messenger in the intracellular compartment.
27 direct evidence for PA dynamics in different intracellular compartments.
28 an be internalized and localized to specific intracellular compartments.
29 tion of the transporter from cell surface to intracellular compartments.
30 entified, although these may function within intracellular compartments.
31 TPase (V-H(+)-ATPase), which modulates pH in intracellular compartments.
32 les and its requirement for acidification of intracellular compartments.
33 or peptide motifs that localize to different intracellular compartments.
34 ins are essential players in the dynamics of intracellular compartments.
35 sicles cycle between the plasma membrane and intracellular compartments.
36  transducer of signals from extracellular to intracellular compartments.
37  apoptosis and delivery of other proteins to intracellular compartments.
38 r to biological pathogens to target specific intracellular compartments.
39  so the folding mechanism can be modified by intracellular compartments.
40 ptors and/or proteins and their ligands into intracellular compartments.
41 e (v-ATPase) is a proton pump that acidifies intracellular compartments.
42 hosphorylated LRP1 primarily originates from intracellular compartments.
43              Intravascular PAF has access to intracellular compartments.
44 of information between the extracellular and intracellular compartments.
45 , and CpG-A and CpG-B accumulate in distinct intracellular compartments.
46 d perhaps for pH regulation in highly acidic intracellular compartments.
47  assessment of oxidant signaling in distinct intracellular compartments.
48 in acute pancreatitis and may require low pH intracellular compartments.
49 asis of the thiol redox environment in their intracellular compartments.
50 etained during ATP7B trafficking between the intracellular compartments.
51 liver zinc to certain metalloproteins within intracellular compartments.
52 coprotein- and dynamin-dependent fusion with intracellular compartments.
53 to mediate their efficient transport between intracellular compartments.
54 rates, Akt needs to be recruited to specific intracellular compartments.
55 lasma membrane of Na,K-ATPase molecules from intracellular compartments.
56  is activated by DNA presented in acidified, intracellular compartments.
57 ertion of CFTR into the plasma membrane from intracellular compartments.
58 smembrane proteins, which reside in distinct intracellular compartments.
59 se typically lysosomal proteases in distinct intracellular compartments.
60 ynthesis of unique metabolites in unexpected intracellular compartments.
61 lization at, and signaling by, G proteins at intracellular compartments.
62  assembles on, and accumulates within, these intracellular compartments.
63 osphorylated caveolin-2 primarily resides in intracellular compartments.
64 identify than proteins that are localized in intracellular compartments.
65 tribution of DRA from the apical membrane to intracellular compartments.
66 atch to the rest of the cell membrane and/or intracellular compartments.
67  and the remainder trafficked to more distal intracellular compartments.
68 le production and redirects processed Gag to intracellular compartments.
69 , the Na(+),K(+)-ATPase was redistributed to intracellular compartments.
70 tence of functional groups of RyR2s in these intracellular compartments.
71 ity of trafficking between cell membrane and intracellular compartments.
72 P in synaptic spines or recruited MT5-MMP to intracellular compartments.
73 r that can carry ligand-decorated "cargo" to intracellular compartments.
74 uggest that autoactive FGFR2 can signal from intracellular compartments.
75 on levels both on the plasma membrane and in intracellular compartments.
76 istant aptamers do not efficiently enter the intracellular compartments.
77 y be internalized and transported to various intracellular compartments.
78 orts for cleavage products to the extra- and intracellular compartments.
79 n previously shown to target VCP to specific intracellular compartments.
80 cadherin complexes from lateral membranes to intracellular compartments.
81 gnate host receptors or entering into acidic intracellular compartments.
82  to targeted degradation of cAMP in specific intracellular compartments.
83 r protein synthesis to occur within discrete intracellular compartments.
84 space or by sequestering cytoplasmic Zn into intracellular compartments.
85  combined with a lipidomic analysis of PA in intracellular compartments.
86 ntrol of ERK signalling exerted at different intracellular compartments.
87 ductance allowing efficient acidification of intracellular compartments.
88  and accumulation of cargoes within discrete intracellular compartments.
89 otides from late endosomes rather than other intracellular compartments.
90 etion-induced accumulation of Na,K-ATPase in intracellular compartments.
91 is inhibitor-induced accumulation of CSCs in intracellular compartments.
92 lfated glycosphingolipids were only found in intracellular compartments.
93 definition of specific trafficking steps and intracellular compartments.
94 ing its internalization from cell surface to intracellular compartments.
95      Recently, TLR2 was found to signal from intracellular compartments.
96 as an impaired maturation and retention into intracellular compartments.
97 dephosphorylate their substrates on specific intracellular compartments.
98 m three compartments in human brain in vivo: intracellular (compartment 1), extracellular (compartmen
99 by the HIV-1 envelope glycoproteins occur in intracellular compartments accessible only to small inhi
100 al cells, is internalized and accumulates in intracellular compartments after renal ischemic injury.
101                The FcRn resides in an acidic intracellular compartment, allowing it to bind IgG.
102 nsition of the hydrophobic brushes in acidic intracellular compartments, allows for triggered intrace
103 termini of GPCRs in the export from distinct intracellular compartments along the secretory pathway.
104 hen lysed, expressed FliC within a protected intracellular compartment and evaded stimulation of FliC
105 eceptor that recognizes its ligand within an intracellular compartment and not at the plasma membrane
106 galovirus (HCMV) acquires its membrane in an intracellular compartment and we show that Stx3-5R stron
107 , which differentially lead them to the same intracellular compartments and adjacent to phagosomes co
108           The third and final wave occurs at intracellular compartments and could be elicited by G pr
109 CIN85 resulted in accumulation of TbetaRI in intracellular compartments and diminished TGFbeta-stimul
110 he N54K mutant was retained primarily within intracellular compartments and displayed dominant or tra
111  this adapter are internalized into distinct intracellular compartments and dissipate rapidly upon TC
112 nd in the plasma membrane as well as various intracellular compartments and it has been suggested to
113  of Npt2a from proximal tubule microvilli to intracellular compartments and lysosomes alongside a PTH
114 life of a cell: from shuttling cargo through intracellular compartments and onto the cell surface, ho
115 ocytic vesicles for trafficking into various intracellular compartments and pathways.
116 ts of the inflammasome machinery in distinct intracellular compartments and release IL-1beta and IL-1
117 aled that the H89G mutation retargets Gag to intracellular compartments and severely inhibits virus p
118                 The proteins act within most intracellular compartments and span the molecular determ
119      These receptor subtypes traffic between intracellular compartments and the plasma membrane and f
120 gulated Ca(2+) channel that shuttles between intracellular compartments and the plasma membrane.
121 bution of alpha3* nAChRs between specialized intracellular compartments and the plasma membrane.
122 membrane protein Atg9 cycles between certain intracellular compartments and the vesicle nucleation si
123 ty to localize to different cell surface and intracellular compartments and their ability to interact
124  are ATP-dependent proton pumps that acidify intracellular compartments and, in some cases, transport
125 stribution of KCNN4c proteins into subapical intracellular compartment, and a biotinylation assay sho
126 n bacterial transporters and transporters of intracellular compartments, and (b) patch clamp and volt
127 PARs including partially assembled AMPARs in intracellular compartments, and electrophysiological app
128 lucidate how molecules enter cells, traverse intracellular compartments, and interact with sites of a
129 alization of P. gingivalis into DC-SIGN-rich intracellular compartments, and MoDCs secrete low levels
130 that Ras and ERK can be activated at various intracellular compartments, and that RTKs can modulate R
131  plasma membrane or through sequestration in intracellular compartments, and that SLC39 family transp
132 nt biological window, target to all relevant intracellular compartments, and to facilitate imaging at
133                                     However, intracellular compartments are crowded by macromolecules
134 echanisms that regulate the acidification of intracellular compartments are key to host defense again
135 curs not only at the cell membrane, but from intracellular compartments as well.
136  (Slo1(VEDEC)) that is typically retained in intracellular compartments, as assessed by cell-surface
137  nanoART that facilitates drug depots within intracellular compartments at or adjacent to the sites o
138 tion of a patch derived from rapid fusion of intracellular compartments at the wound site.
139 tes the import of extracellular S1P into the intracellular compartment before its degradation.
140 TLR3 is located in early endosomes and other intracellular compartments but migrates to LAMP1(+) endo
141 KT9 and NP-hTf were internalized into acidic intracellular compartments but were not localized in EEA
142 nto an endoplasmic reticulum (ER)-associated intracellular compartment, but the mechanisms of HBV ass
143 valently linked heterologous antigens to the intracellular compartment by traversing the plasma membr
144 by uptake from the extracellular towards the intracellular compartment by way of equilibrative nucleo
145 h whereby antigens were targeted to distinct intracellular compartments by receptor-mediated internal
146  promote cAMP diffusion and propagation into intracellular compartments by sequestrating phosphodiest
147 lting in differentiated bacteria enclosed in intracellular compartments called symbiosomes within nod
148  of many viruses is associated with specific intracellular compartments called virus factories or vir
149 shift in water from the extracellular to the intracellular compartment can lead to cerebral edema and
150 ansporters and binding proteins at different intracellular compartments can alter the content and dis
151 ce that Akt activation may take place within intracellular compartments challenges this dogma.
152 rdings, suggesting that steroid diffusion to intracellular compartments competes with receptor potent
153 nce between supply and demand in eukaryotes, intracellular compartments contain metal transporters th
154 eins were almost exclusively detected in the intracellular compartment, contrary to WT netrin-1, whic
155 Finally, we show that BST2 resides within an intracellular compartment corresponding to the Golgi app
156 ch coding for proteins targeted to different intracellular compartments--cytoplasmic (CytCK), mitocho
157 such as annexin V; caspase activation in the intracellular compartment, detected by labeled enzyme su
158 gesting that the early capture of virus into intracellular compartments did not depend on endosomal m
159 C class II broader access to antigens within intracellular compartments distinct from the endosomal n
160 ing a dual role: (i) maintaining channels in intracellular compartments downsizing their surface expr
161 e presence of parallel pathways and multiple intracellular compartments, each having its own ROS sour
162 a Mac1-dependent fashion, and relocated into intracellular compartments enriched in cyclooxygenase1 (
163 , most likely by interacting with M3Rs in an intracellular compartment (ER).
164 IgG3-Av shows that the TfR is directed to an intracellular compartment expressing the lysosomal marke
165 rial toxins require localization to specific intracellular compartments following injection into host
166 n that takes place at the cell surface or in intracellular compartments following virus uptake.
167                              We identify two intracellular compartments for the sequestration of misf
168 e to recycle IL-15.IL-15Ralpha complexes via intracellular compartments, for residual proliferation i
169  allows stabilization of CFTR in a regulated intracellular compartment from which it traffics to the
170     However, for viruses that fuse inside of intracellular compartments, fusion-inhibitory peptides h
171  find that damage triggers rampant fusion of intracellular compartments, generating a barrier that li
172                                          The intracellular compartment harboring Toxoplasma gondii sa
173 ow-pH trigger are modulated by properties of intracellular compartments harboring the virus.
174 art from the cytosol and lysosomes, no other intracellular compartment has been successfully targeted
175      Measurement of changes of pH at various intracellular compartments has potential to solve questi
176 discuss the cross talk between autophagy and intracellular compartments, highlighting recent exciting
177 of membrane receptors and their ligands into intracellular compartments, however, the significance an
178 rhythmia and the retention of Na(v)1.5 in an intracellular compartment in cardiomyocytes.
179 pool of endogenous PC2 redistributes into an intracellular compartment in MDCK cells without any chan
180 ctively, this paper (a) tracks TLR9 to a new intracellular compartment in PLTs and (b) describes a no
181 rodimers occur on the cell surface and in an intracellular compartment in response to SDF-1.
182 , which implies that the acidification of an intracellular compartment in the receiving cells is cruc
183                                 To date, the intracellular compartment in which PG is detected by NOD
184 ually cycles between the plasma membrane and intracellular compartments in basal cells, and the major
185 ribution of old and new proteins marking all intracellular compartments in budding yeasts.
186 lar processes through controlling acidity of intracellular compartments in eukaryotes.
187                            The complexity of intracellular compartments in eukaryotic cells evolved t
188 ates V-ATPase-dependent acidification of the intracellular compartments in human proximal tubular cel
189  cell membrane of resting macrophages and in intracellular compartments in L.
190 rst time that flavocytochrome b localizes to intracellular compartments in macrophages that recycle t
191 rus to assemble and accumulate in apparently intracellular compartments in macrophages.
192 tor that directs target proteins to distinct intracellular compartments in neurons.
193 copper transporter that traffics between the intracellular compartments in response to copper elevati
194           By contrast, MIG-14 accumulates in intracellular compartments in retromer mutants.
195 ing of the transporter to insulin-responsive intracellular compartments in the basal state or that is
196 e we quantified ROS dynamics within specific intracellular compartments in the cytosol and mitochondr
197 n of cholesterol from the plasma membrane to intracellular compartments in the knockdown cells.
198 ot been possible to visualize rapidly moving intracellular compartments in three dimensions in cells.
199                    MT6/MMP25, sequestered in intracellular compartments in unstimulated NK cells, tra
200  distinct pH optima identical to that of the intracellular compartments in which each CD1 isoform res
201    In dim light conditions, AHA2 is found in intracellular compartments, in addition to the plasma me
202 body as expected, but instead accumulates in intracellular compartments including Syntaxin-13- and RA
203       The Sec13 protein functions in various intracellular compartments including the nuclear pore co
204 EK-293 cells, PAT1 is highly concentrated in intracellular compartments, including endosomes, wherein
205 sidency P2XRs also populate the membranes of intracellular compartments, including mammalian lysosome
206  adenosine triphosphatase (ATPase) acidifies intracellular compartments, including synaptic vesicles
207  the ambient redox potentials in the various intracellular compartments, influence the status of redo
208 s the escape of the genetic cargo out of the intracellular compartments into the cytosol.
209 ing of transmembrane receptors to a specific intracellular compartment is conducted by adaptor molecu
210                  The accumulation of AHA2 in intracellular compartments is consistent with reduced H(
211     Targeting SOD to endothelial surface vs. intracellular compartments is desirable to prevent patho
212                        The high viscosity of intracellular compartments is likely to play an importan
213 otein 1 (AP-1) complex in protein sorting in intracellular compartments is not yet completely defined
214 olling signaling from receptors localized at intracellular compartments is still very limited.
215 or (DOPr), a GPCR constitutively targeted to intracellular compartments, is driven to the surface mem
216                 Although localized mostly in intracellular compartments, little is understood regardi
217                                              Intracellular compartments make up roughly two-thirds of
218 ts that defects in protein maturation in one intracellular compartment may be compensated for by adju
219  function, O(2) gradients between extra- and intracellular compartments may vary and play important p
220 t many alpha4beta2 nAChRs, remain in neutral intracellular compartments, mostly the ER.
221                        OSCAR localized in an intracellular compartment of alveolar macrophages togeth
222 (TLR4) was expressed both on the surface and intracellular compartment of HMVEC-Ls.
223 In leaves, MDA occurred predominantly in the intracellular compartment of mesophyll cells and was enr
224 n optical fibre can guide visible light into intracellular compartments of a living mammalian cell, a
225 y trafficked between the plasma membrane and intracellular compartments of both GIP-stimulated and un
226 iesterase regulate cAMP content in different intracellular compartments of cardiac myocytes in respon
227  distributed between the plasma membrane and intracellular compartments of CM/PF neurons.
228 orms to the regulation of cAMP hydrolysis in intracellular compartments of human myocardium and the e
229 T) to monitor GPCR proximity within discrete intracellular compartments of intact living cells.
230 bited significantly enhanced survival in the intracellular compartments of macrophages.
231 ) brains and were localized primarily to the intracellular compartments of neurons.
232 -ATPases affecting the pH of the cytosol and intracellular compartments, particularly those containin
233 nnabinoid CB1 receptor, to be transported to intracellular compartments, possibly via caveolae-relate
234 own that a majority of TF resides in various intracellular compartments, predominantly in the Golgi,
235 how that a majority of TF resides in various intracellular compartments, predominantly in the Golgi.
236  and budding site to CD63(+)/Lamp-1-positive intracellular compartments resulted in lower levels of v
237 g mutants sequester Kv1.5, but not Kv2.1, in intracellular compartments, resulting in a loss of funct
238  to limit fimbrial subunit expression to the intracellular compartment (Salmonella-CFA/I(IC)).
239  A. phagocytophilum and E. chaffeensis to an intracellular compartment secluded from oxygen-dependent
240         The localization of TLR9 and TLR7 to intracellular compartments seems to have a role in facil
241  and -4 form stable heterodimers at distinct intracellular compartments, some of which are completely
242                 Membrane-less organelles are intracellular compartments specialized to carry out spec
243 n appropriately coupled, can give rise to an intracellular compartment-specific sustained Ras activat
244 nd transporters are harbored in membranes of intracellular compartments such as endosomes and lysosom
245 cytized and they were found to reside within intracellular compartments such as endosomes.
246                 The targeting of assembly to intracellular compartments such as multivesicular bodies
247 urface receptors and receptors restricted to intracellular compartments, such as phagosomes and the c
248 no accumulation of AMPA receptor subunits in intracellular compartments, suggesting that folding and
249 ing cell surface biotinylation as well as in intracellular compartments, suggesting that ubiquitylati
250 several that were previously associated with intracellular compartments surrounded by a lipid bilayer
251 orter 4 (GLUT4) trafficking from specialized intracellular compartments, termed GLUT4 storage vesicle
252                  Virions were observed in an intracellular compartment that contains several tetraspa
253 sulted in a redistribution of ferroportin to intracellular compartments that labeled with early endos
254 rgm1 or Irgm3 led to accumulation of Gbp2 in intracellular compartments that were positive for both t
255 BP in neurons targets RGS9-2 to the specific intracellular compartment, the postsynaptic density.
256 ng successful application to the analysis of intracellular compartments, the 2D CWT was further used
257  GLUT4 continually cycles between the PM and intracellular compartments, the maintenance of elevated
258  NMDA and AMPA receptors by sequestration in intracellular compartments, thereby critically reducing
259 a family of Wnt receptors that signal to the intracellular compartment through the cytosolic protein
260 ized AXL by mediating its degradation in the intracellular compartment, thus restricting its exposure
261 ocation of apical NHE3 and V-ATPase from the intracellular compartment to the apical plasma membrane
262  skeletal muscle, FATP1 translocates from an intracellular compartment to the plasma membrane in resp
263 n-stimulated translocation of GLUT4 from its intracellular compartment to the plasma membrane is regu
264 sperm activation, TRP-3 translocates from an intracellular compartment to the plasma membrane to allo
265                                  Neither the intracellular compartment to which the CXCR4-TCR heterod
266 king of the delta-opioid receptor (DOR) from intracellular compartments to plasma membrane in central
267 rters translocate between the sarcolemma and intracellular compartments to regulate substrate metabol
268  skeletal muscle by GLUT4 translocation from intracellular compartments to sarcolemma and t-tubules.
269 PA subtype glutamate receptors (AMPARs) from intracellular compartments to synapses is thought to be
270 eeper" that may control APP trafficking from intracellular compartments to the cell surface.
271 on involves translocation of the enzyme from intracellular compartments to the outer leaflet of the c
272    Slit induces redistribution of Robo1 from intracellular compartments to the plasma membrane in a U
273 cation of the GLUT4 glucose transporter from intracellular compartments to the plasma membrane.
274 in triggers the redistribution of Glut4 from intracellular compartments to the plasma membrane.
275 enhanced surface expression of channels from intracellular compartments to the plasma membrane.
276 zation of the ErbB2 and ErbB3 receptors from intracellular compartments to the plasma membrane.
277 ed to a redistribution of both proteins from intracellular compartments to the plasma membrane.
278 o increased trafficking of transporters from intracellular compartments to the terminal membrane, rep
279 0% of endogenous cellular copper stores from intracellular compartments to the tips of nascent endoth
280  membrane-bound vesicles carry cargo between intracellular compartments, to and from the cell surface
281 aterials to target organs, tissues, cells or intracellular compartments; to co-deliver immunomodulato
282 lator, AS160, stabilizes ENaC in a regulated intracellular compartment under basal conditions, and th
283 se from the fusogenic liposome in the acidic intracellular compartments upon a pH-sensitive membrane
284                 Because TLR7 is expressed in intracellular compartments, viral RNA must be internaliz
285 pH 6.2 and 10mM Ca(2+), conditions mimicking intracellular compartments, VWFpp-VWF binding occurs wit
286 ion in patch pipette solutions perfusing the intracellular compartment was high and elimination of it
287 stasis and were not observed if acidic pH in intracellular compartments was neutralized.
288 teria found on the extracellular surface and intracellular compartments were analyzed individually.
289 in-containing granules were juxtaposed to an intracellular compartment where exocytosed LAMP-1 was re
290 mbling autophagosomes, which seem to form an intracellular compartment where the MOG40-48 epitope is
291 ar self-DNA, accumulated DNA gains access to intracellular compartments where it drives inflammatory
292 uld exist in an oligomeric state but only in intracellular compartments where its concentration is 5-
293 es were long thought to be restricted to the intracellular compartment, where they are used for energ
294 sociation with LL37 enhances DNA uptake into intracellular compartments, where it stimulates TLR9-dep
295  and both these proteins were enriched in an intracellular compartment which also contained Rab5 and
296 modulate K(+) and pH homeostasis of distinct intracellular compartments, which alter membrane traffic
297 sted that HDL promoted TRAM translocation to intracellular compartments, which impaired subsequent si
298 1) heparin blocks synthesis of hyaluronan in intracellular compartments, which prevents the autophagy
299 lization by transferring cytosolic copper to intracellular compartments, while leaving the overall ce
300 ins are delivered efficiently to appropriate intracellular compartments within specific cell types.

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