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1 ma cells (where it is primarily localized to cytosol).
2 m the ER and transport of the virus into the cytosol.
3 iability and it was mostly determined by the cytosol.
4 ontaining putative transport vesicles in the cytosol.
5 olecular NPs was efficiently released to the cytosol.
6 he periplasm when expressed in the bacterial cytosol.
7 tabilization of the PDE6alpha subunit in the cytosol.
8 and does not sequentially accumulate in the cytosol.
9 soforms that generate the cAMP signal in the cytosol.
10 sion of roGFP2 to this organelle besides the cytosol.
11 d alpha/beta heterodimer dissociation in the cytosol.
12 l nuclear-encoded proteins imported from the cytosol.
13 icrotubule (MT) organization across the cell cytosol.
14 rial ubiquitin ligase secreted into the host cytosol.
15 complexes both at the injectisome and in the cytosol.
16 on-promoting activity of MOAG-2/LIR-3 in the cytosol.
17 ted to transport the viral particle into the cytosol.
18 and promote sodium chloride influx into the cytosol.
19 molecule responsible for budding-LD entering cytosol.
20 iana leaves and the complex localized in the cytosol.
21 ransduce signals from the environment to the cytosol.
22 eral means to deliver native proteins to the cytosol.
23 chondrial matrix and export phosphate to the cytosol.
24 and membrane lipids and release them in the cytosol.
25 cids are in rapid exchange with those in the cytosol.
26 ving onto budding LDs and extracting them to cytosol.
27 f unsaturated triacylglycerols (TAGs) in the cytosol.
28 de novo synthesis exclusively occurs in the cytosol.
29 particle (DLP), which they deliver into the cytosol.
30 s translocate from low-pH endosomes into the cytosol.
31 ities for regulating calcium influx into the cytosol.
32 ism by which self-DNA becomes exposed to the cytosol.
33 undergo retrograde trafficking to reach the cytosol.
34 ability to deliver exogenous molecules into cytosol.
35 factors, controlling their release into the cytosol.
36 the endosomal membrane into the host cell's cytosol.
37 also disrupts these organelles to access the cytosol.
38 ytes, but very few bacteria reached the cell cytosol.
39 calizes MOAG-2/LIR-3 from the nucleus to the cytosol.
40 ng virions were partially trapped within the cytosol.
41 from the ER and transport the virus into the cytosol.
42 minal [2Fe-2S] binding domain located in the cytosol.
43 ters could provide 3-phosphoglycerate to the cytosol.
44 A genes, and thus imports all tRNAs from the cytosol.
45 he channel is closed by constrictions in the cytosol.
46 eticulum (ER) and extracts ER-budding LDs to cytosol.
47 se it causes release of cathepsin B into the cytosol.
48 onocytogenes to its replicative niche in the cytosol.
49 tion of S Typhimurium in the epithelial cell cytosol.
50 nd chloroplasts, whereas PGD2 remains in the cytosol.
51 lls, whereas N. munroi CA1a localized to the cytosol.
52 es in, e.g., endosomes (or lysosomes) in the cytosol.
53 ll-length SENP7L, SENP7S is localized in the cytosol.
54 livering therapeutic cargo into the neuronal cytosol.
55 the ER and extracts the LD from the ER-LD to cytosol.
56 e of delivering functional antibodies to the cytosol.
57 transport of internalized antigens into the cytosol.
58 ctional integrity of the Bag6 complex in the cytosol.
59 stent with the modification occurring in the cytosol.
60 n the dimers move from interstitial fluid to cytosol.
61 tine from the lysosomal compartment into the cytosol.
62 owing to probe biophysical properties of the cytosol.
63 ell, and 90% appear to freely diffuse in the cytosol.
64 ty and release of mitochondrial DNA into the cytosol.
65 ation of stored heme from the vacuole to the cytosol.
66 e phagosome membrane and make contact to the cytosol.
67 s and then tracelessly releasing them in the cytosol.
68 dehydrogenase (G6PD) inhibitor affected the cytosol; 24 h exposure to arylmethylamino steroids and G
70 require the import of many proteins from the cytosol, a process that is controlled by phosphorylation
71 ts with superoxide dismutase 2 (SOD2) in the cytosol after synthesis to transfer the enzyme to the mi
72 ow interferon-enhanced immunity protects the cytosol against bacteria and how professionally cytosol-
73 ch form an aqueous cavity extending from the cytosol almost to the endoplasmic reticulum lumen, while
74 quent diffusion and dephosphorylation in the cytosol also serves to suppress the pathway in down-grad
75 hell sequesters enzymatic reactions from the cytosol, analogous to the lipid-based membrane of eukary
76 at penetratin is mostly alpha-helical in the cytosol and acquires a more beta-sheet and random coil c
77 roteins are synthesized as precursors in the cytosol and are imported into mitochondria by five trans
78 ulator of several signaling molecules in the cytosol and as a cofactor of transcription in the nucleu
79 domains of Gea1 and Gea2 toggle roles in the cytosol and at the membrane surface, preventing membrane
81 N terminus, PGD1 and PGD3 accumulate in the cytosol and chloroplasts, whereas PGD2 remains in the cy
84 and activated protein kinase C (PKC) in the cytosol and extracellular signal regulated kinase (ERK)
85 lowed by lysosomal export of free Cbl to the cytosol and further processing to these cofactor forms.
87 creases its sedimentation coefficient in egg cytosol and increases its diffusion coefficient in live
88 e degradation of proteins in the nucleus and cytosol and is an established target for anticancer ther
89 mentous actin structures within the parasite cytosol and labels an extensive F-actin network that con
90 the switch-complex proteins can form in the cytosol and might function as intermediates in assembly.
91 n specific intracellular compartments in the cytosol and mitochondria and determined which scavenging
93 a fluorescent NO-sensor that locates to the cytosol and mitochondria, we observed that NO increased
97 tween melanocytes (where it is found in both cytosol and nucleus) and melanoma cells (where it is pri
98 and recycles macromolecules, signals to the cytosol and nucleus, and is implicated in many diseases.
103 lyase produces acetyl-CoA in the nucleus and cytosol and regulates histone acetylation levels in many
104 tion is necessary to recruit C2GAP1 from the cytosol and retains it on the membrane to locally inhibi
107 ADH to facilitate enhanced glycolysis in the cytosol and that pioglitazone may regulate energy metabo
108 termini of PHO1 are both oriented toward the cytosol and that the protein spans the membrane twice in
110 ometric H2O2 redox sensor roGFP2-Orp1 in the cytosol and the mitochondria of Plasmodium falciparum (P
112 plasmic reticulum (ER) membrane to reach the cytosol and then traffics to the nucleus to cause infect
114 e acidic endo-lysosomal compartment into the cytosol and traffics to its therapeutic destination-the
115 e how assembled tau seeds gain access to the cytosol and whether this access triggers cellular defens
116 mechanism MAGIC (mitochondria as guardian in cytosol) and provide evidence that it may exist in human
117 ion, redistribution of beta-catenin into the cytosol, and a reduced transepithelial electrical resist
118 t escapes from phagosomes, grows in the host cytosol, and avoids autophagy by expressing three determ
119 including the mitochondrial matrix, nucleus, cytosol, and endoplasmic reticulum (ER), with specificit
120 on of Mps1 occurs at kinetochores and in the cytosol, and inactivation of both pools of Mps1 during m
121 es peptide secretion, reimportation into the cytosol, and interaction with the intracellular global g
122 N is a major PI(3,4)P2 phosphatase in Mcf10a cytosol, and loss of PTEN and INPP4B, a known PI(3,4)P2
123 n these cells, copper accumulates in nuclei, cytosol, and mitochondria, causing distinct changes in t
126 don and shoot apical meristem, mainly in the cytosol, and that the epidermis of adt3 cotyledons conta
129 D-M substrates, are retrotranslocated to the cytosol as full-length intermediates during ERAD, and we
130 chloroplast proteins are synthesized in the cytosol as higher molecular weight preproteins and impor
131 ious protein quality-control pathways in the cytosol as well as regulating transcription and histone
133 d not diffuse to the target site through the cytosol, as this would potentially activate undesirable
134 de novo dTMP synthesis does not occur in the cytosol at rates sufficient for DNA replication, support
136 from karyopherin alpha to retain Bag6 in the cytosol but also for preventing TRC35 from succumbing to
137 acidic buffers (pH 5) reduced the pH of the cytosol by 0.8 +/- 0.1 pH units, whereas glycosomal pH d
138 to protein misfolding and aggregation in the cytosol by adjusting gene transcription and a number of
140 rates, pathogen-derived DNA is sensed in the cytosol by cGAS, which produces the cyclic dinucleotide
141 rier to deliver functional antibodies to the cytosol by employing anti-beta-tubulin or anti-nuclear p
142 croautophagic process that protects the host cytosol by entrapping and delivering microbes to a degra
144 ysosomal hydrolysis are then exported to the cytosol by lysosomal transporters, which remain undercha
145 otoxic stress reduces this ubiquitination in cytosol by S13/T330 phosphorylation-dependent translocat
148 idence that overexpression of AaIPPI1 in the cytosol can lead to metabolic alterations of terpenoid b
149 archaea) and Ncs6 (in archaea and eukaryotic cytosols) catalyze the formation of 4-thiouridine (s(4)U
150 -organization of F-actin across Sertoli cell cytosol, causing truncation of actin microfilament, ther
151 The Arabidopsis GLX system involves the cytosol, chloroplasts, and mitochondria, which harbor in
152 erential performance of these sensors in the cytosol compared to the ER of HeLa cells, and identify t
153 by cyclic-GMP-AMP synthase (cGAS) in the DC cytosol, contributing to type I interferon (IFN) product
154 nal acidic (A-) domain that extends into the cytosol, controls receptor specificity, and is highly ph
155 cle is often tightly connected to a membrane/cytosol cycle regulated by the Rho guanine nucleotide di
156 (Ser151) and translocation of CRTC1 from the cytosol/dendrites to the nucleus of hippocampal neurons
157 ated that unlike free drug, which enters the cytosol directly through the cell membrane and then traf
158 r a more oxidized state (NAD(+)/NADH) in the cytosol during GIIS that favors high glycolysis rates.
162 osol against bacteria and how professionally cytosol-dwelling bacteria avoid clearance are insufficie
165 er from chloroplasts to nuclei, avoiding the cytosol, enables photosynthetic control over gene expres
167 f GFP-RAB7 and GFP-RAB8 from endomembrane to cytosol, enhanced binding to RABGDI, and decreased GTP l
170 e number of S. aureus RN6390 bacteria in the cytosol, followed by a decrease shortly thereafter.
173 ransferase domain that is delivered into the cytosol from endosomes via a translocation domain after
176 ular Salmonella gain access to the host cell cytosol from within its membrane-bound compartment to ac
177 yclase catalytic domain (AC domain) into the cytosol, generates uncontrolled toxic levels of cAMP tha
178 s, the export of internalized antigen to the cytosol, has been suggested to be mediated by Sec61.
183 c42, and Rac1/2/3 from cell membranes to the cytosol in U251 (glioblastoma), A549 (lung adenocarcinom
184 y accumulate TAZ in both the nucleus and the cytosol, increase expression of YAP and TAZ connective t
188 dopsis thaliana Moreover, IYO moves from the cytosol into the nucleus in cells at the meristem periph
189 by two mechanisms: direct insertion from the cytosol into the peroxisomal membrane and indirect traff
190 ity relies on the ubiquitin coat surrounding cytosol-invading bacteria functioning as an 'eat-me' sig
192 by intracellular pathogens in the mammalian cytosol is challenging, and that environment remains poo
194 kers [13] obtained evidence that FliG in the cytosol is monomeric and takes on a more compact conform
198 ortation of citrate from mitochondria to the cytosol, leading to cytosolic glucose carbon flow via OA
199 Deficiency of TRADD or its sequestration in cytosol leads to accumulation of gammaH2AX-positive foci
200 ution, trapping it inside the cells into the cytosol, mainly as unreduced Ag(I) bound with molecules
202 eria growing in vitro Further, the host cell cytosol may resemble an anaerobic environment, with tiss
203 -SGTA-Hsp105 complex in promoting SV40 ER-to-cytosol membrane penetration and unveils a role of SGTA
205 on undecaprenyl diphosphate carriers at the cytosol:membrane interface, before export by the ABC tra
206 e tricarboxylic acid (TCA) cycle, and in the cytosol/nucleus as part of the DNA damage response (DDR)
209 n-protein interactions with ubiquitin in the cytosol of a targeted eukaryotic cell, leading to destru
210 , which causes self DNA to be exposed in the cytosol of affected cells, where it activates the DNA se
213 -bet with the adaptor protein 14-3-3z in the cytosol of CD8(+) T cells from patients with SSc reduces
214 Moreover, the d-peptide is retained in the cytosol of cells for several days, whereas the l-peptide
215 multi-protein complexes that assemble in the cytosol of cells upon detection of pathogen- or danger-a
219 S) when both proteins are co-produced in the cytosol of Escherichia coli A 12-amino acid-long peptide
220 one-third of the proteins synthesized in the cytosol of eukaryotic cells are integrated into the plas
222 dium falciparum genomic DNA delivered to the cytosol of human monocytes binds and activates cyclic GM
225 ymersomes to deliver molecules into the cell cytosol of neutrophils without causing cellular activati
227 is used by proteins that store copper in the cytosol of prokaryotes and eukaryotes, where this reacti
231 racterized by the ability to escape into the cytosol of the host cell and to stimulate the formation
235 tion calorimetry performed at cyanobacterial cytosol or meaningful environmental pHs values shows a m
236 m indicator GCaMP6, expressed in presynaptic cytosol or mitochondria, showed that Mrpl40 haploinsuffi
237 Whereas STAT5A typically localizes to the cytosol or nucleus, PDC normally resides within the mito
240 minor adjustments to the composition of the cytosol or the strengths of the intermolecular interacti
242 f intracellular factors originating from the cytosol, organelles, the substrate, neighbors, and the n
243 here a critical role of Hsc70 in SV40 ER-to-cytosol penetration and reveal how SGTA controls Hsc70 t
245 re resistant to external pH changes than the cytosol; placement of cells in acidic buffers (pH 5) red
246 ral enzyme that cleaves nucleic acids in the cytosol, preventing accumulation and a subsequent type I
247 es (e.g., proteins, nucleic acids) into cell cytosol remains a critical challenge for the development
248 show that the polymer network formed in the cytosol resembles a physiological hydrogel-like entity t
250 ndicator, named 'pHerry', in the presynaptic cytosol revealed acid efflux following nerve activity to
252 ADP acts as a strong ATPase inhibitor of cytosol-specific Hsp90 homologs, whereas organellular Hs
253 from the ER lumen or from endosomes into the cytosol, suggesting that the inhibition of cross-present
255 re KS-WNK1-dependent microdomains of the DCT cytosol that modulate WNK signaling during physiological
256 dolysosomal disruption and delivery into the cytosol, thereby greatly improving the detection accurac
257 acts with Nrf2, which sequesters Nrf2 in the cytosol, thereby repressing the transcription of Nrf2-de
258 n peroxidase activity, translocates into the cytosol to engage in the intrinsic apoptotic pathway, an
259 tion factor domain is then released into the cytosol to enter the nucleus and regulate gene expressio
261 lation-dependent translocation of TRAF6 from cytosol to nucleus, where TRAF6 also facilitates the K63
263 r transferring reducing equivalents from the cytosol to the ER, which is required to ensure correct d
264 her systems, the GR is translocated from the cytosol to the mitochondria and that stress and corticos
265 nterferon regulatory factor 7(IRF7) from the cytosol to the nuclei was effectively blocked in the pre
267 bust translocation of both proteins from the cytosol to the plasma membrane, as well as promoting cel
268 n Ura3 mistargeting from mitochondria to the cytosol, to identify small molecules that attenuated pro
269 ing that the fusion and ribosomes are in the cytosol together possibly engaged in protein synthesis.
270 ne, resulting in the pressure-driven flow of cytosol toward the area of detachment and local expansio
271 trikingly, this motor facilitates SV40 ER-to-cytosol transport by constructing a penetration site on
272 llular adaptors, is dispensable during ER-to-cytosol transport of SV40, this domain appears to exert
273 have lost their outer layer and entered the cytosol (uncoated) from those still within membrane vesi
274 rticles can be efficiently released into the cytosol under NIR irradiation, resulting in enhanced ant
277 ic behavior of the CPC in Xenopus laevis egg cytosol using sucrose gradient sedimentation and in HeLa
278 for slow ICWs, which then propagated in the cytosol via a reaction-diffusion process from the endopl
279 cells exchanged plasma membrane proteins and cytosol via a trogocytosis related process leaving both
280 e C is released from the mitochondria to the cytosol via Bax oligomeric pores, a process which is req
281 ial precursor proteins are imported from the cytosol via N-terminal presequences, which are cleaved u
282 ween the sarcoplasmic reticulum (SR) and the cytosol via the sarco-/endoplasmic reticulum Ca-ATPase (
284 aged IP3 The rate of Ca(2+) removal from the cytosol was unaffected by PGE2, but PGE2 attenuated hist
287 strates from the ER lumen or membrane to the cytosol where they are degraded by the 26S proteasome.
288 ases the glucosyltransferase domain into the cytosol, where GTP-binding proteins of the Rho/Ras famil
290 o-translocated through the membrane into the cytosol, where they are poly-ubiquitinated, extracted fr
291 rotranslocated through the membrane into the cytosol, where they are polyubiquitinated, extracted fro
292 d escape from damaged endomembranes into the cytosol, where they seed the aggregation of soluble tau.
293 tylated Skp2 is exclusively localized to the cytosol, which causes hyper-accumulation of the cyclin-d
294 tical during fast removal of Ca(2+) from the cytosol, which is required under stress conditions.
295 he mitochondria and on the PDH bypass in the cytosol, which synthesizes acetyl-CoA from acetate.
296 to be sufficient during transit through the cytosol while still allowing for release of the cargo wi
297 of cytochrome c, Smac/DIABLO and AIF in the cytosol while their levels were decreased in mitochondri
299 izes in the inclusion membrane and faces the cytosol with the active deubiquitinating enzyme domain.
300 ial growth and that, upon access to the host cytosol, WT L. monocytogenes utilized PLCs and ActA to a
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