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1 ses [most likely serine proteases] along the secretory pathway).
2 ture VLDL particles occurs through the Golgi secretory pathway.
3 sential for the movement of IRAP through the secretory pathway.
4 proximal and distal points in the regulated secretory pathway.
5 of GluR trafficking at an early step in the secretory pathway.
6 s), the prominent component in the dendritic secretory pathway.
7 tional modification in proteins entering the secretory pathway.
8 ehaviors simultaneously as they traverse the secretory pathway.
9 n from the PLC and their transit through the secretory pathway.
10 nts and is dependent on the acidic pH in the secretory pathway.
11 eventually traffic out of the ER through the secretory pathway.
12 disulfide formation in proteins entering the secretory pathway.
13 ermines the fate of aberrant proteins in the secretory pathway.
14 d the other with a role in disruption of the secretory pathway.
15 neuropeptide hormones through the regulated secretory pathway.
16 acellular protein phosphorylation within the secretory pathway.
17 ains by sensing the organellar pH within the secretory pathway.
18 new insights into the use of red FPs in the secretory pathway.
19 ulation of their transport through the early secretory pathway.
20 organellar compartments as they transit the secretory pathway.
21 retained by cellular quality control in the secretory pathway.
22 ia a late endosomal/lysosomal unconventional secretory pathway.
23 have a partial secretion block later in the secretory pathway.
24 erologous secretory protein to the regulated secretory pathway.
25 c membrane proteins that are targeted to the secretory pathway.
26 reticulum-to-Golgi trafficking in the early secretory pathway.
27 rograde trafficking in the constitutive-like secretory pathway.
28 on of Rab1 affects Scabrous and Delta in the secretory pathway.
29 posure to the acidic environment of the late secretory pathway.
30 d phosphorylation as it traffics through the secretory pathway.
31 fic fluorescence sensors that traffic in the secretory pathway.
32 roles for protein quality control within the secretory pathway.
33 dial Golgi and traversing the unconventional secretory pathway.
34 hydrophobic signals for localization to the secretory pathway.
35 n of folding-defective proteins in the early secretory pathway.
36 ) for proper folding before release into the secretory pathway.
37 yosin motor activity and is dependent on the secretory pathway.
38 from other cargoes using the "constitutive" secretory pathway.
39 cytokines are not secreted via the classical secretory pathway.
40 ation of the Golgi apparatus that blocks the secretory pathway.
41 gnal peptide for release along the classical secretory pathway.
42 sing the pH gradient maintained within their secretory pathway.
43 otein for AP-3 in formation of the regulated secretory pathway.
44 mer dissociated during transport through the secretory pathway.
45 lly cytosolic proteins were recruited to the secretory pathway.
46 dominantly localized to the ER and the early secretory pathway.
47 saggregating drug these proteins transit the secretory pathway.
48 trafficking through the compartments of the secretory pathway.
49 esis efficiency of mutant channels along the secretory pathway.
50 cellular compartment follow the conventional secretory pathway.
51 exity of organelle movement within the plant secretory pathway.
52 by proprotein convertase(s) (PCs) along the secretory pathway.
53 egating FM domain that face the lumen of the secretory pathway.
54 icking of the many proteins that rely on the secretory pathway.
55 d protein cargo as it traverses the cellular secretory pathway.
56 utated enzyme and its processing through the secretory pathway.
57 se from the LMAN1.MCFD2 complex in the early secretory pathway.
58 egradation clears aberrant proteins from the secretory pathway.
59 ing protein and lipid flux through the early secretory pathway.
60 transmembrane proteins involved in the early secretory pathway.
61 ty, Golgi organization, and flux through the secretory pathway.
62 ematologic, result from defects in the early secretory pathway.
63 from the cell, nonbulky proteins reenter the secretory pathway.
64 d provide the entryway for proteins into the secretory pathway.
65 is secreted from cells by an unconventional secretory pathway.
66 ular specialization at an early stage of the secretory pathway.
67 the conventional endoplasmic reticulum-Golgi secretory pathway.
68 otein (APP) is trafficking through the early secretory pathway.
69 rane-bound compartment to another within the secretory pathway.
70 g and trafficking of proteins that enter the secretory pathway.
71 s, a membrane organelle in the center of the secretory pathway.
72 ant torsinA alters protein processing in the secretory pathway.
73 shown to increase immature APP in the early secretory pathway.
74 for copper increases, especially within the secretory pathway.
75 ng of channels to forward trafficking in the secretory pathway.
76 s copper transport from the cytosol into the secretory pathway.
77 panded repertoire of cargo that transits the secretory pathway.
78 of newly synthesized GluA3 receptors to the secretory pathway.
79 icles is crucial to homeostasis in the early secretory pathway.
80 tes Sec4p, the final Rab GTPase of the yeast secretory pathway.
81 abolic and electrical signals in the insulin secretory pathway.
82 e critical for the evolution of an efficient secretory pathway.
83 ion to the periplasmic space via the general secretory pathway.
84 and trafficking of proteins targeted to the secretory pathway.
85 lain many observed aspects of the eukaryotic secretory pathway.
86 the bloodstream independently of the B-cell secretory pathway.
87 P)-mediated trafficking in the endocytic and secretory pathways.
88 an important regulator in both endocytic and secretory pathways.
89 sors for Ca(2+) and PI(4,5)P2 in a myriad of secretory pathways.
90 ith decreased levels of proteins involved in secretory pathways.
91 b networks will be common to other regulated secretory pathways.
92 mbranes that traffic in the endocytic and/or secretory pathways.
93 port mechanism of T6 and other characterized secretory pathways.
94 al transduction pathways and inhibiting host secretory pathways.
95 for ERES components to rebuild a functional secretory pathway after re-addition of amino-acids actin
97 protein glycosylation reactions in cellular secretory pathways, also act as important extracellular
98 ch is involved in membrane remodeling in the secretory pathway and a known target of sorafenib, was f
99 patially restricted entry into the dendritic secretory pathway and accumulate in recycling endosomes
101 ns appear to be exported through the general secretory pathway and deliver a variety of tRNase toxins
102 Here, we demonstrate that UNC93B1 enters the secretory pathway and directly controls the packaging of
103 ects a vast array of proteins transiting the secretory pathway and diseases arise upon misregulation
104 on correlates with pronounced defects in the secretory pathway and greatly reduces the replication of
105 rd of all cellular proteins pass through the secretory pathway and hence undergo oxidative folding in
108 ird of the eukaryotic proteome traverses the secretory pathway and most of these proteins are N-glyco
109 e rate of MHC class I maturation through the secretory pathway and prolongs the association of MHC cl
110 ce that pro-SdpC is secreted via the general secretory pathway and that signal peptide cleavage is a
111 IP13 transports excess zinc out of the early secretory pathway and that zinc overload in the endoplas
112 m is the port of entry for proteins into the secretory pathway and the site of synthesis for several
113 O-GlcNAc transferase, EOGT, functions in the secretory pathway and transfers O-GlcNAc to proteins wit
114 formed a comprehensive, unbiased analysis of secretory pathways and identified an unconventional lyso
115 ting, P/rds was prohibited from entering the secretory pathways and was retained in the Golgi apparat
116 ht to regulate protein trafficking along the secretory pathway, and demonstrate its importance for th
117 the beta-cell endoplasmic reticulum (ER) and secretory pathway, and ER stress is associated with beta
118 remains associated with TACE throughout the secretory pathway, and is stabilised at the cell surface
119 These genes all encode key regulators of the secretory pathway, and much of our knowledge of the secr
120 ic reticulum (ER), is trafficked through the secretory pathway, and released to generate extracellula
121 c pathway, the protein transport through the secretory pathway, and to the formation of a novel rever
123 onomeric, suggesting that the effects on the secretory pathway are independent of E ion channel activ
124 copper transport from the cytoplasm into the secretory pathway, as well as copper export across the p
125 e identification of a novel regulator of the secretory pathway, bactericidal/permeability-increasing
127 Glycoproteins traversing the eukaryotic secretory pathway begin life in the endoplasmic reticulu
128 in differential membrane ordering along the secretory pathway but also specifically localize diverse
130 oxic protein aggregates that form within the secretory pathway, but not those that form in the cytoso
131 R appears to influence the efficiency of the secretory pathway by affecting ER-mediated quality contr
132 teases have evolved to exploit the pH of the secretory pathway by altering the spatial juxtaposition
137 L-1) is required for actin and P-type ATPase secretory pathway calcium ATPase (SPCA)-dependent sortin
138 us studies have shown that disruption of the secretory pathway can be replicated by expression of ind
140 d collagen II synthesis with upregulation of secretory pathway coat protein complex II components.
141 ting receptors (VSRs) between early and late secretory pathway compartments is regulated by signals i
143 e Rab27a-dependent lysosomal trafficking and secretory pathways contributes to the correction of some
145 complex.trappc11mutants are characterized by secretory pathway defects, reflecting disruption of the
146 urons, we found that after synthesis via the secretory pathway, dendritic APP/BACE-1-containing vesic
147 traffic and organelle integrity in the plant secretory pathway depend on ARF-GTPases, which are activ
148 by regulating the abundance of PHT1s in the secretory pathway destined for plasma membranes, but als
149 begun to uncover how different parts of the secretory pathway directly and indirectly contribute to
150 on of STAT3 prevented the induction of these secretory pathways during pneumonia, with similar result
151 calized overexpression of Sly41 to the early secretory pathway elevates cytosolic calcium levels to s
152 inA contributes to protein processing in the secretory pathway, endocytosis, and the stability of syn
153 brane by establishing check points along the secretory pathway, especially during the export from the
155 product is channelled at the Golgi into the secretory pathway for deposition into the cell wall.
156 ecretion have been described that bypass the secretory pathway for the extracellular delivery of cyto
157 s secreted during adulthood by the canonical secretory pathway from female reproductive glands are ne
158 rience dramatic environmental changes in the secretory pathway, from the endoplasmic reticulum via se
162 ornaviruses to influence the function of the secretory pathway has important implications for host de
163 h results from protein misfolding within the secretory pathway, has a profound effect on cancer cell
164 n identified, the protein kinases within the secretory pathway have only recently been discovered, an
165 ease, multimerization, and polarity of the 3 secretory pathways have only been addressed separately,
167 in vesicle transport at several steps in the secretory pathway; however, its functional roles and eff
168 osylated channels appear to pass through the secretory pathway in a manner comparable with glycosylat
172 into the secretory granules of the regulated secretory pathway in each cell type are required for nut
173 ransition in the lipid landscape divides the secretory pathway in early and late membrane territories
175 cking of protein and lipid cargo through the secretory pathway in eukaryotic cells is mediated by mem
180 matrix (EEM) protein amelogenin disrupts the secretory pathway in the enamel-forming ameloblasts, res
183 (ER) is the entry site of proteins into the secretory pathway in which protein folding occurs and te
185 Other protein maturation processes in the secretory pathway, including ER-localized N-linked glyco
186 US5-2 target multiple components of the host secretory pathway, including VAMP3, RAB5C, RAB11A, SNAP2
187 destroyed Chlamydomonas Golgi, inhibited the secretory pathway, inhibited flagellar regeneration, and
188 NA interference-mediated inactivation of the secretory pathway inhibits bacteroid differentiation.
189 s in the endoplasmic reticulum and regulates secretory pathways, integrins, and Toll-like receptors,
190 om the endoplasmic reticulum/Golgi-dependent secretory pathway into the unconventional secretory path
192 he molecular decision to enter the regulated secretory pathway is a pre-Golgi event controlled by the
194 ry pathway, and much of our knowledge of the secretory pathway is based on this initial discovery.
195 To determine whether the Rab1-dependent secretory pathway is conserved in parasites, we have ana
198 hough most of the machinery acting along the secretory pathway is known and its function generally un
199 l-dependent sorting of proteins in the early secretory pathway is required for dynamic retention of e
200 ust trafficking within the constitutive-like secretory pathway is required for VAMP8- but not VAMP2-m
202 r results have shown that the Rab1-regulated secretory pathway is well conserved, and hemoglobin rece
206 te that the mutation inhibits the ameloblast secretory pathway leading to ER stress and an activated
207 ith machinery to tackle perturbations in the secretory pathway, like the unfolded protein response pa
208 e p62 is cleaved before exit from the acidic secretory pathway, low pH-dependent binding of E3 to the
209 re retained in the early compartments of the secretory pathway: mainly the endoplasmic reticulum, but
210 ation and O-glycosylation of proteins in the secretory pathway may be an important mechanism by which
211 ich occur frequently in the cytoplasm and in secretory pathways, may induce the formation of betaS fi
212 teins localized to the Golgi stack and early secretory pathway, mediate processes including Golgi sta
213 ontrast to endocytosis or recycling, how the secretory pathway mediates the localization of auxin car
219 reagents to identify N-glycans in the early secretory pathway of HeLa cells during subcellular fract
221 To understand the role of LdRab1 in the secretory pathway of Leishmania, we have generated trans
223 actin-mediated organelle movement within the secretory pathway of plant cells, and report on recent a
224 coprotein prM during virus maturation in the secretory pathway of the infected cell, explaining its c
225 ort the hypothesis that TG processing in the secretory pathway of TSHR-hyperstimulated thyrocytes alt
227 little is known about the filamentous fungal secretory pathway or how it might be manipulated for imp
228 o regulate its anterograde routing along the secretory pathway, particularly its export from the ER.
231 ifications during protein biosynthesis along secretory pathways play critical roles in determining th
232 pressing mutant SOD1 activate unconventional secretory pathways, possibly as a protective mechanism.
233 Our results establish Fam20C as the major secretory pathway protein kinase and serve as a foundati
235 the Golgi casein kinase that phosphorylates secretory pathway proteins within Ser-x-Glu/pSer motifs.
236 e of the sharpest evolutionary signatures of secretory pathway proteins, and was therefore critical f
238 ation triggered a dual selection pressure on secretory pathway proteins: while sequons were positivel
239 etion efficacy, although passage through the secretory pathway reduces its cell-penetrating activity.
240 n impairs transporter maturation through the secretory pathway, reduces surface expression, and inhib
241 mmalian proteome that traverses the cellular secretory pathway, regulating glycoprotein folding and f
243 The exocyst is an essential component of the secretory pathway required for delivery of basolateral p
244 sn-linked oligosaccharides in the eukaryotic secretory pathway requires the trimming of nascent glyca
248 FAM20C is a newly identified kinase on the secretory pathway responsible for the phosphorylation of
249 ion in viral egress by targeting VCP and the secretory pathway, resulting in a buildup of virions wit
250 2 within the ER (scFv4B12KDEL) and along the secretory pathway (scFv4B12) reduced the intracellular p
251 g and reveal that a GNL1/GNOM-mediated early secretory pathway selectively regulates PIN1 basal polar
252 liferation arrest associated with an altered secretory pathway (senescence-associated secretory pheno
256 ient to BFA than functioning of the cellular secretory pathway, suggesting that the role of GBF1 in t
257 V1.4, KV3.3, and KV3.4 channels early in the secretory pathway suggests a shared mechanism of channel
258 produce a higher flux of copper through the secretory pathway that balances copper in the cytosol an
259 sg101- and ISG15-dependent checkpoint in the secretory pathway that compromises influenza virus relea
260 A10 may form a complex with neurexins in the secretory pathway that facilitates surface transport of
262 nism of the folding state of proteins in the secretory pathway that targets unfolded/misfolded polype
263 me families for pathogenesis, illustrate the secretory pathway that transports CWDEs out of the funga
265 and from constitutive, basal, and regulated secretory pathways, the latter two via Weibel-Palade bod
266 e focus on the first two compartments of the secretory pathway: the endoplasmic reticulum and Golgi.
267 regulates the dynamics of p115 in the early secretory pathway, thereby controlling trafficking from
268 it the tightly controlled pH gradient of the secretory pathway, thereby regulating activation within
270 uring maturation of the proteins through the secretory pathway, they are modified by the addition of
271 m lumen regulates normal proteostasis of the secretory pathway; they also support therapies targeting
272 iferation arrest, associated with an altered secretory pathway, thought to promote tumor suppression
273 ssing can occur at neutral pH throughout the secretory pathway through the activity of furin-like pro
274 These studies reveal the importance of the secretory pathway to assemble and maintain full-length f
275 coordinately regulate reorganization of the secretory pathway to control cytokine secretion and faci
276 g cotranslational translocation early in the secretory pathway to downregulate receptor levels and in
277 s (PV) requires membranes of the host cell's secretory pathway to generate replication complexes (RCs
278 , p62, which is cleaved by furin in the late secretory pathway to produce mature E2 and a small perip
279 ertase furin requires the pH gradient of the secretory pathway to regulate its multistep, compartment
281 echanisms to adapt the functions of the late secretory pathway to the specific needs of the organism.
282 where Tomt and the Tmcs interact within the secretory pathway to traffic Tmc proteins to the hair bu
283 ther enterovirus, replication by controlling secretory pathway trafficking and Golgi complex morpholo
284 data implicate BPIFB6 as a key regulator of secretory pathway trafficking and viral replication and
285 sing to Abeta requires transport through the secretory pathway, trafficking of the substrate and acce
286 co-factors, because Psd1p re-directed to the secretory pathway undergoes autocatalysis normally and i
287 roteins in directing trafficking through the secretory pathway, we generated fluorescently tagged VSV
288 iroporin, causes disruption of the mammalian secretory pathway when exogenously expressed in cells.
289 e three P4Hs are shown to be targeted to the secretory pathway, where P4H5 forms dimers with P4H2 and
290 ry for the entrance of LH into the regulated secretory pathway, whereas FSHbeta does not traverse the
291 dulate and augment key aspects of the entire secretory pathway, whereas maladaptive UPR outputs trigg
292 s dispensable for COPI function in the early secretory pathway, whereas the N-terminal longin domain
293 olgi fragmentation and impose a block in the secretory pathway which reduces expression of major hist
294 enterovirus 71 (EV71), co-opt the host cell secretory pathway, which controls the transport of prote
295 a set of interconnected organelles form the secretory pathway, which encompasses the terrain that th
296 arge amounts of membrane protein through the secretory pathway, which makes these cells particularly
297 of the intrinsic factors that act along the secretory pathway, which may compromise product integrit
298 gates in Alzheimer's disease form within the secretory pathway while in Huntington's disease and amyo
299 f terminally misfolded proteins in the early secretory pathway yet spares folding intermediates from
300 not depend on membrane traffic in the early secretory pathway, yet requires both Sec23 and Sec24AB.
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