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1 taining KFERQ-like sequences are degraded by chaperone mediated-autophagy.
2 e cytosolic chaperonin complex 2, triggering chaperone-mediated autophagy.
3 tophagy, which prevents STING degradation by chaperone-mediated autophagy.
4 cytosolic chaperone HSC70 and degradation by chaperone-mediated autophagy.
5 /Hsp90/Cdc37/IKK/NF-kappaB pathway to induce chaperone-mediated autophagy.
6 /Hsp90/Cdc37/IKK/NF-kappaB pathway to induce chaperone-mediated autophagy.
7 e key glycolytic enzyme hexokinase-2 through chaperone-mediated autophagy.
8 es lysosomal RhoH uptake and degradation via chaperone-mediated autophagy.
9 ulation of other autophagic pathways such as chaperone-mediated autophagy.
10 hat are degraded by the lysosomal pathway of chaperone-mediated autophagy.
11 s include macroautophagy, microautophagy and chaperone-mediated autophagy.
12 down of proteins targeted for destruction by chaperone-mediated autophagy.
13 els and activities of the main components of chaperone-mediated autophagy.
14  importance of KFERQ motifs in substrates of chaperone-mediated autophagy.
15 cells are macroautophagy, microautophagy and chaperone-mediated autophagy.
16 inding receptors (P62, NBR1, and TAX1BP1) or chaperone-mediated autophagy.
17                              We investigated chaperone-mediated autophagy, a lysosomal import pathway
18 been proposed to be a targeting sequence for chaperone-mediated autophagy, a lysosomal pathway of pro
19                                              Chaperone-mediated autophagy activating molecules stabil
20 a mechanism for pharmacological targeting of chaperone-mediated autophagy activation and suggest a th
21 tes LC3-II and CCT2 interactions, confirming chaperone-mediated autophagy activation.
22 nscriptional program that leads to selective chaperone-mediated autophagy activation.
23                                              Chaperone-mediated autophagy activators molecules activa
24 ntified the mechanism of action of selective chaperone-mediated autophagy activators previously devel
25  information to generate orally bioavailable chaperone-mediated autophagy activators with favorable b
26  and VI, are enriched in lysosomes with high chaperone-mediated autophagy activity as expected for su
27                                              Chaperone-mediated autophagy activity, essential in the
28 abrogating the GPX4 degradation regulated by chaperone-mediated autophagy, alleviating ferroptosis an
29      Furthermore, Nrf2 in astrocytes delayed chaperone-mediated autophagy and macroautophagy dysfunct
30 n mutant p53 expression by the activation of chaperone-mediated autophagy and potential pharmacologic
31 re, we focus on two autophagic pathways, the chaperone-mediated autophagy and the endosomal microauto
32 ptor alpha - a known endogenous inhibitor of chaperone-mediated autophagy - and its co-repressor, nuc
33 old" (22-month-old) rats show lower rates of chaperone-mediated autophagy, and both substrate binding
34 is pivotal to the process of macroautophagy, chaperone-mediated autophagy, and endosomal microautopha
35                          LAMP2 is needed for chaperone-mediated autophagy, and its expression improve
36 for degradation and includes macroautophagy, chaperone-mediated autophagy, and microautophagy.
37 e and a specific type of vacuolar autophagy, chaperone-mediated autophagy, are involved in the degrad
38 nate protein Hsc73 (a key protein marker for chaperone-mediated autophagy), beclin 1 (a mammalian aut
39 phate dehydrogenase, a classic substrate for chaperone-mediated autophagy, by more than 90%, whereas
40                                Inhibition of chaperone-mediated autophagy caused accumulation of inac
41 gradation of perilipin 2 by interacting with chaperone-mediated autophagy chaperone HSC70.
42                                              Chaperone-mediated autophagy (CMA) also mediated resista
43                                              Chaperone-mediated autophagy (CMA) contributes to regula
44                                              Chaperone-mediated autophagy (CMA) contributes to the ly
45                                              Chaperone-mediated autophagy (CMA) declines in ageing an
46 ve identified a compensatory upregulation of chaperone-mediated autophagy (CMA) in different cellular
47                                              Chaperone-mediated autophagy (CMA) is a highly regulated
48                                              Chaperone-mediated autophagy (CMA) is a homeostatic proc
49 mal degradation of the HIF-1alpha subunit by chaperone-mediated autophagy (CMA) is a major regulator
50                                              Chaperone-mediated autophagy (CMA) is a protein degradat
51                                              Chaperone-mediated autophagy (CMA) is a selective autoph
52                                              Chaperone-mediated autophagy (CMA) is a selective form o
53                                              Chaperone-mediated autophagy (CMA) is a selective form o
54                                              Chaperone-mediated autophagy (CMA) is a selective lysoso
55                                              Chaperone-mediated autophagy (CMA) is a selective mechan
56                                              Chaperone-mediated autophagy (CMA) is a selective mechan
57                                              Chaperone-mediated autophagy (CMA) is a selective mechan
58                                              Chaperone-mediated autophagy (CMA) is a selective pathwa
59                                              Chaperone-mediated autophagy (CMA) is a selective type o
60                                              Chaperone-mediated autophagy (CMA) is a selective type o
61                                              Chaperone-mediated autophagy (CMA) is activated in respo
62 tivation, macroautophagy is inhibited, while chaperone-mediated autophagy (CMA) is induced, promoting
63                                              Chaperone-mediated autophagy (CMA) is part of the mammal
64                                              Chaperone-mediated autophagy (CMA) is the most selective
65                                          The chaperone-mediated autophagy (CMA) lysosome subgroup pro
66                                              Chaperone-mediated autophagy (CMA) serves as quality con
67                                              Chaperone-mediated autophagy (CMA) targets soluble prote
68 ed protein kinase (AMPK) phosphorylation and chaperone-mediated autophagy (CMA) that translate into t
69 arge fraction of neuronal tau is degraded by chaperone-mediated autophagy (CMA) whereas, upon acetyla
70                            Here we show that chaperone-mediated autophagy (CMA)(5), a selective form
71           Cancer cells up-regulate their own chaperone-mediated autophagy (CMA), a process that deliv
72             Here, we investigate the role of chaperone-mediated autophagy (CMA), a selective autophag
73                                              Chaperone-mediated autophagy (CMA), a selective form of
74  pluripotency factors OCT4 and SOX2 suppress chaperone-mediated autophagy (CMA), a selective form of
75 ave shown that alpha-syn can be degraded via chaperone-mediated autophagy (CMA), a selective lysosoma
76                                              Chaperone-mediated autophagy (CMA), a selective mechanis
77                              The activity of chaperone-mediated autophagy (CMA), a selective pathway
78     Cystinosis is associated with defects in chaperone-mediated autophagy (CMA), but the molecular me
79 graded during both macroautophagy and during chaperone-mediated autophagy (CMA), the latter of which
80 e found LRRK2 to be degraded in lysosomes by chaperone-mediated autophagy (CMA), whereas the most com
81 al interplay between the circadian clock and chaperone-mediated autophagy (CMA), whereby CMA contribu
82                      LAMP-2A is required for chaperone-mediated autophagy (CMA), which promotes Ag ca
83 utophagy-macroautophagy, microautophagy, and chaperone-mediated autophagy (CMA)-contribute to degrada
84 satellite proteins PCM1 and CEP290 via HSC70 chaperone-mediated autophagy (CMA).
85   Here we find that ER disturbance activates chaperone-mediated autophagy (CMA).
86           We demonstrate that PTEN regulates chaperone-mediated autophagy (CMA).
87  target cytosolic protein for degradation by chaperone-mediated autophagy (CMA).
88 iently degraded via the lysosomal pathway by chaperone-mediated autophagy (CMA).
89 adation through a type of autophagy known as chaperone-mediated autophagy (CMA).
90  70 kDa (hsc70), two essential components of chaperone-mediated autophagy (CMA).
91 ane protein type 2a (lamp2a), a receptor for chaperone-mediated autophagy (CMA).
92 in type 2 A (LAMP2A), two core components of chaperone-mediated autophagy (CMA).
93 sed BCL6 by attenuating BCL6 degradation via chaperone-mediated autophagy (CMA).
94                                              Chaperone-mediated autophagy controls the degradation of
95 lly, HO2 is degraded by the lysosome through chaperone-mediated autophagy, distinct from other HRM-co
96 orm A (Lamp-2a), an established component of chaperone-mediated autophagy, enhanced cytoplasmic autoa
97  transcriptomics validated the activation of chaperone-mediated autophagy genes in PSEN1-E280A.
98 d biological functions of macroautophagy and chaperone-mediated autophagy have been extensively studi
99 omotes the degradation of mutant p53 through chaperone-mediated autophagy in a lysosome-dependent fas
100 PhLP1) chaperone complexes, thereby inducing chaperone-mediated autophagy in mammalian and human canc
101 oncolytic avian reovirus (ARV) p17 activates chaperone-mediated autophagy in Vero and A549 cells by m
102 ls and HIF-1 activity, whereas activators of chaperone-mediated autophagy, including 6-aminonicotinam
103  while a disruption of lysosome function and chaperone-mediated autophagy increased cellular HSD17bet
104 ompanied by impairment of macroautophagy and chaperone-mediated autophagy, increased levels of total
105 sence of macroautophagy, an up-regulation of chaperone-mediated autophagy induced resistance to these
106 ses, yielding fragments that translocate via chaperone-mediated autophagy into the endosomal network
107 f the host protein turnover pathway known as chaperone-mediated autophagy involved in transport of cy
108 bilization of Hspa8 enhances its function in chaperone-mediated autophagy, leading to degradation of
109 , aberrant interactions with tubulin and the chaperone-mediated autophagy machinery as observed by ot
110                                        Thus, chaperone-mediated autophagy modulates the neuronal surv
111 he BCR and cytoplasmic proteins that use the chaperone-mediated autophagy pathway.
112 ocated into lysosomes for degradation by the chaperone-mediated autophagy pathway.
113 -Lys97), overlapping the recently identified chaperone-mediated autophagy recognition motif and a hig
114       In a neuronal cell line, we found that chaperone-mediated autophagy regulated the activity of m
115                                A receptor of chaperone-mediated autophagy regulates glioblastoma stem
116 others (for example, dTAGs(3), Trim-Away(4), chaperone-mediated autophagy targeting(5) and SNIPERs(6)
117 process has selectivity and is distinct from chaperone-mediated autophagy that occurs in lysosomes.
118 his acetylation hindered tau degradation via chaperone-mediated autophagy, thereby leading to its acc
119                To determine if EGF regulates chaperone-mediated autophagy through PI3K signaling, thi
120  protein type 2a that acts as a receptor for chaperone-mediated autophagy was responsible for decreas
121                           In cultured cells, chaperone-mediated autophagy, which is responsible for t

 
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