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1 lity-dependent HIF-alpha degradation via the ubiquitin proteasome system.
2 on of myofibrillar proteins primarily by the ubiquitin proteasome system.
3 stresses can reduce buffering effects in the ubiquitin proteasome system.
4 barrier dysregulation and disruption of the ubiquitin proteasome system.
5 proteins, priming their degradation via the ubiquitin proteasome system.
6 regulatory proteins for destruction via the ubiquitin proteasome system.
7 ABCG1 is ubiquitinated and degraded via the ubiquitin proteasome system.
8 is under dual control via autophagy and the ubiquitin proteasome system.
9 ion of proatrophic genes and proteins of the ubiquitin proteasome system.
10 specific degradation is a key feature of the ubiquitin proteasome system.
11 a cells depends on the elaborately regulated ubiquitin proteasome system.
12 argeting proteins for degradation across the ubiquitin proteasome system.
13 quitination, followed by degradation via the ubiquitin proteasome system.
14 lored how Sestrin-2 is regulated through the ubiquitin proteasome system.
15 show that these proteins are degraded by the ubiquitin-proteasome system.
16 hat exocyst degradation is controlled by the ubiquitin-proteasome system.
17 roteolysis via SUMO-dependent control of the ubiquitin-proteasome system.
18 carefully orchestrated by ubiquitination and ubiquitin-proteasome system.
19 egradation of intracellular proteins via the ubiquitin-proteasome system.
20 aperone-associated misfolded proteins by the ubiquitin-proteasome system.
21 e abundance of four PIF proteins through the ubiquitin-proteasome system.
22 , the bacterial equivalent of the eukaryotic ubiquitin-proteasome system.
23 ed proteins is primarily accomplished by the ubiquitin-proteasome system.
24 ts SUMO-2 conjugation and degradation by the ubiquitin-proteasome system.
25 MI involve accelerated titin turnover by the ubiquitin-proteasome system.
26 eins are not targeted for degradation by the ubiquitin-proteasome system.
27 the nucleus, where they are targeted by the ubiquitin-proteasome system.
28 s is largely dependent on proteolysis by the ubiquitin-proteasome system.
29 protein levels are tightly regulated by the ubiquitin-proteasome system.
30 ation of RB family repressor potency and the ubiquitin-proteasome system.
31 ed to Tip110 protein degradation through the ubiquitin-proteasome system.
32 in degradation of wild type channels via the ubiquitin-proteasome system.
33 ifically inhibited protein processing by the ubiquitin-proteasome system.
34 unction by promoting its degradation via the ubiquitin-proteasome system.
35 es that control USP33 degradation within the ubiquitin-proteasome system.
36 a post-translational level by co-opting the ubiquitin-proteasome system.
37 ation, enhancing its degradation via the K48 ubiquitin-proteasome system.
38 ted into the cytosol for degradation via the ubiquitin-proteasome system.
39 Rad17 has been shown to be regulated by the ubiquitin-proteasome system.
40 g protein, is a versatile participant in the ubiquitin-proteasome system.
41 es that regulate protein degradation via the ubiquitin-proteasome system.
42 tain and modulate the dynamic balance of the ubiquitin-proteasome system.
43 e Entamoeba histolytica harbors an extensive ubiquitin-proteasome system.
44 sulin signaling extends to regulation of the ubiquitin-proteasome system.
45 teins that are slated for degradation by the ubiquitin-proteasome system.
46 were regulated by synaptic activity and the ubiquitin-proteasome system.
47 ocytes because of reduced degradation by the Ubiquitin-proteasome system.
48 idea that its stability is regulated by the ubiquitin-proteasome system.
49 wn that Tip60 is turned over in cells by the ubiquitin-proteasome system.
50 ng protein (Vcp/p97), a key component of the ubiquitin-proteasome system.
51 timuli followed by rapid degradation via the ubiquitin-proteasome system.
52 m35-2HA(ts) are degraded from the MOM by the ubiquitin-proteasome system.
53 ro Hep3B cells appears to be mediated by the ubiquitin-proteasome system.
54 rt lived and is rapidly degraded by the host ubiquitin-proteasome system.
55 structure is regulated and remodeled by the ubiquitin-proteasome system.
56 hway and that its degradation depends on the ubiquitin-proteasome system.
57 1-like (ASK) protein components of the plant ubiquitin/proteasome system.
58 a cellular stress response that engages the ubiquitin/proteasome system.
59 estruction of PSD-localized fragments by the ubiquitin/proteasome system.
60 s in the induction of autophagy-lysosome and ubiquitin-proteasome systems.
61 changes in the cancer cells, which makes the ubiquitin-proteasome system a potential target to enhanc
62 nanobody mediates target destruction by the ubiquitin proteasome system, a process we describe as an
63 se isoforms were efficiently degraded by the ubiquitin proteasome system, an effect reversed by the a
67 BXO25 mediates ELK-1 degradation through the ubiquitin proteasome system and thereby plays a role in
68 ytoplasmic DPPA3 is partially cleaved by the ubiquitin-proteasome system and an N-terminus fragment r
69 an increase of protein breakdown due to the ubiquitin-proteasome system and autophagy activation.
70 ased the expression of the components of the ubiquitin-proteasome system and autophagy in LLC-bearing
71 he increased expression of components of the ubiquitin-proteasome system and autophagy in skeletal mu
72 that p62 mediates the crosstalk between the ubiquitin-proteasome system and autophagy through its bi
73 One module includes genes involved in the ubiquitin-proteasome system and contains SCA genes usual
74 which greatly increase substrate load on the ubiquitin-proteasome system and eventually activate the
75 regulate ribosome abundance through both the ubiquitin-proteasome system and forms of autophagy refer
76 generative diseases and the link between the ubiquitin-proteasome system and neurodegeneration make t
78 is currently great clinical interest in the ubiquitin-proteasome system and ongoing development of s
79 ns show abnormal protein degradation via the Ubiquitin-proteasome system and partially impaired trans
81 amage response pathways by engaging with the ubiquitin-proteasome system and promoting the degradatio
82 egulation of hepatic lipid metabolism by the ubiquitin-proteasome system and suggests COP1 as a poten
83 utophagy-lysosome pathway, although both the ubiquitin-proteasome system and the autophagy-lysosome p
84 nontraditional mitophagy pathways involving ubiquitin-proteasome system and the ubiquitin-binding pr
85 ation and to STUbL-mediated targeting to the ubiquitin-proteasome system and thereby implicate this p
86 levance for biomedical sciences, such as the ubiquitin-proteasome system and various human disease-as
87 that SUMOylation is an integral part of the ubiquitin proteasome system, and expression of the small
88 this analysis included specific genes of the ubiquitin proteasome system, and inhibition of ubiquitin
89 hways involving endo-lysosomal vesicles, the ubiquitin-proteasome system, and autophagy-based or endo
90 he Ca(2+)-dependent protease calpain and the ubiquitin-proteasome system, and causes attenuation and
91 o main cellular processes, autophagy and the ubiquitin-proteasome system, and defective clearance of
92 ular peptides are constantly produced by the ubiquitin-proteasome system, and many are probably funct
93 tability of Axin protein is regulated by the ubiquitin-proteasome system, and modulation of cellular
94 ubiquitination, protein trafficking, and the ubiquitin-proteasome system, and monitored P-gp protein
95 this study, we show that Fbp1 is part of the ubiquitin-proteasome system, and we further investigated
98 Taken together, these results reveal the ubiquitin-proteasome system as a novel regulatory mechan
101 factor Bag1 promotes hERG degradation by the ubiquitin-proteasome system at the endoplasmic reticulum
102 y to lead to its targeted degradation by the ubiquitin-proteasome system because degradation is blunt
103 inking cytosolic antibody recognition to the ubiquitin proteasome system brings this research into sh
104 other major degradative route involving the ubiquitin-proteasome system by eliminating 26S proteasom
105 cultures and found altered levels of several ubiquitin proteasome system components, in particular de
108 scription factor, NAC1, that is subjected to ubiquitin-proteasome system-dependent degradation in pla
111 n between the cytosolic Hsp70 system and the ubiquitin proteasome system during protein triage are no
112 iated factor-1 (FAF1) both have roles in the ubiquitin-proteasome system during NF-kappaB activation,
113 to the destruction of select targets by the ubiquitin-proteasome system (eg, SCF(Skp2)-directed dest
114 homeostasis of MCPH1 in association with the ubiquitin-proteasome system ensures mitotic entry indepe
115 nd related signaling pathways such as hippo, Ubiquitin-proteasome system (ERK5), Tsc1/Tsc2 complex, F
119 umber variation.Eukaryotic cells rely on the ubiquitin-proteasome system for selective degradation of
120 he potential for therapeutic intervention in Ubiquitin Proteasome System function in heart disease is
122 quitin ligases are attractive targets in the ubiquitin-proteasome system, however, the development of
123 hown that ST2L stability is regulated by the ubiquitin-proteasome system; however, its upstream inter
124 hesized proteins are rapidly degraded by the ubiquitin-proteasome system; however, the relationship o
125 or the first time a fine-tuning of FACT by a ubiquitin proteasome system in promoting chromatin reass
126 ese findings suggest a role for CRLs and the ubiquitin proteasome system in suppression of p27 in SI-
127 alysis of RNA-sequencing data identified the ubiquitin proteasome system in the TNF-alpha signaling p
128 a reveal new controls and concepts about the ubiquitin proteasome system in which a ubiquitin-conjuga
129 UVR8 promotes rapid PIF5 degradation via the ubiquitin-proteasome system in a response requiring the
130 tate induced TTF1 protein degradation in the ubiquitin-proteasome system in both HTori3 thyroid folli
131 ts cellular proteins from degradation by the ubiquitin-proteasome system in conditions of stress.
134 ovide further evidence of dysfunction of the ubiquitin-proteasome system in schizophrenia, and sugges
136 dings identify an essential function for the ubiquitin-proteasome-system in spermiogenesis and define
137 ific branches of the endosomal-lysosomal and ubiquitin-proteasome systems, in maintaining the homeost
138 their demise by activating components of the ubiquitin proteasome system, including the E2 ligase LET
139 selectively degraded MEK1/2 by hijacking the ubiquitin-proteasome system, inhibited downstream signal
140 ing the autophagy-lysosomal pathway when the ubiquitin proteasome system is compromised, thus contrib
141 In this study, we provide evidence that the ubiquitin proteasome system is involved in the reduced d
142 crosstalk between protein ISGylation and the ubiquitin proteasome system is not fully understood.
152 es indicate that the overall activity of the ubiquitin-proteasome system is preserved in SBMA models.
160 radation pathways, such as autophagy and the ubiquitin-proteasome system, is associated with various
161 protein ISGylation negatively regulates the ubiquitin-proteasome system, leading to increased produc
162 synapses, Pinto et al. show that the axonal ubiquitin-proteasome system locally regulates the accumu
163 is, the E3 ubiquitin ligase Highwire and the ubiquitin-proteasome system maintain low Tkv protein exp
164 tin-like domains in proteins not part of the ubiquitin proteasome system may bind the proteasome more
165 ation of organelle biogenesis factors by the ubiquitin-proteasome system may constitute an important
166 c deficiency disrupts their folding, and the ubiquitin-proteasome system may help manage this stress.
168 mino acids (aa261-270) that was required for ubiquitin-proteasome system-mediated degradation, among
171 rotein quality control pathways, such as the ubiquitin-proteasome system, mitochondria per se can inf
172 iquitin ligase that functions to promote the ubiquitin-proteasome system of protein degradation and a
174 volving targeted protein removal through the ubiquitin-proteasome system, or selective, whole-chlorop
175 ncoding RNAs (ncRNAs) cosedimenting with the ubiquitin-proteasome system, our approach unveiled ncRNA
176 nes are involved in cytokinin signaling, the ubiquitin-proteasome system pathway, DNA repair and Cu t
178 induced aggregate formation through enhanced ubiquitin proteasome system performance rather than auto
182 (eight patients), and one patient with FTLD-ubiquitin proteasome system positive inclusions (FTLD-UP
183 CR interacts with proteins that regulate the ubiquitin-proteasome system, predominantly with the E3 u
184 study in Caenorhabditis elegans suggests the ubiquitin-proteasome system promotes degradation of the
186 s as promising chemical tools to exploit the ubiquitin-proteasome system, protein target classes asso
187 nd is degraded in the nucleus/nucleolus by a ubiquitin-proteasome system quality control pathway comp
188 ll ubiquitin-like modifier)-modification and ubiquitin-proteasome systems regulate the major events o
189 ng through polycomb-repressive complex 1.The ubiquitin-proteasome system regulates cellular reprogram
191 depletion of the ubiquitin ligase SYVN1, the ubiquitin/proteasome system regulator NEDD8, or the F-bo
193 t induce targeted protein degradation by the ubiquitin-proteasome system represent a new therapeutic
196 The treatment with MG132, an inhibitor of ubiquitin proteasome system, rescues the expression leve
197 osylation causes the inhibition of a nuclear ubiquitin proteasome system responsible for SRF stabiliz
198 report that EXO1 is rapidly degraded by the ubiquitin-proteasome system soon after DSB induction in
199 ligases or E3 enzymes are components of the ubiquitin proteasome system that function during the tra
200 oproteasome is an inducible component of the ubiquitin proteasome system that shapes the repertoire o
201 anical ventilation-induced activation of the ubiquitin-proteasome system, the autophagy/lysosomal sys
202 The stability of Atoh1 was regulated by the ubiquitin proteasome system through the action of Huwe1,
203 cal intervention on E3 ligases.Targeting the ubiquitin proteasome system to modulate protein homeosta
204 ss that serves as a companion pathway to the ubiquitin-proteasome system to degrade long-lived protei
205 that a range of plant pathogens subvert the ubiquitin-proteasome system to enhance their virulence.
206 g the cellular quality-control machinery-the ubiquitin-proteasome system-to remove specific cancer-ca
208 rs to answer fundamental questions about the ubiquitin proteasome system, uncovering that kinase degr
209 Failed AT2 quality control components (the ubiquitin-proteasome system, unfolded protein response,
210 applying inhibitors to selectively block the ubiquitin proteasome system (UPS) and autophagy-lysosoma
211 s a poorly understood alternative arm of the ubiquitin proteasome system (UPS) and is required for mo
212 two most prominent proteolytic systems, the ubiquitin proteasome system (UPS) and the autophagosomal
213 ded proteins that fail to be degraded by the ubiquitin proteasome system (UPS) are redirected to auto
214 t not only is DISC1 turnover elicited by the ubiquitin proteasome system (UPS) but that it is orchest
215 emains unknown, though altered expression of ubiquitin proteasome system (UPS) components have implic
222 activating proline hydroxylase (PHD) and the ubiquitin proteasome system (UPS) in primary rat astrocy
223 isorders, implicating the involvement of the ubiquitin proteasome system (UPS) in their pathogenesis.
231 ental mechanisms of protein homeostasis, the ubiquitin proteasome system (UPS), as it relates to lung
232 rotease-14 (Usp14), a major regulator of the ubiquitin proteasome system (UPS), controls ciliogenesis
233 es, a substrate recognition component of the ubiquitin proteasome system (UPS), have an integral role
234 er, it is unclear whether proteolysis by the ubiquitin proteasome system (UPS), which catalyzes most
236 strains revealed a broad down-regulation of ubiquitin proteasome system (UPS)-related genes, in part
241 Degradation of maternal proteins by the ubiquitin-proteasome system (UPS) accompanies the matern
244 induced unfolded protein response (UPR), the ubiquitin-proteasome system (UPS) and autophagy, appear
246 n of genes involved in mitochondrial (MT) or ubiquitin-proteasome system (UPS) functions were markedl
251 mmalian spermatozoa revealed the role of the ubiquitin-proteasome system (UPS) in the regulation of f
255 egulated protein degradation mediated by the ubiquitin-proteasome system (UPS) is critical to eukaryo
259 mechanisms of protein homeostasis, including ubiquitin-proteasome system (UPS) mediated protein degra
261 ulation of p53 and its E3 ligase MDM2 by the ubiquitin-proteasome system (UPS) promotes carcinogenesi
263 mRNA export, it remains unknown whether such ubiquitin-proteasome system (UPS) regulation of Sub2 occ
264 es and various proteolytic processes such as ubiquitin-proteasome system (UPS) to avoid a build-up of
265 for antifouling paint biocides, inhibits the ubiquitin-proteasome system (UPS) via targeting both 19S
266 Targeted degradation of proteins through the ubiquitin-proteasome system (UPS) via the activities of
267 At the molecular level, an activation of the ubiquitin-proteasome system (UPS) was detected which res
268 d a small-molecule screen, we found that the ubiquitin-proteasome system (UPS) was essential in RMC.
269 n the major protein degradation pathway, the ubiquitin-proteasome system (UPS), and protein synthesis
270 lso known as dendrite pruning-depends on the ubiquitin-proteasome system (UPS), but the specific proc
271 of these compounds is their targeting of the ubiquitin-proteasome system (UPS), known to be essential
274 influences cellular survival and the rate of ubiquitin-proteasome system (UPS)-mediated proteolysis f
285 ardiomyocyte proteostasis is mediated by the ubiquitin/proteasome system (UPS) and autophagy/lysosome
286 st plant interaction is the role of the host ubiquitin/proteasome system (UPS) in the infection proce
287 r HDAC, which is functionally related to the ubiquitin proteasome system via its ubiquitin binding do
288 sponse to mitogens, Tiam1 is degraded by the ubiquitin-proteasome system via the SCF(betaTrCP) ubiqui
290 effect on bona fide native substrates of the ubiquitin-proteasome system was observed from PKG manipu
291 ng an shRNA library targeting enzymes in the ubiquitin proteasome system, we screened for genes that
292 e myoblasts revealed many genes encoding the ubiquitin-proteasome system were up-regulated during myo
293 ubiquitin ligases are key enzymes within the ubiquitin proteasome system which catalyze the ubiquitin
294 ism of regulation that is independent of the ubiquitin proteasome system, which can become occupied w
295 PN1 protein accumulation is regulated by the ubiquitin proteasome system, which is highly dysregulate
297 ells, proteome remodeling is mediated by the ubiquitin-proteasome system, which regulates protein deg
298 y the EWS-FLI1 protein as a substrate of the ubiquitin-proteasome system with a characteristic polyub
299 y pathways impact RB function, including the ubiquitin-proteasome system with deregulated RB destruct
300 way is a highly conserved constituent of the ubiquitin proteasome system, yet little is known about i