ライフサイエンスコーパス: rapid degradation

1 ar targeting of antigen to lysosomes and its rapid degradation.

2 quent, and released tssRNAs are targeted for rapid degradation.

3 endent protein kinase (AMPK), leading to its rapid degradation.

4 rylated 5'-terminus, yet it manages to avoid rapid degradation.

5 slation pathway, which would result in their rapid degradation.

6 the majority of PER proteins are tagged for rapid degradation.

7 d protein synthesis but was a consequence of rapid degradation.

8 ugh failure of myofilament incorporation and rapid degradation.

9 high nuclear levels by protecting them from rapid degradation.

10 n vivo either by assembly in a complex or by rapid degradation.

11 are targeted for translational silencing and rapid degradation.

12 ranslated regions, targeting these mRNAs for rapid degradation.

13 bility complex class I heavy chains (HC) for rapid degradation.

14 o the cytoplasm, and is sufficient to impose rapid degradation.

15 e, generating a complex that is targeted for rapid degradation.

16 y complex (MHC) products, resulting in their rapid degradation.

17 were targeted to the proteasomal pathway for rapid degradation.

18 of EphB4 carboxy-terminal tail and with its rapid degradation.

19 malian cell is limited by low expression and rapid degradation.

20 reas the others were poorly expressed due to rapid degradation.

21 tranded DNA-sensing pathway, followed by its rapid degradation.

22 mbers under normoxic conditions, causing its rapid degradation.

23 or metabolites may have been present despite rapid degradation.

24 rgoing premature translation termination for rapid degradation.

25 UHPLC-PDA/Q-ToF-MS profiles revealed rapid degradation (72-78%) of most intact precursors (ep

26 crosslinkers of hydrogels, hydrogels undergo rapid degradation after sequential exposure to light irr

27 ith observed in vivo ubiquitination and with rapid degradation after treatment with JA.

28 as 5 nucleotides was sufficient to stimulate rapid degradation, although an in vivo tail length of 20

29 o effectively treat diseases; however, their rapid degradation and poor absorption in the gastrointes

30 However, due to rapid degradation and poor bioavailability, its translat

31 ytosolic peptides, thus protecting them from rapid degradation and securing the peptide pool for furt

32 ntibody recycling mechanism, thus leading to rapid degradation and shortened half-life in vivo Here w

33 PTEN to the plasma membrane is coupled with rapid degradation and that the phosphatase domain and th

34 in strong IkappaBalpha phosphorylation, its rapid degradation, and enhanced nuclear translocation of

35 ds to a loss of REDD1 protein because of its rapid degradation, and in part reduced REDD1 expression

36 ascent class I molecules, resulting in their rapid degradation, and this process was found to be depe

37 Acetylated starches films exhibited more rapid degradation as compared with the native starches f

38 an targeting the antisense bound message for rapid degradation, as occurs in most other antisense RNA

39 otein metabolically unstable, leading to its rapid degradation at the inner nuclear membrane.

40 Exposure of 1a-f to O2 caused rapid degradation, but substitution of the unique PMe3 w

41 However, rapid degradation by adenosine deaminase (ADA) limits it

42 green fluorescent protein (GFP) promoted its rapid degradation by ClpXP, attachment of 5-27 C-termina

43 ciate from the PSII complex and then undergo rapid degradation by cysteine and aspartic proteases.

44 vivo half-life of GLP-1 is short because of rapid degradation by dipeptidyl peptidase-IV (DPP-IV) an

45 e in vivo half-life of GLP-1 is short due to rapid degradation by dipeptidyl peptidase-IV (DPP-IV) an

46 mono-phosphate, are controlled through their rapid degradation by diphosphohydrolases and ecto-nucleo

47 However, its rapid degradation by enzymes like dipeptidyl peptidase-I

48 llular matrix-based dressings are subject to rapid degradation by excessive protease activity at the

49 interaction with target DNA and inducing its rapid degradation by Lon protease.

50 nalling motifs for efficient recognition and rapid degradation by Lon.

51 scripts prone to surveillance and subject to rapid degradation by NMD.

52 protect these promising drug candidates from rapid degradation by plasma and intracellular nucleases.

53 ation is typically required to prevent their rapid degradation by proteases in the blood.

54 trate, resulting in multi-ubiquitination and rapid degradation by the 26 S proteasome.

55 that target a subset of the ACS proteins for rapid degradation by the 26S proteasome.

56 ected by Nrd1 and Nab3 is a prerequisite for rapid degradation by the nuclear exosome.

57 bsequent targeting of spliced-out introns to rapid degradation by the nuclear exosome.

58 The loss of toxicity is explained by rapid degradation by the proteasome after retrotransloca

59 compatibility complex (MHC) heavy chains for rapid degradation by the proteasome through a process te

60 continuous synthesis of IkappaBalpha and its rapid degradation by the proteasome through a ubiquitin-

61 PINK1-53) is often overlooked because of its rapid degradation by the proteasome upon its production.

62 ving both to target hundreds of proteins for rapid degradation by the proteasome, and as a dynamic si

63 18-30) as the signal for ER localization and rapid degradation by the ubiquitin (Ub)/proteasome pathw

64 Ralpha) in the nuclear matrix accompanied by rapid degradation by the ubiquitin-proteasome pathway.

65 he loss of REST in the nucleus is due to its rapid degradation by the ubiquitin-proteasome system.

66 that marks dimerization-defective Elk-1 for rapid degradation by the ubiquitin-proteasome system.

67 GAPDH, where it protected telomeres against rapid degradation, concomitant with increased resistance

68 ived beta-galactosidase causes it to undergo rapid degradation, demonstrating that this C-terminal do

69 their gradual depolymerization (unlike their rapid degradation during fasting).

70 zed through caveolin-1 lipid rafts undergoes rapid degradation, effectively decreasing TGF-beta signa

71 essing of the Hh precursor competes with its rapid degradation, explaining the impaired Hh signaling

72 ATF5 protein, which is otherwise subject to rapid degradation, facilitated by both proteasome-depend

73 that involves protecting nascent chains from rapid degradation followed by its folding function in as

74 RNAs of noninfectious SINV particles undergo rapid degradation following infection.

75 NAs need to be actively translated for their rapid degradation following the inhibition of DNA synthe

76 n termination codons (PTCs) are targeted for rapid degradation in all eukaryotes tested.

77 25I-TGF-beta1 undergoes nystatin-inhibitable rapid degradation in CHO-K1 cells but not in CHO-677 cel

78 Target dinitroanilines underwent rapid degradation in PPL porewaters and were transformed

79 role in the protection of telomeres against rapid degradation in response to chemotherapeutic agents

80 site mainly due to poor cellular uptake and rapid degradation in serum.

81 rdered structure that directs the protein to rapid degradation in the core 20 S proteasomes.

82 these proteins need further verification for rapid degradation in vivo, they cluster in chlorophyll a

83 The two variants that undergo the most rapid degradation in vivo, TPMT*2 and *3A, are also the

84 eir CheA proteins were subject to relatively rapid degradation in vivo.

85 nwanted metabolic processes that can lead to rapid degradation in vivo.

86 This turnover is heme-dependent, and rapid degradation involves heme binding to a heme regula

87 determines endocannabinoid signaling, their rapid degradation is expected to control the temporal pr

88 at IkappaBalpha is an unstable protein whose rapid degradation is slowed upon binding to NF-kappaB, b

89 rexpressed Cdc17 that is normally subject to rapid degradation is stabilized by Mcm10 co-overexpressi

90 lopment include poor intracellular delivery, rapid degradation, low target affinity, and membrane tox

91 e, or charge reversal mutations results in a rapid degradation (<30 min) of total protein, confirming

92 r, limb autotomy, and death characterized by rapid degradation ("melting").

93 ng recovery from shock, contrasting with the rapid degradation observed for many exogenous thermolabi

94 s to a transient quiescent state through the rapid degradation of a key proactivation factor.

95 It has previously been shown to cause the rapid degradation of a number of mRNAs that encode prote

96 report that IRE1 independently mediates the rapid degradation of a specific subset of mRNAs, based b

97 Multiple mechanisms, including rapid degradation of a subset of hypomodified tRNAs, acc

98 ntrol mechanisms are in place to trigger the rapid degradation of aberrant polypeptides and mRNAs.

99 ive selection pressure during evolution, via rapid degradation of aberrant transcripts that might yie

100 horylation of ACS2 and ACS6 by MPK6 prevents rapid degradation of ACS2/ACS6 by the 26S proteasome pat

101 mislocalized-mutant tafazzins to include the rapid degradation of aggregation-prone polypeptides that

102 The rapid degradation of alpha A(1-162) by the UPP may preve

103 Despite the rapid degradation of anthocyanins observed within the fi

104 Rapid degradation of antioxidants after 3weeks was obser

105 ants had low Aer expression levels caused by rapid degradation of apparently nonnative subunits.

106 Hence the rapid degradation of ARE mRNAs noted in DeltaICP27 mutan

107 participate in inhibiting or promoting their rapid degradation of ARE mRNAs, and influence cytokine e

108 Rapid degradation of ARE-bearing mRNAs (ARE-mRNAs) requi

109 2 to sublethal oxidative stress results in a rapid degradation of Bcl-2 and cellular inhibitor of apo

110 bset of these inhibitors were found to cause rapid degradation of BCL6, and optimization of pharmacok

111 The rapid degradation of blood ex vivo imposes logistical li

112 f BST2 are ubiquitinated by K5, resulting in rapid degradation of BST2.

113 g of Reaper/Hid/Grim, selectively causes the rapid degradation of c-IAP1 and c-IAP2 but not XIAP and

114 LT treatment causes a rapid degradation of c-Jun protein that follows inactiva

115 egrasyn, a small synthetic molecule, induces rapid degradation of c-Myc protein in MM-1 multiple myel

116 slocated across the ER membrane, causing the rapid degradation of CB1 by proteasomes; this leads to a

117 This suggests that the rapid degradation of cell death-promoting proteins by th

118 o not appear to play any role in the initial rapid degradation of CH(3) NH(3) PbI(3) solar cells unde

119 man cytomegalovirus gene product US11 causes rapid degradation of class I major histocompatibility co

120 The rapid degradation of contaminants within the first minut

121 Cisplatin (DDP) triggers the rapid degradation of CTR1 and thus limits its own accumu

122 DDP triggered rapid degradation of CTR1 in 2008 human ovarian cancer c

123 Exposure to DDP triggered the rapid degradation of CTR1, suggesting that its contribut

124 se control of cytokine expression depends on rapid degradation of cytokine mRNAs, mediated by an AU-r

125 ion was observed, PKC activation resulted in rapid degradation of DAT (t12 = 1-2 h).

126 Rapid degradation of dead bacteria is unlikely to accoun

127 dent activity of EndA is responsible for the rapid degradation of DNA and NETs, and is required for t

128 ntravector antigens to the immune system and rapid degradation of E. coli components.

129 activation of photoreceptor phyB results in rapid degradation of EIN3, the master transcription fact

130 danamycin-based HSP90 inhibitors resulted in rapid degradation of EML4-ALK in vitro and substantial,

131 nt illumination is the dominant force in the rapid degradation of encapsulated perovskite solar cells

132 elop novel therapies that limit the inherent rapid degradation of endogenous apelin peptides and prod

133 or FANCC in leukemic OCI/AML3 cells induced rapid degradation of endogenous NPMc.

134 riments with soil from each field revealed a rapid degradation of FPB to FP.

135 ation of FRH results in hypophosphorylation, rapid degradation of FRQ, as well as low levels of WHITE

136 n of Chlamydomonas gamete membranes leads to rapid degradation of FUS1 and HAP2, proteins required fo

137 Because of the rapid degradation of H2O2 by bacterial catalase, only st

138 l, each of which is sufficient to induce the rapid degradation of HC.

139 otein (pVHL) mediates the ubiquitination and rapid degradation of HIF-alpha (including HIF-1alpha and

140 IM5alphahu), blocks HIV-1 production through rapid degradation of HIV-1 Gag polyproteins.

141 We now report that HIV-1 Vif could induce rapid degradation of human APOBEC3G that was blocked by

142 ] in Drosophila) and ultimately leads to the rapid degradation of hyperphosphorylated isoforms via a

143 s well as biochemical analyses revealed that rapid degradation of hypomodified tRNA is mediated by th

144 o polyubiquitinated proteins, leading to the rapid degradation of I kappa B.

145 DINGS: TNF-alpha treated RASMCs demonstrated rapid degradation of IkappaBalpha (10-30 min), followed

146 ha and IkappaBbeta degradation do not induce rapid degradation of IkappaBepsilon.

147 d cereblon-dependent suppression of IRF4 and rapid degradation of IKZF1, but not IKZF3.

148 NAs with non-optimal codons, consistent with rapid degradation of inefficiently translated mRNAs.

149 dephosphorylation of INrf2Y141, resulting in rapid degradation of INrf2.

150 ing wild-type NSP1 were characterized by the rapid degradation of IRF3 during the replication cycle,

151 d region (3'-UTR) that can contribute to the rapid degradation of labile transcripts.

152 ivo activities, allowing for recognition and rapid degradation of LIN-28 and thus facilitating a swit

153 3.5.1.4.) is the enzyme responsible for the rapid degradation of lipid-derived chemical messengers s

154 alovirus (HCMV1) US11 and US2 proteins cause rapid degradation of major histocompatibility complex (M

155 diator of PE-mediated apoptosis and that the rapid degradation of Mcl-1 unleashes Bak to activate apo

156 inhibition of translation thus involves the rapid degradation of Mcl-1, leading to activation of Bim

157 emarkably, common T-cell stimuli induced the rapid degradation of MCPIP1 in both T-cell lines and qui

158 mising compound (MD-224) effectively induces rapid degradation of MDM2 at concentrations <1 nM in hum

159 organisms remain inaccessible, owing to the rapid degradation of messenger RNA after death.

160 of ribosomal and transfer RNA as well as the rapid degradation of messenger RNA.

161 We demonstrate the visible light-driven rapid degradation of microcystin-LR, one of the most tox

162 cal neurons and demonstrated that Tat causes rapid degradation of microtubule-associated protein 2 (M

163 Furthermore, our study revealed rapid degradation of milk miRNAs in intestinal fluid.

164 disease phenotypes of ATD patients with more rapid degradation of misfolded ATZ and lack of globular

165 Disruption of these complexes results in rapid degradation of Monarch-1 via the proteasome and pr

166 Recognition and rapid degradation of mRNA harboring premature translatio

167 bonuclease Xrn1 act in concert to elicit the rapid degradation of mRNA substrates observed in vivo, a

168 Puf3p promotes rapid degradation of mRNA targets in the fermentable car

169 Vhs caused rapid degradation of mRNAs beginning with cleavages at s

170 ) is an RNA-binding protein required for the rapid degradation of mRNAs containing AU-rich elements.

171 thiolutin in nup116-delta strains revealed a rapid degradation of mRNAs in the nucleus that was suppr

172 ed pathway that leads to the recognition and rapid degradation of mRNAs with premature termination co

173 ndria, recruitment of the 26S proteasome and rapid degradation of multiple outer membrane proteins.

174 to endoplasmic reticulum (ER) retention and rapid degradation of mutant hERG proteins.

175 embryonic fibroblasts substantially restored rapid degradation of mutant SP-C proprotein, whereas tra

176 ations (L22P, T101I, and L408P) by mediating rapid degradation of mutated RPE65s via a ubiquitination

177 ecruitment of ESCRT-I to MVBs results in the rapid degradation of Mvb12.

178 therefore studied if p97 participates to the rapid degradation of myofibrillar proteins during muscle

179 ific case of mK3, it selectively targets the rapid degradation of nascent class I heavy chains in the

180 re impaired in Cox1 maturation and exhibit a rapid degradation of newly synthesized Cox1.

181 Cells lacking Coa2 show a rapid degradation of newly synthesized Cox1.

182 de (MDP) in the bacterial cell wall, induces rapid degradation of Nod2, which confers MDP tolerance i

183 We suggest that rapid degradation of non-poly(A) mRNAs may be primarily

184 f the hybrid 17-18 DeltaIDR exon followed by rapid degradation of nonfunctional prestin protein.

185 t the in vivo activity is sufficient for the rapid degradation of nonstop mRNAs.

186 me function, can markedly delay the normally rapid degradation of nontranslocated secretory and membr

187 to retrieve the CI-MPR, resulting in either rapid degradation of or mislocalization to the plasma me

188 minates, protein phosphatases ABI1/2 promote rapid degradation of OST1 via HOS15.

189 We show that MNNG caused rapid degradation of p21, and this involved the ubiquiti

190 Rapid degradation of P53 ensures the survival of healthy

191 We further demonstrate that this rapid degradation of PDE6 is due to the essential role o

192 The rapid degradation of PDGFRbeta in the LRP1-deficient fib

193 abundance and activity, which is caused by a rapid degradation of Peroxisome proliferator-activated r

194 We further suggest that the more rapid degradation of PERS bypasses PKA regulation and ma

195 o PIF3 has remained undefined but results in rapid degradation of PIF3.

196 phytochrome family of photoreceptors induce rapid degradation of PIFs to promote photomorphogenesis.

197 Subsequently, the rapid degradation of pK3/MHCI secondarily causes the slo

198 kly selected, Muller's ratchet can lead to a rapid degradation of population fitness.

199 -delta trm4-delta double mutant demonstrates rapid degradation of preexisting tRNA(Val(AAC)) accompan

200 Nonsense-mediated mRNA decay (NMD) directs rapid degradation of premature termination codon (PTC)-c

201 the heterogeneity of human diseases and the rapid degradation of proteins in sampled blood.

202 igase, which mediates the ubiquitination and rapid degradation of proteins, and a recombinant, antibo

203 between the high photothermal stability and rapid degradation of PTAs are rare.

204 The rapid degradation of PTAs may address safety concerns bu

205 e CHO-K1 cells, exhibit nystatin-inhibitable rapid degradation of receptor-bound 125I-TGF-beta1), tre

206 es to ClpX for trans-targeting, Vir promoted rapid degradation of Rep by ClpX deleted for the tetheri

207 tide tag encoded by wild-type tmRNA promotes rapid degradation of rescued proteins.

208 models however presents obstacles, including rapid degradation of RNA duplexes in plasma, insufficien

209 virulence-associated genes as well as in the rapid degradation of rnpB read-through transcripts.

210 s inhibit cellular transcription by inducing rapid degradation of Rpb1, a catalytic subunit of the RN

211 ar luminal ATP concentrations significantly; rapid degradation of secreted ATP by ecto- and soluble n

212 A mutation at L341P causes rapid degradation of SLC25A46, which manifests as a rare

213 In addition, rapid degradation of SNRNP70 reduces the localization of

214 us mediates two functions, i.e., it mediates rapid degradation of some mRNAs exemplified by beta-acti

215 respectively, in 20S proteasomes and caused rapid degradation of some of the 26S proteasomal subunit

216 inus from Lon protease, since Lon's normally rapid degradation of SoxS is blocked in the chimera.

217 ro1 binding to Ofd1 is disrupted, leading to rapid degradation of Sre1N.

218 pressed both lon phenotypes and restored the rapid degradation of SulA.

219 mediated mRNA decay was generated to prevent rapid degradation of target mRNA containing premature st

220 lomeres and also show that mechanisms of the rapid degradation of telomeres in response to ceramide i

221 caveolae/lipid-raft-mediated endocytosis and rapid degradation of TGF-beta1, thus diminishing non-lip

222 from the nucleus to the cytoplasm, mediating rapid degradation of the 9-1-1 complex via the 26 S prot

223 0A-P-mediated repression of abrB followed by rapid degradation of the AbrB protein.

224 e, which stabilizes the macrocycle, and (ii) rapid degradation of the C-terminal proteolysis fragment

225 for rILYd4 in promoting internalization and rapid degradation of the complement inhibitor CD59, and

226 omoplasmic 1624C>T-cell lines is caused by a rapid degradation of the deacylated form of the abnormal

227 rine residue 301 promotes ubiquitination and rapid degradation of the E2 protein by the proteasome pa

228 ptide, inhibits EGFR dimerization and causes rapid degradation of the EGFR.

229 RPE cells with IL-1beta or TNF-alpha caused rapid degradation of the endogenous, but not mutant, Ika

230 eavage where they anneal, thereby triggering rapid degradation of the entire message [1-4].

231 ng takes place in endosomes and involves the rapid degradation of the extracellular EphB2.

232 lpha-amylase to the solution resulted in the rapid degradation of the films.

233 slated region of IFN-gamma mRNA and mediates rapid degradation of the IFN-gamma transcript.

234 ding, an inability to localize to PC-HC, and rapid degradation of the Ikaros protein.

235 hat luteolin triggers a superoxide-dependent rapid degradation of the JNK-inactivating phosphatase mi

236 analogue due to its inability to prevent the rapid degradation of the L156F-SSAT protein.

237 on, it has been thought that the products of rapid degradation of the mistakes of protein synthesis (

238 ck of effect at a distant site is due to the rapid degradation of the molecule to inactive fragments.

239 op-forming region previously associated with rapid degradation of the mRNA.

240 Rapid degradation of the mutant tubulin does not elicit

241 l kinase signaling pathways, which favor the rapid degradation of the mutant.

242 eed at a nearly normal rate with concomitant rapid degradation of the new glycan strands.

243 rylation events acts collectively to trigger rapid degradation of the PIF3 protein in response to ini

244 otoactivated phytochromes bind to and induce rapid degradation of the PIFs, indicating that the photo

245 rvation strategies for works of art to avoid rapid degradation of the pigments.

246 This binding results in the rapid degradation of the pK3/MHCI complex by a mechanism

247 rotein; the single amino acid changes led to rapid degradation of the protein.

248 ed its intracellular processing, resulted in rapid degradation of the receptor.

249 ownstream signaling blockade associated with rapid degradation of the SFK LynA.

250 ingle-component system that could induce the rapid degradation of the specific endogenous protein its

251 n of such proteins, based on conditional and rapid degradation of the target protein in vivo, so that

252 nti-hTfR IgG3-Av induces internalization and rapid degradation of the TfR.

253 lut4 prior to induction of sortilin leads to rapid degradation of the transporter, whereas overexpres

254 Rapid degradation of the truncated slow TnT protein, rat

255 The E6 protein of HPV 16 mediates the rapid degradation of the tumor suppressor p53, although

256 In addition, Vpr causes rapid degradation of the uracil-DNA glycosylases UNG2 an

257 with an altered C-terminal sequence promote rapid degradation of the wild-type repressor by inducing

258 n premature termination codons (PTC) and the rapid degradation of their mRNAs by nonsense-mediated RN

259 Their prompt presentation, after rapid degradation of their newly synthesized source prot

260 bidopsis thaliana, we previously showed that rapid degradation of these proteins requires conserved A

261 deficient in both albumin and IgG because of rapid degradation of these proteins, suggesting a lack o

262 d deglutathionylation of MCL1, followed by a rapid degradation of this cell survival molecule.

263 Further studies confirmed the rapid degradation of this channel, having a time constan

264 Thus, rapid degradation of this large misfolded mutant protein

265 We recently reported that ischemia induced rapid degradation of tight junction protein occludin in

266 complex formation, dexrazoxane also induced rapid degradation of Top2beta, which paralleled the redu

267 Rapid degradation of TPHP was observed in CEH exposed to

268 tors (TRAFs) 1, 2, 3, and 6, followed by the rapid degradation of TRAFs 2 and 3.

269 e growth medium with N were accompanied by a rapid degradation of triacylglycerol stored in lipid dro

270 These domains are required for rapid degradation of tumor necrosis factor (TNF) and oth

271 (2) subunits results in the ER retention and rapid degradation of unassembled mutants.

272 d opening of the substrate-entry channel and rapid degradation of unfolded proteins without PAN; howe

273 many instances, small peptides are prone to rapid degradation or aggregation and may lack the confor

274 flammatory cell infiltration that led to its rapid degradation, promoting the infiltration of angioge

275 ion caused alpha1(AD) subunit misfolding and rapid degradation, reducing its total and surface expres

276 at Cdc37 protects nascent kinase chains from rapid degradation shortly after synthesis.

277 or fused to heterologous proteins, exhibited rapid degradation similar to wild-type GADD34, thereby i

278 rylation sites on SCG10 are required for its rapid degradation, suggesting that direct JNK phosphoryl

279 Although the mitofusins Mfn1 and Mfn2 are rapid degradation targets of Parkin, we find that degrad

280 tered holo-iso-1-cytochrome c are due to the rapid degradation that is carried out by a novel proteol

281 odegradable hydrogel is presented, achieving rapid degradation through radical addition-fragmentation

282 ence that Vif binds APOBEC3G and induces its rapid degradation, thus eliminating it from cells and pr

283 because of its limited plasma stability and rapid degradation to inactive metabolites.

284 report that nuclear FL SIRT3 is subjected to rapid degradation under conditions of cellular stress, i

285 In particular, PSCs have demonstrated rapid degradation under illumination, the driving mechan

286 the bulk of solid BBA particles but undergo rapid degradation upon deliquescence/liquefaction at hig

287 shock protein 90 (HSP90) clients and undergo rapid degradation upon HSP90 pharmacological blockade by

288 2 binds with IkappaBalpha and results in its rapid degradation via a non-proteasomal pathway.

289 ion is essential for stabilizing FRQ against rapid degradation via a pathway distinct from its typica

290 proprotein in the endoplasmic reticulum, and rapid degradation via a proteasome-dependent pathway.

291 otein, including a VWLL sequence that causes rapid degradation via the proteasomal system.

292 sed p58 is active but unstable and undergoes rapid degradation via the proteasome.

293 tly to DELLA proteins and targeting them for rapid degradation via the ubiquitin-proteasome pathway.

294 in response to external stimuli followed by rapid degradation via the ubiquitin-proteasome system.

295 lation of D-cyclins, known to initiate their rapid degradation, was reduced in TG mouse islets.

296 Perovskite films based on CH3NH3PbI3 undergo rapid degradation when exposed to oxygen and light.

297 f plant-based fibers to HCl vapor results in rapid degradation with simultaneous crystallization.

298 ly plasma membrane-impermeant and subject to rapid degradation within endosomes and lysosomes upon ce

299 ach to destabilize Asf1p that results in its rapid degradation within minutes of transcriptional repr

300 potent induction of vasoconstriction and its rapid degradation within minutes.