ライフサイエンスコーパス: rapid degradation

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

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

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

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

5 mbers under normoxic conditions, causing its rapid degradation.

6 high nuclear levels by protecting them from rapid degradation.

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

8 are targeted for translational silencing and rapid degradation.

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

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

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

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

13 were targeted to the proteasomal pathway for rapid degradation.

14 s in Cln2 that result in binding to Grr1 and rapid degradation.

15 or metabolites may have been present despite rapid degradation.

16 rgoing premature translation termination for rapid degradation.

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

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

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

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

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

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

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

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

25 nucleotides in biologic media is hampered by rapid degradation and low final concentrations that are

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

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

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

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

30 nd proto-oncogene mRNAs serve as signals for rapid degradation and translational repression.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 in vivo and do not appear to be targeted for rapid degradation by the proteasome.

57 ility complex (MHC) class I heavy chains for rapid degradation by the proteasome.

58 18-30) as the signal for ER localization and rapid degradation by the ubiquitin (Ub)/proteasome pathw

59 e results indicate that Nrf2 is targeted for rapid degradation by the ubiquitin-proteasome pathway an

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

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

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

63 oloenzyme incorporation protects Bgamma from rapid degradation by the ubiquitin/proteasome pathway.

64 Prior to their rapid degradation, class I molecules in K3-expressing ce

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

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

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

68 Moreover, this protein undergoes rapid degradation during germination.

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

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

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

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

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

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

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

76 25I-TGF-beta1 undergoes nystatin-inhibitable rapid degradation in CHO-K1 cells but not in CHO-677 cel

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

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

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

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

81 Polyadenylation of synthetic RNAs stimulates rapid degradation in vitro by using either Chlamydomonas

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

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

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

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

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

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

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

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

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

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

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

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

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

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

99 Despite the rapid degradation of anthocyanins observed within the fi

100 Rapid degradation of antioxidants after 3weeks was obser

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

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

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

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

105 s, the potent transcriptional activities and rapid degradation of ATF6 and VP16 require the VN8 domai

106 s show that exon 7 blocks ubiquitination and rapid degradation of AUF1 proteins, whereas its deletion

107 ergoing M phase exit is sufficient to induce rapid degradation of Aur-A.

108 2 to sublethal oxidative stress results in a rapid degradation of Bcl-2 and cellular inhibitor of apo

109 The rapid degradation of blood ex vivo imposes logistical li

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

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

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

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

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

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

116 olic but not ER stresses slowed the normally rapid degradation of connexins, and led to a striking in

117 The rapid degradation of contaminants within the first minut

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

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

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

121 rictive to permissive temperature results in rapid degradation of CtrA, initiation of DNA replication

122 ults in the enhanced expression of E2F-1 and rapid degradation of cyclin B in the absence of the modu

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

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

125 Rapid degradation of dead bacteria is unlikely to accoun

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

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

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

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

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

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

132 f MCL1 by siRNA-MCL1 was associated with the rapid degradation of fortilin protein, which was found q

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

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

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

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

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

138 Ansamycins caused rapid degradation of HER2 and a concomitant loss in HER3

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 ssive phosphorylation of Per, leading to the rapid degradation of hyperphosphorylated isoforms by the

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

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 dephosphorylation of INrf2Y141, resulting in rapid degradation of INrf2.

149 The rapid degradation of IRAK may serve as a negative feedba

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 In contrast to rapid degradation of LDL and aggregated LDL taken up by

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

154 3.5.1.4.) is the enzyme responsible for the rapid degradation of lipid-derived chemical messengers s

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

156 ARE) in the 3' noncoding region promotes the rapid degradation of mammalian cytokine and proto-oncoge

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

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

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

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

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

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

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

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

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

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

167 rion host shutoff (vhs) protein mediates the rapid degradation of mRNA and the shutoff of host protei

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

186 Rapid degradation of nuclear HIF-1alpha protein levels w

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

188 The rapid degradation of p21 protein during the signalling p

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 ein hdm2 ubiquitinates p53, resulting in the rapid degradation of p53 through the ubiquitin (Ub)-prot

192 The E6 protein of HPV 16 mediates the rapid degradation of p53, although this is not the only

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

222 0A-P-mediated repression of abrB followed by rapid degradation of the AbrB protein.

223 Rapid degradation of the bacteriophage Mu immunity repre

224 nal mechanism, Notch signaling also leads to rapid degradation of the basic helix-loop-helix (bHLH) t

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

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

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

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

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

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

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

232 The Cpe(fat) mutation leads to rapid degradation of the enzyme.

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

234 y proteasome inhibitors, suggesting that the rapid degradation of the F protein is mediated by the pr

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

236 cysteine at Cys-145 was found to lead to the rapid degradation of the hAGT protein in vivo.

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

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

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

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

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

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

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

244 ne for any cysteine residue of AT results in rapid degradation of the mutant protein in vivo.

245 Rapid degradation of the mutant tubulin does not elicit

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

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

248 greatly diminished levels of protein due to rapid degradation of the NQO1*2 protein by the ubiquitin

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

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

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

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

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

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

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

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

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

258 Rapid degradation of the truncated slow TnT protein, rat

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

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

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

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

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

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

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

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

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

268 Thus, rapid degradation of this large misfolded mutant protein

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

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

271 Rapid degradation of TPHP was observed in CEH exposed to

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

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

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

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

276 for VP16-mediated transcription, as well as rapid degradation of VP16 by proteasomes.

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

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

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

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

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

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

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

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

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

286 g of repeated canonical AUUUA motifs confers rapid degradation to many cytokine mRNAs when present in

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

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

289 2 binds with IkappaBalpha and results in its rapid degradation via a non-proteasomal pathway.

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

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

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

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

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

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.