ライフサイエンスコーパス: translation product

1 om the C terminus of the initial full-length translation product.

2 , as well as potential for a psiPTEN-encoded translation product.

3 pression and the folding and activity of the translation product.

4 peptide occurred after Ala-21 in the primary translation product.

5 in the doublet corresponds to a glycosylated translation product.

6 is unstable and appears to be an aborted D1 translation product.

7 es, most similar to the homomultimeric Kv1.1 translation product.

8 are unable to convert to the expected final translation product.

9 nstituent protein is generated as a discrete translation product.

10 ate the 76 kDa mature enzyme from the 90 kDa translation product.

11 , indicating that the latter are not primary translation products.

12 deficiency in plastid ribosomes and plastid translation products.

13 ed rates of synthesis of other mitochondrial translation products.

14 antibodies revealed coimmunoprecipitation of translation products.

15 efficiency and pronounced aggregation of the translation products.

16 ipitation of 35S-methionine-labeled in vitro translation products.

17 ll benefit from the enrichment for authentic translation products.

18 ensional gel analysis of their hybrid-arrest translation products.

19 upon RAN translation, aggregate with the RAN translation products.

20 f stalled translation, and removal of faulty translation products.

21 usands of strong pause sites and unannotated translation products.

22 ript-analysis to experimentally define HHV-6 translation products.

23 re preferentially generated from a subset of translation products.

24 th the parotid hormone-related mRNAs and the translation products.

25 nces that are highly similar to the putative translation products.

26 creased the levels of capped mRNAs and their translation products.

27 have albino leaves and lack plastid rRNA and translation products.

28 chanisms that detect and eliminate deficient translation products.

29 g MHC class I associated peptides from viral translation products.

30 ors NEMF, LTN1 and ANKZF1 markedly boost RAN translation product accumulation from both G4C2 and CGG

31 Perhaps HeT-A translation products act in cis to target the RNA to chr

32 he RQC complex collaborates to clear stalled translation products, advancing insight into cellular pr

33 tral properties of our transcripts and their translation product allow for their straightforward, sim

34 e YKL-39 cDNA predicts a 385-residue initial translation product and a 364-residue mature YKL-39.

35 he cytoplasmic nature of the protcadherin-PC translation product and its propensity to bind beta-cate

36 nents, thereby clearing the cell of improper translation products and defective components of the tra

37 roteins, which support membrane insertion of translation products and early assembly steps into OXPHO

38 t analysis to experimentally define the HCMV translation products and follow their temporal expressio

39 uggested that the 68-kDa form is the primary translation product, and the 63-kDa form may be generate

40 and (High Molecular Weights) are alternative translation products, and have a different subcellular l

41 Unedited rps12 translation products are also detected in other plant sp

42 Its translation products are predicted to belong to a superf

43 These defective translation products are thought to be ubiquitinated at

44 fied in AAT bound to GroEL (or in mAAT fresh translation product) are already present at the early st

45 Epitope-containing translation products as short as 21 amino acids when exp

46 supported the same pattern of mitochondrial translation products as yeast mIF2, and the pattern did

47 to microsomal membranes and were full-length translation products, as shown by sedimentation through

48 ivation of mitochondrial proteases, aberrant translation products, as well as defects in OXPHOS compl

49 ing frame (NSP-ORF) that cleaves the NSP-ORF translation product at a single site to produce two prod

50 The inferred translation product bears highest identity (43-47%) to c

51 t appear to reflect the presence of distinct translation products but rather a significant degree of

52 strates in which ubiquitin forms part of the translation product, but ufd2 mutants have no detected p

53 most genes, one ORF represents the dominant translation product, but we also detect genes with trans

54 Analysis of the truncated translation products by immunoprecipitation with anti-me

55 ranslation of actin cDNA and analysis of the translation products by native-PAGE was used to study th

56 Its in vitro translation product can be folded to produce enzymatic a

57 Our results demonstrate that noncanonical translation products can account for an important fracti

58 er membrane-associated mRNAs, removes faulty translation products causal of disease, and improves mit

59 abort stalled translation, and remove faulty translation products causative of disease in these model

60 In pulse-chase experiments, the primary Vhs translation product comigrated in sodium dodecyl sulfate

61 , and both the mature protein and the exon 2 translation product complemented a hemA mutation.

62 The other, derived from the primary translation product ComS, is thought to be sensed by an

63 The deduced primary translation product consists of 194 amino acids (aa), co

64 that the first 40 amino acids of the primary translation product constitute a mitochondrial targeting

65 Thus, the deduced translation product contained 351 instead of 409 amino a

66 The palC-derived translation product contains 507 amino acids, and the nu

67 trimental effects on levels of mitochondrial translation products correlate with a substantial reduct

68 ectrometry, and Edman degradation identified translation products corresponding to virion-associated

69 The predicted translation product (DdApm1p) shares at least 51.7% iden

70 ss I-peptide complex for each 500-3000 viral translation products degraded.

71 Moreover, the studied novel translation products exhibit temporal regulation similar

72 ome activity is dependent on the size of the translation product expressed in the target cell.

73 sions, which also stain positive for the RAN translation product FMRpolyG.

74 Here, we show that the most abundant RAN translation product, FMRpolyG, is markedly less toxic wh

75 Analysis of the nascent translation products for folding intermediates has ident

76 However, when in vitro transcription/translation products for the Rel proteins are used in an

77 cessing involves modification of the primary translation product from 39 to 42 kDa and at least 3 sub

78 immunoprecipitate an in vitro transcription/translation product from a full-length bamacan cDNA.

79 Based on HPLC separation of radiolabeled translation products from an mRNA encoding a tetrapeptid

80 tudy supports the existence of non-canonical translation products from both intragenic and extragenic

81 Translation products from cDNAs for BC, BCCP, and alpha-

82 Here, we define two novel translation products from the SIV env mRNA that are targ

83 Furthermore, the in vitro translation products from this RNA are very similar to t

84 nine independent cDNAs, and their predicted translation products, from this analysis show no signifi

85 ition of tau or the alternative shorter dnaX translation product gamma showed that tau-, tau2-, or ta

86 ducing discrete [GFP-T2A] and [E2(trunk)-V5] translation products: GFP fluorescence acts, therefore,

87 Its predicted translation product has 364 aminoacyl residues and molec

88 The translation product has 91% identity to a mouse protein,

89 Short-lived protein translation products have been proposed to be the princi

90 The putative translation products have molecular masses of 41,584 and

91 This study shows that mouse Pkhd1 and its translation products have very similar properties to its

92 The predominant translation product in the PEL cell line BCBL-1 derives

93 ociated with decreased (35)S-Met labeling of translation products in isolated mitochondria, whereas t

94 teins resulting in a cleavage of the primary translation products in order to generate the mature try

95 Here we show that mitochondrial translation products in Saccharomyces cerevisiae were sy

96 Pulse-chase labeling of mitochondrial translation products in SCO1 patient fibroblasts showed

97 in vivo pulse labeling of the mitochondrial translation products in the mutant indicate normal expre

98 Pulse labeling and chase of mitochondrial translation products in vivo indicate that Atp6p is less

99 synthesis and turnover of the mitochondrial translation products in wild-type, mutant and revertant

100 The translation product includes the proposed DNA binding an

101 Analyses of genomic DNA, transcripts, and translation products indicate that alternative splicing

102 ponds to residue 20 of the primary CLN2 gene translation product, indicating removal of a 19-residue

103 ptimal cytoplasmic assembly of the resulting translation products into protein multimers.

104 n the insertion of a number of mitochondrial translation products into the inner membrane.

105 ptides that mediate insertion of the nascent translation products into the membrane of the endoplasmi

106 Its deduced translation product is a 124-amino-acid polypeptide shar

107 Moreover, the MIRb-ACE2 translation product is a truncated, unstable ACE2 form,

108 First, the SMT3 translation product is cleaved endoproteolytically to ex

109 s) of DSPP that are cleaved when the initial translation product is converted to DSP and DPP, we perf

110 systems, compared with FV, the FVIII primary translation product is inefficiently transported out of

111 he N-terminal two-thirds of the CTGF primary translation product is not required for mitogenic activi

112 Instead, the primary translation product is phosphorylated to the 58-kDa viri

113 are close, it is likely that the primary tgl translation product is processed and modified in M. xant

114 In the first pathway, the primary translation product is processed to 59.5 kDa, is transpo

115 Each translation product is processed to yield a great divers

116 by a single open reading frame whose initial translation product is proteolytically processed to yiel

117 healthy tissue, abundance of the respective translation products is greatly increased in diseased an

118 ate that the larger DMPK-1 form (the primary translation product) is proteolytically cleaved near the

119 helial AS expression, demonstrating that the translation product itself affects regulation.

120 esult in reduced expression of mitochondrial translation products, leading to the suggestion that thi

121 ted in an open reading frame whose predicted translation product, LpsQ, falls within a large family o

122 tated with unglycosylated gp91(phox) primary translation product made in the presence of tunicamycin,

123 ion stage of Plasmodium indicates that their translation products may have unique roles in hepatocyte

124 moter activity in the form of an alternative translation product MBP-1, which is distinct from its ro

125 roducts of mRNA lacking stop codons [nonstop translation products (NSPs)].

126 ide a molecular explanation for the abnormal translation products observed in CAG trinucleotide repea

127 contains no introns, and yields a conceptual translation product of 231 amino acids, with a predicted

128 open reading frame which predicts a primary translation product of 280 amino acids and a calculated

129 he 2.4-kilobase pair cDNA encodes a putative translation product of 801 amino acids which shows great

130 The translation product of a chimeric green fluorescent prot

131 oprecipitated the in vitro transcription and translation product of a human cDNA clone encoding the n

132 TOP2a/90, the translation product of a TOP2a mRNA that retains a proce

133 cDNA ends, we confirmed TOP2alpha/90 as the translation product of a TOP2alpha mRNA in which a crypt

134 t results in a 1383 bp cDNA with a predicted translation product of approximately 53 kD.

135 The primary translation product of ATP25 is cleaved in vivo after re

136 We show that mp15 is a truncated translation product of COX1 mRNA whose synthesis require

137 An in vitro translation product of DAP-2 cDNA binds specifically to

138 Based on these observations, we suspect a translation product of ext-a1 affects different regulato

139 ecific antiserum, we show that the principal translation product of gag (Pr55(gag)) is cleaved to pro

140 -10), a decapeptide derived from the primary translation product of KISS1 gene, has been reported pre

141 ted an approx. 50-kDa in vitro transcription/translation product of Ld Cht1.

142 Thus, AtMBP-1 is as a bona fide alternative translation product of LOS2.

143 ein is consistent in size with the predicted translation product of metaxin cDNA.

144 The deduced 39-kDa translation product of ORF2 contains a sequence matching

145 The conceptual translation product of ORF2 is predicted to contain an e

146 nation, and for UV repair; (b) the predicted translation product of ORF4 is highly homologous to the

147 The derived translation product of palH contains 760 amino acids wit

148 248-259 of the 349-residue predicted primary translation product of porcine connective tissue growth

149 The primary translation product of the 7.5-kb ash1 transcript is pre

150 eceptor activator RNA protein (SRA1p) is the translation product of the bi-functional long non-coding

151 The major in vitro translation product of the cDNA co-migrated in SDS-PAGE

152 The predicted translation product of the cDNA corresponding to the ant

153 cently, we demonstrated that the full-length translation product of the cDNA encoding mimecan is a co

154 The predicted translation product of the cloned gad-1 gene includes si

155 eation of a premature stop codon so that the translation product of the edited (apoB-48) mRNA contain

156 The translation product of the gene exhibited PME activity i

157 corneal keratan sulfate proteoglycan to be a translation product of the gene producing osteoglycin an

158 We conclude that the full-length translation product of the gene producing osteoglycin is

159 uent analysis identified this protein as the translation product of the human RARbeta(4) transcript.

160 P21ras, the translation product of the most commonly mutated oncogen

161 The primary 300-kDa translation product of the Notch1 gene (p300) is cleaved

162 It is derived from a translation product of the precore/core gene by two prot

163 The predicted translation product of the S. invicta tranferrin (SiTf)

164 The translation product of the S/D3 cDNA shares some feature

165 The predicted translation product of the Thg-1pit gene contains a C-te

166 mARF), previously identified as an alternate translation product of the tumor suppressor p19ARF, depo

167 o produce functional rescue of the truncated translation product of the W1282X mutation, CFTR1281, wi

168 The translation product of this mRNA was not detectable in v

169 The predicted translation product of this ORF has homology to transpos

170 The translation product of traF is related to TraF of RP4, a

171 The translation product of vlmJ exhibits similarity to diacy

172 ilarity to diacylglycerol kinases, while the translation product of vlmK exhibits a weak similarity t

173 The C/EBPbeta mRNA encodes three translation products of 38, 35, and 20 kDa.

174 uence in the same reading frame, to generate translation products of 57 kD and 62 kD.

175 ns, also known as the orexins, are alternate translation products of a single gene.

176 In vitro translation products of ATAPM1 and AtAPP1 have enzymatic

177 cP immunoprecipitated in vitro transcription/translation products of both SAcP-1 and SAcP-2.

178 The predicted translation products of cfa1, cfa2 and cfa3 showed relat

179 Furthermore, the translation products of cusC and additional downstream g

180 h later waves of expression are triggered by translation products of early-expressed genes.

181 The sequences, transcripts, and translation products of malp were compared between clona

182 ontrol Listerin localization, explaining how translation products of mRNA surveillance are efficientl

183 re they release Ub monomers from the primary translation products of poly-Ub and Ub extension genes,

184 The primary translation products of RMAD-1 to -8 are 94- and 96-amin

185 and Shigella flexneri, and in the conceptual translation products of several open reading frames in Y

186 s a substrate for caspase-3 by screening the translation products of small complementary DNA pools fo

187 with an increase in transcripts and de novo translation products of the inducible nitric oxide synth

188 Translation products of the next 11 ORFs showed similari

189 Predicted translation products of the ORFs showed the presence of

190 The translation products of the sense and antisense transcri

191 The transcription/translation products of these fusion vectors in reticulo

192 signated cfa8, cfa9, and tnp1; the predicted translation products of these genes showed relatedness t

193 sed on the high similarity between predicted translation products of these three sequences and known

194 anslation by T cells to directly measure the translation products of uORFs during the ISR.

195 SP-A resulted in both 28 and 29 kDa primary translation products on SDS-PAGE analysis, while transla

196 vegetative and reproductive tissues, but the translation product, ORF239, is present only in reproduc

197 As a result the principal translation products, P2 and P3, are N-terminally trunca

198 However, the frequency of the antisense RAN translation product poly(PR) is comparable between c9ALS

199 The translation products predicted from human, bovine, mouse

200 ously, whereas trypsin digestion of the mAAT translation product produces a pattern of fragments qual

201 us compartments were generated from a single-translation product rather than by alternative translati

202 ly blocked, we calculate that > or =1 in 200 translation products receives an SsrA tag.

203 nate assembly of mitochondrial and cytosolic translation products relies on chaperones and specific f

204 o proteasomal degradation of these defective translation products remains unknown.

205 Examination of the deduced translation product revealed that the PHD, CXXC, coiled-

206 Interspecies comparisons of the predicted translation products revealed rapidly evolving sequences

207 Examination of the predicted translation products reveals a high degree of homology w

208 2452 bases of a 3.1-kb mRNA whose predicted translation product shows 40% identity with mammalian te

209 sigH is expressed as three primary translation products, SigH-sigma(37), SigH-sigma(51), an

210 lated using rabbit reticulocyte lysates, and translation product sigma3 was quantitated by phosphorim

211 firm that the U(S)1.5 protein is a bona fide translation product since it is detected during infectio

212 thern analysis and analysis of hybrid-select translation products suggest that each class has two dis

213 Analysis of the translation products suggests that the extended 5'-UTR o

214 d-borne TgVP1 yields a stable and functional translation product that is competent in aminomethylened

215 on was not spliced, resulting in a predicted translation product that terminates prematurely.

216 N-terminal 65 amino acids (aa) resulted in a translation product that was not targeted or integrated.

217 quences from various primate species defined translation products that are homologous to MICA and MIC

218 n constructs for the full-length initial gtr translation product, the mature protein after transit pe

219 P25 elicit a deficit of ATP9 mRNA and of its translation product, thereby preventing assembly of func

220 is aided by matching similarity of potential translation products to those target proteins.

221 Polycystin-2 translation products truncated at or after Gly(821) reta

222 expressed in the mouse ovary and testis are translation products utilizing the second initiation AUG

223 ra raised against the putative ATS1 and ATS3 translation products verified that ATS1 and ATS3 protein

224 The predicted translation product was a polypeptide (ca. 62 kDa) with

225 The KOB1 translation product was demonstrated to form a tight phy

226 Its deduced translation product was highly similar to PII proteins f

227 The translation product was immunoprecipitated and analyzed

228 Thus, retaining degradation of ssrA-tagged translation products was apparently important enough dur

229 and IN are derived from the same Tf1 primary translation product, we concluded that the excess Gag mo

230 The translation products were combined and dimers isolated b

231 alpha-E259V), and the properties of in vitro translation products were examined.

232 hemical properties of in vitro transcription/translation products were examined.

233 locyte lysate system +/- microsomes, and the translation products were identified by autoradiography

234 from virions was translated in vitro and the translation products were reacted with antibody to alpha

235 slocated with equal efficiency although both translation products were recovered as heterogeneous agg

236 ingly, considerable amounts of mitochondrial translation products were still integrated into the inne

237 Truncated translation products were used to delimit the analysis t

238 cell-free synthesis produced a 62-kD primary translation product, which in the presence of microsomal

239 a 63-kDa proenzyme is synthesized as primary translation product, which is cleaved into a 57-kDa memb

240 ation product of mtmB1 and decreased the UAG-translation product, which nonetheless contained pyrroly

241 shown to encode a 415-amino acid conceptual translation product with a predicted molecular mass of 4

242 0 kb of DNA and that encode a 541 amino acid translation product with extensive sequence similarity t

243 nterfere with its ability to modify aberrant translation products with C-terminal tails which assist

244 erious in heterozygotes, perhaps by creating translation products with dominant negative effects.

245 ts in frame shifts and leads to novel larger translation products with one (for hTGN48) or two (for h

246 ines the precise subcellular localization of translation products within the cell.

247 region of the transcript such that only one translation product would be generated.