ライフサイエンスコーパス: translation product

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

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

3 , as well as potential for a psiPTEN-encoded 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 usands of strong pause sites and unannotated translation products.

20 chanisms that detect and eliminate deficient translation products.

21 re preferentially generated from a subset of translation products.

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

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

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

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

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

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

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

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

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

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

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

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

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

35 Its translation products are predicted to belong to a superf

36 These defective translation products are thought to be ubiquitinated at

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

74 Its predicted translation product has 364 aminoacyl residues and molec

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

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

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

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

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

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

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

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

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

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

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

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

87 The translation product includes the proposed DNA binding an

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

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

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

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

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

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

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

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

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

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

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

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

100 Each translation product is processed to yield a great divers

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

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

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

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

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

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

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

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

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

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

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

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

113 The translation product of a chimeric green fluorescent prot

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

129 248-259 of the 349-residue predicted primary translation product of porcine connective tissue growth

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

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

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

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

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

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

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

137 The translation product of the gene exhibited PME activity i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 The translation product of vlmJ exhibits similarity to diacy

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

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

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

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

157 In vitro translation products of ATAPM1 and AtAPP1 have enzymatic

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

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

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

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

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

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

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

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

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

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

168 Translation products of the next 11 ORFs showed similari

169 Predicted translation products of the ORFs showed the presence of

170 The translation products of the sense and antisense transcri

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

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

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

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

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

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

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

178 The translation products predicted from human, bovine, mouse

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

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

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

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

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

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

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

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

187 2452 bases of a 3.1-kb mRNA whose predicted translation product shows 40% identity with mammalian te

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

206 The translation product was immunoprecipitated and analyzed

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

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

209 The translation products were combined and dimers isolated b

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

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

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

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

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

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

216 Truncated translation products were used to delimit the analysis t

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

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

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

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

221 0 kb of DNA and that encode a 541 amino acid translation product with extensive sequence similarity t

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

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

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