ライフサイエンスコーパス: cDNA fragment

1 ) were used to amplify and clone a rhodopsin cDNA fragment.

2 ain a prostate-specific approximately 339-bp cDNA fragment.

3 reverse transcription-PCR and cloned as four cDNA fragments.

4 the R-RNA transcript by hybridization to its cDNA fragments.

5 from a retroviral library of random rat p53 cDNA fragments.

6 ing radiolabeled probes prepared from the 12 cDNA fragments.

7 ll walls out of 600 differentially expressed cDNA fragments.

8 on of display fragments or to confirm cloned cDNA fragments.

9 ilizing three different backbones with RPS25 cDNA fragments.

10 esulted in the amplification of two distinct cDNA fragments.

11 mbinant adenoviruses containing the rat HO-1 cDNA fragment Ad5-HO-1 were generated by homologous reco

12 From 16,000 cDNA fragments analyzed, 251 (1.6%) were differentially

13 alysis of the longest clone displayed a 2 kb cDNA fragment and encodes a protein of approximately 542

14 Southern hybridizations with a CAS cDNA fragment and fluorescent in situ hybridization (FIS

15 ach, we have identified a novel TIMP-related cDNA fragment and subsequently cloned a fourth human TIM

16 We isolated two cDNA fragments and one full-length cDNA that were induce

17 homologous to the sequence of a fetal brain cDNA fragment, and the remaining six corresponded to jun

18 f 16 unique three-base key codes into the 3'-cDNA fragments, and combined samples were sequenced usin

19 We assembled the overlapping cDNA fragments, and the longest NF2 cDNA, containing all

20 populations are converted to double-stranded cDNAs, fragmented, and ligated to linkers for PCR amplif

21 th different frequencies, the representative cDNA fragments are generated within or near to the prote

22 cDNA fragments are individually labeled so that each mol

23 man RK locus using a bovine rhodopsin kinase cDNA fragment as a probe.

24 Using this cDNA fragment as probe, Northern analysis reveals a ubiq

25 By using one of the isolated cDNA fragments as a screening probe, full-length cDNA of

26 have isolated nine differentially expressed cDNA fragments as confirmed by slot blot, Northern, and

27 hly reproducible primer-specific patterns of cDNA fragments, as well as reproducible duplicate finger

28 The capture of cDNA fragments at the sites of double-strand breaks may

29 se-independent retrotranspositions contained cDNA fragments at their 3' ends that are probably derive

30 ferent decamers and two anchor primers, 2268 cDNA fragments between 200 and 600 bp were displayed.

31 o (AMPV/CO) was generated by assembling five cDNA fragments between the T7 RNA polymerase promoter an

32 We found that chimeric RNA-cDNA fragments can also be detected at 5' end stem-loops

33 Because multiple cDNA fragments can be treated as alleles in a genetic sc

34 A cDNA fragment coding for the pea (Pisum sativum L.) chlo

35 e the TGF-beta-binding site in alpha2M, five cDNA fragments, collectively encoding amino acids 122-13

36 Among the subtracted cDNA fragments confirmed as differentially expressed, th

37 A 2.3-kb cDNA fragment containing a partial coding sequence for A

38 r cDNA library at low stringency with a MDR1 cDNA fragment containing the P-loop and ATP binding site

39 A 68-nucleotide (nt) cDNA fragment containing these elements was inserted bet

40 MmeI endonuclease that creates 20- to 21-bp cDNA fragments, conversion to a double-stranded DNA that

41 l of heat shock promoter HSP70) containing a cDNA fragment corresponding to base pairs 1-309 of IGF-1

42 The cDNA fragment corresponding to the mature (processed) pr

43 A microarray was constructed containing cDNA fragments corresponding to genes known or postulate

44 Complementary DNA (cDNA) fragments corresponding to differentially expresse

45 An 872-bp cDNA fragment, corresponding to the amino acid sequence

46 tags of 10 bases into their corresponding 3' cDNA fragments covering hundred bases.

47 Fifteen unique cDNA fragments encode genes/ESTs that are already known,

48 A 1.2-kb cDNA fragment encoding a platelet 47-kDa protein has bee

49 ning by using NEDD8 as a bait and isolated a cDNA fragment encoding a potent down-regulator of the NE

50 e identification and characterization of the cDNA fragment encoding BDNF protein, and 2) the localiza

51 lysis of placental RNA with a 641 bp apo A-I cDNA fragment encoding most of the 5' region of the apo

52 and sequencing of a 1326<HSP SP = "0.25">bp cDNA fragment encoding the cell-cycle proliferation prot

53 Expression of a cDNA fragment encoding the GRD inhibited the CDC24/CDC42

54 r immunogenicity, a DNA construct in which a cDNA fragment encoding the melanoma epitope MART-1(27-35

55 A cDNA fragment encoding the processed form of the enzyme

56 A series of cDNA fragments encoding Crx protein with deleted C termi

57 lin-resistant clones, 80% of which contained cDNA fragments encoding secreted and membrane spanning p

58 cDNA fragments encoding the carboxyltransferase domain o

59 dehydratase, we also cloned the appropriate cDNA fragments encoding the domains that contain the tra

60 When cDNA fragments encoding the four cysteine-rich ligand-bi

61 A cDNA fragment encompassing the Aequorea victoria green f

62 We have cloned and sequenced two cDNA fragments encompassing the entire coding region of

63 By using this approach, a cDNA fragment extending from the SAGE tag toward the 3'

64 DNA tags or adapters attached to the ends of cDNA fragments for labeling or sequencing, different con

65 technique, we isolated a complementary DNA (cDNA) fragment for the intercellular adhesion molecule 1

66 chain reaction to amplify the corresponding cDNA fragment from a rabbit liver cDNA library.

67 Using differential display PCR (DDPCR), a cDNA fragment from Shigella flexneri serotype 5 that sho

68 levels in the flower, we have sequenced 1587 cDNA fragments from a subtractive floral cDNA library.

69 Polymerase chain reaction amplification of cDNA fragments from P388D1 cells using primers based on

70 EST sequences with the generation of longer cDNA fragments from SAGE tages for gene identification (

71 d by application of the generation of longer cDNA fragments from SAGE tags for gene identification (G

72 a technique called the generation of longer cDNA fragments from serial analysis of gene expression (

73 The cDNA fragments from the known flavonoid genes, except ch

74 Sixteen cDNA fragments from these experiments were sequenced and

75 oncogene from a set of AIDS IBLP-associated cDNA fragments generated by subtractive hybridization wi

76 istant plasmids, which contains an antisense cDNA fragment homologous to the yeast chromosome segrega

77 cDNA fragments homologous to DG42 from zebrafish and mou

78 None of these cDNA fragments, however, shared complete homology with g

79 Rat megalin cDNA fragments I through IV encoding the first through f

80 Sequencing of the cloned genome cDNA fragments identified two single-nucleotide mutation

81 e DNA synthesis and release 3'-azido-blocked cDNA fragments in a process akin to dideoxy-Sanger seque

82 otype than constructs carrying corresponding cDNA fragments in sense or antisense orientation.

83 pressed by introducing a PLD alpha antisense cDNA fragment into Arabidopsis.

84 ectly complementary overhangs partitions the cDNA fragments into non-overlapping subpopulations.

85 human gene originally identified as a 767-bp cDNA fragment isolated from normal ovarian epithelial ce

86 by Northern blot analysis using mouse COX-2 cDNA fragments labeled with 32P as probes.

87 (RT-PCR) was established to amplify a 379-bp cDNA fragment (nucleotides 747 to 1126, coding for amino

88 chain reaction (RT-PCR) was used to clone a cDNA fragment of a putative G-protein-coupled receptor f

89 A cDNA fragment of approximately 180 bp, located 260 bases

90 m invasive tumors when transfected with a 5' cDNA fragment of BEHAB/brevican, but not when transfecte

91 stitutions were created in a cloned NS2B-NS3 cDNA fragment of dengue virus type 2, and the effect of

92 Expression of a 1737-bp cDNA fragment of the hsp60 gene in E. coli resulted in p

93 at model for SCA17 that carries a full human cDNA fragment of the TBP gene with 64 CAA/CAG repeats (T

94 stimate that there are 27 upregulated genes; cDNA fragments of 16 have been isolated.

95 cDNA fragments of erg homologues from guinea pig, rabbit

96 Multiple copies of cDNA fragments of identical sequence become distinct thr

97 e of dynein heavy chains were used to obtain cDNA fragments of rat dynein heavy chains.

98 Sense or antisense cDNA fragments of rat SCF were ligated into an episomal

99 ified by reverse transcriptase-PCR to obtain cDNA fragments of several new granzymes.

100 cDNA fragments of the homologues of the Drosophila head

101 patitis virus strain A59 (MHV-A59), in which cDNA fragments of the RNA genome are assembled in vitro

102 Multiple cDNA fragments of this gene were isolated by hybrid capt

103 k Office has rejected patent applications on cDNA fragments of unknown function from the National Ins

104 ichment and depletion of mismatch-containing cDNA fragments offers a useful approach for detecting co

105 oducibility, predictable spatial location of cDNA fragments on 2-D gels, and the potential for identi

106 A cDNA fragment originally identified in U-937 cells as a

107 orresponding to conserved motifs, two 300-bp cDNA fragments (pBMDR1 and pBMDR2) with a significant se

108 The 20 cDNA fragments represent between 6 and 15 different gene

109 ening of randomly selected clones identified cDNA fragments representing 16 different mold-upregulate

110 Over 135 000 individual cDNA fragments representing an estimated 90% of the tran

111 differential display techniques to identify cDNA fragments representing mRNAs that are induced withi

112 al difference analysis of cDNA to amplify 20 cDNA fragments representing transcripts that were more a

113 ed by a nested suppression PCR, the selected cDNA fragments, representing entire cDNA population, can

114 A putative 278-bp IGFBP-4 cDNA fragment (residues 341-618) of rat) that contains t

115 ed with a 5' conserved 330-base pair UGT2B13 cDNA fragment, resulting in the isolation and characteri

116 Sequencing of the corresponding cDNA fragment revealed that it corresponded to an expres

117 Sequencing of 24 AFLP-cDNA fragments revealed genes with a variety of function

118 egulation from high-throughput sequencing of cDNA fragments (RNA-seq), we developed the mixture-of-is

119 DNA sequencing analyses of 10 subcloned cDNA fragments, selected on the basis of the outcome of

120 Based on the cDNA fragment sequence, a full-length cDNA of 858 bp tha

121 The differentially expressed cDNA fragment showed 99% homology to Homo sapiens CD36 g

122 Nucleotide sequencing of this cDNA fragment showed it to be homologous to that of the

123 2-D gels, and the potential for identifying cDNA fragments solely on the basis of their two-dimensio

124 Of 15,000 mouse cDNA fragments studied, metallothionein (Mt)-1 and Mt2 e

125 irus (15,384 nucleotides) was assembled from cDNA fragments such that an exact antigenome RNA could b

126 CR), we have identified one early responsive cDNA fragment, TDD5, from a 5alpha-reductase-deficient T

127 poptosis, we identified a 326 bp bone marrow cDNA fragment (termed Je2) that suppresses, upon transfe

128 ing this system, we isolated and sequenced a cDNA fragment that encoded mouse lysyl oxidase (LO) and

129 gonucleotide PCR based technique to obtain a cDNA fragment that encodes an ETS domain from a human me

130 mia cell xenograft tumors in vivo, yielded a cDNA fragment that encodes an N-terminal fragment of hum

131 We have previously cloned the cDNA fragment that encodes the complement fixation antig

132 This allowed us to identify a 249 bp cDNA fragment that hybridized to a 4.8 kb mRNA preferent

133 Using differential display, we identified a cDNA fragment that was reproducibly upregulated in vascu

134 iate into smooth muscle cells, we isolated a cDNA fragment that was robustly induced during this diff

135 We repeatedly isolated a 325-bp cDNA fragment that, as determined by Northern analysis,

136 ue has been modified to identify prokaryotic cDNA fragments that are differentially induced by facult

137 The key steps are the generation of random cDNA fragments that are fused to a hairpin linker, cleav

138 cDNA fragments that encode an unknown putative alcohol d

139 duced cell population, however, incorporated cDNA fragments that included genes specifying TAA.

140 , identified 336 of 32,496 and 656 of 32,940 cDNA fragments that showed >or=1.5-fold change in expres

141 on ultra-high-throughput sequencing of 27-bp cDNA fragments that uniquely tag the corresponding gene,

142 We cloned and sequenced three cDNA fragments that were differentially expressed in hea

143 We isolated three opsin-encoding cDNA fragments that were identified with P530, P470, and

144 inc yielded several differentially expressed cDNA fragments that were individually subcloned.

145 ion PCR (DDRT - PCR), we found that a 360 bp cDNA fragment was absent in several c-myc transfected ra

146 A 300 bp specific fragment from the cDNA fragment was chosen to insert into vector pFGC1008

147 The amplified cDNA fragment was cloned into the bacterial expression v

148 This cDNA fragment was identical in amino acid sequence to th

149 Using differential display, a cDNA fragment was identified as being overexpressed in a

150 The cDNA fragment was isolated by using the yeast two-hybrid

151 This cDNA fragment was present in the parental REC (Rat Embry

152 s gene expression and it was proved that the cDNA fragment was relevant to the cellulose biosynthesis

153 The cDNA fragment was subsequently cloned and used as a prob

154 ide whose sequence was deduced from a cloned cDNA fragment was synthesized and used to prepare an ant

155 A retroviral expression library of random cDNA fragments was constructed from cancer cells and use

156 The production of replicative MS2 phage from cDNA fragments was used to assess the viability of MS2 c

157 Using the cDNA fragment, we then isolated a full-length clone from

158 Many novel cDNA fragments were also induced or repressed by lines e

159 PCR-generated CF/chitinase cDNA fragments were cloned and examined for their reacti

160 Overlapping cDNA fragments were generated by the polymerase chain re

161 One hundred fifteen cDNA fragments were identified and shown to represent 90

162 Eleven unique cDNA fragments were identified from YAC B30H3, which spa

163 Numerous cDNA fragments were identified that showed a twofold or

164 A number of novel differentially expressed cDNA fragments were isolated from human papillary thyroi

165 pollen development, a number of Arabidopsis cDNA fragments were isolated using subtractive hybridiza

166 stment for redundancy among clones, 34 novel cDNA fragments were isolated.

167 BC cells expressing stably integrated GADD45 cDNA fragments were obtained and CD437-dependent inducti

168 All cDNA fragments were sequenced and the identities of seve

169 ning of an endothelial cDNA library, and the cDNA fragments were subcloned into prokaryotic expressio

170 n examining a manganese superoxide dismutase cDNA fragment which we detected while evaluating the eff

171 an microvascular endothelial cells (HMVEC) a cDNA fragment with characteristics of the 3'end of mRNA.

172 NA recombination and repair genes, yielded a cDNA fragment with high homology to RAD54.

173 A 130 bp cDNA fragment with sequence similarities to crnA was amp

174 essed sequence tag database was queried, and cDNA fragments with sequence similarity to the Na(+)/Cl(

175 he screen is based on fusion of a library of cDNA fragments with the lysosomal protease cathepsin B (

176 s cloned from M. grisea by identification of cDNA fragments with weak homology to the cDNA of trihydr

177 All 6 cDNA fragments with zinc finger homology had a poly-A ta

178 Two of the 6 cDNA fragments with zinc finger homology hybridized to 3

179 , and E) for simultaneous analysis of 60,000 cDNA fragments, with 12,000 fragments covering full-leng

180 ival motor neuron gene SMN, and of a further cDNA fragment, XS2G3, have been reported in childhood-on