ライフサイエンスコーパス: 5' sequence

1 terminus of the herpes simplex virus 2 UL27.5 sequence.

2 ity required no more than 549 nucleotides of 5 sequence.

3 g of exon 6 to the immediate upstream intron 5 sequence.

4 apparent retention of the entire chromosome 5 sequence.

5 ed at B-Z junctions flanking d(CG)4 and d(CG)5 sequences.

6 p extension to the previously published cDNA 5' sequence.

7 for replication relative to the parental SIN 5' sequence.

8 ne encompassing the entire coding region and 5' sequences.

9 h declining activity upon further removal of 5' sequences.

10 f interchain cross-links in 5'-GGC-3'/3'-CCG-5' sequences.

11 RNA lacked the 3' sequences rather than the 5' sequences.

12 te, there was hypermethylation of H-cadherin 5' sequences.

13 a new cDNA clone for eIF4GI that extends the 5' sequence 340 nucleotides beyond the previously publis

14 Polymorphisms in the 5'-sequence adjacent to the SCN5A gene have been linked

15 sequence to buffer end erosion of essential 5' sequence after the RNA is reverse transcribed onto th

16 rate constants increased for substrates with 5' sequence alterations that reduced ground-state bindin

17 5' sequence analysis revealed several conserved promoter

18 mined that a fusion transcript between novel 5' sequence and exons 4 and 5 of Hmgi-c is created.

19 n mammalian U7 snRNAs because of an extended 5' sequence and has only a limited potential to form a s

20 d is highly sensitive to the identity of the 5' sequence and Mg2+ ions.

21 le-specific ankyrin 1 cDNA composed of novel 5' sequences and 3' sequences previously identified in t

22 Characterization of mRNA 5' sequences and the intron-exon structure of the 5' reg

23 ing locations and mRNA transcript abundance, 5' sequences and translation into proteins to determine

24 sgenic mice carrying a 6.5 kb segment of the 5'-sequence and most of the EPO gene in which lacZ was s

25 te the nucleosome positioning ability of the 5S sequence and detect an enhanced preference for nucleo

26 Exon 1 contains a noncoding 5' sequence, and exon 2 contains the transcriptional sta

27 h transcript and is preceded by an extensive 5' sequence (approximately 0.5 to 2.5 kb) containing sev

28 Only 217 bp of 5' sequence are required for basal adipose tissue-specif

29 In contrast, over 900 bp of Kir6.2 5' sequence are required for similar high level expressi

30 Thus 5' sequences are at risk for terminal erosion while the

31 This identifies the LG4-5 sequences as the region of laminin responsible for sig

32 ed a variant HPS cDNA that contains the same 5' sequence as the published HPS gene and a unique 3' se

33 TbMTr1 favors the spliced leader 5' sequence, as reflected by a preference for A at posit

34 s in a U-tract, and mature scR1 retains a U4-5 sequence at its 3' end.

35 A strands through base recognition while the 5' sequence C(3)AC(3)AC(3)TC(3)A favors formation of a n

36 plasmid contains bC2GnT-M cDNA devoid of the 5'-sequence coding the cytoplasmic tail and transmembran

37 results indicate that miRNAs sharing common 5' sequences, considered to be largely redundant, might

38 and RRV17577 sequences differ in that ORF 67.5 sequences contained in RRV26-95 were not found in RRV1

39 The -20/-5 sequence contains critical 5' sequence elements.

40 The beta-PDE gene 5' sequence contains two distinct transcription start si

41 This 5'-sequence contains a clinically conserved U-1 that we

42 miR-15, miR-16, and miR-195 due to a common 5' sequence critical for target specificity.

43 Y314F) and a splice variant without TEL exon 5 sequences (Deltae5) lacked Grb2 interaction and exhibi

44 cDNA library contained two different extreme 5'-sequences derived from short alternative first untran

45 f N(2)-BPDE-dG formation within the p53 exon 5 sequences did not correlate with the mutational spectr

46 transgenic plants showed that 1190 bp of g10 5' sequence directed preferential expression of GUS in p

47 s shared high VP7 gene sequence homology (<2.5% sequence divergence on both the nucleotide and amino

48 the nucleocapsid protein, were found with 12.5% sequence divergence, while no heterogeneity was obser

49 on and LIS1 partial cDNAs, and therefore its 5' sequence does not represent the LIS1 5' end.

50 Here, we identified two 5' sequence domains that are necessary and sufficient to

51 The two 5' sequence domains were also conserved among geminin or

52 l for the initiation of replication, another 5' sequence element, the 51-nucleotide (nt) conserved se

53 However, the exact kinesin-5 sequence elements that are important for formation of

54 The -20/-5 sequence contains critical 5' sequence elements.

55 te of transcriptional repression to the most 5' sequence encoding the iPLA2gamma holoprotein; (c) ide

56 moter swap transgenic mice that contain IIIB 5' sequences express Fc gamma RIII in neutrophils only.

57 t human GLI2 contains previously undescribed 5' sequence, extending the amino-terminus an additional

58 A initiation site and another located on the 5' sequence flanking stem-loop III.

59 ARPE-19 and D407) in culture to evaluate the 5' sequence flanking the RLBP1 gene.

60 nctional analyses indicate that the proximal 5' sequence flanking the TATA box of the PTP-oc contains

61 The 5'-sequences flanking the human complement component C4

62 The 5' sequences for six established M protein genes--the em

63 nd squirrel monkeys by crossovers that fused 5' sequence from gamma1 with 3' sequence from gamma2.

64 Known 5' sequence from MLL but unknown 3' sequence from chromo

65 Further deletion of the 5' sequence from nucleotide -1336 to -407 (pluc 440), an

66 ESTs) were obtained representing both 3' and 5' sequences from about half that number of cDNA clones.

67 GFbetaR) fusion transcript that incorporated 5' sequences from H4 fused in frame to 3' PDGFbetaR sequ

68 d sequences resulted from the fusion between 5' sequences from the human beta-1,4-galactosyltransfera

69 and RACE were used to acquire the remaining 5'-sequence from RNA isolated from oil gland secretory c

70 The 5' sequence GCCGUU, required for editing of C214 in toba

71 ion from the IIIA gene, and conversely, IIIA 5' sequences have been substituted for the analogous reg

72 nsp3b, although the two proteins share only 5% sequence identity in the homologous sequence regions.

73 These duplicons show 94%-98.5% sequence identity to their ancestral loci.

74 The predicted protein product shows 72.5% sequence identity with the human protein and conserva

75 were in a common chromosomal site and had 98.5% sequence identity with variations occurring mainly in

76 regulatory protein Hha, despite having only 5% sequence identity.

77 coli (NgMltA and EcMltA), which have only 21.5% sequence identity.

78 omain VI and one exon encoding the divergent 5' sequence in another published cDNA clone variant (orp

79 vity is dependent on the 8 nt repeat-derived 5' sequence in the crRNA, but not on the presence of a p

80 In two of the incomplete genes, 5' sequence in the incomplete genes is 3' sequence in th

81 structs containing different lengths of hNET 5' sequence in the presence or the absence of the first

82 Furthermore, the 5' sequence in the proximal promoter region and 3' untra

83 ribozyme to examine the contribution of the 5' sequence in the substrate to HDV ribozyme catalysis.

84 We report that the unique 5' sequences in these mRNA isoforms are encoded in two s

85 ect was observed for RNAs with globin or DEN 5' sequences, indicating no codependency between viral 5

86 In addition, the LRP-5 sequences involved in interactions with Axin are requi

87 One particular (GGXXP)5 sequence is located directly after the RGD motif, and

88 ransgenes incorporating 1.7 kb of additional 5' sequence mimic the endogenous H19 pattern, including

89 ituations is unclear, however, several IGFBP-5 sequence motifs and studies in vitro suggest IGF-indep

90 The other was 4.1 kb long with a unique 5' sequence of 853 bp.

91 lated with repressive chromatin marks in the 5' sequence of a synthetic LINE-1 element.

92 ect binding of SMADs on the highly conserved 5' sequence of DeltaNp63.

93 , indicating that the similarity between the 5' sequence of LIS1 (8-1) and the 3' UTR of 14-3-3 epsil

94 e characterized approximately 3.8-kb genomic 5' sequence of murine SOCS-3, including approximately 2.

95 roid plexus, which was 99 % identical to the 5' sequence of rat ClC-2.

96 lone and characterize the previously elusive 5' sequence of the barley powdery mildew chitin synthase

97 es (5'-GUAAA-3') identical to those from the 5' sequence of the BMV genomic RNA2 and RNA3.

98 erase chain reaction (RACE-PCR) in which the 5' sequence of the human gastric mucin cDNA HGM-1 (1) wa

99 The DNA flanking the 5' sequence of the mouse 1alpha-hydroxylase gene has bee

100 The 5' sequence of this cDNA is identical to the EGFR transc

101 The 5' sequence of vRNA binds to an amino acid sequence cent

102 on studies demonstrated in vivo occupancy of 5' sequences of both genes by IRF8 protein.

103 lucocorticoid regulation of CYP3A5, we fused 5' sequences of CYP3A5 to the chloramphenicol acetyltran

104 Divergence among 5' sequences of DR genes amplified from G. arboreum, G.

105 regulation of ORG expression, we have mapped 5' sequences of mRNA from olfactory epithelium encoding

106 phomas (DLBCLs), leading to mutations in the 5' sequences of multiple genes, including oncogenes.

107 pears to misfire and causes mutations in the 5' sequences of multiple proto-oncogenes, including PIM-

108 M type serology and the previously published 5' sequences of the emm genes of M type reference strain

109 NA transfection data suggested that proximal 5' sequences of the GFAP gene are sufficient to direct h

110 onstructed chimeric genes in which 5.8 kb of 5' sequences of the IIIB gene has been replaced with a h

111 To identify the 5' sequences of the murine coagulation factor VII (fVII)

112 The 3' and 5' sequences of the primer both influenced the efficienc

113 to harbor multiple somatic mutations in the 5' sequences of the S1P(2) gene.

114 e transmembrane and cytoplasmic domains, the 5' sequences of these mucins are identical; however, the

115 converting enzyme (ACE), was identified from 5' sequencing of a human heart failure ventricle cDNA li

116 difications to the major groove of the GGGAA 5'-sequence of the nonscissile strand were introduced an

117 ession to approximately 40,000,000 bases (10(5) sequences) of expressed gene sequence from germinal c

118 nces added to the 5' end of the original SFV 5' sequence or its "deleted" versions.

119 poly(A) tail, suggesting that 500-600 bp of 5' sequence remains to be identified.

120 its normal chromosomal position relative to 5' sequences rescued TCR delta rearrangement.

121 A deletion of the Xist 5' sequence resulted in the loss of somatic X inactivati

122 ase-pair substitutions at positions 4 and/or 5 [sequence: see text] in each 10 bp half site of the sy

123 (5) Sequence-specific assignments of these carbon and nit

124 show that Cmr crRNAs contain an 8 nucleotide 5' sequence tag (also found on crRNAs associated with ot

125 occur in two size forms that share a common 5' sequence tag but have distinct 3' ends that direct cl

126 rsal-neural tube enhancer was located in the 5' sequence that is conserved among mouse, human, chick,

127 These forms differed in 5' sequences that resulted from the alternative use of t

128 ion of a 28-kb contig encompassing 300 bp of 5' sequence, the entire coding region, and 2 kb of 3'-fl

129 -dependent regulon contain a short conserved 5' sequence, the ops element, deletion of which increase

130 The chimeric receptors were mostly M(5) sequence; the amount of M(2) sequence ranged from abo

131 PCR protocols were designed to target 5 sequences unique to the M. gallisepticum ts-11 strain:

132 CD45 minigenes using the CD45 5' sequences up to 19 kilobases upstream of the transcri

133 Inspection of the 5' sequences upstream of the predicated translation star

134 The remaining 5 sequence variants (L134V, S227I, Q228H, R410G, and D41

135 Ten fibulin 5 sequence variants have been associated with AMD and tw

136 that GII.4 subclusters be defined as having >5% sequence variation between strains.

137 d against the aminoterminus of the human FGF-5 sequence was used in Western blot analyses to identify

138 of the U tract with respect to the 3'-UCAAU-5' sequence was critical.

139 spliced smaller transcript with a divergent 5' sequence was expressed specifically in the human feta

140 NGFI-A-binding site; however, a more distal 5' sequence was found to repress basal activity in N1E-1

141 plicing to generate transcripts with varying 5' sequences was detected in the human but not the mouse

142 e the molecular basis of these heterogeneous 5' sequences, we determined the sequence of the alpha hF

143 reporter constructs containing up to 3 kb of 5' sequence were performed in hematopoietic and small-ce

144 The missing 5' sequences were obtained by 5'-rapid amplification of

145 The flanking 5' sequences were rich in G and C ( approximately 80%) a

146 little as 1.5 kb of 3' sequences or 5 kb of 5' sequences were sufficient to confer apoB expression i

147 ic peptides based on each of the IR(2) to IR(5) sequences were produced in rabbits.

148 31 to 38 amino acids that spanned the Phl p 5 sequence, were synthesized, characterized by circular

149 transcribe a cDNA containing the unique Osf2 5' sequence, whereas a second donor splice site gives ri

150 et site duplications and contained conserved 5' sequences, which likely regulate their transcription.

151 effects of substrate analogues with varying 5' sequences, which reside as dangling overhangs outside

152 fficking efficiency was largely dependent on 5' sequences, while translation efficiency involved mult

153 Replacement of the A(5) sequence with a disrupted DNA bending sequence (A(2)T