戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  terminus of the herpes simplex virus 2 UL27.5 sequence.
2 ity required no more than 549 nucleotides of 5 sequence.
3  apparent retention of the entire chromosome 5 sequence.
4 g of exon 6 to the immediate upstream intron 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 l/3' end, and then apically using N-terminal/5' sequences.
10 h declining activity upon further removal of 5' sequences.
11 f interchain cross-links in 5'-GGC-3'/3'-CCG-5' sequences.
12  RNA lacked the 3' sequences rather than the 5' sequences.
13 te, there was hypermethylation of H-cadherin 5' sequences.
14            DSNs were divided into cohorts of 5 (sequence 1-5, 6-10, and so forth).
15 a new cDNA clone for eIF4GI that extends the 5' sequence 340 nucleotides beyond the previously publis
16                         Polymorphisms in the 5'-sequence adjacent to the SCN5A gene have been linked
17  sequence to buffer end erosion of essential 5' sequence after the RNA is reverse transcribed onto th
18 rate constants increased for substrates with 5' sequence alterations that reduced ground-state bindin
19                                              5' sequence analysis revealed several conserved promoter
20 mined that a fusion transcript between novel 5' sequence and exons 4 and 5 of Hmgi-c is created.
21 n mammalian U7 snRNAs because of an extended 5' sequence and has only a limited potential to form a s
22 d is highly sensitive to the identity of the 5' sequence and Mg2+ ions.
23 le-specific ankyrin 1 cDNA composed of novel 5' sequences and 3' sequences previously identified in t
24                     Characterization of mRNA 5' sequences and the intron-exon structure of the 5' reg
25 ing locations and mRNA transcript abundance, 5' sequences and translation into proteins to determine
26 sgenic mice carrying a 6.5 kb segment of the 5'-sequence and most of the EPO gene in which lacZ was s
27 te the nucleosome positioning ability of the 5S sequence and detect an enhanced preference for nucleo
28                  Exon 1 contains a noncoding 5' sequence, and exon 2 contains the transcriptional sta
29 h transcript and is preceded by an extensive 5' sequence (approximately 0.5 to 2.5 kb) containing sev
30                               Only 217 bp of 5' sequence are required for basal adipose tissue-specif
31           In contrast, over 900 bp of Kir6.2 5' sequence are required for similar high level expressi
32                                         Thus 5' sequences are at risk for terminal erosion while the
33                      This identifies the LG4-5 sequences as the region of laminin responsible for sig
34 ed a variant HPS cDNA that contains the same 5' sequence as the published HPS gene and a unique 3' se
35             TbMTr1 favors the spliced leader 5' sequence, as reflected by a preference for A at posit
36 s in a U-tract, and mature scR1 retains a U4-5 sequence at its 3' end.
37 A strands through base recognition while the 5' sequence C(3)AC(3)AC(3)TC(3)A favors formation of a n
38 plasmid contains bC2GnT-M cDNA devoid of the 5'-sequence coding the cytoplasmic tail and transmembran
39  results indicate that miRNAs sharing common 5' sequences, considered to be largely redundant, might
40 and RRV17577 sequences differ in that ORF 67.5 sequences contained in RRV26-95 were not found in RRV1
41                                     The -20/-5 sequence contains critical 5' sequence elements.
42                            The beta-PDE gene 5' sequence contains two distinct transcription start si
43                                         This 5'-sequence contains a clinically conserved U-1 that we
44  miR-15, miR-16, and miR-195 due to a common 5' sequence critical for target specificity.
45 Y314F) and a splice variant without TEL exon 5 sequences (Deltae5) lacked Grb2 interaction and exhibi
46 cDNA library contained two different extreme 5'-sequences derived from short alternative first untran
47 f N(2)-BPDE-dG formation within the p53 exon 5 sequences did not correlate with the mutational spectr
48 transgenic plants showed that 1190 bp of g10 5' sequence directed preferential expression of GUS in p
49 s shared high VP7 gene sequence homology (<2.5% sequence divergence on both the nucleotide and amino
50 the nucleocapsid protein, were found with 12.5% sequence divergence, while no heterogeneity was obser
51 on and LIS1 partial cDNAs, and therefore its 5' sequence does not represent the LIS1 5' end.
52                      Here, we identified two 5' sequence domains that are necessary and sufficient to
53                                      The two 5' sequence domains were also conserved among geminin or
54 l for the initiation of replication, another 5' sequence element, the 51-nucleotide (nt) conserved se
55                   However, the exact kinesin-5 sequence elements that are important for formation of
56        The -20/-5 sequence contains critical 5' sequence elements.
57 te of transcriptional repression to the most 5' sequence encoding the iPLA2gamma holoprotein; (c) ide
58 moter swap transgenic mice that contain IIIB 5' sequences express Fc gamma RIII in neutrophils only.
59 t human GLI2 contains previously undescribed 5' sequence, extending the amino-terminus an additional
60 A initiation site and another located on the 5' sequence flanking stem-loop III.
61 ARPE-19 and D407) in culture to evaluate the 5' sequence flanking the RLBP1 gene.
62 nctional analyses indicate that the proximal 5' sequence flanking the TATA box of the PTP-oc contains
63                                          The 5'-sequences flanking the human complement component C4
64                                          The 5' sequences for six established M protein genes--the em
65 nd squirrel monkeys by crossovers that fused 5' sequence from gamma1 with 3' sequence from gamma2.
66                                        Known 5' sequence from MLL but unknown 3' sequence from chromo
67                      Further deletion of the 5' sequence from nucleotide -1336 to -407 (pluc 440), an
68 ESTs) were obtained representing both 3' and 5' sequences from about half that number of cDNA clones.
69 GFbetaR) fusion transcript that incorporated 5' sequences from H4 fused in frame to 3' PDGFbetaR sequ
70 d sequences resulted from the fusion between 5' sequences from the human beta-1,4-galactosyltransfera
71  and RACE were used to acquire the remaining 5'-sequence from RNA isolated from oil gland secretory c
72                                          The 5' sequence GCCGUU, required for editing of C214 in toba
73 ion from the IIIA gene, and conversely, IIIA 5' sequences have been substituted for the analogous reg
74  nsp3b, although the two proteins share only 5% sequence identity in the homologous sequence regions.
75 piggyBac sequence (pBac(Bd-Kah)) having ~ 94.5% sequence identity to IFP2 was isolated, and it was re
76 mbinant region, spanning spike (S), shows 96.5% sequence identity to the pantropic canine coronavirus
77                  These duplicons show 94%-98.5% sequence identity to their ancestral loci.
78                          AncFMO1, sharing 89.5% sequence identity with human FMO1, was successfully e
79       The predicted protein product shows 72.5% sequence identity with the human protein and conserva
80 were in a common chromosomal site and had 98.5% sequence identity with variations occurring mainly in
81  regulatory protein Hha, despite having only 5% sequence identity.
82 coli (NgMltA and EcMltA), which have only 21.5% sequence identity.
83 omain VI and one exon encoding the divergent 5' sequence in another published cDNA clone variant (orp
84 vity is dependent on the 8 nt repeat-derived 5' sequence in the crRNA, but not on the presence of a p
85              In two of the incomplete genes, 5' sequence in the incomplete genes is 3' sequence in th
86 structs containing different lengths of hNET 5' sequence in the presence or the absence of the first
87                             Furthermore, the 5' sequence in the proximal promoter region and 3' untra
88  ribozyme to examine the contribution of the 5' sequence in the substrate to HDV ribozyme catalysis.
89                    We report that the unique 5' sequences in these mRNA isoforms are encoded in two s
90 eporter constructs containing gRNA or sgRNA2 5' sequences in vivo, which differs from how umbravirus
91 ect was observed for RNAs with globin or DEN 5' sequences, indicating no codependency between viral 5
92                         In addition, the LRP-5 sequences involved in interactions with Axin are requi
93                        One particular (GGXXP)5 sequence is located directly after the RGD motif, and
94 ransgenes incorporating 1.7 kb of additional 5' sequence mimic the endogenous H19 pattern, including
95 ituations is unclear, however, several IGFBP-5 sequence motifs and studies in vitro suggest IGF-indep
96      The other was 4.1 kb long with a unique 5' sequence of 853 bp.
97 lated with repressive chromatin marks in the 5' sequence of a synthetic LINE-1 element.
98 ect binding of SMADs on the highly conserved 5' sequence of DeltaNp63.
99 , indicating that the similarity between the 5' sequence of LIS1 (8-1) and the 3' UTR of 14-3-3 epsil
100 e characterized approximately 3.8-kb genomic 5' sequence of murine SOCS-3, including approximately 2.
101 roid plexus, which was 99 % identical to the 5' sequence of rat ClC-2.
102 lone and characterize the previously elusive 5' sequence of the barley powdery mildew chitin synthase
103 es (5'-GUAAA-3') identical to those from the 5' sequence of the BMV genomic RNA2 and RNA3.
104 erase chain reaction (RACE-PCR) in which the 5' sequence of the human gastric mucin cDNA HGM-1 (1) wa
105                         The DNA flanking the 5' sequence of the mouse 1alpha-hydroxylase gene has bee
106                                          The 5' sequence of this cDNA is identical to the EGFR transc
107                                          The 5' sequence of vRNA binds to an amino acid sequence cent
108 on studies demonstrated in vivo occupancy of 5' sequences of both genes by IRF8 protein.
109 lucocorticoid regulation of CYP3A5, we fused 5' sequences of CYP3A5 to the chloramphenicol acetyltran
110                             Divergence among 5' sequences of DR genes amplified from G. arboreum, G.
111 regulation of ORG expression, we have mapped 5' sequences of mRNA from olfactory epithelium encoding
112 phomas (DLBCLs), leading to mutations in the 5' sequences of multiple genes, including oncogenes.
113 pears to misfire and causes mutations in the 5' sequences of multiple proto-oncogenes, including PIM-
114 M type serology and the previously published 5' sequences of the emm genes of M type reference strain
115 NA transfection data suggested that proximal 5' sequences of the GFAP gene are sufficient to direct h
116 onstructed chimeric genes in which 5.8 kb of 5' sequences of the IIIB gene has been replaced with a h
117                              To identify the 5' sequences of the murine coagulation factor VII (fVII)
118                                   The 3' and 5' sequences of the primer both influenced the efficienc
119  to harbor multiple somatic mutations in the 5' sequences of the S1P(2) gene.
120 e transmembrane and cytoplasmic domains, the 5' sequences of these mucins are identical; however, the
121 converting enzyme (ACE), was identified from 5' sequencing of a human heart failure ventricle cDNA li
122 difications to the major groove of the GGGAA 5'-sequence of the nonscissile strand were introduced an
123      The DNA segment in and at the immediate 5'-sequences of the first exon of variant 2 contains a c
124 aged deep screening of a library of 2.4 x 10(5) sequences of the third complementarity-determining re
125 ession to approximately 40,000,000 bases (10(5) sequences) of expressed gene sequence from germinal c
126 nces added to the 5' end of the original SFV 5' sequence or its "deleted" versions.
127 ental one and suggest that the residual gene 5 sequence present in the mouse-adapted parental virus h
128  poly(A) tail, suggesting that 500-600 bp of 5' sequence remains to be identified.
129  its normal chromosomal position relative to 5' sequences rescued TCR delta rearrangement.
130                       A deletion of the Xist 5' sequence resulted in the loss of somatic X inactivati
131 ase-pair substitutions at positions 4 and/or 5 [sequence: see text] in each 10 bp half site of the sy
132                                             (5) Sequence-specific assignments of these carbon and nit
133 show that Cmr crRNAs contain an 8 nucleotide 5' sequence tag (also found on crRNAs associated with ot
134  occur in two size forms that share a common 5' sequence tag but have distinct 3' ends that direct cl
135    Independent validation confirmed 4 out of 5 sequences that were identified by this strategy, confe
136 rsal-neural tube enhancer was located in the 5' sequence that is conserved among mouse, human, chick,
137                      These forms differed in 5' sequences that resulted from the alternative use of t
138 ion of a 28-kb contig encompassing 300 bp of 5' sequence, the entire coding region, and 2 kb of 3'-fl
139 -dependent regulon contain a short conserved 5' sequence, the ops element, deletion of which increase
140         The chimeric receptors were mostly M(5) sequence; the amount of M(2) sequence ranged from abo
141                                             (5)) sequence type are dominant, endemic(6-8) and associa
142        PCR protocols were designed to target 5 sequences unique to the M. gallisepticum ts-11 strain:
143                CD45 minigenes using the CD45 5' sequences up to 19 kilobases upstream of the transcri
144                            Inspection of the 5' sequences upstream of the predicated translation star
145                                The remaining 5 sequence variants (L134V, S227I, Q228H, R410G, and D41
146                                  Ten fibulin 5 sequence variants have been associated with AMD and tw
147 that GII.4 subclusters be defined as having >5% sequence variation between strains.
148 d against the aminoterminus of the human FGF-5 sequence was used in Western blot analyses to identify
149  of the U tract with respect to the 3'-UCAAU-5' sequence was critical.
150  spliced smaller transcript with a divergent 5' sequence was expressed specifically in the human feta
151  NGFI-A-binding site; however, a more distal 5' sequence was found to repress basal activity in N1E-1
152 plicing to generate transcripts with varying 5' sequences was detected in the human but not the mouse
153 e the molecular basis of these heterogeneous 5' sequences, we determined the sequence of the alpha hF
154 reporter constructs containing up to 3 kb of 5' sequence were performed in hematopoietic and small-ce
155                                  The missing 5' sequences were obtained by 5'-rapid amplification of
156                                 The flanking 5' sequences were rich in G and C ( approximately 80%) a
157  little as 1.5 kb of 3' sequences or 5 kb of 5' sequences were sufficient to confer apoB expression i
158 ic peptides based on each of the IR(2) to IR(5) sequences were produced in rabbits.
159  31 to 38 amino acids that spanned the Phl p 5 sequence, were synthesized, characterized by circular
160 transcribe a cDNA containing the unique Osf2 5' sequence, whereas a second donor splice site gives ri
161 et site duplications and contained conserved 5' sequences, which likely regulate their transcription.
162  effects of substrate analogues with varying 5' sequences, which reside as dangling overhangs outside
163 fficking efficiency was largely dependent on 5' sequences, while translation efficiency involved mult
164                         Replacement of the A(5) sequence with a disrupted DNA bending sequence (A(2)T

 
Page Top