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1 ere identified at the hemagglutinin esterase gene position.
2 ene to the first or second promoter-proximal gene position.
3 d to detect changes in chromosome shapes and gene positions.
4 neered to express RSV F from three different gene positions.
5  information to derive a map of the relative gene positions.
6 on, but not mitosis, is required for correct gene positioning.
7 f different genomic domains favors nonrandom gene positioning.
8  CM-1 were used as "bait" to identify target genes (positions 0324, 0705, 0708, 0808 to 0810, 1016 to
9 nogaster stocks carrying heat shock reporter genes positioned 1.9 and 3.7 kb downstream of lac operat
10  1.0%-5.5%; combined prevalence: 15.10%); E1 gene position 1053 [HR for overall survival (HR(os)): 3.
11 infer NAT2 phenotype from SNPs found in NAT2 gene positions 282, 341, 481, 590, 803 and 857.
12 3.75, 95% CI 1.77-7.95; P(fdr) = 0.0099]; L2 gene positions 4410 (HR(os): 5.32, 95% CI 1.91-14.81; P(
13 oduced between the phosphoprotein and matrix genes (position 5) of the genome to generate rHRSV(B05)E
14  95% CI 2.41-24.98; P(fdr) = 0.0030); and L1 gene positions 5962 (HR(os): 4.40, 95% CI 1.88-10.31; P(
15 he stochastic transcriptional silencing of a gene positioned adjacent to heterochromatin.
16 ased recombination estimates indicate that R genes positioned adjacent to nested long terminal repeat
17 thin the nucleus, but it remains unclear how gene position affects gene expression.
18            Independent manual measurement of gene positions agreed with automatic results in 21 out o
19    Finally, we introduce a novel approach to gene position analysis by employing measures from direct
20  Here we characterized the effect of varying gene position and 2As on the expression of proteins enco
21               However, the interplay between gene position and expression remains incompletely unders
22 to examine any relationship between relative gene position and likelihood of rearrangement.
23                 However, in all three cases, gene positioning and interchromosomal clustering are reg
24                                              Gene positioning and regulation of nuclear architecture
25    Together, these results reveal how radial gene positioning and the compartmentalization of activit
26 r results show that, for all 89 chromosomes, gene positions and gene orientations share a common form
27 enomic linguistic complexity and varies with gene-position and gene-essentiality.
28 ncoding RNAs (lncRNAs) and three-dimensional gene positioning are involved in genome organization and
29 RSV F was expressed from the first or second gene position as the full-length protein or as a chimeri
30                                    The ALL-1 gene positioned at 11q23 is directly involved in human a
31 view, we assess the current knowledge of how gene positioning at different levels of genome organizat
32  These results argue that zip code-dependent gene positioning at the nuclear periphery and interchrom
33  sufficient to allow comparisons of relative gene positions, both tyrRS types occupy equivalent posit
34 we explore the biological meaning of spatial gene positioning by examining the functional link betwee
35                  Investigations of flatliner gene positions, d(N)/d(S) ratios, and phylogenetic trees
36 comparisons against a pooled normal (benign) gene position distribution.
37  transcriptional repression of nearby marker genes (position-effect variegation or silencing).
38 iction and experimental confirmation of tRNA gene position effects at native chromosomal loci.
39 the continuous nature of the centromeric and gene position effects have not yet been studied as a sin
40 icular, we observed a number of CB-dependent gene-positioning events on chromosome 1.
41 table form of NF-kappaB into the vicinity of genes positioned fortuitously near NF-kappaB-binding sit
42 es evidence for the biological importance of gene positioning in the plant kingdom.
43 and intergenic distance, which suggests that gene positions in both yeast and human genomes are optim
44 ge-scale, high-resolution localization of 3D gene positions in single cells.
45 epression of Pol II- and Pol III-transcribed genes positioned in adjacent subtelomeric regions.
46                     Being able to manipulate gene position independently of other changes in differen
47  the user to input manually curated lists of gene position information, DNA sequence or gene homology
48 hypothesis, and support the idea that target gene positioning involves combinatorial interactions tha
49 tween IGHD gene pairing frequencies and IGHD gene position is a near linear one for each IGHJ gene.
50  discuss specific studies demonstrating that gene positioning is a dynamic and highly regulated featu
51                  In contrast, Ste12-mediated gene positioning is regulated independently of DNA bindi
52                                Robustness of gene position measurements to boundary inaccuracies was
53 Pearson correlation coefficients between the gene position measurements were above 0.9 (p < 0.05).
54 n configuration and silencing of euchromatic genes positioned near heterochromatin.
55    RSV F was expressed from the pre-N or N-P gene position of the rHPIV1 vector as a full-length prot
56                   To investigate the role of gene positioning on GAL gene expression, we monitored th
57  various ORF-clustering algorithms, relative gene positions on the chromosome and placement of gene p
58              Sequence similarities, relative gene positions on the chromosome, and metabolic reconstr
59  of multi-omic integration and depend on the gene positions on the chromosome.
60 itch-like control or quantitative control of gene positioning over different time scales.
61  in relation to their functional annotation, gene position, pathway and conservation score.
62                             These interphase gene positioning patterns may be used to identify cancer
63 ar association between evolutionary rate and gene position, suggesting that the evolution of function
64        Here, we resolve this by manipulating gene positions through targeting the nuclear envelope tr
65 identity and synteny analyses suggested that gene position was conserved between both strains.
66 iseases requires combining information about gene position with clues about biological function.
67  for the neomycin phosphotransferase (nptII) gene positioned within Ds followed by a negative selecti
68 s can reshape chromatin folding patterns and gene positioning within the nucleus.
69 or axis in a manner that correlates with the gene positions within the cluster (a feature called coll
70                                              Genes positioned within the telomeric heterochromatin of
71 e of the generally high expression levels of genes positioned within transposed elements, the new tra
72 Maternally defined spatial modes control gap genes positioning, without the classically assumed intri