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1 ual sequence elements, consistent with motor concatenation.
2 incongruent with the phylogeny inferred from concatenation.
3 defined subunit arrangement by using subunit concatenation.
4 e levels but showed significant viral genome concatenation.
5 nes for phylogenetic analyses, singly and by concatenation.
6 simal rotation, and the rules for PMD vector concatenation.
7 mutually exclusive mechanisms: expansion and concatenation.
8 ggests that chunking involves two processes: concatenation, aimed at the formation of motor-motor ass
9 Furthermore, our data showed expansion and concatenation also formed the contractile ring in dividi
10 sus unrooted archaeal topology using protein concatenation and a multigene supertree method based on
11 e results question the exclusive reliance on concatenation and associated practices, and argue that s
12 supported phylogenetic hypothesis using both concatenation and multispecies coalescent approaches (AS
13 on and estimates a tree on each subset using concatenation, and finally produces an estimated species
14 distinct sequences via selective activation, concatenation, and recycling of specific subsequences; a
15 ional viral approach to prevention of genome concatenation; and provide a mechanism for the general i
17 genes, exploring phylogenetic signal through concatenation as well as recently developed consensus ap
18 4 11k and the E4 34k/E1b 55k complex prevent concatenation at least in part by inactivation of the ho
22 e what appears to be an inability to resolve concatenation between chromosomes during meiosis, locali
29 tant to thermal denaturation, allowing their concatenation into long arrays and subsequent recognitio
33 erial species (including P. penetrans) using concatenation of 40 housekeeping genes, with and without
36 r 72 alphaproteobacteria was produced from a concatenation of alignments for 104 well-behaved protein
38 NA replication during G2/M by Top2-dependent concatenation of cohesed chromatids due to their physica
40 ry and spectroscopy techniques confirmed the concatenation of FeS and glycerol-dehydrogenase/nicotina
41 recombination methods rely on the mixing and concatenation of genetic material from a number of paren
43 cal nanoparticles (MNPs-oSUD) consisted of a concatenation of iron oxide cores, with an average size
44 iRNAs for multi-gene knockdown, we show that concatenation of miRNAs targeting different genes is its
45 is is given to the report of progress in the concatenation of molecular logic devices and switches, t
47 ow that, although clusters can be defined by concatenation of multiple marker sequences, barriers to
52 ed to the United Kingdom because of a unique concatenation of risk factors, including: 1) a high rati
53 s can be estimated under conditions in which concatenation of sequence data will positively mislead p
55 f correct classification was obtained by the concatenation of spectral, physico-chemical, and instrum
57 rotein, enhanced Nano-lantern (eNL), made by concatenation of the brightest luciferase, NanoLuc, with
60 ng reaction resulting in intein excision and concatenation of the flanking polypeptides (exteins) wit
62 s shows that this occurs as a consequence of concatenation of the transforming DNA, in planta, prior
63 types from Exome Sequencing Project alone or concatenation of the two panels over quality score-based
66 onstruction of an artificial gene encoding a concatenation of tryptic peptides (QCAT protein) from se
67 ion in protein, which is approximated by the concatenation of two binomial distributions of (13)C and
69 ert with the 55 kDa product of E1b, prevents concatenation of viral genomes in infected cells, inhibi
71 a single frequency but in which, through the concatenation of wavelets, the phase changes randomly ev
72 We systematically identified each SNP in concatenations of all backbone ORFs in 7 newly or previo
73 identification, multiple sequence alignment, concatenation, phylogenetic tree estimation, and post-tr
74 how that template-directed ligation and high concatenation rates counter compositional bias and shift
75 vitro V(D)J recombination and adenoviral DNA concatenation, two processes that rely on cellular DNA d
77 of E4 ORF3 in the regulation of virus genome concatenation via inhibition of cellular double-strand b
78 cyclic ring closure and the dimer-dimer ring concatenation were accomplished through formation of dis
79 tor putamen positively correlated with chunk concatenation, whereas a left-hemisphere frontoparietal
80 rent gene trees, phylogenomic studies couple concatenation with practices such as rogue taxon removal
81 was an aggregate increase in chunk strength (concatenation) with training, suggesting that subcortica
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