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1 ical in macroevolutionary research, and they allow us to begin to answer the proposal of George Gaylo
2                            These unique mice allow us to further our understanding of ALS by separati
3 orms of NorM in a phospholipid lipid bilayer allow us to identify the nature of the drug-protein/ion-
4  to maximise signalling robustness, and will allow us to make increasingly complex biological compute
5 r each of these eight conserved residues and allow us to propose a sequential, base-catalysed mechani
6           Careful sample handling techniques allow us to quantitatively detect HIF-1alpha in samples
7 d chemical reactivity, such defects may also allow us to selectively functionalize the material and s
8                                  Our results allow us to understand the role of individual mutations
9                             Genetic analysis allowed us to assign most of the new modification sites
10                 This ultrasensitive workflow allowed us to collect thousands of biochemical data poin
11                                         This allowed us to construct quantum dot molecules whose coup
12                        Our studies have also allowed us to define a set of maternal mRNAs that are de
13    Detailed phenotyping of patients with FMD allowed us to demonstrate that FMD is a systemic disease
14                                   This model allowed us to develop and validate new hypotheses about
15                       Microarray comparisons allowed us to establish a list of genes regulated in ten
16 nced high-throughput genomic approaches have allowed us to examine the microbiota in an unprecedented
17  conservation of the TCR interaction surface allowed us to exploit deep-sequencing information to com
18                      Our integrated approach allowed us to gather a complete view of the complex chro
19 rging the human data sets with the fly genes allowed us to identify disease-associated mutations in s
20                               These proteins allowed us to identify encoding neurons several days aft
21                            Spectral analysis allowed us to identify signals from multiple levels of t
22 ins and restoration of the wild-type alleles allowed us to identify target genes involved in this ant
23 ibutes of the graph to train a decision tree allowed us to increase accuracy of SNP calls further.
24 rometry, and integrative structure modeling, allowed us to position and orient all eIF3 components on
25    Mining data from the 1000 Genomes Project allowed us to precisely estimate copy numbers of the RNU
26 essential function for this binding site and allowed us to propose a model for the binding of the gro
27 D-phnF intergenic region of M. smegmatis has allowed us to propose a quantitative model for repressor
28 encing, using a DNA barcoding technique that allowed us to quantify independent integration events.
29                                  This system allowed us to rapidly compare the ability of 12 differen
30 embling the unmapped reads pooled by biotype allowed us to recover some divergent genomic regions pre
31                                         This allowed us to simultaneously monitor the expression of m
32 ts of their respective molecular structures, allowing us to compare the intact tissues at atomic leng
33 rk databases are of increasing importance in allowing us to contextualise data sets emerging from tra
34    We analyzed a panel of 43 chimeric NAIPs, allowing us to map the NAIP domain responsible for speci
35 its hepatocyte growth without cell division, allowing us to study cell size in vivo using transcripto
36 f action might lead to important information allowing us to understand the link between HTLV-1 HBZ an
37 almonella enterica and Staphylococcus aureus allows us to build a modular framework containing 204 tr
38                                         This allows us to calculate the relative contribution from du
39 novel approach, termed AAV Barcode-Seq, that allows us to characterize phenotypes of hundreds of diff
40          This approach of hybrid integration allows us to combine the strength of p-type carbon nanot
41 N termini with a pair of fluorophores, which allows us to determine the Sb2 length and geometry.
42 fic copy number estimates obtained by falcon allows us to draw detailed conclusions regarding the clo
43 s that stabilize boundaries between TADs and allows us to identify and genetically validate key struc
44 derstanding of the genetic code and splicing allows us to identify likely candidates, but interpretin
45 pulsed excitations of the disordered samples allows us to identify long-lived localized modes and sho
46 is close match between theory and experiment allows us to infer and subsequently build a 2-node netwo
47 stHap leverages a new similarity metric that allows us to precisely measure distances between pairs o
48 y, the identification of 'who infected whom' allows us to quantify key characteristics such as incuba
49 individual links into a broader network that allows us to understand how these components interact.
50                                         This allows us to use a continuous separation process with he

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