ライフサイエンスコーパス: allowed us to

1 es of the Cp(X)Rh(III) catalysts were systematically varied allowed us to apply multivariate linear regression algorithms

2 r details of promoter recognition by sigma(N) The structure allowed us to build and refine an improved sigma(N)-holoenzym

3 Incorporation of proteomic evidence allowed us to change the designation of more than 87 predicte

4 n relation to transgenerational epiallelic stability, which allowed us to classify chromosomal targets of epigenetic regu

5 computational evidence in the context of experimental data allowed us to conclude that three chemosensory pathways in P.

6 Differential gene-expression analysis has allowed us to confirm the relevance of these targets for EOC

7 tive comparisons of the binding preferences of 400 peptides allowed us to construct a position-specific scoring matrix (P

8 of an azobenzene photoswitch moiety led to structures that allowed us to control their activity against Escherichia coli

9 ing stage in the sequential vapor deposition growth process allowed us to cool the existing 2D crystals to prevent undesi

10 +/- 3.1 years of age) showed similar sulci patterns, which allowed us to delineate the mFPC areas in them.

11 This allowed us to derive the spectrum of the non-equilibrium (det

12 nd 3D digital models for the larval, pupal and adult stage, allowed us to describe the morphogenetic changes shaping the

13 Microprobe CE-ESI-MS of <0.02% of the single-cell content allowed us to detect approximately 230 different molecular fe

14 thiolated aptamer to achieve the required selectivity that allowed us to detect LYS in human serum.

15 d) and DPPH (2,2-diphenyl-1-picryl-hydrazyl-hydrate), which allowed us to determine the ability to scavenge free radicals

16 Measurement of this deflection at multiple epochs allowed us to determine the mass of Stein 2051 B-the sixth-ne

17 ntal compensations found in constitutive Drd2(-/-) mice and allowed us to directly evaluate the participation of D2R in s

18 This method allowed us to dissect the concerted process of E1-E2-catalyze

19 ing (fMRI) with a previously developed Stroop protocol that allowed us to dissociate reductions in Stroop interference ba

20 The high-resolution transcriptome atlas allowed us to distinguish between CAM-related and non-CAM gen

21 osting tree ensemble (GDBT) was applied to the samples that allowed us to distinguish between different genders, ethnicit

22 le mice before and after a 7 d monocular deprivation, which allowed us to examine both the depression component (Dc-ODP)

23 The rigid bicyclic skeleton of 2,4-methanoprolines allowed us to follow the through-bond impact of the substitue

24 A time-sampled approach allowed us to (i) reconstruct theoretical haplotypes in the s

25 22 were known to carry a germline BRCA1 or BRCA2 mutation, allowed us to identify an additional 22 tumors with somatic l

26 y, then we developed and validated a UPLC-MS/MS method that allowed us to identify and quantify for the first time a dipe

27 This approach also allowed us to identify metabolic limiting steps, which could

28 d on univariate (ANOVA) and multivariate analyses (OPLS-DA) allowed us to identify new potential volatile markers related

29 The prolonged intermediate state allowed us to identify protein substrates that have biased af

30 The high resolution of the structure allowed us to identify small but important differences at int

31 Next-generation sequencing technologies have allowed us to identify somatic mutations that initiate BE and

32 Conversely, untargeted metabolomics allowed us to identify two withanolides and one fatty acyl gl

33 ent anti-Stokes Raman spectroscopy (CARS) microspectroscopy allowed us to locally identify acylglycerols as the main cons

34 of virally encoded mutant green fluorescent proteins, which allowed us to measure the rates of selectively neutral mutati

35 The unique composite allowed us to miniaturize the sensor and couple it with a Pt

36 Our approach allowed us to monitor fast blinking of an organic dye, the di

37 recent high-throughput genome-wide mapping approaches have allowed us to more comprehensively recognize potential enhanc

38 These techniques allowed us to observe both a systematic underrepresentation a

39 inst the National Cancer Institute's 60-cell line panel and allowed us to obtain an X-ray co-crystal structure of the syn

40 Here, we have adopted a fragment-based strategy that allowed us to obtain high-quality NMR data providing, to our

41 The use of a one-pot reaction allowed us to overcome potential problems with individual ste

42 Moreover, the model allowed us to replicate the kinetics of junctional conductanc

43 A protein kinase A (PKA) biosensor allowed us to resolve minute PKA activity microdomains on the

44 In combination with FRET it allowed us to reveal and characterize the dynamics of what ha

45 These findings allowed us to select lyophilized flowers (A) for further chee

46 These cell-derived nanovesicles allowed us to separate single membrane receptors while mainta

47 rted in the literature, the great sensitivity of this model allowed us to show unambiguously that a methyl appears bigger

48 The high-throughput multiplex assay allowed us to simultaneously measure FcgammaR dimer-binding A

49 This approach also allowed us to study the properties of distinct AML subclones,

50 These maps, complemented with genetic perturbations, allowed us to uncover TRUB1 and PUS7 as the two key PUSs acti