ライフサイエンスコーパス: how to use

1 We describe how to use 3View for studying collagen fibril organizati

2 "specification problem") and the problem of how to use a computer to simulate the progress of the sy

3 psychoeducational intervention, were taught how to use a pillbox, and were given written instruction

4 Finally, we show how to use a reference fluorophore for the correction of

5 Before grasping and demonstrating how to use a specific tool, participants passively viewe

6 In this protocol, we describe how to use a time-correlated single-photon counting (TCS

7 Finally, we describe how to use a user-friendly and easily accessible web ser

8 The challenge is how to use advanced molecular understanding with limited

9 developing the ability of the brain to learn how to use an implant may be as important as further imp

10 The focus of this review is on how to use and apply microarrays to these situations.

11 ecreased?" Their findings leave us uncertain how to use and interpret these measures to track changes

12 ation was not independent of tumor features, how to use BRAF V600E to manage mortality risk in patien

13 lines provide conflicting recommendations on how to use bronchodilators to manage childhood acute whe

14 ng approach more appropriate for determining how to use chromatography most efficiently in one's own

15 This protocol also describes how to use confocal microscopy to visualize mitophagy in

16 In this protocol, we discuss how to use data obtained in affinity purification-mass s

17 This protocol explains how to use DAVID, a high-throughput and integrated data-

18 r fluids adequately to a transplant patient; how to use direct vasoactive agents; how to manage the i

19 o provide guidance to oncology clinicians on how to use effective communication to optimize the patie

20 In this paper, the authors demonstrate how to use empirical methods appropriate for EBQP tables

21 At the same time, critical information on how to use established drugs like nelfinavir and efavire

22 Finally, we outline how to use exosomes to efficiently deliver siRNA in vitr

23 Although strategies for how to use guidelines to improve care are increasingly w

24 iders seek guidance from economic studies on how to use health care resources wisely.

25 We describe how to use hidden Markov models to evaluate multilocus t

26 Our approach shows how to use high-throughput data to calculate accurately

27 his note we provide a step-to-step guide for how to use HIVcleave to identify the cleavage sites of a

28 We show how to use information theory to validate simple stimulu

29 rce code of the program and documentation on how to use it are freely available to non-commercial use

30 rception as probabilistic inference, we show how to use knowledge of the psychophysical task to make

31 an introduction for scientific experts about how to use mental models research with intended audience

32 This protocol describes how to use microengraving to screen mouse hybridomas to

33 red their personal experiences and advice on how to use modeling effectively.

34 newer areas of inquiry attempting to define how to use molecular-genetic features of individual tumo

35 We illustrate how to use our model to examine previously uncharacteriz

36 Moreover, we show how to use our package to easily perform Connectivity Ma

37 In this protocol, we describe how to use our previously reported gelatin-based O2-cont

38 from plants and provide recommendations for how to use our results.

39 Thus, MBBC users are not required to know how to use Ox, R or C++, but they must be pre-installed.

40 been studied for 200 years, understanding of how to use parallel flows to augment the capabilities of

41 ers and clinicians should carefully consider how to use PFS data in balancing potential benefits agai

42 We describe how to use PLINK, a tool for handling SNP data, to perfo

43 We detail how to use prior knowledge to bound the number of detect

44 In this paper, we describe how to use PROBEmer, the computational methods it employ

45 ticle, we provide a step-by-step guidance on how to use PS methods.

46 We describe how to use public protein databases and molecular modeli

47 A Readme file, which explains how to use pViz with examples, is available as Supplemen

48 In addition, new video tutorials describe how to use RDP features.

49 rrent work-up of lymphocytosis and highlight how to use recently identified prognostic tools to strat

50 We show how to use reference 450k datasets to estimate cell type

51 We show how to use relativistic motion to generate continuous va

52 icians and patients are often confused about how to use results of studies in individual cases.

53 s an overview of the algorithm and describes how to use Scalpel to perform highly accurate indel call

54 In this protocol we describe how to use several popular features of Vaa3D, including

55 In this protocol, we show how to use small-scale transient transfection and fluore

56 ich entrants submitted strategies specifying how to use social learning and its asocial alternative (

57 inding sites, suggesting that adjustments of how to use such metrics are required.

58 Here, we show how to use suffix array-based methods that have formed t

59 As we continue to learn how to use targeted therapies in the context of genomic

60 nonlinear interactions, but it was not clear how to use that information to obtain quantitative insig

61 Here, we detail how to use the 'novel tank' test to assess behavioral in

62 We present a set of protocols showing how to use the 3DNA suite of programs to analyze, rebuil

63 We demonstrate how to use the computational environment R to integrate

64 entists, a step-by-step guide is provided on how to use the current web server to generate their desi

65 of when to order testing, what to order and how to use the data in real time remains an area for fut

66 Examples of how to use the database to identify Drosophila genes rel

67 njector is prescribed, education on when and how to use the device should be provided.

68 erstands the concept of occupancy factor and how to use the dosing charts, our model facilitates appl

69 when and how to introduce fluorine but also how to use the effects of fluorine for a desirable resul

70 exists in each marker interval, we describe how to use the expectation-maximization algorithm to exa

71 interval at most one crossover, we describe how to use the expectation-maximization algorithm to exa

72 We show how to use the expectation-maximization algorithm to fin

73 l as its recent development, particularly in how to use the general formulation of PseAAC to reflect

74 Not all participants could learn how to use the Icare HOME device, but for those who coul

75 This protocol covers how to use the intrinsic circular dichroic properties of

76 We describe how to use the Kimura distribution in mitochondrial gene

77 Finally, we show how to use the library to extract SWATH data with the op

78 n of the method and give several examples of how to use the modules in specific cases.

79 The authors show how to use the MSM parameter estimates and contrasts to

80 In particular, we show how to use the multigeneration-wrinkled substrate for se

81 beled coalescent tree (PLCT) and demonstrate how to use the PLCT to evaluate the feasibility of a gen

82 The user can quickly see how to use the pressure for speed or for more theoretica

83 effector transgenes in tissues of interest, how to use the Q system in conjunction with the GAL4 sys

84 ssues will be experimentally manipulated and how to use the Q system to perform mosaic analysis.

85 assays has led to potential confusion about how to use the results for clinical decision making.

86 forward, one of the many challenges will be how to use the results of molecular profiling to guide p

87 Extensive video tutorials on how to use the site are available through http://www.met

88 inst new viral strains is vital for deciding how to use the stockpile.

89 ish SoNar-expressing cells, and then discuss how to use the system to quantify the intracellular redo

90 the reader will find a brief description on how to use the various scripts and programs.

91 This protocol describes how to use the viral protein families catalog ( approxim

92 entists, a step-by-step guide is provided on how to use the web server to obtain the desired results

93 This protocol is a step-by-step guide on how to use the Web-server predictors in the Cell-PLoc pa

94 step-by-step protocol guide was provided on how to use the web-server to get the desired results wit

95 ibe how these human-powered systems work and how to use them effectively in scientific domains.

96 and insect cells as well as instructions on how to use them in stable isotope dilution mass spectrom

97 benefit our studies of individual genes, and how to use them to improve our understanding of developm

98 est suit their needs, where to get them, and how to use them to their best advantage.

99 d synthesis, as well as practical details of how to use them with living cells.

100 ral-fluid-based HIV test kits, instructed on how to use them, and encouraged to distribute a test kit

101 rmative resources for scientists-IF you know how to use them.

102 ed them rather than clear instructions about how to use them.

103 As an example of how to use these approaches, in this article we use a co

104 However, how to use these biomarkers is still being debated, espe

105 eractions were analyzed to better understand how to use these characteristics to extract how biomolec

106 our objective was to provide a framework for how to use these data correctly in a spatial meta-popula

107 How to use these databases effectively is an open questi

108 e already established, guidance is needed on how to use these drugs in patients already receiving ant

109 ment between health care providers regarding how to use these indices.

110 Clinicians need to know how to use these modalities and monitor them properly, e

111 We conclude with considerations on how to use these new agents to treat non-AIDS-defining c

112 We then discuss how to use these parameters in the optimal design of pea

113 e such as PLINK, R or Haploview, we describe how to use these popular tools for handling single-nucle

114 everal other FST estimators, and we describe how to use these statistics to produce a rooted tree of

115 tegies have shown promise, but guidelines on how to use these strategies optimally are lacking.

116 We also presented a framework to outline how to use these three algorithms to obtain collaborativ

117 This protocol describes how to use this approach to determine how efficiently a

118 Finally, we outline how to use this approach to investigate which targets po

119 ers, and will hopefully provide insight into how to use this biomarker more productively by distingui

120 rotocol we describe the synthesis of CS1 and how to use this chemical tool to investigate intracellul

121 ol, we describe the synthesis of MitoPY1 and how to use this chemical tool to visualize mitochondrial

122 s to ascertain the source of vision loss and how to use this clinical information to help guide the s

123 We further show how to use this framework to create simple models with a

124 sponsible for complex disease phenotypes and how to use this information to develop new and specific

125 Five case studies are provided to illustrate how to use this information to inform responses to real-

126 We demonstrate how to use this knowledge to refine these methods and im

127 form, in vitro detection of ATP and GTP, and how to use this platform to realize intracellular ATP an

128 A current challenge is how to use this structural information for the rational

129 This protocol describes how to use this system, which provides a powerful tool f

130 This protocol describes how to use this system; the time required for lysing the

131 linicians to have a fuller sense of when and how to use time-limited trials.

132 This protocol describes in detail how to use TopHat and Cufflinks to perform such analyses

133 itional mouse model of epilepsy, we describe how to use transcranial US to disrupt electrographic sei

134 Here, we describe how to use Transmission Electron Microscope (TEM) to obt

135 This review focuses first on how to use troponin, which at present is the best valida

136 domains of life and provides an example for how to use various experimental techniques to rapidly le