ライフサイエンスコーパス: learn more about

1 oteomes will be an extremely powerful way to learn more about a particular protein's structure, its f

2 fills or a desire to receive help refilling, learn more about asthma control, or speak with an asthma

3 To learn more about autotrophic growth of methanococci, we

4 onosubstituted dianionic phosphates, both to learn more about basic properties intrinsic to this impo

5 Two bindin genes were sequenced to learn more about bindin introns.

6 To learn more about biological pathways that are potentiall

7 neutrophil entry during lung injury and are learning more about cellular interactions during inflamm

8 Clinicians are learning more about chronic pancreatitis but are enterin

9 ination treatment strategies, it is vital to learn more about coexpression of both inhibitory and sti

10 Finally, we stress the importance of learning more about coverage measurement to strengthen t

11 ed gain-of-function Cpx* mutants in order to learn more about Cpx signal transduction.

12 Thus, learning more about cytokine-mediated regulation of esta

13 The challenge for the future will be to learn more about dose, duration, and mechanism of action

14 As we learn more about fMRI related to pain, functional connec

15 To learn more about FTi and to identify novel regulators in

16 To learn more about functional contributions made by Blimp1

17 obile elements are becoming useful tools for learning more about genome evolution and gene function.

18 To learn more about holocentric chromosome structure and fu

19 To learn more about how BFP protein expression is induced d

20 To learn more about how cells regulate production of nitrit

21 seed that contribute to seed dormancy and to learn more about how dormancy and germination are regula

22 To learn more about how Dsh can discriminate between these

23 To learn more about how dyneins are targeted to specific si

24 To learn more about how FXIIIa selects its targets, a matri

25 To learn more about how the cytosolic domains regulate chan

26 To learn more about how these two processes determine wheth

27 More than 85% (175 [87.9%]) wanted to learn more about how to prevent skin cancer.

28 As we learn more about how to refine our present resistance ma

29 clinical trials offer a unique resource for learning more about individual susceptibility and develo

30 To learn more about islet vulnerability in the immediate po

31 To learn more about its effect on cellular proliferation an

32 udy, we analyzed the lasB promoter region to learn more about lasB activation by LasR and PAI.

33 In answering these questions we may hope to learn more about mechanisms of genome plasticity and ada

34 To learn more about metals in ALS, we determined the metall

35 To learn more about MLK3 regulation and its signaling pathw

36 To learn more about Mot3 function, we have performed a synt

37 To learn more about Mus101, we have initiated an analysis o

38 To learn more about mutations that can suppress the spt21De

39 To learn more about NBD structure and function, we introduc

40 ative genomics of helminth genomes to aid in learning more about nematode genomes, as well as drug, p

41 To learn more about p53's transactivator function in vivo,

42 ed with inflammatory bowel diseases (IBD) to learn more about pathogenesis.

43 To learn more about pathogenic PV autoantibodies, we isolat

44 at high risk and offer key opportunities to learn more about pediatric nephrolithiasis, thereby fuel

45 To learn more about regulation of hilA, we isolated Tn5 mut

46 To learn more about silencing, we investigated mating type

47 and progression, but also as a biomarker to learn more about specific treatment responses and pharma

48 To learn more about Spt3-TBP interactions in vivo, we have

49 To learn more about such control, we initiated studies of p

50 To learn more about switching, we measured the fraction of

51 To learn more about TAO/KIN-18 function, we studied how exp

52 his issue, took an epidemiologic approach to learn more about the 8q24 region.

53 To learn more about the action of these important complexes

54 To learn more about the BAM complex, we solved structures o

55 biologists interested in these topics should learn more about the basic structure of drug development

56 ther optimization should be possible when we learn more about the binding requirements at the active

57 ciliate protozoan Tetrahymena thermophila to learn more about the biochemical characteristics of RNas

58 To learn more about the biochemical composition and activit

59 To learn more about the biochemistry of the human enzyme an

60 They also provide the opportunity to learn more about the biology of DM which had previously

61 creatic surgery is a fascinating field as we learn more about the biology of the conditions that affl

62 Additional studies are required to learn more about the biology of these diseases, which ma

63 essing and internal cognitive state, we must learn more about the brain areas supporting attentional

64 To probe the cross-bridge cycle and to learn more about the cardioplegic agent BDM (2,3-butaned

65 n view of this continuing controversy and to learn more about the cell interactions during rib morpho

66 To learn more about the characteristics, origin, and possib

67 To learn more about the compensatory mechanism by which vir

68 This evolution continues, as we learn more about the complex interplay between patient a

69 As we learn more about the complexities of immune responses, n

70 To learn more about the cross-talk that must be occurring b

71 To learn more about the determinants of this increasingly i

72 therapy holds much promise in SLE and as we learn more about the disease and apply the lessons learn

73 n mediators and receptors also expands as we learn more about the disease processes that are either i

74 l continue to be reviewed and modified as we learn more about the disease to better perform this risk

75 To learn more about the distribution and possible regulator

76 To learn more about the dynamics of soluble Abeta economy i

77 To learn more about the effects of repetitive magnetic stim

78 egulation by OxyR and illustrate the need to learn more about the ensembles of binding sites and tran

79 idual metabolic networks is increasing as we learn more about the enzymes that are active in particul

80 To learn more about the epidermal antigens targeted by Ro a

81 To learn more about the epimerization process, the structur

82 To learn more about the essential role of Cdc7 kinase in th

83 nd lifetime nonsmokers can be enhanced as we learn more about the etiologic mechanism(s) of lung canc

84 To learn more about the evolutionary effects of the duplica

85 To learn more about the function and regulation of small he

86 individual mutations separately in vitro to learn more about the function of the kindlin-3 protein.

87 To learn more about the function of the NTSFs in species wh

88 To learn more about the function of the Spt4/Spt5 complex a

89 To learn more about the function of these genes in auxin re

90 erated mice lacking MDC9 (mdc9(-/-) mice) to learn more about the function of this protein during dev

91 To learn more about the function of Tim18p, we screened for

92 As we learn more about the functional expression of nicotinic

93 To learn more about the functional requirements of this com

94 In an effort to learn more about the functional role of this protein, we

95 To learn more about the functions and regulation of CenH3,

96 orker and haploid male honeybees (drones) to learn more about the genetic architecture of the overall

97 To learn more about the genomic organization of regions sur

98 To learn more about the gliding motor, we sheared cells to

99 To learn more about the importance of ascorbate in the accl

100 To learn more about the interaction between these proteins,

101 To learn more about the mechanism and specificity of isoAsp

102 To learn more about the mechanism of action of PEG, we anal

103 To learn more about the mechanism of hepadnavirus replicati

104 To learn more about the mechanism of the DnaB transfer reac

105 the use of this approach we will be able to learn more about the mechanisms by which methylation pat

106 To learn more about the mechanisms by which this pathogen c

107 To learn more about the mechanisms controlling neurite outg

108 6-31+G) study was undertaken in an effort to learn more about the mechanisms controlling the regiosel

109 To learn more about the mechanisms involved in establishing

110 nt medical practice mandates that physicians learn more about the mechanisms of trastuzumab-induced c

111 To learn more about the mechanisms that regulate entry into

112 To learn more about the miRNAs of mammals, we sequenced 60

113 e technology, to address these questions and learn more about the molecular functions of each of the

114 To learn more about the molecular mechanism of H3K56 acetyl

115 The current studies were carried out to learn more about the molecular motors responsible for LP

116 We will learn more about the natural history of the disease and

117 the questions and opportunities it opens to learn more about the nature of phage-bacterial coevoluti

118 kers rely on available technology and, as we learn more about the neurobiological correlates of neuro

119 To learn more about the pathogenesis of Alport disease, we

120 t-partum patients is likely to improve as we learn more about the pathogenesis of these disorders.

121 Our objective was to learn more about the pathophysiology of severe meningiti

122 ent research using tissue and cell models to learn more about the plasma delivery of RONS into biolog

123 To learn more about the possible function of Hsp93 during p

124 To address this possibility in vivo and to learn more about the potential physiological roles of CK

125 and provide direction for those desiring to learn more about the precise topics.

126 To learn more about the problem, we studied a group of chil

127 To identify and learn more about the protein encoded by HCMV UL46, we ha

128 To learn more about the regulation of contraction of collag

129 To learn more about the regulation of H blood group express

130 To learn more about the relation between diabetes and cance

131 To learn more about the requirement for subplate neurons in

132 The goal of this study was to learn more about the risk factors and short- and long-te

133 As we learn more about the RNA codes and maps that guide the a

134 To learn more about the role of chromatin in P cytotype rep

135 To learn more about the role of denitrification in these an

136 To learn more about the role of GGT in metabolism in vivo,

137 To learn more about the role of GR3 in salt-stress toleranc

138 f this heterogeneity will become clear as we learn more about the role of NK cells in cattle disease

139 To learn more about the role of protein methylation during

140 To learn more about the role of STAT-5B in vessel wall remo

141 To learn more about the role of STATs in the mitogenic and

142 To learn more about the role of these compounds, we have ex

143 Therefore, to learn more about the role of this pathway in vivo, we ge

144 To learn more about the roles of PDK1, we generated mice th

145 To learn more about the roles of the conserved proline resi

146 To learn more about the roles of the tentacles in ribosome

147 To learn more about the shared function, we sought new muta

148 To learn more about the signaling pathways involved, we did

149 To learn more about the sites of blocker binding and about

150 ls, further field research is recommended to learn more about the sources of transmission and the eff

151 To learn more about the specificity of this intercompartmen

152 In order to learn more about the STAT-3-cPLA(2) axis in motogenic si

153 To learn more about the structural and functional significa

154 cal processes, there is an important need to learn more about the structural features relevant to the

155 Drosophila gene in the erg subfamily and to learn more about the structure and biological function o

156 To learn more about the structure and function of eIF3 we h

157 To learn more about the structure of the DNA terminus at Te

158 To learn more about the structure, expression, and function

159 To learn more about the targets of Cn (Cn) and calcium/calm

160 To learn more about the telomeric function of proteins from

161 The goal of this study was to learn more about the transfer mechanism by defining the

162 s in humans, providing a strong incentive to learn more about the underlying causes.

163 Here we set out to learn more about the underlying mechanism by which Cat-p

164 n and development is expanding rapidly as we learn more about the unique properties associated with t

165 The reasons are simple: 1) we need to learn more about the world around us; and 2) a robust an

166 In recent years, we have learned more about the complex interactions that occur b

167 armers who had attended a brief workshop and learned more about the forecasts were significantly more

168 four decades, it is fair to say that we have learned more about the lysosomal system of cells through

169 At the same time, we learned more about the regulatory networks of H. influen

170 indicate some of the resources available for learning more about the advanced capabilities of these p

171 Learning more about the cells that enable parasitic worm

172 In this regard, learning more about the immune components of these disea

173 osomic humans (45,X) and mice (39,X), we are learning more about the influences of X-linked imprinted

174 While we are still learning more about the myriad clinical presentations in

175 brains of 12 human subjects, with the aim of learning more about the position and variability of the

176 imed at nonspecialists who are interested in learning more about the potential and impact of NMR spec

177 Learning more about the regulation of TEMs by the tumor

178 Interested in learning more about the starvation response, we cloned a

179 logical disorders is likely to improve as we learnt more about the spectrum of this entity in the las

180 sought to study their C. elegans homolog to learn more about their functions.

181 remain a vexing treatment dilemma, but as we learn more about their natural history, more thoughtful

182 19 genes implicated in early development, to learn more about their potential role in specifying and

183 isparities, health care professionals should learn more about them and the roles they can play in eli