ライフサイエンスコーパス: understanding of

1 iated with HLA class I-DSA could improve our understanding of ABMR and be useful for diagnostic or th

2 ms and tissue types will further improve our understanding of ancient DNA breakdown dynamics.

3 uld be a valuable step towards improving our understanding of anxiety disorder vulnerability.

4 he potential to improve our surveillance and understanding of asthma.

5 his, it has become apparent that our initial understanding of AT1R signaling is oversimplified.

6 ochar use highlight the need for an improved understanding of biochar's impacts on soil NO emissions.

7 A major gap in our understanding of biodiversity-ecosystem function relatio

8 Collectively, these results add to our understanding of CaM-dependent regulation of RyR2 as wel

9 Comprehensive understanding of capsid-host interactions that promote o

10 A deeper understanding of Cas9 activation and its cleavage mechan

11 themselves is important for our mechanistic understanding of cell biology.

12 A-seq data can be powerful for improving our understanding of cell identity control.

13 in therapeutic development, and fundamental understanding of cellular behavior during hypoxia.

14 rofiling with great potential to improve our understanding of cellular heterogeneity through discover

15 fill gaps in trait coverage will improve our understanding of changes in fine-root traits across spac

16 tions related to the application of SERS for understanding of chemical processes at the nanoscale, wi

17 e alone remains poor, reflecting our limited understanding of cis-regulatory grammar and hampering th

18 ons can inform disaster preparedness and the understanding of climate change consequences.

19 vide a candidate entry point toward a better understanding of cognitive architectures.

20 er measurements of network structure and our understanding of collective phenomena.

21 findings have important implications for the understanding of compartmentalized cAMP signalling.

22 Great strides have been made in the understanding of complex networks; however, our understa

23 However, neuroscientific understanding of cross-modal plasticity following cochle

24 human pancreatic beta-cells, broadening our understanding of cytokine-induced beta-cell apoptosis in

25 In addition to extending our basic understanding of DATs and their role in cocaine reinforc

26 scovery and could lead to more comprehensive understanding of disease etiology.

27 ch is absolutely essential for improving our understanding of disease mechanisms contributing to risk

28 ing pathways, with implications for improved understanding of disease recurrence and therapeutic resp

29 These fundamental understandings of dose effect on the in vivo transport o

30 ABSTRACT: To improve our understanding of early disease mechanisms and to identif

31 emarkably common in early human embryos, our understanding of early embryonic somatic mutations is ve

32 possible model, given the available data and understanding of ecological structures.

33 bon budget in China's forests and for better understanding of effects of climate and stand characteri

34 bstrates, as foundational to the mechanistic understanding of emerging PBP2a resistance mutations.

35 pect this insight will decisively change our understanding of essential phenomena occurring within th

36 des a structural framework for a mechanistic understanding of eukaryotic ribosome assembly in the mod

37 While an understanding of evolutionary processes in shifting envi

38 e exploited as a model system towards better understanding of F. pseudograminearum-wheat interaction.

39 requently begin in childhood/adolescence, an understanding of fear-extinction learning in children is

40 An understanding of fluid transport through porous material

41 or FND and PTSD symptoms and may advance our understanding of FND.

42 PCA for clinical genetic testing, expanding understanding of genetic contribution to aggressive PCA,

43 We review the current understanding of genomics in myelodysplastic syndromes (

44 clear and represent a major challenge to our understanding of glacial climates.

45 e efforts will contribute to a more complete understanding of global carbon and nitrogen cycling and

46 have important implications for our current understanding of healthy and adaptive brain processing.

47 These findings may have implications for our understanding of how altered folate availability causes

48 However, we lack an understanding of how an interface can select some ligand

49 ng cellular ATP production, and advances our understanding of how defective FA signaling contributes

50 eighboring mesenchymal partners provides new understanding of how different cell types are maintained

51 ng cardiac specification is critical for our understanding of how heart formation is initiated during

52 tuberculosis enzyme, augmenting our current understanding of how M. tuberculosis meets its nutrient

53 ctin-mitochondria interaction, enhancing our understanding of how mitochondria properly localize in a

54 either FTD or NCL, in part because of a poor understanding of how mutations in genes such as GRN cont

55 Results extend the understanding of how organic carbon and nitrite loads mo

56 this single-cell approach provides a better understanding of how prostate cancer cells respond heter

57 Our model enables an analytical understanding of how Red Queen dynamics emerge in our se

58 In order to gain a better understanding of how resistance to DNA methylation from

59 behavior and pathology, but we lack a basic understanding of how sex differences in the human cerebe

60 Together, these models provide a biophysical understanding of how stem cell scaling is maintained dur

61 This necessitates further understanding of how T follicular helper cells are regul

62 ed view of motor cortex may lead to a better understanding of how the brain controls movement.

63 Two recent papers advance our understanding of how the cancer genome evolves as the pr

64 individual isoforms, necessitating a deeper understanding of how the distinct transcriptional progra

65 Here, we highlight recent advances in our understanding of how the genome folds inside the 3D nucl

66 Our work advances understanding of how the TRF2(TRFH) domain orchestrates

67 across different temperatures would advance understanding of how thermally activated processes contr

68 r interpretations of forest dynamics and our understanding of how these forests are responding to glo

69 tity of these genetic factors, improving our understanding of how they shape retinal function.

70 protein acetylation dynamics is critical for understanding of how this modification influences protei

71 esistance that would be helpful for a better understanding of how to manage antibiotic-resistant bact

72 The results extend our understanding of human CSF flux and open important clini

73 nnotate the human genome and to increase the understanding of human disease.

74 revolutionizing approaches to gain a better understanding of human diseases.

75 le and has begun making contributions to the understanding of human intestinal transport in normal ph

76 Discoveries leading to an improved understanding of immune surveillance of the central nerv

77 pproaches to contribute substantially to the understanding of important human diseases.

78 roptosis in macrophages, and revises current understanding of independent and collaborative functions

79 Further understanding of innate allorecognition and its conseque

80 A better understanding of intrauterine conditions that influence

81 With our evolving understanding of intrinsic resistance, people have succe

82 of centriole components have accelerated our understanding of its assembly, function, evolution, and

83 e drug reaction will further our mechanistic understanding of its development and potentially lead to

84 ostic tools for Alzheimer disease and better understanding of its neurobiology.

85 We discuss how growing understanding of key anatomic sanctuaries for the virus

86 lasticity or TGP) may occur, we have limited understanding of key aspects of TGP, such as the environ

87 is critical to health, making furthering our understanding of L-R development an important concern.

88 nodulation, have led to major changes in our understanding of legume taxonomy.

89 It is demonstrated that SERS provides a deep understanding of living cells as well as their microenvi

90 ines recent work that has contributed to our understanding of LOS-deficiency and compares it to studi

91 ing Alzheimer's disease (AD) requires a deep understanding of mechanisms affecting complex brain syst

92 A major bottleneck limiting understanding of mechanisms and consequences of cell dea

93 ors and coregulators, can profoundly improve understanding of mechanisms underlying genetic associati

94 a valuable resource to advance our molecular understanding of meiosis.

95 Current understanding of mercury (Hg) dynamics in the Arctic is

96 This study provides new understanding of methanotrophic responses to methane sta

97 se questions will provide a greater level of understanding of miRNA biology and critical insights int

98 a has been implicated in aging, but a deeper understanding of mitochondrial dynamics and mitophagy du

99 the Drosophila visual system, where a deeper understanding of molecular mechanisms allows for the gen

100 This research will impact our understanding of morbillivirus-related immunosuppression

101 To gain understanding of MRN in cancer, we engineered mice with

102 However, our understanding of N deposition effects on microbial commu

103 Our finding can enrich our understanding of nanoscale energy transfer in molecular

104 d light harvesting (8-16) require a thorough understanding of (nanoscale) heat flow.

105 erstanding of complex networks; however, our understanding of natural microecologies is limited.

106 y their differential actions may advance our understanding of nervous system disorders and suggest st

107 brings a new perspective to molecular-scale understanding of neurodegenerative diseases.

108 wledge in these areas lag behind our current understanding of neuroprotection and vascular biology in

109 dimers as the key antigenic target, and deep understanding of neutralizing mechanisms, multiple vacci

110 e of interest and valuable data for a better understanding of OST-catalyzed N-glycosylation.

111 key issues that require resolution for full understanding of pathogenic autoimmunity.

112 Disease heterogeneity and poor understanding of pathogenic mechanisms hampers the ident

113 An improved understanding of pathogenic pathways in AKI may identify

114 mitations, there has been an increase in the understanding of pathophysiology and important risk fact

115 nt paradigm shifts that have transformed our understanding of pediatric ocular motor disease at the p

116 Developing a greater understanding of personal and environmental factors that

117 ctly in a single nanostructure, limiting our understanding of phonon coupling with photons and plasmo

118 ans.This study sought to advance the current understanding of placental vitamin D metabolism and its

119 h sufficiently long values of T2 requires an understanding of precisely how the position of nuclear s

120 e and rhizosphere of plants, a more detailed understanding of predator-prey interactions, changes in

121 hways within the brain and provide a limited understanding of primary odor detection.

122 s to simian immunodeficiency virus (SIV), an understanding of processes that promote successful cross

123 s, significant progress has been made in the understanding of proteasome assembly, structure, and fun

124 Thus, this study contributes to our understanding of protein function within different Norov

125 Further understanding of risk factors, presentation, optimal man

126 However, a general understanding of RNA localization has been hindered by a

127 Critically, our understanding of ROS-mediated PTP oxidation is not yet s

128 have important implications for fundamental understanding of RVFV virulence.

129 predominant one concerning questions on the understanding of science, the main goal, the stage of in

130 Over the past 50 years in pharmacology, an understanding of seven transmembrane (7TMR) function has

131 Nevertheless, significant gaps remain in our understanding of several crucial aspects of MP exposure

132 y gene in 1990 triggered a revolution in our understanding of sex determination.

133 A more thorough understanding of sex-specific cardiovascular differences

134 FEM) modeling has been undertaken to enhance understanding of SICM as an electrochemical cell and to

135 e about RTK interactions and can further our understanding of signal transduction across the plasma m

136 has significant global implications for our understanding of soil N cycling pathways and N2 O produc

137 cies-level effects, ultimately improving our understanding of spatial community dynamics.

138 Increased understanding of specific diabetes phenotypes and genoty

139 ingly, the physiological and pharmacological understanding of specific motoneuronal contributions to

140 pulating the epigenome to facilitate further understanding of stem cell biology and engineering of st

141 e manner, with the aim of obtaining a deeper understanding of stem cell fate computation, in order to

142 identification advanced much faster than our understanding of stem/progenitor cells.

143 resent an important avenue for advancing our understanding of substance abuse disorders.

144 A-4 pathway are therefore required to inform understanding of such immune dysregulation syndromes.

145 the production, manipulation, and scientific understanding of such remedies.

146 that can contribute to a more comprehensive understanding of symbiosis as a major driving force of e

147 There is limited understanding of the associations between systemic medic

148 formation has prevented a detailed molecular understanding of the assorted ANT-associated diseases, i

149 n, it is imperative that we develop a better understanding of the basic biology of this parasite and

150 model mice in vivoSIGNIFICANCE STATEMENT Our understanding of the basis for intellectual impairment i

151 ivo functions of ADAR enzymes, informing our understanding of the biological importance of A-to-I edi

152 ion of gene models will not only further our understanding of the biological processes of this plant

153 physiological measurements, has improved our understanding of the biological responses during drought

154 Further understanding of the biological tropism with cells and p

155 ing deconstruction not only provide a better understanding of the cell wall architecture but also is

156 thcare costs inherent in device use, a clear understanding of the clinical benefits relative to costs

157 ation and transmigration, which advances our understanding of the complex contribution of CtsB to ang

158 ents, are paving the way for a more complete understanding of the complex events that help build the

159 Our findings add a new chapter to the understanding of the complex molecular mechanism underly

160 The present study advances our understanding of the complex signalling mechanisms invol

161 Our understanding of the conservation and divergence of the

162 An understanding of the current-day magnitude of each compo

163 Work with this model system has enriched our understanding of the cyclopropanation-Cope rearrangement

164 However, a detailed understanding of the DDR at a physiological level is lac

165 However, our understanding of the development and maintenance of chol

166 d midlife exposures will further advance our understanding of the disease.

167 In one such approach, an understanding of the distal and geometric relationships

168 results suggest large biases in our current understanding of the distribution, area and volumes of t

169 ial to provide epidemiologists with a deeper understanding of the divergent pathways via which neighb

170 complementary methods which provide a better understanding of the domain wall motion.

171 ingle-molecule approaches have increased our understanding of the dynamic behavior of complex multipr

172 cial and ecological factors, and enhance our understanding of the dynamics of natural populations.

173 This study significantly enhances our understanding of the EAV carrier state in stallions by u

174 A better understanding of the ecological and agronomic factors un

175 e effects in social species will improve our understanding of the ecological and evolutionary implica

176 eralisation and the development of a broader understanding of the ecology and evolution of mutualisms

177 genes duplicated in Trisomy 21 and a lack of understanding of the effect of disease pathology on the

178 This study sought a better understanding of the effect of the definition of T2MI on

179 ecent studies that advance the knowledge and understanding of the effects of various environmental fa

180 void this issue is hindered by an inadequate understanding of the electrically-induced wrinkling defo

181 A comprehensive understanding of the environmental cues that regulate FC

182 1):1-9) was an important contribution to the understanding of the epidemiology of cardiovascular dise

183 To gain a deeper understanding of the evolution of gene transcription in

184 Our understanding of the exoskeleton formation provides a un

185 This study facilitates our understanding of the fate and transformation of IAPP in

186 Our understanding of the frequency of large earthquakes at t

187 Yet our understanding of the function of facilitation remains la

188 these findings contribute to our fundamental understanding of the functional interplay between host E

189 ved issue, even though it is critical to the understanding of the functional properties of MSMAs.

190 We have a limited understanding of the genetic and molecular basis of evol

191 during development, contributing to improved understanding of the genetic etiology of familial tooth

192 on sequencing has substantially enhanced our understanding of the genetics of primary brain tumors by

193 ications may be accomplished through a sound understanding of the hemodynamic and physiological conse

194 An improved understanding of the heterogeneity of presenting symptom

195 w the EBV life cycle and discuss our current understanding of the immune response to EBV in healthy,

196 AR1-AtZED1 protein complex provides a better understanding of the immune signaling hub controlled by

197 An evolving understanding of the immunopathogenesis of multiple scle

198 described by Glorius et al., builds a broad understanding of the impact of individual functional gro

199 s, patients and their families, for a better understanding of the impact this disease has on a person

200 Our results provide a fundamental understanding of the information-theoretic nature of the

201 scover new catalysts by obtaining a detailed understanding of the initial steps of CO2 electroreducti

202 cidating cerebellar function will require an understanding of the interactions, both short- and long-

203 logy provides a better and more quantitative understanding of the intracellular behavior of drug-load

204 ant use in biotechnology, we lack a detailed understanding of the kinetics of nucleic acid hybridizat

205 Recent studies have enhanced our understanding of the linkage of oxygenation and metazoan

206 aking place throughout the tropics, improved understanding of the magnitude and spatial variation in

207 n the scalability, stability and fundamental understanding of the materials.

208 ular homeostasis and therapy, our structural understanding of the MBS CC interaction with LZ PKG-1alp

209 As a next step toward an understanding of the mechanism by which IreB regulates r

210 tural products contain chlorine and thus, an understanding of the mechanism of its introduction into

211 Improved understanding of the mechanism of long-distance iron sig

212 A thorough understanding of the mechanism of this efficient enzyme

213 A further understanding of the mechanism underlying HBoV1 helper-d

214 Considerable advances in our understanding of the mechanisms and functions of rapid-e

215 These findings may improve our understanding of the mechanisms involved in rotor-guided

216 This disease has improved understanding of the mechanisms of lung fibrosis, and of

217 es have not significantly contributed to our understanding of the molecular basis of trainability.

218 This study improves the current understanding of the molecular evolution, divergence, an

219 Taken together, our results extend the understanding of the molecular mechanism of transcriptio

220 A key problem here is a general understanding of the molecular mechanisms accompanying t

221 linical challenge and may relate to the poor understanding of the molecular mechanisms involved.

222 To improve our limited understanding of the molecular mechanisms of filament as

223 Advances in understanding of the molecular mechanisms that underlie

224 However, until recently, deficiencies in our understanding of the nature of these cell populations, c

225 To broaden our understanding of the Neolithic transition across Europe,

226 There is growing understanding of the oncogenic and tumor suppressive fun

227 This work not only deepens our understanding of the online commercial networks, but als

228 dedness, implying a fundamental shift in our understanding of the ontogenesis of hemispheric asymmetr

229 These results extend our understanding of the origins of cooperativity and stabil

230 In less than a decade, understanding of the pathogenesis and management of this

231 past decade has seen significant advances in understanding of the pathogenesis and progression of lun

232 light how such improvements enable a greater understanding of the pathogenesis of disease and the rea

233 The findings are important for the understanding of the pathogenesis of VTE.

234 Our understanding of the pathophysiological basis of chronic

235 A better understanding of the pathophysiology of DWMI is therefor

236 Recent advances in the molecular understanding of the pathophysiology of systemic mastocy

237 he lower urinary tract and contribute to our understanding of the pathophysiology of urinary retentio

238 explore several new ideas that could improve understanding of the phenotypic and genotypic difference

239 This gap in knowledge stems from a lack of understanding of the physics of surface structures inter

240 omputation devices will be aided by a better understanding of the physics underlying material behavio

241 nst antithrombin polymerization, an improved understanding of the polymerogenic intermediates is cruc

242 xpression/function, could be improved by the understanding of the properties of the cancer secretome,

243 This article reviews recent advances in our understanding of the proteasome's multistep ATP-dependen

244 Through a fundamental understanding of the redox reaction mechanism in Li2 MnO

245 postmortem human brain cells and further our understanding of the regulome and the impact of neuropsy

246 To gain a better understanding of the relationship between measured level

247 ndividual variability, necessitates a deeper understanding of the relationship between stimulation pa

248 egions throughout plant genomes will advance understanding of the relationship between TF binding, ch

249 es in photosynthetic infrastructure, but our understanding of the relative effects of these factors a

250 our simple model contribute a more intimate understanding of the response and consequence of rotatin

251 brain structures which are essential to the understanding of the result statistics from the analyses

252 ng survivors of explosions, but with limited understanding of the resulting retinal pathologies.

253 A better understanding of the risk factors and movement patterns

254 s lack effective therapies despite increased understanding of the role factors such as an overactive

255 novel strategy could greatly facilitate our understanding of the role of BMP in biological systems.

256 A growing understanding of the role of DAMPs in directing the immu

257 Despite considerable understanding of the role of each cell type in the proce

258 ted with patient survival would increase the understanding of the role of glioma cancer stem cells (G

259 Our work has the potential to improve our understanding of the role of global methylation in human

260 Our work provides an improved understanding of the role of ionic correlations in NP as

261 ere is a fundamental gap in our quantitative understanding of the role of local ECM size and arrangem

262 n and repair, the mechanistic and functional understanding of the role of PARPs in different biologic

263 This work contributes to a better understanding of the roles of different viral proteins i

264 Current understanding of the specific organic constituents in th

265 The current understanding of the specificity of the bacterial class

266 of theoretical mathematical models toward an understanding of the system's regulatory properties.

267 nits and antigenic epitopes to gain a better understanding of the technology at a molecular level.

268 e climates, which will require a mechanistic understanding of the trade-offs that determine trait div

269 dings have enabled a deeper and more precise understanding of the transcriptional mechanisms that ind

270 unity-based surveillance allows for a better understanding of the true burden and seasonality of dise

271 th, is an important yield component, but our understanding of the underlying genes and mechanisms is

272 A better understanding of the underlying molecular mechanisms wou

273 cant advantages that allow for a fundamental understanding of the underlying physics of a system.

274 s comprehensive analysis extends our current understanding of the ureteric branch tip niche.

275 A fuller understanding of the virus life cycle is important to ai

276 Gaining a better understanding of the WGS data, and how that data is util

277 These findings not only advance our understandings of the nano-bio interactions in kidneys b

278 Understanding of their development is of high interest f

279 en instrumental to enable advanced molecular understanding of their intriguing properties.

280 hiadiazoles are likely to result if a deeper understanding of their preferred patterns of molecular a

281 reported RGGT inhibitors, rationally improve understanding of their structure-activity relationship.

282 tools that assess function have improved our understanding of these cascades.

283 A fuller understanding of these effects and the characterization

284 The detailed understanding of these interactions will not only provid

285 A precise understanding of these layers of control has important i

286 utionary and genetic approaches will improve understanding of these symbiotic associations and, in th

287 h over the previous decades has improved our understanding of this complex arrhythmia while unravelin

288 This work further expands our understanding of this complex multifaceted transcription

289 Further understanding of this differential regulation will enhan

290 aminergic neurons and contribute to a better understanding of this functionally complex group of neur

291 hange is a promising new approach but better understanding of this mechanism of action is needed.

292 This Review will discuss our current understanding of this metabolic supportive function of o

293 e epidemiology of SJS/TEN contributes to the understanding of this still underinvestigated severe ski

294 work opens the door to a detailed atomistic understanding of transformation reactions in even larger

295 toward our expanding cellular and molecular understanding of type-2-cell-mediated immunity, as well

296 ation of these interactions could expand our understanding of viruses and be exploited for epidemiolo

297 These results enhance our understanding of vRNA assembly and the role of cytoskele

298 n be experimentally validated to improve our understanding of what triggers and maintains the growth

299 m(6)A) RNA modifications in mRNA requires an understanding of when and where in the life of a pre-mRN

300 atients, it is necessary to develop a better understanding of where patients seek care.