ライフサイエンスコーパス: functional diversity

1 either directly or indirectly via changes in functional diversity.

2 a given cell, which may be related to their functional diversity.

3 hese biotic crises in coupling taxonomic and functional diversity.

4 ity of the soil microbial population and its functional diversity.

5 processes relates to successional changes in functional diversity.

6 ural features that might correlate with this functional diversity.

7 tem, are found in all tissues and show great functional diversity.

8 for structural stability and a full range of functional diversity.

9 ontribution of NTB-A costimulation to T cell functional diversity.

10 interneurons show an enormous structural and functional diversity.

11 t classes of HOXA1 targets, which may create functional diversity.

12 n of hundreds of receptor types implies high functional diversity.

13 rtebrate pre-mRNAs to generate proteins with functional diversity.

14 ned to facilitate synthetic manipulation and functional diversity.

15 roportion of dead bacteria in depth, and low functional diversity.

16 ytes (RMPs), with substantial phenotypic and functional diversity.

17 our knowledge of microbial phylogenetic and functional diversity.

18 constrain or expand polyamine structural and functional diversity.

19 acilitate re-inspection of IFN molecular and functional diversity.

20 m networks that contribute to structural and functional diversity.

21 des, is not limited with respect to observed functional diversity.

22 modules, resulting in extreme structural and functional diversity.

23 lly integrate a wide array of structural and functional diversities.

24 can exist as different conformers, favoring functional diversity, a moonlighting property arising fr

25 l transitions that can be used to understand functional diversity across the kinesin superfamily.

26 rotein mechanochemistry and for interpreting functional diversity across the kinesin superfamily.

27 Mapping functional diversity advances our understanding of the b

28 Their structural and functional diversity allows KChs to play diverse roles i

29 However, anatomical gradients suggest a functional diversity along the CA3 transverse axis.

30 Increased functional diversity ameliorated negative effects of pre

31 e assessed, revealing molecular evidence for functional diversity among individual RTs.

32 Here we investigate functional diversity among neurons in the anterior fundu

33 Thus, previously unrecognized functional diversity among physiologic innate immune cel

34 quence similarity, indicating structural and functional diversity among them.

35 n in a dose-dependent manner, and there is a functional diversity among them.

36 ransplantation, the molecular determinant of functional diversity among various alleles is unclear.

37 y owing to their almost unlimited structural/functional diversities and stimuli-responsive pore archi

38 n the body showing tremendous anatomical and functional diversity and are actively involved in mainta

39 Here we show that fish functional diversity and biomass of top predators are si

40 hannels play an important role in generating functional diversity and control of cell surface express

41 distinct, specialized cell types to generate functional diversity and cope with changing environmenta

42 ear but are critical for understanding their functional diversity and determining why Rb has unique t

43 community-weighted mean plant traits, trait functional diversity and divergence, and species richnes

44 e present the current knowledge of routes to functional diversity and DNA binding specificity, includ

45 n the near future, with cascading impacts on functional diversity and ecosystem function.

46 molecular structures as a means to increase functional diversity and gain an evolutionary advantage

47 Recent information has revealed the functional diversity and importance of mitochondria in m

48 ons of the analytic techniques for capturing functional diversity and interrogating the taxonomy of p

49 rannual precipitation variability effects on functional diversity and its consequences for ecosystem

50 The functional diversity and mechanistic complexity, as well

51 Recent studies have begun to explore the functional diversity and mechanistic role of these large

52 lassification scheme-independent measures of functional diversity and modeling cities as social netwo

53 tested for interactions between the loss of functional diversity and nutrient enrichment on ecosyste

54 This provided a means to compare functional diversity and organismal ecology in the human

55 eprogramming to enriched FR and demonstrates functional diversity and overlap of the Populus PHYB1 an

56 e show that stability depended critically on functional diversity and patterns of guild interaction,

57 an help to unravel the adhesome's remarkable functional diversity and plasticity.

58 This article explores the functional diversity and redundancy in a bacterial metac

59 ersity partitioning was used to characterize functional diversity and redundancy within (alpha), betw

60 st-translational S-nitrosylation may provide functional diversity and specificity to S100A1 and other

61 Rs in Zika virus proteome, which provide the functional diversity and structural plasticity to viral

62 ness, including shifts in trophic structure, functional diversity and symbiont composition.

63 mework to relate structural heterogeneity to functional diversity and, beyond neural dynamics, are ge

64 anges in the abundance, taxonomic diversity, functional diversity, and phylogenetic diversity of bird

65 al variety of cells is matched only by their functional diversity, and reflects the complex interplay

66 adaptations in the motor that allow for this functional diversity are not known, due, in part, to the

67 Much of this functional diversity arises in the inner plexiform layer

68 losing taxonomic, phylogenetic, genetic, and functional diversity as a result of human appropriation

69 hy, which may ultimately lead to a mosaic of functional diversity as well as rare species diversity a

70 ies, resulting in homogenization and reduced functional diversity at a landscape scale.

71 of 1,2-dihydropyridines with wide structural/functional diversity at the ring and featuring mono, dou

72 -translational processing are used to create functional diversity between BMPs within and between spe

73 romise of single-cell genomics in uncovering functional diversity between cells and in deciphering ce

74 l to account for the contribution of MGBv to functional diversity between frequency-organized cortica

75 To infer the structural and functional diversity between Pf12 and the other 11 6-Cys

76 have proven to be a powerful tool to predict functional diversity between PMEIs, allowing the discove

77 blooms often harbor significant genetic and functional diversity: bloom populations may undergo gene

78 Given their functional diversity, BMCs constitute a rich source of m

79 gle tissue, fibroblasts exhibit considerable functional diversity, but it is not known whether this r

80 Tree canopy chemistry underpins forest functional diversity, but the interactive role of phylog

81 High sequence variation causes BabA functional diversity, but the underlying structural-mole

82 Here, we probe the principles enabling this functional diversity by exploiting the natural divergenc

83 executing translation, the ribosome exhibits functional diversity by modification of just a single rR

84 n assumed to be buffered against declines in functional diversity by the ability of the species-rich

85 es from hybridization based rules, and their functional diversity can be significantly expanded throu

86 ensive FGAs have been applied to analyze the functional diversity, composition, structure, and metabo

87 hat dominant plant traits, rather than trait functional diversity, control the fate of added N in the

88 nd that these properties are also related to functional diversity, defined by depth of proteins withi

89 pathogenic Beauveria spp., shows remarkable functional diversity, displaying antimicrobial, antivira

90 ert soils typically had the lowest levels of functional diversity (diversity of protein-coding gene c

91 hematopoietic system that display remarkable functional diversity encompassing innate immune response

92 rther analyses of plant LIMEs revealed their functional diversity, encompassing elements found near r

93 ling is essential for understanding cortical functional diversity, especially in the highly complex p

94 This large degree of functional diversity even between cells with the same sp

95 he methods most commonly used to assess this functional diversity ex vivo and to recover specific cel

96 nism of CCoAOMTs and provide a basis for the functional diversity exhibited by type 2 plant OMTs that

97 Patterns of tropical forest functional diversity express processes of ecological ass

98 Both can be functionally defined using the functional diversity (FD) and functional identity (FI) o

99 Functional diversity (FD) and phylogenetic diversity (PD

100 f canopy traits yielded a map of forest beta functional diversity for land-use analysis.

101 The implications of this functional diversity for the regulation of neuronal proc

102 tical mechanism for expanding regulatory and functional diversity from a limited number of genes, and

103 Assessing functional diversity from space can help predict product

104 es we demonstrate the potential of assessing functional diversity from space, providing a pathway onl

105 These results show that functional diversity had additional effects on both plan

106 Recently, isotype functional diversity has been linked to a "tubulin code"

107 matic flow cytometry was used to analyze the functional diversity (ie, CD107, CD154, interleukin 2, t

108 odel to study IFN evolution in molecular and functional diversity in coping with dramatic environment

109 future efforts to delineate the emergence of functional diversity in enzyme superfamilies, provide cl

110 rnative splicing that greatly enhances their functional diversity in excitable cells.

111 ng ecosystem recovery and the maintenance of functional diversity in future scenarios is very limited

112 ing is an important mechanism for generating functional diversity in genes.

113 ously unappreciated degree of phenotypic and functional diversity in human Treg cells that allows sub

114 ray of mechanisms through which EBV achieves functional diversity in its relatively small, compact ge

115 hat each distributional group contributes to functional diversity in proportion to their species rich

116 Using path analysis, we found that functional diversity in regeneration traits (fire tolera

117 over, the existence of subclonal genetic and functional diversity in some human cancers such as leuke

118 ns in environmental stress supported greater functional diversity in stress-response pathways than so

119 factors establish cell-type specificity and functional diversity in terms of motor neuron identities

120 eal both redundant and unique nonoverlapping functional diversity in TGF-beta isoform signaling that

121 ld expect to see a great deal of irreducible functional diversity in the brain at multiple spatial sc

122 e characterization of baseline microbial and functional diversity in the human microbiome has enabled

123 ving both the DHp and the CA domains suggest functional diversity in the regulation of HisKA and HisK

124 These findings reveal new functional diversity in the SAM-dependent methyltransfer

125 This study underscores the structural and functional diversity in the UDG superfamily.

126 Functional diversity in thermal affinity within the pisc

127 The processes that led to functional diversity in these lineages, which may contri

128 he DC lineage and predicted regulators of DC functional diversity in tissues.

129 ly in succession, phylogenetic diversity and functional diversity in two leaf traits exhibited the st

130 Functional diversity increased in the Ordovician and, es

131 We find that functional diversity increased more slowly than would be

132 h taxa and for each distributional category, functional diversity increases with species richness, wh

133 e of the first direct empirical evidence for functional diversity increasing resilience at large spat

134 rait data for spiders and beetles and used a functional diversity index (FRic) to test for nonrandomn

135 ion of global marine microbial taxonomic and functional diversity is a primary goal of the Global Oce

136 This functional diversity is attributed to the ability of bet

137 This functional diversity is consistent with schizophrenia's

138 the intact retina, we show that bipolar cell functional diversity is generated by the interplay of de

139 lexity to the mechanisms by which BK channel functional diversity is generated.

140 but a similarly deep understanding of their functional diversity is lacking.

141 ss, although the decline in phylogenetic and functional diversity is less severe.

142 is functionally heterogeneous and that this functional diversity is lost after neonatal thymectomy.

143 was discovered nearly three decades ago, its functional diversity is still not completely understood.

144 A key to functional diversity is the enzymes' ability to divert f

145 A molecular pathway by which NO accomplishes functional diversity is the selective modification of pr

146 At the base of such functional diversity is the subtle balance between diffe

147 Functional diversity is thought to enhance ecosystem res

148 ive loss of species, and of phylogenetic and functional diversity, is highest when habitable area dis

149 To understand the overall landscape of their functional diversity, it is important to establish a com

150 pancies reveal both (1) the inconsistency of functional diversity levels among different taxa and (2)

151 This functional diversity makes therapeutic targeting of memo

152 Univariate and multivariate functional diversity measures were poorly explained by a

153 ironmental conditions, and how taxonomic and functional diversity mediate these changes.

154 their outstanding structural, chemical, and functional diversity, metal-organic frameworks (MOFs) ha

155 l processes, yet drawing a global picture of functional diversity, microbial community structure, and

156 The appearance of functional diversity might be explained by task heteroge

157 structural features that may underlie subtle functional diversity observed for the two orthologues.

158 hanisms that regulate the conformational and functional diversity of actin filaments in living cells.

159 vertebrates and exhibit some of the greatest functional diversity of all vertebrates.

160 xalogenesis and constitute an example of the functional diversity of an enzyme for survival and adapt

161 Functional diversity of associated reef fish communities

162 gress has been made toward understanding the functional diversity of bacterial microcompartment (MCP)

163 of anthropogenic inputs on the taxonomic and functional diversity of bacterioplankton communities in

164 predict hotspots of taxonomic diversity and functional diversity of bird communities in European cou

165 constituent protein domains, foregrounds the functional diversity of BMCs and provides a reference fo

166 egration; (5) dual process theories; and (6) functional diversity of brain regions/networks and cogni

167 nation with satellite data to understand the functional diversity of C3 and C4 grasses by comparing b

168 y of taxa is important for understanding the functional diversity of C3 and C4 grasses, and should ha

169 These results highlight the functional diversity of CD1-restricted T cells circulati

170 gene batteries define the morphological and functional diversity of cell types in the nervous system

171 sult in the morphological, connectional, and functional diversity of cells.

172 aching events, threatening the integrity and functional diversity of coral reefs.

173 These data highlight the functional diversity of core components of front-line ca

174 The functional diversity of cytoplasmic dynein is in part at

175 or complexes, revealing new insight into the functional diversity of Daam proteins and how canonical

176 The functional diversity of deubiquitinating enzymes (DUBs)

177 ulfide bonds, but only more recently has the functional diversity of disulfide bonding in extracellul

178 The geometric and functional diversity of DNA nanostructures created to da

179 olved to coadapt specificity and affinity to functional diversity of domain-peptide interactions.

180 itation in the modification of taxonomic and functional diversity of ecological communities, and indi

181 The functional diversity of eukaryotic viruses infecting a s

182 average fruit size tracks the taxonomic and functional diversity of frugivorous birds and mammals.

183 The temporal characteristics and functional diversity of GABAergic inhibition are determi

184 arch agenda to improve future assessments of functional diversity of global fisheries.

185 cent findings highlighting the metabolic and functional diversity of HDL subspecies.

186 esides histone acetylation, has added to the functional diversity of histone modifications.

187 echniques, we explored the heterogeneity and functional diversity of human Tregs in healthy donors an

188 ells, explains the remarkable complexity and functional diversity of human Tregs.

189 ty of humanized models for understanding the functional diversity of human tumors.

190 We examined how the functional diversity of identified dopaminergic neurons

191 eural circuits is the extreme anatomical and functional diversity of interneurons.

192 mputation, it is essential to understand the functional diversity of its odor receptors.

193 tantaneous net ecosystem CO2 exchange and 3) functional diversity of leaf N concentration as estimate

194 Overall, we demonstrate considerable functional diversity of MAIT cell responses, as well as

195 make key contributions to the structural and functional diversity of mammalian proteomes.

196 plex and intriguing evolutionary pattern and functional diversity of mammalian ribonuclease than prev

197 This study reveals not only functional diversity of MATE transporters and regulatory

198 class I gene loss and dramatic reduction in functional diversity of MHC genes would explain why chee

199 Given the synthetic and functional diversity of MOCs and BCPs, our method should

200 hlighted greater complexity, plasticity, and functional diversity of mononuclear phagocytes (MPCs), i

201 rtic hemoglobinase, this work focuses on the functional diversity of multiple Ixodes ricinus cathepsi

202 e myosin II isoforms, suggesting that a rich functional diversity of myosin II motors may exist in ne

203 on initiation as a mechanism to increase the functional diversity of NPC components.

204 ne methylation patterns underlie much of the functional diversity of nucleosomes in eukaryotes, and a

205 histone lysine acylation marks increase the functional diversity of nucleosomes well beyond acetylat

206 Together, these results reveal a functional diversity of PF synapses, which use different

207 zoan parasite Toxoplasma gondii expanded the functional diversity of pore-forming proteins.

208 al 'silent code' mechanism that controls the functional diversity of protein isoforms.

209 native splicing, which greatly increases the functional diversity of protein species.

210 To study functional diversity of proteins encoded from a single g

211 Our results demonstrate that the functional diversity of proteins with a common fold can

212 indicates that splice variants increase the functional diversity of proteins.

213 Alternative inclusion of exons increases the functional diversity of proteins.

214 tates of numerous GPCRs, contributing to the functional diversity of receptors.

215 n as a new factor responsible for increasing functional diversity of S100A1 and helps explain the rol

216 very of productivity after wildfire than the functional diversity of seed mass or species richness.

217 tures, we reveal through genomic editing the functional diversity of several GATA switch enhancers in

218 The functional diversity of skin requires the synthesis of l

219 The functional diversity of SMRs underscores both the varied

220 network topology contributes to the observed functional diversity of subicular pyramidal cells during

221 lls, the molecular mechanisms underlying the functional diversity of T(H)17 cells are not fully under

222 cularly in the context of ACs, and about the functional diversity of TAM receptors.

223 The structural and functional diversity of the assemblies is influenced by

224 The functional diversity of the CBP/p300 interactome provide

225 synaptic plasticity, axonal arborization, or functional diversity of the circuit.

226 ain compartments, which in part accounts for functional diversity of the DA system.

227 rovide the structural basis for studying the functional diversity of the dorsal striatum and disrupti

228 nd disease, and highlight the structural and functional diversity of the FKBPs.

229 The study demonstrates the molecular and functional diversity of the GABAAR system within the mou

230 Moreover, these findings highlight functional diversity of the hypusine system compared wit

231 factor expression with CD4(+) Th2 cells, but functional diversity of the ILC2 lineage has yet to be f

232 The functional diversity of the INO80 complex can, in part,

233 anges in composition, metabolic activity and functional diversity of the microbial assembly.

234 These results illuminate the functional diversity of the PLRV-host protein interactio

235 anscription factor could produce significant functional diversity of the protein.

236 Thus, ApA contributes to the functional diversity of the proteome without changing th

237 mportance if we are to gain insight into the functional diversity of the proteome.

238 Compared to the functional diversity of the regulon of the other general

239 The dazzling functional diversity of the rumen microbiota was reflect

240 the global distribution of microbes and the functional diversity of their communities cannot be robu

241 This suggests that the genomic and functional diversity of these organisms lies largely in

242 ependent control mechanisms may underlie the functional diversity of these variants and explain an el

243 tructural details that help explain the wide functional diversity of this ABC transporter subfamily.

244 monstrated a physiological importance of the functional diversity of TnT isoforms.

245 to various regulatory stimuli and highlight functional diversity of transcription factors that bind

246 particular, we discuss the context-dependent functional diversity of Tregs, the developmental origins

247 inue to be identified and further expand the functional diversity of UBL pathways in cellular homeost

248 ng unreported catches were large (changes in functional diversity of up to 46%).

249 xpressed genes; investigate expressional and functional diversity of vascular tissue preferential gen

250 c diversity (FDQ) to evaluate the effects of functional diversity on the ABP in the Northern Tibetan

251 vidual neurons of the brain, contributing to functional diversity or to an unexplained burden of neur

252 ed catches had little impact on global-scale functional diversity patterns.

253 We determined the functional diversity profiles of the soil biota (i.e., m

254 increasing a library's structural, and thus functional diversity, rather than only its size.

255 In addition to the anatomical and functional diversity, recent studies have shown the mech

256 ns unknown whether species' contributions to functional diversity relate to their network roles.

257 h-diversity systems, such as tropical reefs, functional diversity remains highly vulnerable to specie

258 oid bacteria are common, but the genetic and functional diversity resulting from polyploidy is unknow

259 urther, a protein cluster guided analysis of functional diversity revealed that richness decreased (i

260 e method for generating protein sequence and functional diversity, SCHEMA recombination can be used t

261 onmental filtering, make predictions for how functional diversity should vary at the alpha (within lo

262 Functional diversity showed a positive response to incre

263 NS, providing insights into their origin and functional diversity.SIGNIFICANCE STATEMENT We investiga

264 mpared with Simpson's index of diversity and functional diversity, species richness (SR) showed stron

265 t spaces, can be used in ecophenotypical and functional diversity studies, and may reveal novel patte

266 n to the PIF pocket, thus displaying greater functional diversity than is displayed by PIFtides conju

267 rophilin family, show greater structural and functional diversity than the canonical B7 receptors.

268 ey sometimes result in substantial losses of functional diversity that could have severe consequences

269 nsory neurons show incredible phenotypic and functional diversity that is initiated early by cell-aut

270 otransmitter receptors is thought to provide functional diversity that may be important in patterning

271 Deubiquitinases are proteases with a wide functional diversity that profoundly impact multiple bio

272 determined input-specifically, generating a functional diversity that sculpts excitatory transmissio

273 roviding blueprints for the evolutionary and functional diversity that shapes the biosphere.

274 rray of diverse phenotypes, including enzyme functional diversity, that help to subvert obstacles pre

275 Functional diversity, the extent of functional differenc

276 Despite their cellular and functional diversity, they arise from a common field of

277 ty composition, evolutionary relatedness and functional diversity, this study found strong evidence t

278 fundamentally similar structure, but achieve functional diversity through variable regions that deter

279 Whether somatic mutations contribute functional diversity to brain cells is a long-standing q

280 survey of soil taxonomic, phylogenetic, and functional diversity to date, this study demonstrates th

281 nd altered epigenetic programmes that impart functional diversity to individual cells.

282 ensitive properties to the channel providing functional diversity to the cytoskeletal control of tran

283 fisheries, bycatch and discards) influences functional diversity trends in global fisheries.

284 The evolution of miRNA processing and functional diversity underscores the dynamic nature of m

285 uous method to map regional patterns of tree functional diversity using combined laser scanning and i

286 al colonization patterns were determined and functional diversity was assayed via measurements of pot

287 A key element of ecosystem functional diversity was ensured by the presence of diff

288 Multivariate functional diversity was ineffective in predicting ecosy

289 Fish species richness and functional diversity were among the strongest predictors

290 d that temporal differences of taxonomic and functional diversity were more pronounced than spatial o

291 Both species and functional diversity were positively related to the ABP.

292 y in terms of modularity, responsiveness and functional diversity, which enables direct comparisons w

293 hina, and quantified microbial taxonomic and functional diversity with shotgun metagenome sequencing.

294 uence macrophage development, activation and functional diversity, with consequences in disease and h

295 within a single voxel, present a new view of functional diversity within a local neural population.

296 m small-scale experiments to ask whether the functional diversity within a range of woodland and fore

297 l bases and functional implication of such a functional diversity within a single protein family rema

298 s this question, we explore the evolution of functional diversity within the Roundabout (Robo) family

299 nto triterpene cyclization, revealing hidden functional diversity within triterpene synthases.

300 we used the trogocytosis phenomenon to study functional diversity within tumor-specific T cell clones