ライフサイエンスコーパス: -adapted

1 ity, in which acidogenic, aciduric, and acid-adapted bacterial species promote a pathogenic environme

2 review presents current knowledge for an age-adapted immunosuppression based on both, experimental an

3 may have significant implications for an age-adapted immunosuppression.

4 LCI determined by age-adapted multiple breath washout techniques and MRI studi

5 but did not affect the expression of already-adapted motor commands.

6 In contrast, high-altitude-adapted Quechua- and Aymara-speaking inhabitants of the

7 his zinc finger is impaired in high-altitude-adapted Tibetans, suggesting that their adaptation to hi

8 om fetal growth restriction seen in altitude-adapted Andean populations.

9 rical stimulation that includes an amplitude-adapted pulse train which induces force enhancements wit

10 ulation power harmonics during the amplitude-adapted pulse train.

11 eat of displacement by another strain of ant-adapted bacteria.

12 ulting transgenic plants with an Arabidopsis-adapted PM pathogen.

13 pe current species richness of Africa's arid-adapted taxa.

14 directed antibodies that recognize the avian-adapted H1 strain in current influenza vaccines but not

15 ere we investigate accessibility of the best-adapted genotype in the general case of K > 2 units.

16 that lead from a given genotype to a better-adapted genotype are important measures of accessibility

17 smissibility with the 2014 initial wild bird-adapted clade 2.3.4.4 virus, with potential acquisition

18 support the hypothesis that PLVA is a bobcat-adapted virus which is less fit in mountain lions and un

19 t species tested, including even albino cave-adapted species.

20 We amputated appendages in a variety of cave-adapted and surface-dwelling arthropods.

21 nd bulk stable carbon isotope values of cave-adapted shrimp suggest that carbon from methanotrophic b

22 logical and genetic characterization of cell-adapted PDCoV strains.

23 Following LT, CF-adapted Pseudomonas strains, potentially originating fro

24 We investigated whether CF-adapted Pseudomonas populations invade the donor microbi

25 press genetic recombination and establish co-adapted gene complexes, or supergenes.

26 insights into the genome evolution of a cold-adapted diatom from the Southern Ocean, Fragilariopsis c

27 Our twin findings-that the sexes of a cold-adapted species respond differently to modern climate fo

28 st clade 1 H5N1 viruses on an Ann Arbor cold-adapted (ca) backbone that induced long-term immune memo

29 ical activity, indicating that they are cold-adapted.

30 A live attenuated, cold-adapted (ca) H3N8 vaccine virus was generated by reverse

31 ry dipterans) relative to small-bodied, cold-adapted taxa (e.g., chironomids and oligochaetes).

32 ifreeze proteins (AFPs) protect certain cold-adapted organisms from freezing to death by selectively

33 odelling, to investigate how two common cold-adapted bird species, willow and rock ptarmigan (Lagopus

34 t memory CD4 T cell formation following cold-adapted influenza vaccination is boosted when Ag is admi

35 d use appears to exacerbate declines in cold-adapted bird and butterfly species, and prevent increase

36 As found in cold-adapted enzymes, this phenotype likely compensates for a

37 ect the hypothesis that anammox is more cold-adapted than denitrification in our study system.

38 igher rates at low temperatures for the cold-adapted enzyme.

39 l protein-coding gene segments from the cold-adapted temperature-sensitive master donor virus A/Ann A

40 in the common experimental site, where cold-adapted populations produced roots with greater absorpti

41 cool shifts in temperature class where cool-adapted Acer saccharum increased and temperature neutral

42 -genome exon sequence analysis of 31 culture-adapted parasite lines associated amplification of the p

43 hermore, we found that a highly cell culture-adapted HCV strain was able to achieve a complete viral

44 patocyte cultures with a highly cell culture-adapted HCV strain.

45 f is present in the majority of cell culture-adapted PEDV strains but is missing in emerging field is

46 kably, reverse-genetics-derived cell culture-adapted PEDVAVCT12 harboring uncleavable N displayed gro

47 rived from naturally occurring, cell culture-adapted, or genetically modified live attenuated ASFV.

48 ne of this virus containing all nine culture-adapted mutations had 10-fold-higher levels of RNA repli

49 e clinical isolates and a short-term-culture-adapted strain.

50 We found that the culture-adapted mutation in p7 promoted an increase in the size

51 ype (WT) PoSaV Cowden strain, tissue culture-adapted (TC) PoSaV has two conserved amino acid substitu

52 t U.S. PEDV strain PC21A, the tissue culture-adapted PC177 (TC-PC177) contains a 197-amino-acid (aa)

53 igs than those induced by the tissue culture-adapted strain.

54 0(4) to 10(5) free opsin molecules in a dark-adapted rod cell-a number that is three orders of magnit

55 the retina in vivo and find that basal dark-adapted concentrations are not affected.

56 ifference in frequency response between dark-adapted and light-adapted flies, resulting in high-frequ

57 e median junctional conductance between dark-adapted rods is approximately 140 pS, regardless of the

58 atients were determined using chromatic dark-adapted Goldmann VFs (CDA-GVFs).

59 G, light-adapted achromatic and 2-color dark-adapted perimetry, and microperimetry.

60 vision according to results of 2-color dark-adapted perimetry.

61 ual cycle) was similar to that of cones dark-adapted in the intact eye (with both the RPE and retina

62 nsitivity of salamander and mouse cones dark-adapted in the isolated retina (with only the retina vis

63 l suction electrode recording displayed dark-adapted kinetics.

64 Here we found that rods excite dark-adapted DACs across a wide range of stimulation intensit

65 free calcium concentrations typical for dark-adapted rods.

66 analysis, levels of 11-cis-RAL in fully dark-adapted heterozygous KI mice were similar to that in WT

67 solated from Arabidopsis thaliana WT in dark-adapted and high-light-stressed (NPQ) states, we find th

68 ting in high-frequency response also in dark-adapted flies.

69 cells (ONalphaGCs and sOFFalphaGCs) in dark-adapted mouse retinas with elevated intraocular pressure

70 Retinal ganglion cells (RGCs) in dark-adapted retinas show a range of threshold sensitivities

71 hat ligand binding of 11-cis-retinal in dark-adapted Rho was essentially irreversible with a half-lif

72 ngle quantal responses displayed normal dark-adapted kinetics, but rods were only half as sensitive a

73 ge-free, room temperature structures of dark-adapted (S1), two-flash illuminated (2F; S3-enriched), a

74 We present the 2.3 A structure of dark-adapted D217E ASR, which reveals significant changes in

75 ted flies to low frequencies typical of dark-adapted flies.

76 wide range of sensitivities in the same dark-adapted conditions, suggesting a divergence of the rod p

77 d and cone responses (the a-wave of the dark-adapted ERG protocol of 12.0 cd/s/m2) was longer (mean d

78 o -17.9 muV]; P=.003; the a-wave of the dark-adapted ERG protocol of 12.0 cd/s/m2: mean difference, -

79 d and cone responses (the a-wave of the dark-adapted ERG protocol of 3.0 cd/s/m2: mean difference, -4

80 s, taken using a digital camera through dark-adapted pupils using a standard protocol and the same eq

81 a, M-cones and melanopsin contribute to dark-adapted DAC responses with a similar threshold intensity

82 ecies, particularly Smicrodontum in long-day-adapted cultivars.

83 m species in the diversification of long-day-adapted tetraploid potatoes, showing that extant natural

84 for SAMD9L in regulating IFN-driven, demand-adapted hematopoiesis.

85 anisms that pattern leaf thickness in desert-adapted tomato.

86 on population developed from the wild desert-adapted Solanum pennellii and domesticated tomato (Solan

87 coreference resolution system with a domain-adapted system produced results that are consistent with

88 -measure of 0.14 (B3), while a simple domain-adapted rule-based system achieved an F-measure of 0.42.

89 Mesic ecosystems, lacking drought-adapted species, did not show an intrinsic asymmetric re

90 the pulse-response behaviour of the drought-adapted biota of these systems, a response that is estim

91 xpression divergence between upland (drought-adapted) and lowland (mesic) ecotypes of the perennial C

92 at has been linked to diversification in dry-adapted plants.

93 zing antibodies than those produced from egg-adapted viruses, extending the established benefits of c

94 ifferences in glycosylation between H3N2 egg-adapted vaccines and circulating strains likely contribu

95 ted in ferrets and humans exposed to the egg-adapted 2016-2017 H3N2 vaccine strain poorly neutralize

96 idic environment) at higher pHs, but the egg-adapted strains become less acid stable at lower pHs.

97 o decreasing pH, while the fusion of the egg-adapted strains Udorn and X:31 is strongly dependent on

98 a clade 3C.2a H3N2 strain; however, the egg-adapted version of this viral strain lacks the new putat

99 ls, which have developed various environment-adapted structures and materials through natural selecti

100 , cell viability and growth; and (6) ethanol-adapted E. coli cells restore the majority of these redu

101 ic data of both ethanol-stressed and ethanol-adapted E. coli cells with computationally predicated et

102 have investigated stress effects in fasting-adapted species.

103 A ferret-adapted revertant (HA1-H17Y/HA2-R106K) regained airborne

104 vaccinating human subjects with a fibroblast-adapted mutant of human CMV (HCMV).

105 responses were only elicited by a fibroblast-adapted rhesus CMV vector with limited tissue tropism; a

106 uman subjects vaccinated with two fibroblast-adapted HCMV vaccines.

107 nofluorescence staining combined with filter-adapted FISH after filtration enrichment.

108 wildland-urban interface to developing fire-adapted communities.

109 Using an fMRI-adapted social approach-avoidance task, this study ident

110 which would have allowed forests and forest-adapted species to expand.

111 llenging the guinea pigs with salivary gland-adapted GPCMV.

112 0,000 times the 50% lethal dose (LD50) of gp-adapted EBOV, and naive gps were then introduced as cage

113 golden hamster model of MHF using a hamster-adapted MARV variant Angola.

114 of both "healthcare-acquired and healthcare-adapted pathobiota." Under this framework, the criticall

115 Our findings suggest that herbivore-adapted savannas evolved several million years before fi

116 Given that EpaX is enriched in hospital-adapted isolates, this study points to the importance of

117 Host-adapted and host-restricted bacterial clades evolve from

118 range of host species, while others are host-adapted, infecting particular hosts(1).

119 which R. equi virulence is conferred by host-adapted plasmids.

120 fed larvae, fed nymphs and in mammalian host-adapted organisms cultivated in dialysis membrane chambe

121 l-associated ancestor and the mammalian host-adapted pathogenic Brucella species.

122 gene expression is a common feature of host-adapted pathogenic bacteria.

123 that harbor a low burden of persistent host-adapted spirochetes and/or residual antigen.

124 As a prototypic host-adapted airborne pathogen, Mycobacterium tuberculosis tr

125 bility outside the host, reflecting the host-adapted lifestyle and person-to-person transmission of t

126 mpur, Malaysia, and compared it with a human-adapted laboratory line (A1-H.1) derived from the P. kno

127 A human-adapted P. knowlesi line invades human RBCs independentl

128 Streptococcus pneumoniae is a human-adapted pathogen that encounters terminally sialylated g

129 lutinin (HA) proteins of seal H3N8 and human-adapted H3N2 viruses to respiratory tissues of humans an

130 sulting in a clear distinction between human-adapted and avian influenza viruses.

131 sum virus (MCV), the only known extant human-adapted poxvirus, causes a long-duration infection chara

132 tivation pH of 5.3, similar to that of human-adapted isolates from late 2009-2014.

133 Several human-adapted bacterial pathogens use a phasevarion (ie, a pha

134 s an essential virulence factor of the human-adapted bacterial pathogen Salmonella Typhi (6,7) , the

135 i, which was in direct contrast to the human-adapted H3 that bound mainly to the trachea.

136 ctivation, and further clarify how the human-adapted poxvirus MCV can so effectively evade antiviral

137 Motility studies established that the human-adapted typhoidal S. Typhi, S. Paratyphi A, and S. Senda

138 is not known about the biology of this human-adapted bacterial pathogen and the complexity of the dis

139 that Halobacterium salinarum, a hypersaline-adapted archaeal organism, grows exponentially at the si

140 d for ADCC against cells infected with a lab-adapted HIV-1 isolate (HIV-1NL4-3), a primary HIV-1 isol

141 re engineered into Gag from a subtype B, lab-adapted provirus or Gag from a subtype C primary isolate

142 ted vaccines focus on glycoproteins from lab-adapted strains, which may poorly reflect primary viral

143 these mutations, G147R, in the NA of the lab-adapted A/WSN/33 (H1N1) strain while we were passaging a

144 Surprisingly, these two commonly used lab-adapted strains produced drastically different titers in

145 he patient's viral isolate and by laboratory-adapted HIV-1 strains.

146 661 against Plasmodium falciparum laboratory-adapted strains (mean IC50 32 nM), Ugandan field isolate

147 ve been carried out in only a few laboratory-adapted lines.

148 P phase variation have focused on laboratory-adapted E coli strains and have been limited in the numb

149 troviral response against several laboratory-adapted and clinical HIV-1 isolates.

150 ome sequences of eleven long-term laboratory-adapted parasite strains were examined, revealing four i

151 Thus, it appears that the laboratory-adapted H3 strains tested may have evolved to compensate

152 under viruses, in contrast to the laboratory-adapted NL4-3 virus.

153 eviously identified as VFs in the laboratory-adapted reference strain H37Rv and shown to confer lysoz

154 amino-acid difference between the laboratory-adapted ROD10 and ROD14 Envs controlled the enhancement

155 These laboratory-adapted strains of HCMV generally exhibit restricted tro

156 and the generation of high-titer, laboratory-adapted viruses with diminished virulence in animal mode

157 this pathogen are conducted with laboratory-adapted strains which may not be representative of the s

158 Light-adapted rdgC mutant flies showed relatively high S936-TR

159 that are used for photochemistry for a light-adapted measurement from a pulse amplitude modulation fl

160 Under dark- and light-adapted conditions, patients use rod-mediated pathways.

161 ency response between dark-adapted and light-adapted flies, resulting in high-frequency response also

162 essed in etiolated, light-exposed, and light-adapted plants.

163 t-adapted variants from ancestral blue light-adapted ones.

164 tcome measures would include chromatic light-adapted psychophysics, with attention to the photorecept

165 tandard combined, standard flash cone, light-adapted 3.0 Hz flicker and red cone responses were analy

166 tandard combined, standard flash cone, light-adapted 3.0 Hz flicker and red cone responses were up to

167 retinography (ERG) and multifocal ERG, light-adapted achromatic and 2-color dark-adapted perimetry, a

168 f a dark state LOV monomer and a fully light-adapted LOV dimer.

169 ltiple occasions, giving rise to green light-adapted variants from ancestral blue light-adapted ones.

170 Until now, descriptions of how light-adapted retinal circuitry maintains a preponderance of s

171 atomic-level structural model of a low-light-adapted chromatophore vesicle from Rhodobacter sphaeroid

172 S936D) ) set the frequency response of light-adapted flies to low frequencies typical of dark-adapted

173 of dense cone dysfunction detected on light-adapted perimetry and multifocal ERG but with near-norma

174 with a dense relative scotoma noted on light-adapted static perimetry in the left eye.

175 teady-state absorption contours of the light-adapted monomeric bR in nanodiscs composed of different

176 Qualitative analysis of the light-adapted mouse retina with mass spectrometry revealed mor

177 barrier are significantly lower in the light-adapted state.

178 little impact on the forward (dark- to light-adapted form) photoreaction was observed, the change in

179 n exposure followed by TGFbeta induces liver-adapted TRM, including their signature high expression o

180 eana seeds were collected from eight locally-adapted populations in 2015 and 2016.

181 The survival of macrophage-adapted chlamydiae correlates with the multiplicity of i

182 us polymerase to levels similar to mammalian-adapted polymerase.

183 cific genetic changes were discovered in MIL-adapted parasites, including deletions at the LdMT trans

184 achievement, in concert with a mitochondria-adapted CRISPR/Cas9 platform, could prompt a revolution

185 Here, using a mouse-adapted African ZIKV strain (Dakar 41519), we evaluated

186 Previously, we generated a mouse-adapted EV71 (mEV71) capable of infecting 12-week-old in

187 onorgestrel (LNG), and infected with a mouse-adapted H1N1 (maH1N1) virus.

188 receptor transgenic mouse (2D2) and a mouse-adapted human influenza virus to test the hypothesis tha

189 In 2014, we developed a mouse-adapted MARV, Angola variant through serial passaging in

190 A mouse-adapted SARS-CoV (SARS-CoV-MA15) lacking the envelope (E

191 t systemic and airway challenge with a mouse-adapted strain of Ebola virus.

192 ting animal models by characterizing a mouse-adapted strain of EV71.

193 s when the tumor was inoculated with a mouse-adapted strain of ZIKV.

194 ssages through the lungs of KI mice, a mouse-adapted virus emerged (MERSMA) that grew in lungs to ove

195 eered mice was then used to generate a mouse-adapted virus that replicated efficiently within the lun

196 ajority of wild-type (strain EGDe) and mouse-adapted (InlA(m)-expressing) L. monocytogenes recovered

197 n of BALB/c mice with a bioluminescent mouse-adapted EV71 construct (mEV71-NLuc) resulted in a lack o

198 We utilized a non-mouse-adapted DENV-3 Thai human isolate to develop a lethal in

199 of neurotropic disease based on a non-mouse-adapted human isolate, which can be used to investigate

200 gests that murine models utilizing non-mouse-adapted isolates can be obtained for all four DENVs.

201 8 days before a homologous H5N1 and/or mouse-adapted EBOV challenge, as well as a heterologous H5N1 c

202 challenged with homologous H5N1 and/or mouse-adapted EBOV.

203 Here, we demonstrate that the mouse-adapted Ci67 VP40 more potently antagonizes IFN-alpha/be

204 am/1203/04 (VN1203), and the NA of the mouse-adapted H1N1 influenza virus A/Puerto Rico/8/34 (PR8) in

205 The mouse-adapted MARV exhibits many of the hallmarks of MARV dise

206 ted mice against lethal challenge with mouse-adapted Ebola virus (ma-EBOV) in a dose-dependent manner

207 minutes after a lethal challenge with mouse-adapted EBOV or selected H5N1 influenza viruses from cla

208 6A or 8 and then coinfected them with mouse-adapted H1N1 influenza A virus (PR/8/34).

209 and were sequentially challenged with mouse-adapted influenza virus H1N1/A/Puerto Rico/8/1934 and St

210 rom mouse brains with three different murine-adapted scrapie strains (Chandler, 22L, and Me7) and sys

211 antibody reacts differently to three murine-adapted scrapie strains.

212 Therefore, mutation-adapted U1 snRNA gene therapy can be a promising method

213 an activate surface mediated immunity in non-adapted hosts and contribute to non-host resistance.

214 However, on non-adapted hosts, effectors can be detected as non-self by

215 ergetic processes are under selection in PAH-adapted fish from the most contaminated ER site and ex v

216 study of positron emission tomography (PET)-adapted salvage therapy with brentuximab vedotin (BV) an

217 PET-adapted sequential salvage therapy with brentuximab vedo

218 biomarker for development of first-line PET-adapted approaches in FL.

219 assessed the feasibility and activity of PET-adapted salvage therapy with brentuximab vedotin, follow

220 In this phase 2 study of PET-adapted therapy with BV and augICE for relapsed/refracto

221 spleens of guinea pigs in vivo, a guinea pig-adapted SUDV variant (SUDV-GA) uniformly lethal to these

222 te that transmission of viruses that are pre-adapted to the HLA molecules expressed in the recipient

223 domonas fluorescens SBW25, that had been pre-adapted or not to the compost for 48 days.

224 of habitats in severe disequilibrium by pre-adapted individuals, rather than by gradual adaptation f

225 estication occurred through selection of pre-adapted low dormancy phenotypes from the wild.

226 We discuss implications for race-adapted cancer screening programs and clinical trials to

227 lysis of DCE MR imaging and DWI, the BI-RADS-adapted reading algorithm, which adapted ADC thresholds

228 produce long-lasting bacteremia in reservoir-adapted (natural host or passive carrier of a microorgan

229 evolutionary information with the resolution-adapted structural recombination approach of Rosetta, ca

230 ata were collected using age- and respondent-adapted versions of the PediQUEST Memorial Symptom Asses

231 Response-adapted therapy based on interim PET imaging after two c

232 r 2 chemotherapy cycles (PET2) in a response-adapted design.

233 o therapeutic futility and allowing response-adapted treatment strategies.

234 cal trial in Hodgkin lymphoma (HL) (Response-Adapted Therapy in Advanced Hodgkin Lymphoma [RATHL]).

235 imaging to determine the utility of response-adapted therapy for stage III to IV classic Hodgkin lymp

236 onto a more intensive regimen (PET response-adapted therapy), remains to be confirmed.

237 Particular attention is given to response-adapted therapy, which is emerging as a cornerstone of c

238 dapt treatment in a clinical trial: Response-Adapted Therapy in Advanced Hodgkin Lymphoma (RATHL).

239 Phase 3 Trial of Systematic Versus Response-adapted Timed-Sequential Induction in Patients With Core

240 Risk-adapted treatment and follow-up contributes to a favorab

241 provide consensus recommendations for a risk-adapted approach to WM, using a grading system.

242 A risk-adapted strategy could help identify high-risk patients

243 We describe the results of a risk-adapted, response-based therapeutic approach from the Br

244 After risk-adapted treatment strategies, especially in early-stage

245 Treatment should be risk-adapted.

246 a multidisciplinary approach, coupling risk-adapted intensive neoadjuvant and adjuvant chemotherapie

247 ized trials largely support the current risk-adapted therapeutic strategies in early-stage HL.

248 iPET result may potentially help design risk-adapted therapies in patients with aggressive lymphomas.

249 stic models that can be used to develop risk-adapted treatment approaches for patients with ENKTL bei

250 an unmet clinical need by allowing for risk-adapted patient management.

251 on has served to identify subgroups for risk-adapted postremission therapy, but the initial treatment

252 arker-based scores can be used to guide risk-adapted therapy at the onset of acute GVHD.

253 n are part of prognostic scores guiding risk-adapted consolidation strategies, HL at initial diagnosi

254 w for the possibility of individualized risk-adapted therapy.

255 ard treatment toward an individualized, risk-adapted therapy regime.

256 is information should be used to inform risk-adapted therapy and to assist in screening to reduce lon

257 be the future basis for development of risk-adapted GVHD treatment strategies.

258 with Deauville 4 should be the focus of risk-adapted investigational therapies.

259 s it as a reliable biomarker to support risk-adapted clinical trials.

260 s essential for optimizing therapy with risk-adapted approaches.

261 NP were consistently found mutated in rodent-adapted Ebola virus strains.

262 rmore, most data come from studies on rodent-adapted prion strains, making current understanding of t

263 petent rodents, these models rely on "rodent-adapted" viruses that have been passaged several times t

264 ea pigs against lethal challenge with rodent-adapted EBOV.

265 knowledge of diversity across other savanna-adapted species, as well as with palaeoclimate and paleo

266 cs in both TLR4-stimulated normal and sepsis-adapted human blood monocytes and mouse splenocytes.

267 oughput genome-wide translocation sequencing-adapted repertoire sequencing (HTGTS-Rep-seq), to quanti

268 We first demonstrate that serpentine-adapted plants exhibit dramatically altered elemental ac

269 latitudes, where late-flowering but southern-adapted varieties have high winter mortality.

270 e full-length human isoforms from suspension-adapted HEK cells.

271 e a potential risk to public health if swine-adapted viruses with H1N1pdm09 genes also have an increa

272 a potential risk for public health if swine-adapted viruses with H1N1pdm09 genes have an increased r

273 rbation approaches from the popular symmetry-adapted perturbation theory scheme.

274 ispersion energies determined using symmetry-adapted perturbation theory (SAPT), while the induction,

275 Computed tomography-adapted Leaman score (CT-LeSc) was developed to quantify

276 and 4 were previously identified in tropical-adapted and commercial breeds, respectively.

277 Transverse tubules (t-tubules) are uniquely-adapted membrane invaginations in cardiac myocytes that

278 ionary time not to defend against vertebrate-adapted pathogens but instead to counteract infection by

279 nflammasome-evasion strategies of vertebrate-adapted pathogens.

280 e-dependent susceptibility of cold- and warm-adapted amphibian species to the fungal pathogen Batrach

281 he greatest susceptibility of cold- and warm-adapted hosts occurred at relatively warm and cool tempe

282 s between pathogens and their cold- and warm-adapted hosts should occur at relatively warm and cold t

283 l rates (e.g. metabolism) for cool- and warm-adapted species, and independent of latitude or elevatio

284 taxa and a higher proportion of large, warm-adapted species (i.e., snails and predatory dipterans) r

285 widespread poleward expansions by many warm-adapted generalists.

286 th communities increasingly composed of warm-adapted species.

287 These data suggest that warm-adapted species carry a significant survival advantage a

288 n the relative composition of cold- vs. warm-adapted species in a local assemblage [the community tem

289 d and temperature neutral changes where warm-adapted Acer rubrum increased.

290 ersity might be necessary to instruct a well-adapted immune response and regulated inflammatory respo

291 A well-adapted repertoire should be tuned to the pathogenic env

292 ay explain the difficulty in developing well-adapted lines carrying Wsm1 despite improved tolerance t

293 tudied Ethiopians, a population that is well-adapted to HA hypoxic stress.

294 bular recognition system of 4, which is well-adapted to the native conformation of DOPC.

295 to TB transmission than a particularly well-adapted strain.

296 minated by Warnstorfia fontinaliopsis, a wet-adapted moss commonly found in the Antarctic Peninsula.

297 Wetland-adapted trees are known to transport soil-produced metha

298 ns in situ and their controls in two wetland-adapted tree species (Alnus glutinosa and Betula pubesce

299 fer an early diversification of modern xeric-adapted forms.

300 Using a yeast-adapted pCAMBIA0380 Agrobacterium vector, we have constr