ライフサイエンスコーパス: evolve to

1 n competition experiments, a 50%:50% mixture evolved to 70%:30% (WT/mutant) for A(H1N1) and 88%:12% f

2 Some patients with fibrotic HP may evolve to a progressive phenotype, even with complete ex

3 s with an initial apolar geometry eventually evolve to a whole gamut of network morphologies based on

4 w-pathogenicity H7N9 avian influenza viruses evolved to a high-pathogenicity phenotype in China.

5 e ortholog with the highest initial activity evolved to a less-optimal and phenotypically distinct ou

6 Disease mapping has evolved to a powerful field in epidemiology and public h

7 Materials science evolves to a state where the composition and structure o

8 volume/low resistance circulation, gradually evolving to a state of circulatory decompensation usuall

9 s the isocyanide to facilitate deprotonation evolving to a zwitterion that traps pai-electrophiles in

10 generation genome-driven clinical trials can evolve to accelerate our understanding of cancer biology

11 extensive mechanisms that gut symbionts have evolved to access nutrients and the potential for unexpe

12 h- and brackish-adapted fauna must emigrate, evolve to accommodate local habitat changes, or are regi

13 ing a rationale for how the LBD binding site evolved to accommodate diverse amino acids, thus laying

14 the novel hypothesis that the unjammed phase evolved to accommodate fluid-like migratory dynamics dur

15 nd its associated translational factors have evolved to accommodate greater participation of proteins

16 a-molecular protein assembly that has likely evolved to accommodate the high membrane curvature.

17 Thus, two mechanisms have evolved to accomplish the reisomerization: one involving

18 analogous mechanisms that have independently evolved to achieve the same goal of stabilizing the epig

19 ggests that the fifth-wave H7N9 viruses have evolved to acquire novel traits with the potential to po

20 bodies, or the cytoskeleton, they have also evolved to act as part of the plant's defense system to

21 These evolved to active metasurfaces in which light-wavefront

22 Our results indicate that CARD11 has evolved to actively coordinate scaffold opening and the

23 Most populations evolved to allocate a smaller proportion of carbon to gr

24 Birdsong has evolved to allow assessment of conspecific quality in nu

25 y conserved, dedicated molecular network has evolved to allow differentiated cells to re-enter the ce

26 Neuromodulation evolved to allow for such flexibility by dynamically upd

27 Pharmacodynamic improvements are evolving to allow biasing ligands to activate specific d

28 Endogenous circadian clocks have evolved to anticipate 24 hr rhythms in environmental dem

29 Being aware that such enzymes have evolved to approach perfection, chemists are interested

30 he frequency with which strains successfully evolved to assimilate the foreign DNA.

31 eatures, and extensive cortical encephalitis evolving to atrophy.

32 d their hosts can be antagonistic, where TEs evolve to avoid silencing and the host responds by reest

33 Persistent pathogens have evolved to avoid elimination by the mammalian immune sys

34 We propose that 53BP1 has evolved to avoid mutagenic repair outcomes and does so b

35 lost in the Asian haplotype, which may have evolved to balance the antagonistic RETN effects on path

36 ein, the furin cleavage site and D614G, have evolved to balance virus infectivity, stability, cytopat

37 Of patients who did not evolve to BD, 4 died after an unexpected cardiac arrest

38 A successful mutation leading to cancer must evolve to be adaptive, enabling a cancer cell to send a

39 ay in mammals; however, how this pathway was evolved to be functional from its origin is still largel

40 evolution, we found that No Care larvae had evolved to be more cooperative, whereas Full Care larvae

41 dies is key to demonstrating how amino acids evolved to be mostly left-handed in living organisms on

42 e, suggesting that ADAMTS13 and VWF have not evolved to be optimal enzyme-substrate pairs.

43 ther, in BRAF(V600E)-positive melanoma cells evolved to be resistant to BRAF and/or MEK1/2 inhibitors

44 Many mammals have evolved to be social creatures.

45 s a principal component of teeth(1), and has evolved to bear large chewing forces, resist mechanical

46 he potential concern that HPgV will, itself, evolve to become disease-causing by permitting mutant di

47 The island rule predicts that small animals evolve to become larger on islands, while large animals

48 ecome larger on islands, while large animals evolve to become smaller.

49 How did brains evolve to become so complex, and what is their future?

50 Cytochrome c (Cyt c) has evolved to become an important electron-transfer protein

51 ugh neofunctionalization, the SRG family has evolved to become differentially regulated by the key im

52 uggesting that the enzymes have continuously evolved to become more potent resistance genes.

53 RNA sequences suggesting that they may have evolved to bind more complex RNA structures.

54 rs are oligonucleotide sequences that can be evolved to bind to various analytes of interest.

55 Neural signaling pathways that evolved to bolster cognition in settings of food insecur

56 e demonstrate the novel strategies that have evolved to both thread an OTU fold and recognize a ubiqu

57 natural product biosynthetic workaround that evolved to bypass a missing precursor and re-establish i

58 re-type-A and pre-type-B, which consequently evolved to cagPAI type-A and type-B, respectively; impor

59 How do ABC transporters evolve to carry such diverse molecules and what variatio

60 cidation of the mechanism by which H. pylori evolved to carry multiple copies of cagA helps to provid

61 h joint inflammatory symptoms and 14 (43.8%) evolved to chronic arthralgia.

62 hese highly autophagy-dependent cancer cells evolve to circumvent loss of autophagy by upregulating N

63 However, as ablative technologies evolve to circumvent this stalemate, safer, and more eff

64 (Danaus plexippus), that have independently evolved to colonize plants that produce cardiac glycosid

65 Nervous systems have evolved to combine environmental information with intern

66 sed frequently in the United States, and has evolved to commonly include paired exchanges, particular

67 coding framework assuming that neurons have evolved to communicate signals optimally given natural s

68 tory coevolution, whereby the nuclear genome evolves to compensate for the deleterious alleles in the

69 parental care can determine whether siblings evolve to compete or to cooperate.

70 gon is a bona fide postprandial hormone that evolved to concurrently and synergistically work with in

71 We conclude that LeuRS-I may have evolved to confer a selective advantage under the extrem

72 he climate changes and management frameworks evolve to consider climate impacts.

73 pressure), the modular perovskite structure evolves to construct crystallographically defined quantu

74 r support the idea that the termination area evolved to contain fork fusion-mediated pathologies.

75 uss how this 'living' set of guidelines will evolve to continually address new developments in neurop

76 emblies of dedicated clock proteins form and evolve to contribute to the generation of clocks that fu

77 strate known as LITTLE ZIPPER 2 (ZPR2)-which evolved to control the activity of the class-III homeodo

78 We propose that the EPFL2 signaling module evolved to control the initiation and regular, equidista

79 As a result, multiple factors have evolved to control this process.

80 damental puzzle of human evolution is how we evolved to cooperate with genetically unrelated stranger

81 veloped in the same maternal environment and evolved to coordinate the timing of germination and the

82 is suggests that phenological plasticity has evolved to cope with fluctuations in the optimum, despit

83 e-body energy homeostasis, but they have not evolved to cope with the continuous, chronic, nutrient s

84 How the planarian immune system has evolved to cope with these potential pathogens is not we

85 rection of SPECT reconstructions, ultimately evolving to correction techniques that would enable abso

86 ytoplasm of host cells, O. tsutsugamushi has evolved to counter adaptive immunity.

87 maternal) inheritance of cytoplasmic genomes evolved to curtail such selfish replication by minimizin

88 ress histones in a naive system that has not evolved to deal with nucleosomal structures: Escherichia

89 CD) model which predicts that species should evolve to defend territories against heterospecific riva

90 regulatory and often redundant pathways have evolved to detect and respond to human movement, here we

91 Numerous techniques have evolved to determine the concentration of potassium brom

92 Such a mechanism may have evolved to disable repair functions and may be a decisiv

93 echanisms for thick filament activation have evolved to disrupt the interactions that establish the r

94 and found that different starting genotypes evolved to distinct evolutionary outcomes.

95 hanisms not only give clues to how STING has evolved to distinguish between self and foreign, but the

96 that delete or inactivate the transgene may evolve to dominate the vaccine virus population both dur

97 why fungi, rather than unicellular bacteria, evolved to dominate decay of recalcitrant, nutrient poor

98 This is the first CBCR-derived NIR FP evolved to efficiently bind endogenous biliverdin chromo

99 Animals' sensory systems evolved to efficiently process information from their en

100 and innate immune signaling pathways have co-evolved to elicit coordinated responses.

101 Each of these organs has evolved to employ unique branching strategies to achieve

102 twork in the human brain and how it may have evolved to enable complex speech remain unknown.

103 d although the amygdala and cingulate cortex evolved to enable emotion and cognition in both, an evid

104 herein demonstrate that the NPC, which first evolved to enable the biochemical communication between

105 ding argues that our perceptual systems have evolved to encode environmental stimuli in the most effi

106 Plant viruses evolved to encode viral suppressors of RNA silencing (VS

107 of RNAi, cDNA, and chemical libraries, have evolved to encompass a larger biological and chemical sp

108 uits for biological neural routines, but has evolved to encompass the hardware implementation of algo

109 gue that positive emotions such as gratitude evolved to encourage individuals to fulfill cooperative

110 pitopes, suggesting that the antibodies have evolved to engage multiple polymorphic variants of DBP.

111 the ADP-binding function acquired by CxD7L1 evolved to enhance blood-feeding in mammals, where ADP p

112 We suggest that this sex determiner evolved to enhance the meiotic drive of the B chromosome

113 tuent enzymes in the fusion protein may have evolved to ensure a robust but time-limited cOA-activate

114 mposed by the final structure and might have evolved to ensure efficient, timely folding of a highly

115 Our findings suggest that various PSMs have evolved to ensure fast and efficient biofilm formation t

116 resent with seizures, but the probability of evolving to epilepsy is relatively small.

117 removal is among the mechanisms viruses have evolved to escape host immunity.

118 use viral mRNA methyltransferases that have evolved to escape the host's cell immunity response foll

119 longstanding question is how influenza virus evolves to escape human immunity, which is polyclonal an

120 y change in the host antiviral protein as it evolves to escape the effects of viral antagonists.

121 create a persistent global disease burden by evolving to escape immunity induced by prior infections

122 However, cancers evolve to evade immune detection.

123 messenger RNA (mRNA) and protein expression, evolved to evade immune recognition.

124 , including Mycobacterium tuberculosis, have evolved to evade or exploit autophagy, but the precise m

125 Cancer cells have evolved to evade these immunoregulatory mechanisms by up

126 ns of one-component regulatory proteins have evolved to exert control over RNA-binding ANTAR domains.

127 Nonequilibrium interacting systems can evolve to exhibit large-scale structure and order.

128 The gut microbiome and host have evolved to exist in balance and cooperation, and there i

129 Organisms that have evolved to exist under these pressures typically exhibit

130 that rhizobia can subvert plant defenses and evolve to exploit hosts.

131 However, the virus rapidly evolves to exploit the IFN-alpha response for its replic

132 horus (C-P) lyase pathway, an enzyme complex evolved to extract phosphate from phosphonates.

133 Human feet have evolved to facilitate bipedal locomotion, losing an oppo

134 static and anti-inflammatory activities that evolved to facilitate bloodfeeding, but also modulate th

135 lly concerned supernatural agents culturally evolved to facilitate cooperation among strangers in lar

136 ect chemically mediated behaviours that have evolved to facilitate crucial ecological processes.

137 plication, recruitment, and diversification, evolved to facilitate electron transfer and catalysis at

138 ancestrally, sex-specific immune modulation evolved to facilitate survival of the pregnant person in

139 ntation of the mature neutrophil nucleus has evolved to favor migration through narrow pores as found

140 el also suggests a potential reason why life evolved to favor the enrichment of potassium: so living

141 nificant for understanding how microbes have evolved to fill specific ecological niches within a host

142 e feed-forward loop (FFL) is hypothesized to evolve to filter out short spurious signals.

143 of RCO targets reveals that auto-repression evolved to fine-tune RCO activity and that RCO dissects

144 Low contact order proteins evolve to fold cotranslationally.

145 present in the charophycean green algae and evolved to form overlapped and divergent phylogenetic gr

146 Thus, antimony naturally evolves to form optimal nanostructures for alloy anodes,

147 a novel gene with unknown origin, oskar has evolved to fulfil a crucial role in insect germ cell for

148 Symmetrical protein cages have evolved to fulfil diverse roles in nature, including com

149 erstanding how these highly similar pathways evolved to fulfill different roles.

150 speculate that the caveolae-lipid system has evolved to function as a general stress-sensing and stre

151 owever, it remains unclear why influenza NAs evolved to function as Ca(2+)-dependent tetramers that d

152 A prime example of a visual system evolved to function in specific light environments is th

153 dient, we hypothesize that some transporters evolved to harness this 'slip' mechanism to increase sub

154 ed to the ribozyme-based RNase P, but it has evolved to have distinct cellular roles.

155 e energy for growth and maintenance and have evolved to have multiple pathways to produce energy in r

156 to cell viability, molecular chaperones have evolved to help nascent polypeptides fold correctly and

157 TGP evolved to help organisms cope with environmental stress

158 Only 1.6% of patients evolved to HF with reduced LVEF.

159 We hypothesize that viruses, having evolved to hijack the host cellular machinery for cataly

160 n and illustrate how DNA polymerase beta has evolved to hinder Fapy*dGTP insertion.

161 This occurs because faster adapting species evolve to hold onto their initial ranges (i.e., monopoli

162 Numerous ancillary tests have evolved to improve accurate classification of histopatho

163 s conserved in On-Off DSGCs; however, it has evolved to include On-Off DSGCs encoding upward and down

164 Trade agreements in the 21st century have evolved to include provisions that affect domestic publi

165 ct of modern life, clinical trials will also evolve to incorporate these tools, meeting participant e

166 lesion synthesis (TLS) polymerases that have evolved to incorporate nucleotides opposite DNA lesions.

167 Parental care behavior evolves to increase the survival of offspring.

168 s of deep neural networks (DNNs) continue to evolve to increasingly impressive levels.

169 a condition-dependent male ornament that has evolved to indicate immunocompetence.

170 d shed light on how the plastid proteome has evolved to influence plastid morphology and biochemistry

171 ports the novel concept that M. tuberculosis evolved to inhibit autocrine type I IFN signaling to eva

172 te viral replication.IMPORTANCE Viruses have evolved to inhibit cellular DNA damage response pathways

173 sensory stimuli that rodent nervous systems evolved to interpret.

174 However, how photosynthetic seasonality evolved to its current state, and what role climatic con

175 d domesticated amidase effector 2 (dae2)-has evolved to kill mammalian skin microbes with remarkable

176 speculation that protein sequences may have evolved to limit the population of partially folded stat

177 A subpopulation repeatedly evolved to lose the ability to synthesize organosulfurs

178 peach-allergic patients in both populations evolved to LTP-Allergy and showed an early onset.

179 osition in humans and that secretory IgA has evolved to maintain a diverse and stable gut microbial c

180 ensive compared with the jammed phase, which evolved to maintain a solid-like non-migratory state tha

181 rier (BBB), a specialized neurovascular unit evolved to maintain brain homeostasis.

182 The human stress response has evolved to maintain homeostasis under conditions of real

183 nserved protein quality control process that evolved to maintain secretory pathway homeostasis during

184 To avoid mistranslation, editing mechanisms evolved to maintain tRNA aminoacylation fidelity.

185 ctions with cellular membranes, viruses have evolved to manipulate lipid signaling and metabolism to

186 Enteric pathogens have evolved to manipulate the interface between the host and

187 e favouring nutrient-storage pathways, which evolved to maximize energy utilization and preserve adeq

188 that integral helical membrane proteins have evolved to maximize their fitness with cotranslational f

189 hypothesize that all four ZAP isoforms have evolved to mediate distinct antiviral and/or cellular fu

190 We speculate that the EDTEE motif might have evolved to mediate resistance against retroviruses that

191 tial that elaborate circulatory systems have evolved to minimize diffusion distances within tissue.

192 n elegant strategy that Escherichia coli has evolved to minimize metabolic stress that results from t

193 However, the virus has evolved to minimize the immunogenicity of conserved epit

194 mate OAS1 as a model for how immune pathways evolve to mitigate costs and observed a surprising frequ

195 yst nematodes are endoparasites that have co-evolved to modify host plants to create sophisticated fe

196 ents, such as peptide toxins, appear to have evolved to modulate physiologically relevant targets by

197 sphatase parameters are consistent with Vip1 evolving to modulate levels of 1-IP(7) and 1,5-IP(8) Ind

198 arget-site resistance (NTSR) mechanisms have evolved to most herbicide classes.

199 In evolving to obligate intracellular dependence, Chlamydia

200 t sap-feeding insects are widespread, having evolved to occupy diverse environmental niches despite e

201 of NGS data and visualization tools need to evolve to offer the scientific community fast and conven

202 that mechanical activation of these pathways evolved to orchestrate vascular development but also dri

203 rajectories under which an epigenetic switch evolved to outcompete genetic adaptation, shedding light

204 estigate how an IFN-hypersensitive virus can evolve to overcome IFN-beta-mediated blocks targeting th

205 e a common evolutionary origin and that they evolved to parasitise monocot plants from a common dicot

206 arranged in specific network topologies have evolved to perform a diverse array of cellular functions

207 ferent enzymes and even entire pathways have evolved to perform alternative chemical reactions to pro

208 s the optimal treatments of NASH will likely evolve to personalized therapy once we understand the me

209 otility, and show how the outer domains have evolved to play a role not previously found in other bac

210 at least some archaeal histone paralogs have evolved to play distinct and conserved functional roles,

211 is generally assumed that each organism has evolved to possess a unique ribosomal RNA (rRNA) species

212 nt geographic regions revealed that ICP1 has evolved to possess one of two syntenic loci encoding an

213 mitophagy and mitochondrial biogenesis, have evolved to preserve mitochondrial homeostasis under phys

214 the editing domain of I/L/VRSs had primarily evolved to prevent infiltration of Nva into modern prote

215 erlying supergene that determines colour has evolved to prevent phenotypes from "dissolving" into con

216 ve model, tapping perceptual mechanisms that evolved to process physical events in the real world, ma

217 nal centres, the structures in which B cells evolve to produce antibodies with high affinity for vari

218 fter polyploidization, Gossypium hirsutum L. evolved to produce a higher fiber yield and to better su

219 w patterns in more distant teleosts may have evolved to produce a stunningly diverse array of pattern

220 that the filamentous fungus P. graminis has evolved to produce fungal suppressors of RNA silencing a

221 alls short of considering how culture itself evolves to produce indigenous psychologies fitted to par

222 in turn supports the idea that hosts readily evolve to promote host-beneficial defensive microbiomes.

223 d social agency between parents and infants, evolved to promote infant survival.

224 ltiple strategies that the immune system has evolved to promote the separation between symbiotic micr

225 to aerobic environment, cellular mechanisms evolved to protect against iron-mediated oxidative damag

226 te-driven priming of mucus barriers may have evolved to protect from subsequent infections with multi

227 sults suggest that antibody-accessible loops evolved to protect key extracellular regions of LptD, bu

228 ss of cell fitness, cellular safeguards have evolved to protect the genome, especially during sensiti

229 ogether, these findings suggest that SOC has evolved to protect the hypertrophic chondrocytes from th

230 eins; their extreme kinetic stability likely evolved to protect the lens from the initiation of aggre

231 sistance represent two strategies that hosts evolved to protect themselves from pathogens.

232 We propose that this mechanism may have evolved to provide protection from potentially harmful t

233 The wood from which it comes has evolved to provide structural support for the tree and t

234 example of plasticity of regulatory networks evolving to provide an adapted response in each individu

235 The rupture evolved to pulse-like as it propagated at a relatively s

236 concentrations of anti-rubella IgG have also evolved to rapid, high-throughput binding assays, which

237 Bamboo grasses have evolved to rapidly deposit this combination of thick and

238 tic environment in which preneoplastic cells evolve to reach their full tumorigenic potential.

239 Visual systems have evolved to recognize and extract features from complex s

240 pha-d-manno-heptose) suggests the lectin has evolved to recognize distinct bacterial species.

241 G protein-coupled receptors (GPCRs) have evolved to recognize incredibly diverse extracellular li

242 progress that the theoretical descriptor has evolved to reconcile the observed differences between ex

243 ork has survived the end of the Cold War and evolved to reflect the new geopolitical context.

244 l unclear how their morphological structures evolve to regulate their functionality.

245 rom ancient gene duplications of RAD51, have evolved to regulate and promote RAD51 function.

246 We propose that the NRPD1 N-terminus motif evolved to regulate Pol IV function in genome surveillan

247 ndings, we propose that prion-like LCRs have evolved to regulate protein phase behavior and to protec

248 Therefore, deuterosomes may have evolved to relieve, rather than supplement, the centriol

249 Several pathways have evolved to repair these cytotoxic lesions by rejoining b

250 This suggests that KSHV has evolved to replicate independently of the activity of AP

251 y target 15 EBV promoters that have uniquely evolved to require XPB for activity, providing an additi

252 ry is an evolutionary process by which weeds evolve to resemble domesticated crop plants and is thoug

253 that some A. varius populations have rapidly evolved to resist or tolerate Bd infection.

254 taxa, and several high-altitude natives have evolved to resist the depressive effects of hypoxia on V

255 h as immunological responses might have thus evolved to respond accordingly to dietary surplus and de

256 ts cognition is that signaling pathways that evolved to respond adaptively to food scarcity are relat

257 scriptional regulators that prokaryotes have evolved to respond to environmental challenges.

258 itch may represent an ancient mechanism that evolved to restrict genetic recombination during sexual

259 ame, our understanding of adipose tissue has evolved to reveal a complex structure with distinct type

260 ns are evolutionary puzzles: how do proteins evolve to satisfy multiple functional constraints?

261 rily by ADP-glucose pyrophosphorylase, which evolved to satisfy metabolic requirements of a particula

262 Severe congenital neutropenia (SCN) evolves to secondary myelodysplastic syndrome (sMDS) and

263 jockey family retrotransposons may actually evolve to "selfishly" overreplicate in the genomes that

264 allosteric transcription factors (aTFs) have evolved to sense and respond sensitively to a variety of

265 vely rare in the intestinal epithelium, have evolved to sense and respond to these commensal microbes

266 rs that can move on tracks within cells have evolved to serve this role.

267 gnized as emotional expressions because they evolved to signal emotional information in situations th

268 ed faculties, evolved for social bonding, or evolved to signal mate quality - are incomplete or wrong

269 Yet, because pain evolved to signal threats to survival, it should be mala

270 s spread by a few mosquito species that have evolved to specialize in biting humans, yet the precise

271 nd suggest that various GNAT toxins may have evolved to specificaly target other if not all individua

272 ay for them grows, conservation will have to evolve to stay relevant in the age global change-induced

273 ular and anatomical features synergistically evolve to suit an animal's environmental context.

274 Tree architecture has evolved to support a top-heavy above-ground biomass, but

275 lecular machinery for dopamine secretion has evolved to support fast and slow signaling modes, with f

276 ombination and nuclear restorer alleles that evolve to suppress them.

277 To understand how different DNs evolve to surround core amyloid plaques, we monitored th

278 that this non-coding-RNA-dependent mechanism evolved to survey the microbial environment of the worm,

279 t is well-understood that many bacteria have evolved to survive catastrophic events using a variety o

280 Archaea have evolved to survive in some of the most extreme environme

281 and plant species, efficient strategies have evolved to synthesize, construct and integrate composite

282 opulations, and if bacterial collectives can evolve to take up DNA despite selfish elements.

283 can suggest why (i) mutations are likely to evolve to target it; (ii) inhibitors can straightforward

284 The discovery that one bacterial effector evolved to target ATG16L1's engagement in intracellular

285 appa(2)-cis-P,P-[xant(P(i)Pr(2))(2)]}, which evolve to the dihydride-silyl derivatives IrH(2)(SiR(3))

286 ologies, and next-generation sequencing have evolved to the point where more than two-thirds of conge

287 nding of the unique solutions Plasmodium has evolved to these challenges and discuss the remaining qu

288 Molecular motors have evolved to transduce chemical energy from ATP into mecha

289 ost sulfite reductase suggest that phage Fds evolved to transfer electrons to cyanobacterially encode

290 How Pooideae evolved to transition from tropical to temperate biomes

291 ll surface; hence, diverse secretion systems evolved to transport the hydrophilic molecules to their

292 NCE Protein shells of viruses (capsids) have evolved to undergo specific changes to ensure the timely

293 comprehensive examples of species adaptively evolving to urbanization.

294 bility with the translation apparatus, which evolved to use alpha-L-amino acids.

295 aracoccus, Pseudomonas, and Alcaligenes have evolved to use DMF as a sole carbon and nitrogen source

296 Why CoV evolved to use peptidases as their receptors is unknown,

297 racteristics and hearing sensitivity have co-evolved to utilise higher frequencies in forest environm

298 stability, and both DNA and RNA viruses have evolved to utilize epitranscriptomic modifications as a

299 , suggests that Mononegavirales have broadly evolved to utilize LLPS as a common strategy to assemble

300 s, proteins, and other biomolecules and have evolved to withstand large amounts of physical force and