ライフサイエンスコーパス: wild

1 meerkats (Suricata suricatta) living in the wild.

2 and there is currently little data from the wild.

3 ding infections may be ancient, preserved in wild Agaricus populations, which act as reservoirs for s

4 l samples obtained from 11 types of animals (wild, agricultural, and domesticated) and treated efflue

5 cated allele causes later flowering than the wild allele under short day and exhibits a signature of

6 erentially expressed genes between whorls in wild and cultivated Camellia.

7 We estimated that our wild and cultivated grape samples diverged approximately

8 ates, cause disease in both in humans and in wild and domesticated animals, and are being engineered

9 isease in humans, but can be asymptomatic in wild animals.

10 to silks from domesticated (Bombyx mori) and wild (Antheraea mylitta) silkworms, a variety of previou

11 Similar effects during the mating season in wild Arctic foxes may affect mating behavior and reprodu

12 e is variability for circadian traits in the wild barley lines.

13 We tested poultry, wild bird, and environmental samples from case patient h

14 North American wild birds are an important reservoir of influenza A vir

15 uses of subtypes H5 and H7 into poultry from wild birds have the potential to mutate to highly pathog

16 mplex mixtures has not been characterized in wild birds.

17 The invasive potential of the wild boar therefore probably lies on the reproductive, d

18 ly focus on livestock, but must also include wild boar.

19 apa-B, the bonobo ortholog of HLA-B, for six wild bonobo populations.

20 Microbiome profiling of wild-caught sand flies will be of great help in the inve

21 re) and to the origin of introduced species (wild-caught species show higher invasiveness than captiv

22 ed and silenced, while COL2D is repressed in wild cottons but highly expressed due to methylation los

23 n (Oncorhynchus kisutch) with those of their wild counterparts in two geographically distant rivers.

24 ng immigration in a habituated population of wild dwarf mongooses (Helogale parvula) [5]; sentinels (

25 nd consequences of variation in body mass of wild female Svalbard reindeer (Rangifer tarandus platyrh

26 ding the importance of proper preparation of wild game prior to ingestion is warranted.

27 transmission of human respiratory viruses to wild great apes, causing high morbidity and, occasionall

28 Many wild growing species present high beta-glucan contents,

29 Here, we show that wild-living bonobos are endemically Plasmodium infected

30 Strategies to sustainably manage wild meat hunting in both protected and unprotected trop

31 -site application for the tissue analysis of wild muskellunge.

32 rmance monitoring paid off, as the number of wild poliovirus (WPV) cases detected in Nigeria were red

33 ncertainty about whether or not all types of wild polioviruses had been eradicated, but it might incr

34 Alternatively, wild pollinators could recognize an exclusive signature

35 ed for animal pollination, understanding how wild pollinators utilize resources across environments c

36 of the toolkit for animal model analyses of wild population data sets.

37 Using replicate wild populations with differing levels of sexually antag

38 observe the effects of natural selection in wild populations.

39 The prehistory of wild potato use, leading to its domestication and divers

40 t glacial Ca limits vegetative growth in the wild progenitors of both C3 and C4 founder crops.

41 e and body mass throughout the full cycle in wild recaptured shrews (Sorex araneus).

42 of 147 cotton accessions, including diverse wild relatives, landraces, and modern cultivars, and con

43 y domesticated beans of adaptive traits from wild relatives.

44 large and complex genomes of crops and their wild relatives.

45 has been paid to the origins and history of wild rice itself.

46 We argue that wild rice populations should be considered a hybrid swar

47 dmium, zinc, manganese and iron in white and wild rice samples.

48 In line with this hypothesis, many presumed wild rice varieties show remnants of the effects of sele

49 generally assumed that populations of living wild rice, O. rufipogon, are descendants of the ancestra

50 ork to individual-based long-term data for a wild rodent population and show that despite a positive

51 (ISAV), spreads easily throughout farmed and wild salmonids, constituting a significant economic burd

52 Wild silk from Antheraea mylitta meets these demands to

53 s induced to high levels during long days in wild species, but not in cultivated tomato because of ci

54 s encompassing breeding lines, landraces and wild species, we characterize genome-wide variation.

55 of experimental studies, now bridging to the wild through field experiments.

56 tabolomics along with functional genomics in wild tomato unreveal potential role of steroidal glyco-a

57 er binding to CNS synaptosomes isolated from wild type (wt) mice treated with NIR light was significa

58 sue) were found in LanCL1 knock-out, TKO and wild type (WT) mouse brains, suggesting that LanCL prote

59 GFR was assessed in conscious TRPC6 wild type and knockout mice, and in anesthetized rats wi

60 carefully selected genes with their drugs in wild type and mutant forms.

61 some EBV-associated cancers, p53 tends to be wild type and overly expressed; however, the effects of

62 displays a hyperactive phenotype relative to wild type and overproduces a number of compound families

63 itro, however, IFN-gamma production by naive wild type and tristetraprolin-deficient CD8(+) T-cells i

64 delayed germination as compared to grains of wild type barley.

65 Overexpression of FoxO in wild type cardiomyocytes induced murf1 expression and ca

66 n cryo electron microscopy (cryo-EM) maps of wild type CPMV containing RNA-2, and of naturally-formed

67 genotype followed by introgression into the wild type does not result in the same level of silencing

68 cid (DHA), a representative omega-3 PUFA, in wild type hairless mice induced expression of the Nrf2 t

69 tions of inflammatory cytokines, compared to wild type hearts.

70 have led to a SLO3 variant that differs from wild type in both pH and intracellular Ca(2+) sensitivit

71 observed in cortical pyramidal neurons from wild type mice was conspicuously reduced in TASK(-/-) mi

72 o the vasculature or diluted into blood from wild type mice.

73 HA digestion in wild type NSC cultures or in the SGZ induces increased N

74 ation, and CD44-null as well as HA-disrupted wild type NSCs demonstrate delayed neuronal differentiat

75 Studies on NS1 wild type or mutant alone or in recombinant RSVs demonst

76 Accordingly, the activity of the wild type RUNX2 promoter was decreased upon methylation

77 icantly lower for SERT-DeltaN32 than that of wild type SERT and SERT-DeltaN22.

78 EVS evoked relaxation of wild type stomachs, but the predominant response of W/W(

79 cause the ohr mutant was more sensitive than wild type to 3-morpholinosydnonimine hydrochloride (SIN-

80 remarkably reduced compared with that of the wild type, however, the mRNA levels of the wild-type and

81 ed currents that inactivate more slowly than wild type, indicating that increased cation permeability

82 step in ethylene biosynthesis compared with wild type.

83 ut 10(-9.0) m produced the same effect as in wild type.

84 silencing as direct transformation into the wild type.

85 xpress mCherry, which distinguishes from the wild type.

86 ent (Nlrp3(-/-)) and NLRP3 inhibitor-treated wild-type (C57BL/6) mice.

87 igated the VtE-induced amelioration of DN in wild-type (DGKalpha(+/+)) and DGKalpha-deficient (DGKalp

88 Uremic wild-type (KL(fl/fl) ) and knockout (Prx1-Cre;KL(fl/fl)

89 plaque morphologies similar to those of the wild-type (WT) A24 Cruzeiro strain in BHK cells, and bot

90 Wild-type (WT) and B cell-deficient mice received ovalbu

91 Ear thickness of wild-type (wt) and Sucnr1-deficient (Sucnr1(-/-) ) mice,

92 Wild-type (WT) and TG mice received vehicle or BACE inhi

93 ssion of FOXO transcription factors in three wild-type (WT) and three HD induced-pluripotent stem cel

94 Nephrotoxic serum nephritis was induced in wild-type (WT) and ubiquitin-binding deficient ABIN1[D48

95 t close in response to darkness but exhibits wild-type (WT) behaviour when exposed to abscisic acid (

96 hrombosis model, we found that compared with wild-type (WT) control and nonhematopoietic DREAM knocko

97 ice exhibited enhanced mortality compared to wild-type (WT) controls, while mice lacking the necropto

98 s by RNA sequencing of ATXN2Q127 mice versus wild-type (WT) littermates.

99 es by an increase of 10-300 fold compared to wild-type (WT) merozoites.

100 time corresponding to peak LCN2 induction in wild-type (WT) mice injected with LPS, Lcn2(-/-) mice ch

101 b1)-deficient and FXII-deficient mice and in wild-type (WT) mice pretreated with a PKal inhibitor pri

102 adiponectin gene knockout (Adipoq(-/-) ) and wild-type (WT) mice were crossed to produce pregnant mou

103 ressure during rest and activity compared to wild-type (WT) mice, and smaller responses to chemorecep

104 In wild-type (WT) mice, LY2828360 (3 mg/kg per day i.p. x 1

105 When inoculated into naive wild-type (WT) mice, this persistently circulating CHIKV

106 Compared with the wild-type (WT) rat, Cyp3a1/2 expression was completely a

107 eratures above the conversion temperature of wild-type (wt) virions.

108 aptive immunity, and protection of mice from wild-type (WT) WNV infection.

109 rdial infarction (PMI) HF model evaluated in wild-type (wt-PMI) and Nod1(-/-) mice (Nod1(-/-)-PMI).

110 lammatory cytokines than those infected with wild-type 874391.

111 Patients and Methods Mutation analyses (wild-type [WT] and mutant) for TP53, KRAS, and EGFR were

112 gineered strain with a strain containing the wild-type ACT1 promoter.Genetic isolation of a genetical

113 ated by examining the effect of E6APC820A on wild-type activity and single-turnover pulse-chase kinet

114 sponse to ischemic stress that is similar to wild-type aged hearts (i.e., impaired ischemic AMPK acti

115 h FcRn-binding albumin variant compared with wild-type albumin.

116 To what extent the wild-type allele contributes to leukemogenesis is unclea

117 putative Wag31 target demonstrated that the wild-type allele was dominant and showed no synergy with

118 7) or a low ratio (0.05 to 0.7) of mutant to wild-type alleles (ITD [high] and ITD [low], respectivel

119 pha-synuclein overexpressing model harboring wild-type alleles of GBA, A53T-SNCA mouse model) were ex

120 llen and associated food allergies, a single wild-type allergen does not provide a complete solution.

121 Wild-type and cathepsin K knockout mice were rendered di

122 on Ca(2+) imaging in hippocampal area CA1 of wild-type and Df(16)A(+/-) mice, an animal model of 22q1

123 Wild-Type and dominant-negative-DISC1 (DN-DISC1) mice we

124 Comparative infection with wild-type and epithelial cell receptor-blind viruses dem

125 ing GCaMP6s, we found no differences between wild-type and Fmr1 KO mice in overall whisker-evoked act

126 IL-15 equally sustains wild-type and Il7ra(-/-) ILC survival in vitro and compe

127 Both wild-type and mutant ANO5 protein localize to the endopl

128 e wild type, however, the mRNA levels of the wild-type and mutant cells were comparable.

129 h-clamp to explore biophysical properties of wild-type and mutant KV 3.1 channels.

130 Viruses containing wild-type and mutant MN/10 or BJ/92 hemagglutinins (HAs)

131 n (Gfap(R236H)(/+)) (and thus expresses both wild-type and mutant protein).

132 essing no MECP2 (MECP2-KO), congenic pair of wild-type and mutant RTT patient-specific induced plurip

133 By combining wild-type and mutant subunits in various asymmetric conf

134 We transfected HEK293T cells with pyrin and wild-type and mutated WDR1 Mutant protein formed aggrega

135 ed Huh7 cell lines which ectopically express wild-type and NEDDylation-deficient HBx and found that N

136 thotopically injected breast cancer cells in wild-type and RAGE-knockout C57BL6 mice.

137 By analyzing activated murine wild-type and Rheb-deficient CD4(+) T cells, as well as

138 Furthermore, SSRIs protected both wild-type and SERT knockout mice from behavioral despair

139 and proteomes of primary mouse B cells from wild-type and STAT6-deficient mice cultured for 4 d in t

140 o infection of gastric epithelial cells with wild-type and VacA-deficient H. pylori strains, treatmen

141 e immunity against subsequent infection with wild-type bacteria.

142 ells in the lung and draining lymph nodes in wild-type BALB/c mice after RSV infection.

143 it was suboptimal compared with that seen in wild-type bone marrow (BM)-transplanted OS mice in perip

144 elease, was detected during acute hypoxia in wild-type but not Cox4i2(-/-) PASMCs.

145 embryonic fibroblasts by reconstitution with wild-type but not mutant FKBP65 that lacks intact PPIase

146 In isolated wild-type cardiomyocytes, Cx43 protein content decreased

147 ffer between tumour samples from variant and wild-type carriers.

148 fficient and less deleterious alternative to wild-type Cas9 for gene-knockout studies.

149 acterize the magnetosome arrangement in both wild-type cells and DeltamamJ mutants, which exhibit dif

150 Wild-type cells are required for the active elimination

151 athways in the stem cell compartment and how wild-type cells limit the proliferation of mutant cells

152 ial drug susceptibilities of KRAS mutant and wild-type cells, and predict relapse based on increased

153 n2 is constantly localized to the nucleus in wild-type cells.

154 Rgamma expression in knock-out cells than in wild-type cells.

155 SMARCA4/BRG1 mutant but not of SMARCA4/BRG1 wild-type cells.

156 gnificantly less MHCII, and grew faster than wild-type clones in s.c. and orthotopic xenograft models

157 cally significant changes between pallid and wild-type control.

158 central nervous system, and their respective wild-type controls to photothrombotic stroke.

159 Compared with wild-type controls, HAT-L4-deficient newborn mice had gr

160 female late-stage R6/2 mice and age-matched wild-type controls.

161 ectrophoresis from A36V mutant than from the wild-type core protein.

162 NF or TNF receptors are outcompeted by their wild-type counterpart.

163 ells proliferate more efficiently than their wild-type counterparts in response to BCR cross-linking.

164 unction in NOD2(-/-) CVB3 mice compared with wild-type CVB3 mice.

165 mice induced a severe myocarditis similar to wild-type CVB3 mice.

166 Mice harboring wild-type Cyp24a1 (BVE(Cyp24a1-wt)) developed PTC at 5 w

167 C1-64 on the plasma membrane distribution of wild-type DAT and two non-functional DAT mutants, R60A a

168 F conformation, reduced the concentration of wild-type DAT in filopodia.

169 pression and activity of TACE were lower, in wild-type DCs (wtDCs) than in TNF knockout (TNFko) DCs.

170 Although virtually all AMLs with wild-type DNMT3A displayed CpG island hypermethylation,

171 cortical patches that rapidly disassemble in wild-type embryos.

172 d ligand binding affinity, compared with the wild-type enzyme, demonstrating that substrate binding t

173 TM is sufficient to promote DNA synthesis in wild-type fat body cells.

174 solubility-enhancing mutations that maintain wild-type fitness with an accuracy of 90%.

175 ested primary FLT3-ITD NK-AML in contrast to wild-type FLT3 NK-AML.

176 s that are caused by these perturbations the wild-type function of genes can be elucidated.

177 Remarkably, upon restoration of near wild-type FXN levels, we observed significant recovery o

178 % increase in fusion compared to that of the wild-type gBcyt while arginine substitutions had wild-ty

179 ress this deficit, we generated samples of a wild-type GPCR (A2AR) that are deuterated apart from (1)

180 ently detected by antibodies elicited by the wild-type HA from viruses selected as the vaccine candid

181 is the first detailed case report suggesting wild-type HIV-1 infection despite good adherence, eviden

182 Q mutations have serum half-lives as long as wild-type human IgG1.

183 Importantly, secretion of wild-type human SOD1 and the ALS-linked mutant in human

184 metabolic alterations in glioblastomas with wild-type IDH are poorly understood.

185 n and cynomolgus FcgammaRs compared with the wild-type IgG1 antibody.

186 As compared with wild-type infected mice, CD151-null infected mice exhibi

187 hree orders of magnitude for the full-length wild-type KcsA, a pH-gated bacterial channel, in membran

188 yzing the expression of pRGA::GFP-RGA in the wild-type Landsberg erecta background, we demonstrate th

189 in animals with striatopallidal knock-out to wild-type levels, suggesting a dependence on adenosine r

190 While wild-type lint fiber trichome cells contained long longi

191 ted to the Golgi and activated by Rab29 than wild-type LRRK2.

192 ion, and cells lacking NRP2 are deficient in wild-type LUJV infection.

193 In wild-type mammals, approximately 60% of cells have recom

194 Lentiviral complementation with wild-type MDH2 cDNA restored MDH2 levels and mitochondri

195 Conversely, overexpression of wild-type METTL3, but not of a catalytically inactive fo

196 owed less neurological deficit compared with wild-type mice (n=6).

197 amin D) each increased serum FGF23 levels in wild-type mice and in mice with global deficiency of the

198 were lower in Brd4 heterozygous mice than in wild-type mice at 21 days after birth.

199 he differential CT responses in IgA(-/-) and wild-type mice disappeared after intestinal microbiota e

200 In wild-type mice fed an unsupplemented ad libitum diet, ag

201 Wild-type mice initially learnt, but with prolonged trai

202 eosinophils from fungal allergen-challenged wild-type mice maintain a distinct cytokine profile, and

203 Moreover, overexpression of DLST in wild-type mice protected against cardiac hypertrophy and

204 Wild-type mice showed increased myocilin expression in t

205 Wild-type mice subjected to IL-17A neutralization and IL

206 not observed in Ig-treated Rag1(-/-) mice or wild-type mice treated with anti-type I IFNR alone.

207 ly, both the renal injury and dysfunction in wild-type mice undergoing iAKI is significantly ameliora

208 knock-out and heterozygous mice compared to wild-type mice using RNA-seq; and (iii) morphological an

209 nia, we found that goal-oriented learning in wild-type mice was supported by stable spatial maps and

210 toward either M1 or M2 macrophages in vivo, wild-type mice were injected with gamma interferon (IFN-

211 [KO]), iNOS-deficient (iNOS KO), and C57BL/6 wild-type mice were orally infected with A. actinomycete

212 was significantly reduced after treatment of wild-type mice with CSP, and uPA-deficient mice were unr

213 mage at doses that caused minimal effects in wild-type mice, and adoptive transfer of gammadelta T ce

214 lanar cell polarity genes Vangl2 and Ptk7 In wild-type mice, collagen-fibril bundles appear within a

215 Indeed, compared with wild-type mice, MLKL knockout mice displayed more severe

216 increased serum glycolate concentrations in wild-type mice, rats, and nonhuman primates.

217 expression caused no significant changes in wild-type mice, suggesting that Hjv is not a limiting fa

218 Compared with wild-type mice, the cell surface levels of Cav1.2 in the

219 V-Cre, and in NBQX- and rapamycin-pretreated wild-type mice, these compounds blocking alpha-amino-3-h

220 reater percentage of affected limbs than the wild-type mice.

221 ttractant CXCL1 in their lungs compared with wild-type mice.

222 rse was significantly attenuated compared to wild-type mice.

223 oduction and sperm motility in knock-out and wild-type mice.

224 ate sodium for 7 days and were compared with wild-type mice.

225 e more resistant to bacterial infection than wild-type mice.

226 express low NR2E3 relative to the livers of wild-type mice.

227 ferent in Ormdl3(Delta2-3/Delta2-3)/CC10 and wild-type mice.

228 ofoundly reduced rapid eye movement sleep in wild-type mice; these effects were eliminated in Taar1 k

229 By using both IL-10-deficient and wild-type mothers, we showed that both inoculum and geno

230 Given that wild-type mouse myosin VIIa is a slow, high-duty ratio,

231 study, Calhm1 knockout, Panx1 knockout, and wild-type mouse nasal septal epithelial cells were grown

232 levels of MT1-MMP were engineered to express wild-type MT1-MMP, a phosphomimetic mutant (T567E), or a

233 doplasmic reticulum (ER) stress in both KRAS wild-type normal pancreas cells, as well as in KRAS muta

234 decreased nucleosome interactions similar to wild-type nucleosome arrays.

235 and postnatal n-6/n-3 PUFA ratio exposure in wild-type offspring under standard maternal dietary fat

236 rated transgenic zebrafish models expressing wild-type or A152T-tau, where A152T caused neurodegenera

237 Expression of the wild-type or edited allele of AMD1 but not un-editable a

238 Primary cultures of hepatocytes derived from wild-type or hepatocyte-specific furin, PC5/6, or comple

239 efects were rescued upon the reexpression of wild-type or kinase-dead CDK19.

240 Indeed, BCL6 represses the expression of wild-type p53 and its target genes in GBM cells.

241 a conditional AP2-G knockdown line and NF54 wild-type parasites at multiple stages of development, w

242 rization in Cox4i2(-/-) PASMCs compared with wild-type PASMCs, which could be normalized by the appli

243 predicted resistance to ibrutinib with only wild-type patients responding (P = .002).

244 Ectopic expression of wild-type Pdcd4 and Pdcd4(157-469), a deletion mutant th

245 Interestingly, overexpression of the wild-type PDGFRA was even more potent in promoting trans

246 ause 78% of human MPNSTs have expression of wild-type PDGFRA, whereas only 5% harbor activating muta

247 gain and biochemical analyses comparable to wild-type pigs.

248 getative SAM In agreement, SP-overexpressing wild-type plants exhibited precocious doming of vegetati

249 Overexpressing PEX1 in wild-type plants impaired growth, suggesting that excess

250 in higher endogenous iron concentration than wild-type plants in both brown and white grains.

251 y are morphologically indistinguishable from wild-type plants.

252 e NTD equilibrium can be shifted back to its wild-type position by mutation at a secondary site with

253 = 533 nm) absorption maxima relative to the wild-type protein (lambdamax = 527 nm).

254 f fibroblasts with a lentivirus encoding the wild-type protein partially rescued the deficiency of GP

255 nts decreased cell proliferation relative to wild-type protein.

256 econstitution of PTEN-null cells with either wild-type PTEN or a catalytically dead mutant stabilizes

257 s similar to those for animals infected with wild-type R. typhi and develop comparable pathology and

258 We show that wild-type RAS amplification increases receptor tyrosine

259 orporation into DHFR and IkappaB-alpha using wild-type ribosomes, and the elaborated proteins could s

260 GreA factors activate RNA cleavage by wild-type RNAPs to similar levels.

261 ed more efficiently by IFN-beta than was the wild-type S. aureus, and immunoblotting showed that IFN-

262 ption factors, particularly in SDHD promoter wild-type samples.

263 We found that injection of fluorescent wild-type SOD1 (wt SOD1YFP) or monomeric mutant G85R SOD

264 acteria-specific (P25 CD4(+) TCR transgenic) wild-type spleen cells into sanroqueRag1(-/-) mice actua

265 rated in different genetic backgrounds (e.g. wild-type strain versus knockout strain).

266 rt succumbed to infection with a more recent wild-type strain, indicating that immune responses to th

267 on increased cytarabine resistance of a KRAS wild-type subclone.

268 Wild-type T. denticola and the purified PF triggered act

269 Whereas wild-type Teff cells upregulated Mdr1 in the ileum, thos

270 143K were found to be more thermostable than wild-type TK.

271 control mice (NT) and in mice carrying human wild-type torsinA (hWT) or mutant torsinA (hMT).

272 ly, this mutation was able to sustain 15% of wild-type transport activity, when the catalytic glutama

273 M) are known to be more aggressive than KRAS wild-type tumors.

274 tion at a secondary site with restoration of wild-type two-pronged binding of the UBXD1 adaptor prote

275 antly in its deprotonated form when bound to wild-type VAO, but predominantly in its protonated form

276 ors display a different behavior against the wild-type versus V27A mutant A/M2 channels, and (ii) the

277 growth of the escape mutant viruses with the wild-type virus revealed that some escape mutants posses

278 346 mutant maintains similar antigenicity to wild-type virus, opening the possibility for its use as

279 K166Q showed superior growth to that of the wild-type virus.

280 retained fitness during coinfection with the wild-type virus.

281 Comparisons of cells from wild-type vs. AE3(-/-) mice show that AE3 (present in hi

282 e, the high pelleting temperatures challenge wild-type xylanases.

283 Third, treatment of wild-type yeast cells with E9591 or LMT generated cellul

284 ntrations of K(+) and Na(+) , as compared to wild-type Z. xanthoxylum grown under 50 mm NaCl.

285 one in one centre, assessed plasmid VRC5283 (wild-type Zika virus).

286 ted isolated intestinal tissue from C57BL/6 (wild-type) and Cftr(-/-) mice in Ussing chambers and mea

287 more physiological excitation rates than the wild-type, and the generation of early-after-depolarisat

288 Complementation with wild-type, but not mutagenized, C1qbp restored OXPHOS pr

289 ted colonic HbetaD1 and HbetaD2 release from wild-type, but not Takeda GPCR 5(-/-), mice.

290 grik1-2 grik2-1) that grows similarly to the wild-type, enabling us to evaluate the function of GRIKs

291 (line M20) injected in the hippocampus with wild-type, H50Q, G51D or A53E alphaS fibrils displayed i

292 afish embryos overexpressing mutant, but not wild-type, PDGFRA, suggesting a mechanism through which

293 -type gBcyt while arginine substitutions had wild-type-like fusion levels in an in vitro gB/gH-gL cel

294 ed by comparing melanoma cells infected with wild-type-like VZV or hyperfusogenic mutants.

295 and for the intermediate risk genotype NPM1 wild-type/FLT3 without internal-tandem duplications (EFS

296 study of both cancer-bearing mouse models in wild types and their corresponding control types, emphas

297 t when the fitness values of the mutants and wild types are anti-correlated across environments.

298 r brief bouts of activity and sleep than the wild-types.

299 in reproductive performance is ubiquitous in wild vertebrate populations and has important consequenc

300 esearch has recently shown that macaques and wild vervet monkeys respond strongly to partially expose