ライフサイエンスコーパス: the synthesis of

1 The key step in the synthesis of 1 and 2 is the reaction of the dianion

2 Three routes were devised for the synthesis of 1 at the various stages of the program.

3 e, this study provides a synthetic route for the synthesis of 1,20S(OH)2D3 using the intermediate 1al

4 is is a simple and efficient methodology for the synthesis of 1,3,5-triazines in good to excellent yi

5 For the synthesis of 1,3-disubstituted allenes, the propyne

6 A new approach for the synthesis of 1,4-dicarbonyl compounds is reported.

7 We herein report the synthesis of 12 variations of the PLA-poly(ethylene

8 HA delays the onset of seizures by promoting the synthesis of 17beta-estradiol in the brain.

9 echanism, was translated into a protocol for the synthesis of (18)F-radiolabeled aliphatic CF3-contai

10 ne step formal [3+2]-annulation protocol for the synthesis of 2,3-disubstituted indolines is describe

11 fucosyl (FucN3) donors, valuable synthons in the synthesis of 2-acetamido-2-deoxyfucose (FucNAc) cont

12 The synthesis of 2-AP is discussed alongside the attempt

13 A mild method for the synthesis of 2-quinolinones via hydroarylation of N-

14 We report on the synthesis of [2]rotaxanes driven by stabilization of

15 of the MBH bromides has been demonstrated in the synthesis of 3,4-dihydro-2H-pyrido[1,2-a]pyrimidines

16 A method for the synthesis of 3-fluoroindoles from N-arylamines subst

17 Methodology has been developed for the synthesis of 3-propanaldehydes through a five-step p

18 ed at an isolated rate of 1.2 mg min(-1) for the synthesis of 4-nitrobenzylaldehyde from 4-nitrobenzy

19 rimidine as a detachable directing group for the synthesis of 7-hydroxyindole.

20 We report here the synthesis of 7-phenoxy-substituted 3,4-dihydro-2H-1,

21 detected an early 2.8 kb M25 mRNA directing the synthesis of a 105 kDa M25 protein, and confirmed th

22 the exsA mRNA and Sr0161 leads to a block in the synthesis of a component of the T3SS apparatus and a

23 Here, we report the synthesis of a down-conversion luminescent rare-eart

24 eloped methodology has been illustrated with the synthesis of a family of bicyclic fluorinated 1,3-am

25 species by channeling these oxidants toward the synthesis of a functionally equivalent binuclear Mn(

26 Here, we report an enzyme-based method for the synthesis of a library of 15 different CS oligosacch

27 unprecedent use of the protecting groups in the synthesis of a naturally occurring compound.

28 Here we report the synthesis of a new carbocyclic mechanism-based coval

29 trand polymerase sometimes recycles to begin the synthesis of a new Okazaki fragment before finishing

30 Here, we report the synthesis of a new water-soluble ratiometric Cu(II)

31 eting decapeptide WxEAAYQkFL, here we report the synthesis of a novel cyclic peptide analogue cyclic

32 Here we report the synthesis of a panel of 2-aryl-5-carboxytetrazole-ly

33 lable solvothermal technique is reported for the synthesis of a photocatalytic composite material con

34 ere an optimal feedback strategy to regulate the synthesis of a protein to ensure that an event will

35 The synthesis of a pyrene-tethered TEMPO derivative (TEM

36 yl, R = NC(t)Bu2) for kinetic stabilization, the synthesis of a rare terminal Fe(IV) nitride complex

37 We report here the synthesis of a robust and porous metal-organic frame

38 Herein, we report the synthesis of a series of 14 interpenetrated Zr and H

39 Here, the synthesis of a set of oligorhamnan fragments is repo

40 e present the one-pot two-step procedure for the synthesis of a set of pyrazolo[3,4-d]pyrimidine prod

41 The synthesis of a small set of beta-lactams containing

42 Once assembled, the synthesis of a sulfonamide by reacting 4-chlorobenze

43 The synthesis of a third class of unnatural amino acids,

44 alpha-Imino esters are useful precursors for the synthesis of a variety of types of natural and unnat

45 Here we report a general strategy for the synthesis of a wide range of highly fluorinated biph

46 new multicomponent procedure was applied to the synthesis of (a)chiral bulky unsymmetrical unsaturat

47 ent addition could find broad application in the synthesis of academically and industrially important

48 s, and a key macrocyclic intermediate toward the synthesis of acerogenin A.

49 The synthesis of acetyl-CoA depends primarily on the PDH

50 ein and mRNA regulation of C' components and the synthesis of active C' 3a (C3a) in normal primary hu

51 ing a new insight into possible pathways for the synthesis of active functional microreactors in the

52 e synthesis provides a flexible approach for the synthesis of agrochemicals and pharmaceuticals, as d

53 , no investigations have been performed into the synthesis of alkaloids containing this structure.

54 We describe herein the synthesis of all C13/14 diastereomers of this spiro

55 e take advantage of a recent breakthrough in the synthesis of alpha,beta-unfunctionalised 4,4-difluor

56 access to boron chemotypes, we report herein the synthesis of alpha- and beta-aminocyano(MIDA)boronat

57 lactic acid bacteria use sucrose to catalyze the synthesis of alpha-glucans with different linkage co

58 Finally, the synthesis of ammonium-based oriented calix[2]rotaxan

59 transformation of the cyanide group allowed the synthesis of an advance intermediate of correspondin

60 using a modified Julia reaction then enabled the synthesis of an advanced synthetic intermediate cont

61 In particular, the synthesis of an ester-functionalised Ar-BIAN ligand

62 A straightforward and general method for the synthesis of annulated thiophene, dibenzothiophene,

63 isothiocyanyl alanine ((NCS)Ala = Ita), for the synthesis of another class of unnatural amino acids,

64 hemistry on human tissue specimens justified the synthesis of antibody-functionalized drug delivery v

65 and functional group transformation complete the synthesis of aphanorphine and its analogue over eigh

66 se future applications, a key requirement is the synthesis of appropriate materials in the form of th

67 The synthesis of aptamers by chemical approaches opens u

68 ge approach has been successfully applied to the synthesis of arylborane molecules 4a-c, oligomers 8a

69 enantioselective organocatalytic method for the synthesis of atropisomeric biaryls by a cation-direc

70 We demonstrate the synthesis of Au nanostar dimers with tunable interpa

71 We could extend the methodology for the synthesis of benzothieno[3,2-b]indoles starting from

72 extensively investigated as nucleophiles for the synthesis of beta-substituted carbonyl derivatives.

73 with aryl pinacol boronic esters, leading to the synthesis of biaryl derivatives in good yields.

74 major challenge, especially when it comes to the synthesis of bioactive molecules.

75 rovides a simple, metal-free alternative for the synthesis of biologically interesting arylated heter

76 This is a good alternative for the synthesis of biologically relevant glycoconjugates.

77 ation of an oscillatory chemical reaction to the synthesis of block copolymers.

78 Progress in the synthesis of boron nanostructures suggests that the

79 and intersected an established precursor in the synthesis of brevianamide B.

80 The synthesis of bulk crystals, thin films and nanostruc

81 by dehydrogenative aromatization, completed the synthesis of calothrixin B.

82 ve appeared as attractive building units for the synthesis of carbohydrate metal-organic frameworks (

83 studies in olefin metathesis have focused on the synthesis of catalysts that can overcome the inheren

84 o l-DOPA, which is the rate-limiting step in the synthesis of catecholamines, such as dopamine, in do

85 By combining experimental results on the synthesis of CdSe nanoplatelets with theory predicti

86 nctioned in growth-relevant processes and in the synthesis of cell wall-building components such as a

87 s have revealed some 30 proteins involved in the synthesis of cellular [2Fe-2S] and [4Fe-4S] clusters

88 The synthesis of ceramic materials combining high porosi

89 n constitutes a straightforward protocol for the synthesis of certain phenyl-substituted carboxylic a

90 cGAS catalyzes the synthesis of cGAMP, which functions as a second mess

91 , this reactivity has not been leveraged for the synthesis of challenging molecules.

92 ion is one of the most important methods for the synthesis of chiral amines.

93 eta-borylated amides are useful synthons for the synthesis of chiral beta-hydroxylated, beta-fluorina

94 The dominant method for the synthesis of chlorins has entailed the derivatizatio

95 The synthesis of cholesterol and fatty acids (FA) in the

96 these geometrically defined enamides toward the synthesis of cis vicinal amino alcohols and tetrasub

97 ia photochemistry on semiconductor minerals, the synthesis of clays was demonstrated at low temperatu

98 rol of the autocatalytic process involved in the synthesis of colloidal metal nanocrystals.

99 Despite its universal role in the synthesis of colloidal nanocrystals, it is still poo

100 roved through evolution, ultimately enabling the synthesis of complete DNA genomes.

101 t industries ranging from micropatterning to the synthesis of complex biomaterials and sequence-contr

102 quaternary centers is a common challenge in the synthesis of complex materials and natural products.

103 The synthesis of complex oligosaccharides is often hinde

104 portant driving force behind the progress in the synthesis of complex oligosaccharides.

105 The synthesis of complex protein-based bioconjugates has

106 matic and enzymatic cascade reactions enable the synthesis of complex stereocomplementary 1,3,4-trisu

107 antioenriched structures that can be used in the synthesis of complex target molecules.

108 ctivity and regioselectivity were studied in the synthesis of conjugated linoleic acid (CLA) partial

109 The synthesis of conjugated polymers from direct (hetero

110 e formation of desmoplastic reaction through the synthesis of connective tissue and extracellular mat

111 Here we present the synthesis of crystalline K2Pentacene and K2Picene by

112 ia a polycondensation approach, which allows the synthesis of CTFs under mild conditions from a wide

113 y functional theory calculations reveal that the synthesis of Cu(I) halide double perovskites may ins

114 development of new routes to organoboranes, the synthesis of current candidates is generally limited

115 Herein, we report the synthesis of cyclic-oligophenylene-based nanopropell

116 on of PE facilitates the turnover of SAM for the synthesis of cysteine and glutathione through transs

117 than did SbCCR1, which could imply a role in the synthesis of defense-related lignin.

118 e convergent-divergent iterative methods for the synthesis of dendrimers and dendrons containing ethy

119 ultisegment coupling cascade is designed for the synthesis of densely substituted 4-alkoxy quinolines

120 An assembly line strategy for the synthesis of deoxypolypropionates has already been d

121 To improve on 1, we report the synthesis of dihydro-4-pyranone 2, dihydro-4-pyridon

122 the template coupled with opportunities for the synthesis of diversely functionalized heterocyles fr

123 aea, cis-PT is the first enzyme committed to the synthesis of dolichyl phosphate, an obligate lipid c

124 r the formation of similar invaginations for the synthesis of dsRNA precursors of highly abundant vir

125 thereof may be promising building blocks for the synthesis of electron transport materials.

126 olution process offers a general approach to the synthesis of enantioenriched atropisomeric materials

127 i-responsive "smart" hydrogels, here we show the synthesis of entirely protein-based photoresponsive

128 observed racemization, which occurred during the synthesis of flavone-amino acid hybrids, was success

129 l reactions opens the possibility to control the synthesis of fluorescent quantum defects using light

130 The synthesis of four nitronyl nitroxide (NN) biradicals

131 ith hexanol and the best IL was selected for the synthesis of four other n-alkyl esters with differen

132 Here, we report the synthesis of four surfactant-directed mesoporous sil

133 d herein is an efficient synthetic route for the synthesis of functionalized 2-benzyl benzo[b]furans

134 reaction enables a new bond construction for the synthesis of functionalized furans.

135 actions serve as protected intermediates for the synthesis of functionalized glycosides.

136 The synthesis of glucose esters with palmitic acid, laur

137 n essential role in metabolism by catalyzing the synthesis of glutamine from glutamate and ammonia.

138 The synthesis of glycans and the sorting of proteins are

139 reby regulating cellular ceramide levels and the synthesis of glycosphingolipids (GSLs) in cellular m

140 then mixed with zinc acetate hexahydrate for the synthesis of graphene/zinc oxide nanocomposite by so

141 monstrating the utility of this approach for the synthesis of heterofunctional glycomacromolecules.

142 rostyrene and 5-oxohexanal was developed for the synthesis of hexahydro-6H-benzo[c]chromenones with f

143 l offers a direct and practical strategy for the synthesis of high-value allylic amine building block

144 A mild method for the synthesis of highly functionalized [3]-[6]dendralene

145 The method has been applied to the synthesis of highly functionalized amide-containing

146 Herein, a strategy for the synthesis of highly luminescent dual mode upconverti

147 ations in late biosynthetic steps leading to the synthesis of highly oxygenated triterpenoids.

148 straightforward protocol is demonstrated for the synthesis of highly substituted oxazoles from readil

149 The synthesis of homopropargylic alcohols under metal-fr

150 ng materials, enables a modular approach for the synthesis of imidazoles.

151 Imbalances in the synthesis of individual subunits result in orphans.

152 l 1,2-diamination of alkynes is achieved for the synthesis of indole-cyclic urea fused derivatives th

153 is method has a broad scope and enables both the synthesis of isolable silanes and the conversion of

154 s, and a number of carbonylative methods for the synthesis of ketones and esters, among others.

155 dergo a massive cell division event in which the synthesis of ladders of sporulation septa convert mu

156 The synthesis of LDs occurs with TAG-synthesizing enzyme

157 The synthesis of linear and (1 --> 6)-branched beta-(1 -

158 The synthesis of location must account for this frequenc

159 s) have been applied as ancillary ligands in the synthesis of luminescent gold(I) chalcogenide cluste

160 PSS), which catalyzes the committed step for the synthesis of major phospholipids via the CDP-diacylg

161 This work provides a general strategy for the synthesis of metal oxide nanocrystals, balancing the

162 procedure provides a controllable method for the synthesis of mMOF thin films (modified electrodes) c

163 We report the synthesis of modifiable NAM carbohydrate derivatives

164 lective iodine-mediated cascade reaction for the synthesis of multifunctional polyheterocyclic system

165 veloped in this work can also be extended to the synthesis of N-OMP/SiO2 nanocomposites, mesoporous S

166 plied to the thermoelectric field, including the synthesis of nanoparticles of suitable materials wit

167 thod developed here may also aid in modeling the synthesis of nanostructured materials through self-a

168 of this rearrangement and its application in the synthesis of natural and bioactive products.

169 rst time a general overview of approaches to the synthesis of natural product analogues is presented.

170 aminoacyl-tRNA-dependent enzymes involved in the synthesis of natural products.

171 n them that enables new or exotic processes (the synthesis of new functional materials and structures

172 Here, we report the synthesis of new indirubin 3'- and 5'-derivatives in

173 itically affects our natural environment and the synthesis of new materials.

174 as confinement reaction vessels to template the synthesis of new nanosheet structures.

175 analysis as a preliminary screening tool for the synthesis of new non-immunostimulatory nanocarriers.

176 Upregulation of TSP-4 does not require the synthesis of new protein, is not caused by decreased

177 We demonstrate the synthesis of NH3 from N2 and H2O at ambient conditio

178 nt-free induced self-assembly technology for the synthesis of nitrogen-doped ordered mesoporous polym

179 nsition metal sites (TMSs) in carbon enables the synthesis of noble-metal-free electrocatalysts for c

180 The obtained allyl alcohols were applied in the synthesis of nonracemic alpha-tertiary allylamines v

181 od opens a wide range of applications toward the synthesis of nonribosomal natural products and other

182 hesis and drug discovery are demonstrated in the synthesis of novel analogues of natural product (-)-

183 Herein, we demonstrate the synthesis of novel highly porous N-doped carbon nano

184 aterials, and is a significant technique for the synthesis of novel materials and fundamental researc

185 tial for naphthazarin as a building block in the synthesis of novel organic electronic materials.

186 molybdenum and the use of these reactions in the synthesis of novel organic substances.

187 CN) as the source of carbon and nitrogen for the synthesis of nucleotide, amino acid and lipid buildi

188 damental metabolic hub in cells that enables the synthesis of nucleotides and amino acids and epigene

189 todissociation during dry periods, mean that the synthesis of nucleotides and their polymerization in

190 TBP-chromatin binding events associated with the synthesis of one RNA molecule across Pol II genes, s

191 gy was successfully realized, culminating in the synthesis of oridamycin A and oridamycin B.

192 and root hair initiation and elongation and the synthesis of other receptors.

193 rahydrofuran intermediates have been used in the synthesis of other strychnos alkaloids, no investiga

194 enine phosphonate and can be expanded toward the synthesis of other types of 3'-fluoro nucleoside pho

195 mmodity in itself as well as a feedstock for the synthesis of other valued chemicals.

196 liquid metals as a reaction environment for the synthesis of oxide nanomaterials with low dimensiona

197 e mutations reduce MRPS34 protein levels and the synthesis of OXPHOS subunits encoded by mtDNA.

198 ron deficient olefins has been exploited for the synthesis of phenylpropanoid natural products.

199 Beyond its function for the synthesis of phosphatidylcholine (PC), the methylati

200 The synthesis of phosphatidylcholine (PC), the most abun

201 alpha), the rate-limiting enzyme involved in the synthesis of phosphatidylcholine (PC).

202 t out to take a different approach and mimic the synthesis of phospholipids using abiotic but highly

203 red to fatty acids, much less is known about the synthesis of phospholipids, which is essential for m

204 To enable the synthesis of phosphorylated proteins for in vitro st

205 eported, very few advances have been made in the synthesis of phosphorylated TNA compounds.

206 Herein, the first catalytic method for the synthesis of POEs using air- and moisture-stable vin

207 mal [2 + 2 + 2] cycloaddition strategies for the synthesis of polycyclic pyridine derivatives are des

208 links the inositol pyrophosphate pathway to the synthesis of polyphosphate in acidocalcisomes, and m

209 P site and play a critical role in promoting the synthesis of polyproline peptides.

210 We previously reported the synthesis of polysubstituted chiral oxazepanes in th

211 , we developed a concise synthetic route for the synthesis of polysubstituted naphthalenes starting f

212 gene, which encodes an elongase involved in the synthesis of polyunsaturated fatty acids, including

213 During one such early expedition on the synthesis of porphyrin, Woodward proposed that conde

214 ded by X-ray structure-based design, enabled the synthesis of potent pyridone and macrocyclic pyridon

215 gaea) to biotic and abiotic stresses include the synthesis of prenylated stilbenoids.

216 The synthesis of previously unknown derivatives of boran

217 There was significant inhibition in the synthesis of proinflammatory cytokines with a concor

218 At first, the synthesis of propargylic amines via the Cu(I)-cataly

219 rence (RNAi) therapeutic agent that inhibits the synthesis of proprotein convertase subtilisin-kexin

220 we describe a "click chemistry" approach for the synthesis of PROTACs.

221 stress response is able to rapidly shut down the synthesis of proteins in eukaryotic cells.

222 y AdoCbl, even under growth conditions where the synthesis of pseudoCbl is favored.

223 Herein, we demonstrate the synthesis of Pt shell on titanium tungsten nitride c

224 A four-step protocol for the synthesis of pyrazolo[1,5-a]pyrazines has been devel

225 his method provides an efficient approach to the synthesis of pyrrolidines, structural units prevalen

226 An efficient domino approach for the synthesis of pyrrolobenzoxazine derivatives is descr

227 To this end, we describe the synthesis of reduced iron-hydride/carbonyl complexes

228 tion of lutein esters with linoleic acid and the synthesis of regioisomers at position 3'.

229 chemical cycles and a promising resource for the synthesis of renewable bioproducts from atmospheric

230 num monoaryloxide chloride complexes enables the synthesis of representative biologically active mole

231 Some serve on-site for the synthesis of retinoic acid, a hormone-like compound,

232 Phe) or methyl jasmonate (MeJ) could improve the synthesis of secondary metabolites.

233 Here we describe the synthesis of seven oligosaccharides as the minimal s

234 We describe the synthesis of several substituted N-(pivaloyloxy)alko

235 We report the synthesis of single-crystal iron germanium nanowires

236 ation of asymmetric copper catalysis towards the synthesis of six distinct oligomeric polypyrroloindo

237 However, the synthesis of small iNPs in a controllable manner rem

238 ial reactivity in catalytic processes toward the synthesis of small molecules.

239 The synthesis of stable organic polyradicals is importan

240 The molecular mechanism that initiates the synthesis of starch granules is poorly understood.

241 The synthesis of stereodefined beta-aminophosphines havi

242 A straightforward strategy allows for the synthesis of storable bicyclic (alkyl)(amino)carbene

243 anslation is rapidly reprogrammed to enhance the synthesis of stress mitigators and is again altered

244 ulose strengthening, callose deposition, and the synthesis of structural defense proteins, proposed a

245 Yet, the synthesis of structurally well-defined, core-fucosyl

246 ducts with m-CPBA is an efficient method for the synthesis of substituted bicyclo[4.3.1]deca-2,4,8-tr

247 The synthesis of substituted gamma- and delta-lactams vi

248 This approach is also utilized for the synthesis of substituted indenes selectively deutera

249 Herein we report the synthesis of such a complex.

250 Increasing research efforts are devoted to the synthesis of such colloidal capsules, by which the i

251 Subsequently, recent progress in the synthesis of such NPs from a variety of inorganic co

252 ics and describe the most recent advances in the synthesis of tetrazine and dienophile coupling partn

253 methodology has been successfully applied to the synthesis of the 3,4-dihydroquinazoline-containing a

254 The synthesis of the A-B-cis,B-C-trans-annulated cyclohe

255 two-chamber technology expands the method to the synthesis of the aforementioned structures with (13)

256 h respect to pH and temperature, allowed for the synthesis of the anticonvulsant ilepcimide with up t

257 Mitoribosomes perform the synthesis of the core components of the oxidative ph

258 The synthesis of the cubic gauche allotrope of high ener

259 cyclisation reactions have been employed for the synthesis of the E and F rings of the complex natura

260 The synthesis of the fluoranthene monomers was carried o

261 The synthesis of the full family of bromothiazoles has b

262 The synthesis of the gamma-secretase modulator MK-8428 (

263 Herein, we report the synthesis of the mixed-valent organometallic copper

264 pled with ascorbate catabolism, and controls the synthesis of the moss cuticle, which prevents desicc

265 Finally, the synthesis of the most odorous and pleasant stereoiso

266 this process, and examine its application to the synthesis of the natural product aphanamal.

267 ature of this approach was demonstrated with the synthesis of the natural products, spruce alkaloid a

268 The synthesis of the plate starts with the fusion of ves

269 Yet the synthesis of the requisite geometrically defined ena

270 The synthesis of the s-TCO precursor was best achieved t

271 o-step process occurs in minutes and enables the synthesis of the squares [Pt4(en)4(N intersectionN)4

272 A divergent strategy for the synthesis of the tricyclic 6,7-diaryltetrahydro-6H-b

273 The synthesis of these complex diazenes was made possibl

274 The synthesis of these new bipyrroles comprises three st

275 cient domino reaction has been developed for the synthesis of thiochromenes through Cu-catalyzed in s

276 e utility of the catalyst is demonstrated in the synthesis of trans-1,2-, cis-1,2-, and 2-deoxy-beta-

277 PAP), which catalyzes the committed step for the synthesis of triacylglycerol in Saccharomyces cerevi

278 We herein report the synthesis of two double cavity polypyridyl [Pd3(L)4]

279 The synthesis of two flexible bis-porphyrin cages 3 and

280 The synthesis of two new radical-bridged compounds [Co3(

281 We report the synthesis of two new selenophene-containing ladder-t

282 This protocol describes the synthesis of two transition metal complexes, [Ir{dF(

283 e kinase-induced phosphorylation of IRF3 and the synthesis of type I IFNs.

284 We recently reported that TRIM6 promotes the synthesis of unanchored K48-linked polyubiquitin cha

285 The synthesis of unnatural amino acids with small side-c

286 These reactions allow for the synthesis of useful building blocks from simple comp

287 A simple and efficient strategy for the synthesis of various 1,4-disubstituted tetrahydro-be

288 re shown to be versatile building blocks for the synthesis of various fluorinated products.

289 ehydes, and cyclic ketones was described for the synthesis of various fused quinoline, benzoquinoline

290 Herein, we extend this study to the synthesis of various glycosidic linkages using diffe

291 The present route also enables the synthesis of various lamellarin analogues devoid of

292 his enzyme could be a potential catalyst for the synthesis of various oligosaccharides.

293 lene halides employed in these reactions for the synthesis of various thieno-fused heterocycles were

294 solutions that have been developed to enable the synthesis of various unique cyclopropane natural pro

295 This method enables the synthesis of varying polymeric structures under iden

296 ery versatile Suzuki-Miyaura reaction toward the synthesis of very electron-poor products, making the

297 pared by dynamic covalent chemistry) and for the synthesis of viologen-based materials.

298 ollowing VACV infection, followed swiftly by the synthesis of viral DNA within discrete cytoplasmic f

299 rminal sequence deletions are able to direct the synthesis of viral proteins, but not genomic RNAs, i

300 However, these 5' deletions greatly reduced the synthesis of viral RNA in vitro, which was detected