ライフサイエンスコーパス: full length

1 h C3 cyclizing the chain when it reaches the full length.

2 tter disease classification, suggesting that full-length 16S gene assemblies are a powerful alternati

3 Dirichlet process clustering to reconstruct full-length 16S gene sequences from metagenomic sequenci

4 RAMBL first realizes the access to full-length 16S gene sequences in the near-terabase-scal

5 ems for the Baselines Initiative (6,177 near full-length 16S rRNA gene sequences and 9.4 million high

6 Here, we demonstrate that the full-length 5 UTR of the zorO type I toxin hinders its o

7 strains revealed that FplA is expressed as a full-length 85-kDa outer membrane-embedded protein or as

8 ent with experimental findings on inhibiting full-length Abeta fibrillation.

9 othing is known about their interaction with full-length Abeta(1-40/42) .

10 r experimental counterparts obtained for the full-length Abeta1-40 peptide.

11 Full-length acetylation-mimic tau showed increased prope

12 rmations of the active and inactive forms of full-length AfGcHK in solution, we investigated the intr

13 ails of photoactivation, we investigated the full-length Agp1 bacteriophytochrome from the soil bacte

14 Whereas the function of full-length Akt3 isoform (Akt3/+S472) is well-characteri

15 was added to the CS-AMEL hydrogel to cleave full-length amelogenin during the growth of enamel-like

16 roglutamylated amyloid-beta11-x fibrils than full-length amyloid-beta fibrils.

17 le N-terminally truncated amyloid-beta40 and full-length amyloid-beta40 accumulation showed an almost

18 red to pathological ageing, whereas cortical full-length amyloid-beta42 accumulation was comparable b

19 at N-terminally truncated amyloid-beta42 and full-length amyloid-beta42 accumulations distributed dif

20 n areas, especially some limbic areas, while full-length amyloid-beta42 tended to accumulate more in

21 tercellular adhesion molecule-1 and endocan [full-length and cleaved p14 fragment]) were obtained bef

22 ractions from metastatic IECs contained both full-length and cleaved TLR3, demonstrating surface expr

23 Full-length and conserved C-terminal delta peptide fragm

24 ons (R565W and L640R) in the context of both full-length and N-terminally truncated (DeltaNT) G1.

25 iptional activity and protein levels of both full-length and splice-variant AR.

26 UGA redefinition to control the synthesis of full-length and truncated SELENOP isoforms.

27 ariable efficiencies to control synthesis of full-length and truncated SELENOP isoforms.

28 R with the molecular structure of an intact, full-length, and functional receptor.ligand complex.

29 gth proteins into constant region loops of a full-length antibody or an antigen-binding fragment (Fab

30 n G (IgG) were fabricated using well-defined full-length antibody-polymer conjugates (APCs).

31 We also studied a soluble form of the full-length approximately 7-kDa cytoplasmic C terminus i

32 tely 23- to 24-kDa protein diminish, and the full-length, approximately 45-kDa K15P protein accumulat

33 Here we report that a cDNA encoding a full-length, approximately 45-kDa K15P reporter protein

34 clinical CRPC, the expression levels of the full-length AR (twofold, P < 0.05) and the AR splice var

35 sociated with ARV7 and AR(v567es) as well as full-length AR.

36 apid cell-death induction in vivo requires a full-length ASC.

37 Here we expanded the number of available full-length baboon STLV-1 sequences from one to three an

38 ivatable unnatural amino acids, we show that full-length BACE1, independently of its subcellular loca

39 report that BH3-only proteins bind inactive full-length BAK at mitochondria and then dissociate foll

40 Full-length barcodes obtained from all three century-old

41 d PWM (Position Weight Matrix) stacking, for full-length binding motif prediction.

42 topological investigations of membrane-bound full-length bitopic protein complexes under physiologica

43 To validate its activity, a small amount of full-length BoNT/X was assembled by linking two non-toxi

44 Transfection of cells with full-length CaM slightly increased the ability of estrog

45 CD33 generates two splice variants: a full-length CD33M transcript produced primarily by the "

46 stingly, the expression of CD40LG and active full-length CD40 was increased in the disease tissues, w

47 omplex isoforms because it fails to sequence full-length cDNA copies of RNA molecules.

48 The full-length cDNA encodes a type-I IPPI containing a plas

49 Here, we report the full-length cDNA sequence of croaker elovl4, which conta

50 rapid amplification of cDNA ends (RACE) and full-length cDNA sequencing, revealed four independent p

51 tudy, we have isolated and characterized the full-length cDNA, gDNA and a putative promoter of a RIOK

52 Here, two ELO full-length cDNAs (TmELO1, TmELO2) from the yellow mealw

53 ina RNA-seq and Pacific Biosciences (PacBio) full-length cDNAs to identify 104,091 high-confidence pr

54 Here we report the structure of a full-length class B receptor, the calcitonin receptor, i

55 we recombinantly expressed murine and human full-length CLEC3As as well as truncated forms of CLEC3A

56 ile birds, using a lentivirus containing the full-length coding sequence of the human NR2B subunit.

57 on, NMR, and small-angle x-ray scattering on full-length ColN and its fragments.

58 the sporozoites, combined with the flexible full-length conformations of CSP, may provide the sporoz

59 Moreover, the full-length constructs isomerized before ADP release, wh

60 nstrated that cytoplasmic LANA isoforms were full length, containing the N-terminal nuclear localizat

61 1 particles much more efficiently than their full-length counterparts.

62 emical interrogation of the structure of the full length CTD of Drosophila melanogaster, which we con

63 tein Alpha 1- 20 kDa), which is required for full-length Cx43 trafficking, but by an unknown mechanis

64 mparisons of spectra of IL-8 (1-66) bound to full-length CXCR1 (1-350) and to N-terminal truncated co

65 Our experiments with full-length Cya and its cytosolic domain link the mutati

66 ffect of membrane on the interaction between full-length cytb 5 and cyt c for the first time.

67 ese two proteins were generated from (i) the full-length dbpA gene combined with the invariable regio

68 InsP7 kinase/InsP8 phosphatase activities of full-length diphosphoinositol pentakisphosphate kinases

69 po11 protein to various DNA-binding modules: full-length DNA binding proteins, zinc fingers (ZFs), tr

70 e also determined the structural envelope of full-length DnaB (GstDnaBFL) in solution.

71 of the truncated RRM2 domain compared to the full-length domain, consistent with previous experimenta

72 ritical for relieving the auto-inhibition of full-length Drs2p, whereas the 1-104 N-terminal residues

73 that lentiviruses can be used for permanent full-length dystrophin gene therapy, which presents a si

74 optimising foamy virus vectors carrying the full-length dystrophin open-reading frame for transducti

75 a4beta2 nicotinic receptors in vitro, as did full length ectodomain of the rabies virus glycoprotein.

76 65kDa truncated protein isoform that opposes full-length eIF2Bepsilon to inhibit global translation.

77 s were superior to Apelin-13, likely because full-length ELA enabled a distinctive regulation of pitu

78 IMPORTANCE We report here that a stable full-length enterovirus 71 (EV71) reporter construct was

79 o prevent proteolytic processing generated a full-length enzyme that is active in vitro toward a solu

80 An electron microscopy structural model of full-length ERdj3 shows that these tetramers are arrange

81 Here, we report the crystal structures of full length Escherichia coli RapZ at 3.40 A and 3.25 A,

82 ogen-deuterium (H/D) exchange MS (HDX-MS) of full-length Escherichia coli DXPS to provide a snapshot

83 for simultaneous binding of both domains in full-length ETV4.

84 Here, crystal structures of a full-length eukaryotic UGGT reveal four thioredoxin-like

85 Lumacaftor partially stabilized purified full-length F508del-CFTR and slightly delayed deactivati

86 Compared with purified wild-type CFTR, the full-length F508del-CFTR was about 10 degrees C less the

87 d N-terminal 70 kDa fragment (rF70K) and the full-length fibronectin (rFN).

88 The amounts of rescued full-length FIX protein for the p.W240X ( approximately

89 were derived from 128 667 intron-containing full-length FLNC reads, including a large number of AS e

90 ease needed to generate active NRG1 from the full-length form.

91 present, one being a cleavage product of the full-length form.

92 lalanine (azF) into N-terminal residues of a full-length functional human GLP-1R in mammalian cells.

93 ases of the Clk family control the supply of full-length, functional mRNAs coding for a variety of pr

94 ne-anchored FZD4 CRDs and oligomerization of full-length FZD4, which requires the integrity of CRD pa

95 hese mutations reduced surface expression of full-length G1 but not G1-DeltaNT in HEK-293 cells.

96 Results of in vitro and in vivo assays using full-length GabR support the conclusion that AFPA is an

97 While the full-length GAD1 transcript (GAD67) has been implicated

98 is anticorrelated with the expression of the full-length GAD1 transcript.

99 es may better delineate type 1 diabetes than full-length GAD65 (fGAD65) autoantibodies.

100 ere we report the 3.0 A crystal structure of full-length GCGR containing both the extracellular domai

101 These insights into the full-length GCGR structure deepen our understanding of t

102 In addition, the full-length genome sequence was generated for 116 strain

103 ty >85% or >80%, according to the partial or full-length genome sequence, respectively.

104 The full-length genomic and subgenomic RNA strands were dete

105 recapitulate the genetics of HD, having two full-length, genomic human HTT transgenes heterozygous f

106 Hu128/21 mice have two full-length, genomic human HTT transgenes heterozygous f

107 ent a small-angle X-ray scattering model for full-length GLS2.

108 ictions about the functional behavior of the full-length GluK2/K5 receptor, which we confirmed via el

109 CA45, while exhibiting negligible binding to full-length GP, bound a proteolytically remodeled GP wit

110 We show that both full-length GSDMB and the N-terminal domain bind to nitr

111 Furthermore, full-length GST-mu1A and the GST-mu1A C-terminal domain,

112 However, full-length GST-mu1A did not bind to the phospho-L-selec

113 separate quantitation of non-phosphorylated full-length guide strands from 5-phosphorylated forms th

114 equencing technology can be used to generate full-length HCV envelope sequences at the single-molecul

115 gle cells, the unique task of assembling the full-length heavy and light chain sequences from single

116 le human B cells to scRNA-seq, assembled the full-length heavy and the light chains, and experimental

117 pared to single-host viruses, using 244 near-full-length HEV genomes.

118 ated by normal mode analysis from one of the full-length HiLpoA molecules but even better agreement w

119 pture strategy for purification of unspliced full-length HIV RNA-protein complexes preserved in vivo

120 were not measurably different from those of full-length HjLPMO9A, indicating that the presence of th

121 ual phosphorylation and acetylation sites in full-length Htt constructs.

122 y of a CD3 T cell-dependent bispecific (TDB) full-length human IgG1 therapeutic antibody targeting CL

123 Full-length human immunodeficiency virus type 1 (HIV-1)

124 rms, we overexpressed and purified the three full-length human isoforms from suspension-adapted HEK c

125 ntroduction of equivalent stop codons in the full-length human L1 sequence leads to the expression of

126 Here we present two structures of full-length human TRPM4 embedded in lipid nanodiscs at

127 t two electron cryo-microscopy structures of full-length human TRPML1: a 3.72-A apo structure at pH 7

128 nucleic acid (NA) binding and processing by full-length hUPF1.

129 Plants constitutively expressing full-length HWS-but not a truncated version lacking the

130 Here, we show that co-expression of full-length IcsA and the Shigella membrane protease IcsP

131 Perivascular access and distribution of full-length IgG could be enhanced by intrathecal co-infu

132 n hippocampal neurons, the overexpression of full-length IL1RAPL1 and mutants lacking part of C-termi

133 ontains 146 putatively active L1 elements or full length intact L1 elements (FLIs).

134 tes, are retrotranslocated to the cytosol as full-length intermediates during ERAD, and we have inves

135 le real-time sequencing, characterization of full-length JCPyV genomes in urine and plasma samples fr

136 Full-length JCPyV sequences were not retrieved from plas

137 Although full-length K15P is approximately 45 kDa, numerous lower

138 We also solved the crystal structure of full-length KGA and present a small-angle X-ray scatteri

139 ta, proteolysis experiments performed on the full length KpOmpA as well as on its membrane domain, re

140 ports the expression and purification of the full-length L protein of RABV and the characterization o

141 2 can selectively bind evolutionarily young, full-length L1s located within transcriptionally permiss

142 We now report the crystal structure of a full-length lipid A phosphoethanolamine transferase from

143 -terminal domains showed similar efficacy as full-length LN-511.

144 Purified, full-length LRH-1, as well as isolated ligand binding do

145 expression of the complete 61 domains of the full-length LRP1 ectodomain.

146 dies on a pathogenic mutation that generates full-length M1 and M87 proteins, truncated M1 was notabl

147 alizes at the tip of filopodia like myosin-X full-length (M10(Full)).

148 of the inter-helical channel motion of both full-length M2 and the transmembrane domain of M2.

149 For the full-length M2 channel, the rate is increased from appro

150 Without these shorter isoforms, full-length MAVS is prone to spontaneous aggregation and

151 , blocking Nix-mediated mitophagy stabilizes full-length MAVS, which aggregates spontaneously and ind

152 equired for GAG-dependent oligomerization of full-length MCK-2.

153 known to activate the p53 pathway and impede full-length MDM2's negative regulation of p53.

154 binding constants of GCAP1 and GCAP2 to the full-length membrane-bound guanylate cyclase type 1.

155 The full-length, membrane-bound CH120.6 Env is indeed stable

156 The first X-ray structure of the full-length mISG15 protein is also reported and highligh

157 this site selectively impair proteolysis of full-length MKKs yet have no impact on cleavage of short

158 Starting from a sequence, it first generates full-length models using I-TASSER by iterative structura

159 uctural insight into chemical degradation in full-length monoclonal antibodies and the high-resolutio

160 e present a pseudo-atomic model structure of full-length MotB in its activated form.

161 11, which is formed after HDAC inhibition as full-length MRE11 is downregulated.

162 ed inner surfaces that can package their own full-length mRNA genomes.

163 usion-based transfer mechanism, we find that full-length mRNAs undergo direct cell-cell transfer via

164 ence, this work supports the hypothesis that full-length mRNAs undergo transfer between cells through

165 bstitutions, which lead to the expression of full-length mutant proteins that accumulate in cancer ce

166 LOVDab robustly recruits human full-length myosin VI to various organelles in vivo and

167 we studied the single molecule movement of a full-length myosin-X construct with leucine zipper at th

168 These results suggest that the lever-arm of full-length myosin-X is flexible enough to processively

169 nad5 rather than nad5T1 causing loss of the full-length nad5 transcript, and degradation of nad5 los

170 we perform electrophysiological analysis of full-length NMDARs with a glycosylation-preventing GluN1

171 In total, 145 522 mapped full-length non-chimeric (FLNC) reads were analyzed, res

172 Here we report the crystal structures of full-length NS5 and its polymerase domain at 3.0 A resol

173 ibril interface residues in viruses encoding full-length NSs completely abrogated intranuclear filame

174 rs otherwise tightly bound carotenoid to the full-length OCP apoprotein, resulting in formation of ph

175 our knowledge, this is the first report of a full-length octameric MCM helicase.

176 steine labelling and linkage analysis to the full length of Bak in mitochondria.

177 es the binding activity, suggesting that the full length of the alpha-helical regions of Hic is requi

178 We deduced the full-length of the RBM28 cDNA sequence and profiled its

179 Amplification and cloning of the full-length of the sodium channel gene in pyrethroid res

180 Full structural characterization of the full-length oligomeric p53 is challenging because of its

181 ting the thermodynamics of hybridization for full-length oligonucleotide-template alignments - thermo

182 s African trypanosomiasis and contains three full-length oligosaccharyltransferase (OST) genes; two o

183 ressed in Arabidopsis, the overexpression of full-length OsbZIP48 in rice transgenics reduced the pla

184 ion 6 of the vlsE gene (DbpA/C6) and (b) the full-length ospC gene (OspC).

185 f isoprostanoid moieties that are present in full-length oxygenated PAPC species, we used an inhibito

186 oding sequence has been replaced with either full-length P. vivax VK210 or the allelic VK247 csp that

187 mARF alone or M45A-mutated (smArf-deficient) full-length p19(Arf) proteins.

188 els with available crystal structures of the full-length p53 (fl-p53) tetramer bound to three differe

189 The full-length p53 protein is largely inactive in stem cell

190 RNA can modulate the aggregation of p53C and full-length p53.

191 in adult pancreatic acinar cells by using a full-length pancreatic elastase promoter-driven Cre.

192 e still has the ability to rescue similar to full-length Pcdh15a.

193 gly, expressed low or intermediate levels of full-length PD-1 in the tumor environment.

194 n codon (PTC) that prevents synthesis of the full-length peptide are considered more likely to mount

195 507) phosphorylation (that does not apply to full-length PKCdelta) in structurally organizing diverse

196 region interacts with RNA in the context of full length PKR.

197 Contrary to the full-length polypeptide, in fact, the DFNKF sequence is

198 Here, we expressed and purified full-length porcine INSL3 (pINSL3) using a silkworm-base

199 ing NS cleavage increased association of the full-length prodomain with Gbb15, resulting in a concomi

200 Full-length prophages clustered into four major groups a

201 alleles responded to treatment and produced full length protein, in some cases more than 50% relativ

202 as they are likely less immunogenic than the full-length protein and more convenient to produce.

203 the arrangements of the PCM subunits in the full-length protein dimer in solution differ significant

204 hese results demonstrate that insertion of a full-length protein into non-CDR loops of antibodies pro

205 N-P gene position of the rHPIV1 vector as a full-length protein or as a chimeric form with its TMCT

206 rom the first or second gene position as the full-length protein or as a chimeric protein with its tr

207 as codon optimized and expressed either as a full-length protein or as an engineered chimeric form in

208 atalyzed deacetylation of singly-acetylated, full-length protein substrates, revealing that HDAC8 sub

209 cated form of this enzyme suggested that the full-length protein was required for correct lipid subst

210 mulated higher ATP hydrolysis rates than the full-length protein, indicating that binding to MinD is

211 Compared with the activity of the full-length protein, the C-terminal helicase domain had

212 ite for GCAP1 with similar affinities as the full-length protein, whereas GCAP2 did not bind to this

213 on may contribute to light activation of the full-length protein.

214 ion of the affected gene and production of a full-length protein.

215 fication influences a disordered region of a full-length protein.

216 foundation for understanding recognition of full-length proteins by HDACs.

217 alidated the interface in the context of the full-length proteins in solution.

218 generate bifunctional antibodies by grafting full-length proteins into constant region loops of a ful

219 g post-translational modifications (PTMs) in full-length proteins is a challenge, especially in the c

220 HDAC8 substrate selectivity for peptides and full-length proteins suggest that HDAC8 substrate prefer

221 rate selectivity in the context of peptides, full-length proteins, and protein-nucleic acid complexes

222 ct the substrate selectivity of HDAC8 toward full-length proteins.

223 dentified multiple sets of independent, near-full-length proviral sequences from cART-treated individ

224 ificant expression originating from 15 HML-2 full-length proviruses, through four modes of transcript

225 However, the crystal structure of full-length PSMalpha3, solved de novo at 1.45 angstrom r

226 on of the PTEN C2 domain mimicked effects of full-length PTEN but a membrane-binding defective mutant

227 was used to reconstruct the assembly of the full-length RagA(GTP):RagC(GDP) dimer bound to Ragulator

228 Full length rAhAI showed differential inhibition against

229 l isoforms based on the number of supporting full-length reads with those of annotated isoforms and e

230 P) increases oligomerization compared to the full length receptor (EphA2FL-GFP).

231 ctions occurring in the dynamic, native, and full-length receptor state.

232 ation, an endpoint robustly activated by the full-length receptor.

233 gen synthase kinase 3beta (GSK3beta) via the full-length receptor] and its congener 3-(1H-imidazol-4-

234 k of structural information on activated and full-length receptors.

235 ation and functional characterization of the full-length Red1 protein.

236 fragments N-R2 and N-R6 bind to L1 and that full-length Reelin and its N-terminal fragment N-R6 prot

237 Here, we report that full-length Reelin and its N-terminal fragments N-R2 and

238 ertain populations are more likely to harbor full-length, replication-competent provirus.

239 high resolution in Saccharomyces cerevisiae Full-length resection requires Exo1 exonuclease and the

240 Two distinct nearly full-length Rhizobiales genomes were identified in leaf-

241 and purification system for isolation of the full-length RhoGC protein expressed in HEK293 cells in d

242 logically relevant role in the regulation of full-length RhoGC.

243 Loss of full-length RIM2alpha in a RIM2alpha mutant mouse only m

244 esulting synthetic nucleocapsids package one full-length RNA genome for every 11 icosahedral assembli

245 s possessed more sialidase activity than did full-length rNanI, further supporting the proteolytic ac

246 otoxin and beta toxin more strongly than did full-length rNanI.

247 aden hydrogel pulp-like tissue constructs in full-length root canals for dental pulp regeneration.

248 In contrast, full-length RSV F expressed from the pre-N position was

249 However, the vector expressing full-length RSV F from the pre-N position was immunogeni

250 All peptides, as well as full length Sap6, demonstrated amyloid properties, and a

251 , we demonstrate that the NADase activity of full-length SARM1 is required in axons to promote axonal

252 , we derive a pseudo-atomic structure of the full-length Scc2-Scc4 complex.

253 Two RNAs were studied: the full-length segment 5 (+)RNA and a shorter construct con

254 7S has SUMO isopeptidase activity but unlike full-length SENP7L, SENP7S is localized in the cytosol.

255 have been reported, the atomic structures of full-length separase and especially the complex with sec

256 In this study, we cloned a full-length sequence for the Gnih precursor of a flatfis

257 We report the full-length sequence of two chicken source influenza A (

258 The L1Base database contains annotated full-length sequences of LINE-1 transposons including pu

259 n the CID/UVPD data, UVnovo assigned correct full-length sequences to 83% of the spectral pairs of do

260 INB7 cDNA carrying the mutation and promoted full-length SERPINB7 protein synthesis in NPPK keratinoc

261 ptic peptides, cleavable SIL peptides, and a full-length SIL protein were compared for internal calib

262 the cryo-electron microscopy structure of a full-length Slo1 channel from Aplysia californica in the

263 promotes exon 7 inclusion and thus increases full length SMN expression.

264 SMNDelta7 protein, but from which functional full length SMN protein is produced at very low levels (

265 ne and thus promotes increased production of full-length SMN protein.

266 This enables characterization of the full-length SOS protein, which has not previously been s

267 igand ectodysplasin A (EDA) is produced as 2 full-length splice variants, EDA1 and EDA2, that bind to

268 oplastic localization similar to that of the full-length SS4 protein.

269 sa1, which suggests how Sec72 interacts with full-length Ssa1.

270 O have been solved, efforts to elucidate the full-length structure of NEMO have proved difficult due

271 ntain and transmit [SWI(+)] independently of full-length Swi1.

272 In in vitro fusion assays using full-length t- and v-SNAREs embedded in liposomes, Gbeta

273 on but also inhibit the ability of exogenous full-length tau fibrils to seed intracellular tau in HEK

274 We propose that, in full-length TDP-43, association between folded N-termina

275 e pseudoknot does not form in the context of full-length TER in the absence of TERT, due to formation

276 Full length TET1 (TET1FL) has a CXXC domain that binds t

277 Because full-length TFPI associates with FV in plasma, we hypoth

278 We identified 176 849 full-length transcript isoforms from 44 968 gene models

279 tome annotation and generates manual-quality full-length transcript models at high-throughput scales.

280 Gene annotations were updated using 111,000 full-length transcripts obtained by single-molecule real

281 est in gene coverage and number of recovered full-length transcripts.

282 , number of chimeras and number of recovered full-length transcripts.

283 nal equivalents of tetramers (i.e. dimers of full-length transporters) have also been reported.

284 ular transfer of excess free RNAs, including full-length tRNAs and other small ncRNAs.

285 electron microscopy (cryo-EM) structure of a full-length TRPML3 channel from the common marmoset (Cal

286 In vitro reconstitution of TSP1 with either full-length TSP1 or 3TSR, an anti-angiogenic TSP1 fragme

287 Full-length uPAR is released from the cell surface, but

288 at >50% of the efficiencies of an HIV-1 near full-length vector.

289 The truncated and full-length versions of DrDps were also compared on the

290 Increasing full-length viral RNA abundance or distribution had litt

291 the cytoplasmic abundance or distribution of full-length viral RNAs on Gag trafficking and assembly i

292 in trans In contrast, artificially tethering full-length viral RNAs or surrogate gag-pol mRNAs compet

293 or both minimal synthetic viral circuits and full-length virus.

294 Here, 283 full length wheat AAT genes representing 100 distinct gr

295 chroism spectroscopy confirmed that purified full-length wild-type CFTR is folded and structurally re

296 more than three orders of magnitude for the full-length wild-type KcsA, a pH-gated bacterial channel

297 The full-length winter Hvvrn1 allele was strongly down-regul

298 ein [VSVm] versions) that express either the full length ZIKV envelope protein (ZENV) alone or includ

299 For biochemical validation, a full-length ZmTps21 was cloned, heterologously expressed

300 rt the cryo-electron microscopy structure of full-length ZntB from Escherichia coli together with the