ライフサイエンスコーパス: full length

1 By using V4 and full-length 16S ribosomal RNA sequencing of a series of

2 were studied using the PacBio sequencing of full-length 16S rRNA gene.

3 resent high-resolution cryo-EM structures of full-length 5-HT(3A)R in complex with palonosetron, onda

4 The X-ORF can be translated in full-length (61-amino-acid) or truncated (41-amino-acid)

5 d for reactivity to two types of antibodies, full-length 7S IgY and 5.7S IgY, which has a truncated F

6 eceptor gene, in enhancing expression of the full-length 7TM mMOR-1 through a chaperone-like function

7 -1G regulates expression and function of the full-length 7TM mu-opioid receptor.

8 ns have been solved individually; however, a full-length A3G structure has been challenging.

9 To better mimic oligomers of full length Abeta, we use an orthogonal protecting group

10 rillizing Abeta (1-30) peptide recapitulates full-length Abeta stereoselective cellular uptake, allow

11 nd thus better mimic the oligomers formed by full-length Abeta.

12 In the presence of CRISPR-Cas immunity, full-length AcrIIA1 uses its two-domain architecture to

13 main dimerization interface in all variants, full-length AfGcHK variants bearing the Y15A or Y15G sub

14 isolates possessed mixed PfRh2b deletion and full-length alleles.

15 We present FLAIR (Full-Length Alternative Isoform analysis of RNA), a comp

16 Previously, we have demonstrated that full-length AMELX forms higher-order supramolecular asse

17 We report here that full-length amisyn forms a stable SNARE complex with syn

18 cases revealed increased phosphorylation of full-length amyloid precursor protein and its associated

19 In contrast, full length and truncated arrestin-3 form trimers and hi

20 Our results provide the first glimpse of a full-length and functional BAX(O), revealing structural

21 ng by evaluating the taxonomic resolution of full-length and mini-barcodes and to determine a thresho

22 values of 0.4% and 0.55% were defined using full-length and mini-barcodes, respectively.

23 se 1 (TBK1), that efficiently phosphorylates full-length and N-terminal HTT fragments in vitro (at S1

24 dentification to analyze the interactomes of full-length and truncated forms of RAG1 in pre-B cells.

25 aemia and prostate cancer that expressed the full-length androgen receptor (AR).

26 Moreover, negative-stain EM with full-length antibodies disclosed a stable, ring-like ant

27 ar multipole moments and charge asymmetry of full-length antibodies instead of only localized charges

28 ple preparation procedure applicable to both full-length antibody therapeutics and antibody-antigen c

29 toward the plasma membrane, and (3) requires full-length APC for this relocalization.

30 The expression of full-length APC in SW480 colorectal cancer cells (SW480+

31 d toward the local Wnt cue in CRC cells with full-length APC, but not if APC was truncated or deplete

32 neration of sAPPbeta and increased levels of full-length APP (flAPP), indicative of reduced processin

33 We found that full-length APP is cleaved in EVs incubated in the absen

34 fold higher affinity (30 nM) compared to the full-length aptamer (124 nM), with a limit of detection

35 TEM and cryo-EM to determine 3D maps of the full-length Aquifex aeolicus FtsH protease.

36 o ARSi and genetic chances and expression of full length AR (AR-FL) vs. AR-V7 were evaluated in a ser

37 Full-length AR and AR-V7 transcription activation requir

38 tably, the humanized mice expressed both the full-length AS3MT that catalyzes iAs methylation and the

39 filled projections more effectively than did full-length ASAP1.

40 ogenic HTT but not of HTT exon 1 fragment or full-length ATXN3.

41 Here, we describe the conformation of full-length Bcl-xL.

42 t when expressed alone in HEK293F cells, the full-length beta3-subunit forms trimers in the plasma me

43 e variant-gene-disease associations from the full-length biomedical literature and designs an evidenc

44 erage (88-99%) in the HDX-MS experiments for full-length BM3 and its component domains in both the li

45 A crystal structure of full-length BM3 enzyme is not available in its monomeric

46 Finally, full-length BoNT/B containing two tryptophan mutations i

47 we demonstrate that HPV-16 E2 Y138E bound to full-length Brd4 but not to the Brd4 CTM.

48 Accordingly, in full-length Bs-FtsZ, the CTL acts as a spacer that spati

49 f drug binding on the global conformation of full-length BTK are unknown.

50 uncover a range of conformational effects in full-length BTK induced by a panel of active site inhibi

51 g the compact autoinhibitory conformation of full-length BTK, shifting the conformational ensemble aw

52 f p73 alternative splicing and show that the full-length C terminus of p73 is essential for hippocamp

53 Actin in complex with full-length CAP2 is predominately ATP-bound.

54 e five exon 5-associated seven transmembrane full-length carboxyl terminal variants, MOR-1B1, MOR-1B2

55 We report nanopore sequencing of full-length cDNA from CLL samples with and without SF3B1

56 horbol ester (PMA) and transduction with the full-length cDNA of GLS2.

57 Here, we generated over 10,000,000 full-length cDNA sequences at a median accuracy of 97.9%

58 Evidence of reduced expression of the full-length CFL2 transcript was also observed in the mus

59 mutations also partially restores folding of full-length CFTR.

60 tical role of this motif in the context of a full-length channel chimera, Nav1.9-Ct49aa(Nav1.7), whic

61 Here, we extract full-length chicken ASIC1 (cASIC1) from cell membranes u

62 scriptional repressors and by activating the full-length Ci or Gli proteins.

63 Structures of full-length class B receptors were determined in complex

64 chromosomes, only 34 of which contain the 51 full-length coding regions.

65 We identify the full-length coding transcripts of CACNA1C in human brain

66 recapitulate key aspects of the behavior of full-length Colalpha2(I) constructs.

67 of domain-based contact prediction with the full-length contact prediction improved the performance

68 Expression of the full-length CpMMS19 was able to complement the thermosen

69 propagates up to the DNA recognition lobe in full-length CRISPR-Cas9.

70 ept that the capping strategy can be used on full-length cryo-EM fibril structures.

71 microscopy structure of CsgG in complex with full-length CsgF shows that the 33 N-terminal residues o

72 e kinase (CKB) bound to ASB9-ELOB/C, and for full-length CUL5 bound to the RING protein, RBX2, which

73 te in Cx43 (M213L mutation), which generates full-length Cx43, but not GJA1-20k.

74 overy of the geometry of the complex between full-length CXCR4, a prototypical CXC receptor and drive

75 However, the structure of a functional full-length CYP102A1 enzyme remains to be determined.

76 Moreover, full-length CYP102A1 is highly dynamic, existing in mult

77 Finally, we found that the full-length DDX43 helicase prefers DNA or RNA substrates

78 erentiation with TGF-beta and 1,25diOHvitD3, full-length Dicer became abundant together with varying

79 ts that downsized variants could replace the full-length domain.

80 trophy (FSHD) results from expression of the full-length double homeobox 4 (DUX4-FL) retrogene in ske

81 Mainly due to lack of a full-length double-domain APOBEC structure, it is unknow

82 by inhibiting the proteolytic processing of full-length Drosophila Ci or mammalian Gli proteins to n

83 We cloned the full-length EB1 cDNA for its overexpression in the testi

84 A chimeric VSV expressing the full-length EBOV GP (VSV-EBOV) containing the MLD was su

85 the inhibitory effect of PSGL-1 required its full-length ectodomain.

86 insight into the phosphorylation patterns of full-length EGFR.

87 Expert central readers assigned each full-length endoscopy videos 1 endoscopic Mayo score (eM

88 Seven hundred and ninety-five full-length endoscopy videos were prospectively collecte

89 res to predict eMS and UCEIS from individual full-length endoscopy videos.

90 rained to predict levels of UC severity from full-length endoscopy videos.

91 ich targets only viral maturation, but lacks full-length Env and Gag immunogens, can prevent intravag

92 ociated urethritis; for a subset of samples, full-length env genes were generated for sequence analys

93 acilitate greater targeting specificity than full-length enzymes alone.

94 o substantiate this finding, we analyzed the full-length FERM domain and a series of truncated FERM c

95 tics of fibronectin fragment FNIII(8-14) and full-length fibronectin (FN) on CH(3)-, OH-, COOH-, and

96 Vac14 in vivo and retains some functions of full-length Fig4.

97 erization of split pairs of FRB or FKBP with full-length FKBP or FRB, respectively, by rapamycin.

98 ngle-genome amplification, and sequencing of full-length (FL) envelope HIV.

99 Under mild conditions, full-length (fl) mouse TIA1 spontaneously oligomerizes t

100 ing to classify because the minimal level of full-length (FL) transcripts required for normal functio

101 Despite that, the actin-bundling site in the full-length (FL) villin protein remains unidentified.

102 ransfection, we show increased levels of the full-length GAA transcript, acid-alpha-glucosidase prote

103 structures of heterodimeric and homodimeric full-length GABA(B) receptors.

104 identified evidence of positive selection on full length gamma-c clade genes.

105 specific T cell activity was observed in the full-length gB protein and mRNA-LNP groups, though not i

106 were administered 3 sequential doses of the full-length gB protein with an MF59-like squalene-based

107 capsulated nucleoside-modified mRNA encoding full-length gB.

108 -electron microscopy structures of the human full-length GB1-GB2 heterodimer: one structure of its in

109 ype C that constitutes the oldest HIV-1 near full-length genome recovered to date.

110 This lack of full-length genomes hampers our ability to understand th

111 In addition, full-length GiKIN14a has significantly higher stepping a

112 ines, ABCC4 knockdown and inhibition reduced full-length GLI3 levels.

113 Here, we present Cryo-EM structures of the full-length GlyR protein complex reconstituted into lipi

114 lar dynamics simulations of fusion between a full-length hemagglutinin proteoliposome and a lipid bil

115 Furthermore, although the full-length hERG variant, hERG1a, has been widely used t

116 report the cryo-EM structure of recombinant full-length hIAPP fibrils.

117 constructed from the various segments of the full-length hIAPP peptide; however, only a few have thei

118 We obtained near full-length HIV-1 genome sequences from people living wi

119 The viral protein Gag selects full-length HIV-1 RNA from a large pool of mRNAs as viri

120 We obtained 6078 near full-length HIV-1C genome sequences from 6075 PLWH.

121 letely prevents in vitro phase separation of full-length hnRNPA2 and aggregation of the disease-assoc

122 LINE-1s, as well as increased expression of full-length hominid-specific LINE-1s that produce bidire

123 lecular basis for the differences based on a full-length homology modeling approach.

124 ufficient to cause inclusion formation since full-length HTT and HTTex1 with expanded polyQ are both

125 with expanded polyQ are both toxic although full-length HTT remains diffuse while HTTex1 forms inclu

126 the brain, regardless of truncation sites in full-length HTT.

127 e recombinant expression and purification of full-length human FMRP, FXR1P, and FXR2P from Escherichi

128 ution, peptide-free crystal structure of the full-length human GLP-1R in an inactive state, which rev

129 tions in vitro into phase-separated forms of full-length human hnRNPs (TDP-43, FUS, hnRNPA2) and thei

130 we compare the effects of expressing mutant full-length human HTT (fl-mHTT) to the effects of mutant

131 Here, we report a solution structure of the full-length human Orc6 (HsOrc6) alone and in a complex w

132 e, we developed a mouse model by inserting a full-length human PRSS1R122H gene, the most commonly mut

133 ity of KB105, a gene therapy vector encoding full-length human TGM1, to deliver functional human TGM1

134 We produced and isolated full-length IDOL protein, which displayed high autoubiqu

135 ing of an active submarine channel along its full length in Bute Inlet, Canada.

136 220 OR open reading frames, 20 of which are full length, intact OR genes, and found a large ratio of

137 en made in understanding the architecture of full-length ion channels and the structural and biophysi

138 ic mutations in SF3B1 are known, identifying full-length isoform changes may better elucidate the fun

139 that addresses both challenges for targeted full-length isoform sequencing applications using collec

140 The full-length isoform, MR1A, can activate MAIT cells, whil

141 a strategy to define complete portfolios of full-length isoforms encoded by individual genes.

142 overall efficiency of chitin degradation by full-length Jd1381 depended on its chitinase and LPMO ac

143 the distinct disease mutation which reshapes full-length kinase conformations, affecting their activi

144 rovides additional mechanistic insights into full-length kinase functions by reporting protein-protei

145 ows the tracking of conformation dynamics of full-length kinases in intact cells and real time.

146 , and live-cell imaging, we demonstrate that full-length kindlins can oligomerize (self-associate) in

147 same core structure as fibrils formed by the full-length LC domain.

148 Here we report a crystal structure of the full-length LCI1 membrane protein to reveal LCI1 structu

149 Full-length LGR4 formed a tight complex with ZNRF3 and R

150 However, direct evidence for RSPO-bound, full-length LGR5 interacting with these E3 ligases in wh

151 the target amplicons demonstrated that both full-length library (565 bp) and mini-barcodes (193 bp)

152 Full length lubricin (~300 kDa), was efficiently digeste

153 oth the autologous synthetic peptide and the full-length Luk toxin homologues.

154 The solution of the full-length M1 structure, the identification of critical

155 The structure of full-length M1, and how it oligomerizes to mediate the a

156 5)N-(15)N J-couplings of (15)N His37-labeled full length M2 (M2FL) protein from Influenza A virus emb

157 We have previously shown that full-length MAGP-1 binds active TGFbeta-1 and some BMPs.

158 from > 19,000 protein-coding genes, abundant full-length, mature tRNAs and other structured small non

159 in the mitochondrial membrane, competes with full-length Mcl-1 protein with regards to its antiapopto

160 l1(DeltaIEC) mice); these mice and mice with full-length Mcl1 (controls) were raised under normal or

161 Among various deletion mutants, only full-length Mdm4 was able to support DNA replication for

162 The full-length MECOM transcript, MDS1-EVI1, is not expresse

163 in Mecp2R294X mice was sufficient to elicit full-length MeCP2 protein expression in peripheral tissu

164 Unexpectedly, full-length MeCP2 protein failed to bind GT-rich sequenc

165 418 in Mecp2R294X mice induced expression of full-length MeCP2 protein in the mouse brain.

166 ients receiving DC vaccines expressing three full-length melanoma antigens (MAs) was performed.

167 erization through disulfide formation of the full-length mini-protein and show the coiled-coil region

168 current anti-miRNA (antimiR) reagents target full length miRNAs, here we investigate novel nanopartic

169 l-angle solution X-ray scattering to produce full-length models of membrane-anchored Hck.

170 However, high-resolution structures of full-length monomeric M1 and the matrix layer have not b

171 Here we show that m(6)A can be mapped in full-length mRNAs transcriptome-wide and reveal the comb

172 responsible for nuclear localization within full-length MSH3.

173 of a complex between human caspase-1 and the full-length murine GSDMD.

174 Here, using CRISPR/Cas9 to truncate full-length mutant HTT in HD140Q knock-in (KI) mice, we

175 the cATS class, for "complete" ATS, harbors full-length nascent transcripts.

176 We then tested a full-length native Ab heavy chain encoding the same 17-r

177 Crystallization of both chimeric and full-length native heavy chain-containing Abs provided s

178 immune responses comparable to those of the full-length native polysaccharide.

179 We show that full-length NiV phosphoprotein is tetrameric, and we sol

180 We detected 3,400 full-length NLR loci, of which 1,560 were confirmed as e

181 re, we report the first crystal structure of full-length nsp10 from the arterivirus PRRSV, which has

182 s, Arg111His, Phe112Tyr, and Ala115Val (AgRP full-length numbering), were incorporated into the pepti

183 Although wild-type full-length NUP98 is a member of the nuclear pore comple

184 Taking advantage of long reads spanning the full length of mRNA transcripts, we provide support for

185 erence from short reads that do not span the full length of the isoform.

186 n a RACE PCR-based approach and cloned three full-length OSC transcripts from cork (QsOSC1-3).

187 In chloroplasts, the full-length OsCYP20-2 promotes OsFSD2 forming homodimers

188 OSBPL1 encodes the full-length oxysterol-binding protein-related protein OR

189 ur real time single molecule measurements of full length p53 tetramers binding DNA reveal the paramet

190 pressed UBQLN2 selectively lowered levels of full-length pathogenic HTT but not of HTT exon 1 fragmen

191 CryoEM structure reconstruction of the full-length PCBP2 in complex with SLIVm solved to 6.1 an

192 provided similar cell survival ratio as the full length PfCCT protein.

193 erization of a secreted, soluble, and stable full-length PfCSP (containing 4 NVDP and 38 NANP repeats

194 The recombinant full-length PfCSP, denoted PfCSP4/38, was produced initi

195 ded Gly-zipped TMD2/TMD2 dimer), and for the full-length pinholin protein before being triggered (Gly

196 The host protease furin cleaves the full-length precursor S glycoprotein into two associated

197 Here, we report the structure of full-length PrgA, which shows that PrgA protrudes far ou

198 ion and the resulting read-through increases full-length product formation.

199 ion in vitro but is required to synthesize a full-length product.

200 that are poorly functional and read-through, full-length products.

201 Full-length ProQ bound all six RNAs similarly, while the

202 mpact of PGRN mutations on the processing of full-length prosaposin to individual saposins, which are

203 ore quantitative and structural studies with full length protein.

204 s substrate and the crystal structure of the full-length protein at 1.85 angstrom resolution revealed

205 licing can increase endogenous expression of full-length protein by preventing naturally occurring no

206 ed glycans in the S1 subunit compared to the full-length protein could indicate differences in the gl

207 ical 2-dimensional (2D) crystal lattice, but full-length protein crystallizes multiple orders of magn

208 o its size and complexity, expression of the full-length protein has been difficult, leading to focus

209 relate the experimentally observed yield of full-length protein in the FPA assay to the force exerte

210 found that although the dimerization of the full-length protein is preserved via the kinase domain d

211 nts show that the inter-domain linker in the full-length protein promotes oligomerization and thus ma

212 of repeat-specific Abs compared to a nearly full-length protein vaccine (FL-CSP).

213 which the arrested protein is converted into full-length protein with a Bell model of force-induced r

214 ion of three Pfs48/45 proteins including the full-length protein, the 6C domain fragment and the 6C d

215 -196 C1 PrP construct, in the absence of the full-length protein, were susceptible to Delta(Spont) pr

216 ubstrate proteins to a similar degree as the full-length protein.

217 mpanied by marked cytotoxicity, requires the full-length protein.

218 c ribosomal readthrough of PTCs to produce a full-length protein.

219 however, have largely focussed on refolding full-length proteins from artificially induced denatured

220 but how this relates to the function of the full-length proteins is unclear.

221 n NMR-based approach to monitor oxidation in full-length proteins under denaturing conditions, as dem

222 and on real datasets from droplet-based and full-length protocols, and show that it yields biologica

223 Nearly full-length proviral amplification and sequencing (NFL-P

224 Through nearly full-length proviral amplification and sequencing (NFL-P

225 (PBM) that is required in the context of the full-length, purified Par-6-aPKC complex.

226 consisting of Rab5, RabGDI and a complex of full length Rabex5/Rabaptin5 was necessary to pattern Ra

227 has been resolved(16), the structure of the full-length receptor and its transmembrane signalling me

228 ocyte glycoprotein epitope MOG(35-55) or the full-length recombinant human MOG protein, the latter re

229 uorescence energy transfer assay against the full-length recombinant protein kinase PfCLK3, and 11 an

230 veloped and does not require strain-specific full-length reference antigens or antibodies; instead, s

231 Recently, crystal structures of full-length rhesus macaque A3G variants were solved whic

232 HIV-1 full-length RNA (HIV-1 RNA) plays a central role in vira

233 that are important for the encapsidation of full-length RNA into viral particles.

234 When CaM is bound to full-length RyR1, either purified or in SR membranes, st

235 Insertion of the full-length S protein gene in two different MeV genomic

236 , IgG, and IgM indirect ELISAs to detect the full-length S protein or S receptor-binding domain (S-RB

237 ith SARS-CoV-2, and the vaccine encoding the full-length S protein resulted in >3.1 and >3.7 log(10)

238 reater than either IgM or IgA titers for S1, full-length S, and S-RBD in the overall population.

239 t the cryo-electron microscopy structures of full-length SARM1 proteins.

240 apped the in vivo RNA-RNA interactome of the full-length SARS-CoV-2 genome and subgenomic mRNAs.

241 2) nanoparticle vaccine composed of trimeric full-length SARS-CoV-2 spike glycoproteins and Matrix-M1

242 dified mRNA (mRNA-LNP) vaccines encoding the full-length SARS-CoV-2 spike protein or the spike recept

243 ation-deficient simian adenovirus expressing full-length SARS-CoV-2 spike protein.

244 The full-length sequence of TmMYB3 and partial promoter sequ

245 apping of evolutionary trajectories based on full-length sequences.

246 inus and potentially some functions with the full-length Sfl protein encoded by the host gene.

247 re, using next-generation sequencing of near-full-length single HIV-1 genomes and corresponding chrom

248 and the final DNA boosters delivered a near-full-length SIVmac239 genome capable of assembling nonin

249 Assays with full-length Skp1 substrates reveal substantial differenc

250 The full-length Slit (Slit-FL) is cleaved into Slit-N and Sl

251 Recombinant full-length spike protein and nucleoprotein were digeste

252 candidates from Novavax, which is based on a full-length spike protein formulated in polysorbate 80 d

253 The full-length Spike protein functioned inefficiently with

254 accine that encodes the prefusion stabilized full-length spike protein of the severe acute respirator

255 nd a lateral flow immunoassay (LFI) based on full-length spike protein.

256 which encodes a membrane-anchored SARS-CoV-2 full-length spike, stabilized in the prefusion conformat

257 These defects can be fully rescued by full-length Spindly, but not by variants with mutations

258 In this work, we present the first full-length structural model of tetrameric SinR using a

259 A large degree of fluctuation in the full-length structure is observed, indicating hinge bend

260 Here, we present the full-length structure of PfMyoA in two states of its mot

261 Here we present the full-length structure of the Class 1 OLD nuclease from T

262 Recently, several full-length structures of ionotropic glutamate receptors

263 re than half of the transcript isoforms lack full-length support and instead rely on inference from s

264 In full-length Syt1, both Pb(2+)-complexed C2 domains assoc

265 Here, we present a crystal structure of a full-length talin head in complex with the beta3-integri

266 Full length TANGO1 is a transmembrane protein localised

267 cs to generate libraries of natively paired, full-length TCRalphabeta clones, from millions of primar

268 Both full-length TDP-43 and its CTD are also known to form st

269 Previously, we showed full-length TDP-43 forms spherical oligomers and perturb

270 domain), formed upon proteolytic cleavage of full-length TDP-43 in the nucleus and subsequent transpo

271 cifically modulate the enzymatic activity of full-length TDP1 while not affecting the activity of a t

272 formed insoluble inclusions that sequestered full-length TDP43 via preserved N-terminal interactions.

273 an N-terminally truncated TET1 protein and a full-length Tet1 (Tet1(FL) ) transcript encoding canonic

274 338-nucleotide protein-free RNA structures: full-length Tetrahymena ribozyme, hc16 ligase with and w

275 entiation program similar to deletion of the full-length TF.

276 e immunity, and determine the structure of a full-length TIR-STING fusion from the Pacific oyster Cra

277 the updated reference tomato genome found 34 full-length TPS genes and 18 TPS pseudogenes.

278 Full-length transcript analysis links multiple alternati

279 Rs and splice isoforms, we identified 28,858 full-length transcript isoforms.

280 rimental evidence showed both a reduction in full-length transcript levels and an increase in levels

281 ion of the silencing cassette results in the full-length transcript of 901 nucleotides containing a 2

282 genes, and (ii) the difficulty of obtaining full-length transcript sequences.

283 actor Cubitus interruptus accumulates in its full-length, transcription activating form.

284 in alternative transcript identification of full-length transcripts in short-read RNA-Seq data, whic

285 function tolerates substantial reduction in full-length transcripts, helping to determine the pathog

286 y 120-fold and annotate it using 6.5 million full-length transcripts, thus improving our understandin

287 S) can overcome these limitations by reading full-length transcripts.

288 Electron microscopy of the full-length ULK1 complex shows that the FIP200 coiled co

289 yme, hc16 ligase with and without substrate, full-length Vibrio cholerae and Fusobacterium nucleatum

290 As expected, full-length vinculin and talin are autoinhibited and do

291 ere we studied the interactions of activated full-length vinculin with actin and the way it regulates

292 iral RNA after ART discontinuation with near full-length viral DNA from peripheral blood and lymph no

293 entally validated epitopes sequences on 3985 full-length viral genomes revealed 19 highly conserved e

294 r retroviruses, HIV-2 packages two copies of full-length viral RNA during virus assembly and efficien

295 y of Yorkie WW domains interactions with the full-length Warts PPXY domain, and numerous PPXY motif v

296 ans complementation of heterokaryons using a full-length wild-type allele of the CpRbp1 gene resulted

297 This report describes the effects of full-length, wild-type APC (fl-APC) on cell-cell adhesio

298 RNA sequencing confirmed the lack of full-length WT1 in all fusion positive samples as well a

299 he cryo-electron microscopy structure of the full-length WzmWzt transporter from Aquifex aeolicus bou

300 his antiterminator activity may help produce full-length Xist RNA while rendering the Xist locus resi