ライフサイエンスコーパス: fragment of

1 iamonds, based upon data from an exceptional fragment of a diamond-bearing peridotite, its clinopyrox

2 based on a fragment of a fertile leaf preserved in Burmese amber th

3 h selectivity, ii) tightly bind a structured fragment of a housekeeping gene mRNA, and iii) cleave it

4 RPA and its complex with the antigen-binding fragment of a parasite growth inhibitory antibody.

5 ies are known from Antarctica, a new dentary fragment of a pelagornithid bird from the middle Eocene

6 using a single-chain variable region (scFv) fragment of a specific antibody was developed.

7 RIP enables a protein fragment of a transmembrane precursor to function at a n

8 to both the stem-loop probe and the targeted fragment of a ZIKV amplicon.

9 rimental conditions, select the constituting fragments of a crystal.

10 ger Dryas (YD) impact hypothesis posits that fragments of a large, disintegrating asteroid/comet stru

11 By incrementally docking overlapping fragments of a ligand, DINC allowed predicting binding m

12 oid must be a rubble pile formed from impact fragments of a parent body with microporosity(9) of appr

13 Recombinant fragments of a rabbit coronavirus (RbCoV-HKU14) were ide

14 Homolog fragments of a rodent CoV were also observed at 8.9-kDa

15 Consequently, both fragments of a subunit can be selectively destroyed thro

16 These fragments of activity reappear on a compressed timescale

17 than at 24 h, and the majority mapped to the fragment of aflatoxin efflux-pump gene.

18 rminal portion, the C-terminal tyrosine-rich fragment of ALIX-PRD forms amyloid fibrils and viscous g

19 In solution, the N-terminal fragment of ALIX-PRD is dynamically disordered.

20 The 12-28 fragment of amyloid beta was used to show that as the ch

21 ory marker) and low sAPPbeta (a soluble beta fragment of amyloid precursor protein) in cerebrospinal

22 ucture to 1.8 angstrom resolution of the Fab fragment of an affinity-matured human monoclonal antibod

23 ans of antigen recognition, in which the Fab fragment of an antibody acts as an adaptor, linking a hu

24 t that is thought to have assembled from the fragments of an ancient collision.

25 ous rubble-pile object generated from impact fragments of an undifferentiated aqueously altered paren

26 route affording more than a gram of a major fragment of anti-HIV agents rubriflordilactones A and B

27 F(ab')2-only fragments of anti-CD47 antibodies failed to induce phago

28 w method for covalent immobilization of half-fragments of antibodies on silicon modified by 3-glycido

29 trode surface and HT-2 toxin antigen binding fragment of antibody (anti-HT2 (10) Fab).

30 Previously, we used the scFv fragment of antibody 237 as a chimeric antigen receptor

31 nti-HT2 immune complex single-chain variable fragment of antibody fused with alkaline phosphatase (an

32 sing a structurally homologue apolipoprotein fragment of apoA-I (4F) complexed with Abeta(M1-42) and

33 of endogenous beta-cleaved carboxy-terminal fragment of APP (APP-betaCTF).

34 ediated by the beta cleaved carboxy terminal fragment of APP (APP-betaCTF, C99).

35 script, we propose that the 99-aa C-terminal fragment of APP (C99), when delivered to the ER for clea

36 hypothesis proposes that a small amphipathic fragment of APP, the amyloid beta-protein (Abeta), self-

37 the levels of the membrane-bound C-terminal fragments of APP from both alpha-secretase cleavage (alp

38 The amino-terminal fragment of Ara h 1, a member of a family of small anti-

39 allergen independent of the carboxy-terminal fragment of Ara h 1.

40 action was due to the 5-7 kDa amino-terminal fragment of Ara h 1.

41 ed from automatically reconstructed cellular fragments of arbitrary size and shape.

42 cal extracts was around 20-220bp compared to fragments of around 600bp for the more easily visualized

43 Chondritic meteorites are fragments of asteroids, the building blocks of planets,

44 An N-terminal fragment of ATG2A that supports lipid transfer in vitro

45 Fragments of bacterial peptidoglycan (muramyl peptides)

46 ire new bodies can be regenerated from small fragments of blood vessels.

47 We hypothesized that fragments of both TMS(2)S and HMDS had carried out the r

48 Restoration of growth in hyphal fragments of both wild-type and ftsZ mutant hyphae can o

49 Fragments of buttons do not pair, suggesting that combin

50 re, we compare C5a and a modified C-terminal fragment of C5a, C5a(pep), in terms of G-protein couplin

51 anercept at the middle-up level of analysis (fragments of ca. 25-30 kDa).

52 cy of CD11b or Ly-6C/Ly-6G-specific variable fragments of camelid heavy chain-only antibodies (VHH) c

53 of the chemical syntheses of oligosaccharide fragments of cellulose, hemicellulose, pectin, and arabi

54 lts in dimers, trimers, tetramers, or longer fragments of chains of face-sharing octahedra in the cry

55 arify these relationships by studying larger fragments of cheetah mtDNA, both from an Indian cheetah

56 respond to OS via recognition of proteolytic fragments of chloroplastic ATP synthase, termed inceptin

57 lements that can capture, merge and relocate fragments of chromosomal DNA.

58 n have thus restricted vertebrate studies to fragments of circuits.

59 loped a technically robust assay targeting a fragment of COL6, which was elevated in serum from patie

60 n to have biological activities, including a fragment of complement C3, the spasmogenic C3f, which wa

61 However, the identification of small fragments of cone outer segments within the RPE led us t

62 th and without bound ligand of a recombinant fragment of conglutinin's C-terminal carbohydrate-recogn

63 agExtract), tandem mass spectrometry (MS/MS) fragments of corresponding native and uniformly labeled

64 Diamonds and their inclusions are unique fragments of deep Earth, which provide rare samples from

65 (SCC) EVs were enriched with the C-terminal fragment of desmoglein 2 (Dsg2), a desmosomal cadherin o

66 ion, we generated a panel of oligosaccharide fragments of different lengths and tested them with poly

67 Each long fragment of DNA is only sparsely covered by reads, no in

68 the other hand, the highly homologous Klenow fragment of DNA polymerase I containing an engineered gp

69 t reasonably good efficiency with the Klenow fragment of DNA polymerase I, and we identify thermostab

70 these clones revealed that they all share a fragment of DNA with homology to the genome of Bacteroid

71 g short DNA reads sourced from the same long fragment of DNA; subsequently, the tagged reads are sequ

72 ess can result in the exchange of very large fragments of DNA between the participating cells.

73 characterization and visualization of small fragments of DNA in processed botanical materials and wi

74 ode into clusters that represent single long fragments of DNA.

75 barcodes match reads from roughly 2-20 long fragments of DNA.

76 g signals of dentin sialoprotein (N-terminal fragment of DSPP) were decreased in the dentin matrix, t

77 lution of 2.5 A of a complex between the Fab fragments of E1 and HM14c10 and provide the first detail

78 lution of 2.5 A of a complex between the Fab fragments of E1 and HM14c10 provides the first detailed

79 l degranulation, and IgG1 or antigen-binding fragments of each anti-SEE enhanced degranulation by the

80 In fragments of early copper artifacts (third-second millen

81 d not detect robust increases in proteolytic fragments of ECM proteins in either setting.

82 mined the solution structure of a C-terminal fragment of eEF-2K, eEF-2K(562-725) that encodes two alp

83 Fragments of Ef-Tu retain binding capabilities to host p

84 We exposed fragments of eight Acropora millepora colonies (genotype

85 N and increases the levels of the C-terminal fragment of EMCN 3- to 4-fold.

86 Release of the C-terminal fragment of EMCN by TNF-alpha treatment was blocked by c

87 Furthermore, fusion of short fragments of EWSR1 to FLI1 is sufficient to recapitulate

88 The obtained glycoconjugates are related to fragments of exopolysaccharide galactosaminogalactan (GG

89 iscs) of the NGLs and their affinities for a fragment of family 51 carbohydrate-binding module (CBM)

90 ion and early fiber breakage, and that small fragments of fibers can play an important role in the pr

91 dynamic process in which participants replay fragments of fine-grained temporal patterns and are able

92 cts with a calpain-cleaved carboxyl-terminal fragment of FLNA.

93 trate that acutely introducing an N-terminal fragment of FMRP into BCs normalizes GABA release in the

94 s undergoing primed adaptation, spacer-sized fragments of foreign DNA are associated with Cas1.

95 mmune system that functions by incorporating fragments of foreign DNA into CRISPR arrays.

96 c elements, prokaryotes must first integrate fragments of foreign DNA into their genomic CRISPR array

97 course of CRISPR interference Cas3 generates fragments of foreign DNA that are recognized by the Cas1

98 rated from much longer S1-nuclease sensitive fragments of foreign DNA that require Cas3 for their pro

99 er adaptation, the Cas1-Cas2 complex selects fragments of foreign DNA, called prespacers, and integra

100 y alter their genomes by incorporating small fragments of foreign DNA, called spacers, into CRISPR lo

101 he other in complex with a tagged C-terminal fragment of Galpha.

102 ransposable elements (TEs) regularly capture fragments of genes.

103 e are able to quantitatively detect a 563 bp fragment of genomic DNA of Mycobacterium avium subspecie

104 NA repair and an accumulation of cytoplasmic fragments of genomic DNA.

105 irely precluded production of the N-terminal fragment of HDAC4 but also promoted Ca(2+)/calmodulin-de

106 the cardio-protective N-terminal proteolytic fragment of HDAC4 is enhanced in vivo in patients with d

107 Reexpression of the N-terminal fragment of HDAC4 prevents HDAC4-dependent diabetic card

108 ential step for production of the N-terminal fragment of HDAC4, which was attenuated by Ca(2+)/calmod

109 used with the initially insoluble N-terminal fragment of hepatitis C virus' E2 protein were tested.

110 table mutant of hGal1 (hGal-1), a C-terminal fragment of hGal-3 (hGal-3C) and hGal-7), with known HMO

111 table mutant of hGal1 (hGal-1), a C-terminal fragment of hGal-3 (hGal-3C), hGal-7, and an N-terminal

112 hGal-3 (hGal-3C), hGal-7, and an N-terminal fragment of hGal-9 (hGal-9N), were measured using electr

113 A 17-residue N-terminal fragment of htt(e1) (N17) has been suggested to play a c

114 udy, we sought to identify a minimal soluble fragment of HuCR1, which retains the complement regulato

115 e we report the X-ray crystal structure of a fragment of human ADAR2 comprising its deaminase domain

116 own interactions between a C-terminal domain fragment of human galectin-3 (hGal-3C) and three human s

117 R6/2 mice contain an N-terminal fragment of human huntingtin with an expanded polyQ and

118 y-relevant NHP brain circuits by packaging a fragment of human mutant HTT, the causative gene mutatio

119 RATIONALE: Recombinant fragment of human surfactant protein D (rfhSP-D) has bee

120 Fragments of interest are sequenced by default, while DN

121 adaptation, the Cas1-Cas2 complex integrates fragments of invader DNA as spacers in the CRISPR array.

122 Despite two crystal structures reported on fragments of IRBP and decades of research, the overall s

123 both undecorated and labelled with a soluble fragment of its cellular receptor, feline junctional adh

124 ATCC 27405, with both SAM and an N-terminal fragment of its peptidyl-substrate at 2.04 A resolution.

125 Because only fragments of its habitat are accessible to humans, this

126 plex with rhesus CD4 and the antigen-binding fragment of ITS90.03 at 2.5- angstrom resolution reveale

127 F(ab')2 but not Fc fragments of IVIG induced death of human neutrophils, wh

128 The F(ab')2 fragment of K9.361 did not induce anaphylaxis, even afte

129 interaction study of the C-dots and the DNA fragment of lambda bacteriophage was performed, and the

130 Thick fragments of laminar crustacean cuticle are scattered wi

131 a histolytica kills human cells by ingesting fragments of live cells until the cell eventually dies,

132 Substituting FRRV into a fragment of LL37, a natural substrate of OmpT, led to a

133 We found that an extracellular fragment of low-density lipoprotein receptor-related pro

134 n from tissue necrosis in a shorter congenic fragment of Lsq-1 (C.B6-Lsq1-3).

135 of the nAChR alpha1 subunit bound by the Fab fragment of mAb35, a reference monoclonal antibody that

136 ulting in production of the N-terminal 34 aa fragment of MARF1 (Fig.

137 ave implicated calpain-dependent proteolytic fragments of menin, the product of the MEN1 tumor suppre

138 ircumsporozoite protein (CSP) and the 42-kDa fragment of merozoite surface protein 1 (MSP-1(42)) of P

139 trated in the synthesis of a tetrasaccharide fragment of Micrococcus luteus teichuronic acid containi

140 s such as microbes, metabolites, toxins, and fragments of microorganisms are present ubiquitously in

141 Draft genomes are assemblies that contain fragments of misassembled regions (gaps).

142 1-3], and they have been restricted to short fragments of mitochondrial DNA.

143 were tested in NMRI mice transplanted with a fragment of mouse adenocarcinoma (MAC13).

144 stal structures of an anaerobically prepared fragment of mouse viperin (residues 45-362) complexed wi

145 of the human genes, including small RNAs and fragments of mRNAs and long noncoding RNAs (lncRNAs).

146 port an experiment in which separating short fragments of musical discourse by vertical white gaps in

147 the accumulation of an amyloidogenic exon-1 fragment of mutant huntingtin (mHTTx1) modulates the exp

148 Rare surviving fragments of mycelium, usually around branches, appear t

149 and Neandertals has resulted in introgressed fragments of Neandertal DNA in the genomes of present-da

150 humans and study the effects of introgressed fragments of Neandertal DNA on this phenotype.

151 evaluated deuterium uptake data from the Fab fragment of NISTmAb reference material (PDB: 5K8A ) from

152 w research suggests that a highly inhibitory fragment of Nogo-A is generated by the amyloid precursor

153 Treatment with a soluble fragment of NRP1 (sNRP1) prevented ANGPTL4 from binding

154 ostic criterion by which to identify ancient fragments of oceanic crust, and as a constraint on the f

155 he nuclear translocation of an intracellular fragment of ODZ1 through proteolytic cleavage by signal

156 nhibit activity in context of the DH/PH-DEP1 fragment of P-Rex1 and interacts with the DH/PH domains

157 AgA are naturally occurring amyloid-forming fragments of P1 and WapA, respectively.

158 mpared with the 140-kDa N-terminal catalytic fragment of p261 (p261N), which we kinetically character

159 1, Y1H screens were performed with a genomic fragment of P5CS1, containing 1.2-kB promoter and 0.8-kb

160 Intermittent administration of a fragment of Parathyroid hormone (PTH) activates osteobla

161 t negative membrane-anchored C-terminal tail fragment of PC1 elevated NHA2.

162 eptide GGP817 containing glucagon fused to a fragment of peptide YY (PYY) acted as a triagonist at th

163 Signature fragments of PGN are proinflammatory through engagement

164 itic meteorites, which in turn are primitive fragments of planetary bodies.

165 e recent structure of a catalytically active fragment of PLCepsilon, provide the first evidence that

166 We further identified fragments of PRC2-binding lncRNAs that are enriched with

167 amyloidogenic peptides, namely, the 106-126 fragment of prion protein (PrP(106-126)) and the human i

168 Vasoinhibins are N-terminal fragments of prolactin that prevent BRB breakdown during

169 PAP(248-286) is a peptide fragment of prostatic acid phosphatase and has been repo

170 smaller, soluble but relatively hydrophobic fragments of protein (plasmin-generated protein fragment

171 re believed to be solely derived from linear fragments of proteins, but this concept was challenged s

172 uggest that Hippocamp is probably an ancient fragment of Proteus, providing further support for the h

173 natural agonists of PTHR1, and an N-terminal fragment of PTH, PTH(1-34), is used clinically to treat

174 f otherwise poorly active N-terminal peptide fragments of PTH by conjugating them to nanobodies (VHHs

175 cations to concise preparation of the linear fragment of pumiliotoxin B (myotonic, cardiotonic) and e

176 e to obtain the removal efficiency of NOx by fragments of pyrolyzing PE.

177 olubility assessment of tens of thousands of fragments of recombinant DISC1.

178 cbC-penDE complex and partial duplication of fragments of regulatory genes.

179 on various preparative steps to generate DNA fragments of required concentration, purity and average

180 The route proceeds by condensing fragments of reversed polarity relative to conventional

181 Robo and show that the cleaved extracellular fragment of Robo can function as a ligand for SYG-1/Neph

182 ow that neurons can release an extracellular fragment of Robo upon cleavage to attract glia during mi

183 etween genotypes introgressed by chromosomal fragments of Robusta and non-introgressed genotypes.

184 RPT1 interact in vitro, and the interacting fragment of RPT1 carries a PfPKG consensus phosphorylati

185 The N-terminal Gly-rich fragment of rSp0032 and the C-terminal His-rich fragment

186 anine-valine-phenylalanine-alanine (AVFA), a fragment of RuBisCO.

187 esent the crystal structure of an N-terminal fragment of Saccharomyces cerevisiae Hsp104 with the N d

188 we map the interaction of N- and C- terminal fragments of Sca2 and their contribution to actin bindin

189 ments covalently linked to one another or to fragments of secretory granule proteins or other islet-d

190 mediated decay (NMD) and xrn4 accumulates 3' fragments of select NMD targets, despite the lack of the

191 terize origin firing statistics from Okazaki fragment (OF) sequencing data.

192 report the amplification of discrete target fragments of several kilobases at 37 degrees C from both

193 Our convergent approach couples two achiral fragments of similar complexity and employs an enantiose

194 Using 23 promoter fragments of six UPR marker genes in a high-throughput e

195 Five nearly identical fragments of specialized bone tools, interpreted as liss

196 nly the matured (and not elongating) Okazaki fragments of stalled forks.

197 of full-length STIM1 or a STING-interacting fragment of STIM1 suppressed the function of dominant ST

198 slab dehydration using two suites of exhumed fragments of subducted, oceanic lithosphere.

199 Here, we present the structure of the Fab fragment of such an antibody.

200 helial glycocalyx, releasing heparan sulfate fragments (of sufficient size and sulfation to bind BDNF

201 .67 megabytes of information stored in short fragments of synthetic DNA using a portable nanopore seq

202 eir evolved variants, focusing on the Klenow fragment of Taq DNA polymerase (Klentaq).

203 be on the gold sensing chip and the unpaired fragment of target DNA works as a trigger to initiate th

204 ntify plasma concentrations of an N-terminal fragment of tau (NT1) in a large, well-characterized coh

205 PAGE, so too are detergent-insoluble, 37 kDa fragments of tau(9).

206 smic inclusions of the prion-like C-terminal fragments of TDP-43 CTD (TDP-43 C-terminal domain), form

207 , the target protein, or a synthetic epitope fragment of that protein, provides a template for select

208 f the neuropeptide NAPVSIPQ (NAP), an active fragment of the activity-dependent neuroprotective prote

209 We found the free N-terminal fragment of the adhesion G protein-coupled receptor (GPC

210 ffect, as well as leaving the rest targeting fragment of the affibody to specifically bind tumor over

211 eered enzyme in the synthesis of a dipeptide fragment of the antibiotic enduracidin.

212 e solved a structure of the toxin bound to a fragment of the antitoxin to 1.50 angstrom.

213 We also synthesized the short N-terminal fragment of the atypically split CL intein by solid-phas

214 wledge available for the central proteolytic fragment of the cascade, C3b.

215 e, we investigate the binding processes of a fragment of the coronavirus spike protein receptor bindi

216 901 nucleotides containing a 210 bp inverted fragment of the DvSSJ1 gene, the formation of a double-s

217 We previously reported that a fragment of the extracellular matrix protein agrin promo

218 testinal pathogen Vibrio cholerae A nontoxic fragment of the first 386 aa of cholix was genetically f

219 Endorepellin, the C-terminal fragment of the heparan sulfate proteoglycan perlecan, i

220 By sequencing a subgenomic fragment of the HIV-1 envelope from study participants i

221 ro spontaneously by a 9.7-kDa unglycosylated fragment of the human prion protein.

222 cised ~ 15 kilobases of DNA that contained a fragment of the integrated vector sequence and the neigh

223 Here, we develop a monomeric C-terminal fragment of the lambda repressor as a novel fluorescent

224 o-EM reconstruction of an ~160-kD N-terminal fragment of the lipid transport protein VPS13 reveals an

225 -mer RNA probe specific for a characteristic fragment of the mitochondrial DNA D-loop region of horse

226 ylogenetic trees and time trees containing a fragment of the NS5B region of these and 374 circulating

227 eer-specific primer/probe system targeting a fragment of the nuclear MC1-R gene was designed.

228 Cambodia and after successful DNA extraction fragment of the nuclear rhodopsin gene (RH1) and 9 micro

229 The time-dependent change in the mass of any fragment of the polypeptide chain depends uniquely on th

230 atriuretic peptide [P < .001] and N-terminal fragment of the prohormone brain natriuretic peptide [P

231 Next, a hexasaccharide fragment of the Pseudomonas aeruginosa exopolysaccharide

232 We report on a fragment of the quasicrystal-bearing CV3 carbonaceous ch

233 Increased p25, a proteolytic fragment of the regulatory subunit p35, is known to indu

234 efficients for RNA molecules (pseudoknots, a fragment of the rRNA, and the aptamer domain of the aden

235 pectrum probably overlaps with a derivatized fragment of the same metabolite, and D is modified propo

236 ineered adenoviruses containing a functional fragment of the shear-responsive endothelial nitric oxid

237 corticoid triamcinolone acetonide (TA) and a fragment of the small heterodimer partner (SHP).

238 rids by sandwich hybridization of a specific fragment of the Sola l 7 allergen coding sequence with a

239 eyes, we sample only a small and incomplete fragment of the visual world, which needs to be contextu

240 nd our results suggest that mutations in the fragment of the vp2 gene were not required for infection

241 Cloning and sequencing of nearly full-length fragments of the 16S rRNA gene showed that some of the s

242 structure of a SUZ12-RBBP4 complex bound to fragments of the accessory subunits PHF19 and JARID2.

243 f insoluble, fibrillar aggregates of peptide fragments of the amyloid precursor protein (APP), typica

244 the degradation of intracellular C-terminal fragments of the amyloid precursor protein via the MVB/l

245 rom bacteriophages, but they instead package fragments of the entire bacterial genome without prefere

246 However, treatment of Y7A KI mice with Fab' fragments of the function-blocking anti-CLEC-2 antibody,

247 the 3' ends of mRNAs and silence substantial fragments of the genome.

248 nd partitioning of large single-stranded DNA fragments of the homologous chromosome pairs allows for

249 embrane permeation and structural effects of fragments of the human IAPP and several rat IAPP mutants

250 olecules and precise cleavage and removal of fragments of the integrated proviral DNA from the genome

251 roteins by searching minimal common sequence fragments of the interacting protein pairs.

252 Nested 0.5- and 1.0-kilobase (kb) deletion fragments of the ITPR3 promoter were inhibited by NF-kap

253 affold-hopping, synthesis, and evaluation of fragments of the lead compounds and property-focused opt

254 shrew, Tupaia longipes, that inhabits forest fragments of the Lower Kinabatangan Wildlife Sanctuary,

255 parasite subpopulation, which have acquired fragments of the M. nemestrina associated subpopulation

256 We assessed variation in fragments of the mitochondrial (mt) genes cytochrome c o

257 ons by selection of the appropriate specific fragments of the mitochondrial DNA region and capture pr

258 Here, we show that those particles represent fragments of the plasma membrane that are pulled away an

259 cture of the ZIKV virion in complex with Fab fragments of the potently neutralizing human monoclonal

260 undergoes proteolytic cleavage and processed fragments of the protein are released into the extracell

261 leaved form, as membrane-spanning C-terminal fragments of the proteins.

262 elopment and reintroduced variably truncated fragments of the pxr region to test for their ability to

263 This is particularly true when fragments of the same gene are annotated as distinct gen

264 pairs of genes that are highly likely to be fragments of the same gene.

265 flicting phylogenetic signals from different fragments of the SCMV genome, so it is not appropriate t

266 Fragments of the shell membrane and cuticle are both pre

267 and structure elucidation of small molecule fragments of the stereochemically complex chlorosulfolip

268 As these T cells recognize fragments of the virus that are highly conserved and les

269 ermined through both peptide and oxonium ion fragments, of the desialylated Abeta1-15 or Abeta1-17 gl

270 s are typically quantified using carboxylate fragments of their fatty acid moieties produced by highe

271 tures of the EV71 virion in complex with Fab fragments of these potent and protective antibodies reve

272 E) than controls, as well as the presence of fragments of these proteins not found in controls, sugge

273 We investigated fragments of three diamond-bearing ureilites (two from t

274 uctures of the allergens in complex with Fab fragments of three murine mAbs that interfere with IgE A

275 RISPR editing identified a carboxyl-terminal fragment of thrombospondin-1 as an unexpected SMAP compo

276 Previous studies indicate that larger fragments of Tiam1, such as the region encompassing the

277 Recombinant APC and soluble fragments of TM (sTM) have been tested in settings assoc

278 Tagging N-terminal fragments of TMC1 with Aquaporin 3 (AQP3) and GFP fusion

279 polymerase chain reaction amplification of a fragment of tpi and bg genes.

280 In addition, a truncated fragment of trans-RA16 (S3) was identified, which exhibi

281 mensional structure in the presence of small fragments of tRNA (tRFs).

282 in (IL)-6, IL-10, pentraxin (PTX) 3, soluble fragment of tumor necrosis factor-like weak inducer of a

283 Split-TurboID consists of two inactive fragments of TurboID that can be reconstituted through p

284 he 106-residue LIN28:let-7 interaction (LLI) fragment of TUT4.

285 ose to build an artificial double helix from fragments of two strands connected by covalent linkages

286 and pit formation and release of C-terminal fragment of type I collagen from cells cultured on bone

287 ype III collagen, the unhydroxylated quarter fragment of type III collagen, and synthetic peptides as

288 proic acid, aprotinin, and the aminoterminal fragment of urokinase-type plasminogen activator.

289 e candidate PAMVAC is based on a recombinant fragment of VAR2CSA, the Plasmodium falciparum protein r

290 3 domain-containing proteins bind to another fragment of VEEV HVD.

291 I stoichiometry has been uncertain, and only fragments of VI have been identified in the virion struc

292 A 354-bp DNA fragment of VP1, an effective marker for diagnosing the

293 -bound A1 single domain and A1A2A3 tridomain fragment of VWF under shear stress in an ex vivo shear f

294 A1, A2, and A3 domains, an A1A2A3 tridomain fragment of VWF, plasmin-cleaved dimers of VWF, multimer

295 insic dynamics of A1 observed in recombinant fragments of VWF are conserved in plasma-derived VWF.

296 the common structural scaffold the chemical fragments of well-known antiepileptic drugs such as etho

297 esigned biotinylated probes to capture large fragments of Wolbachia DNA for sequencing using PacBio t

298 Thus, when expressed in mouse ESCs, a 5' fragment of Xist that contains Repeat-A sequesters RNA f

299 roughput sequencing of libraries composed of fragments of yeast genes to identify polypeptides that a

300 with an ATP analogue, RNA, and a C-terminal fragment of Yra1 (Yra1-C) at 2.6 A resolution.