ライフサイエンスコーパス: fragment of

1 thern analysis revealed that in these cells, fragments of 16S and 23S rRNA accumulate to high levels,

2 lly cleaved to generate two major C-terminal fragments of 35 and 25 kDa.

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

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

5 3, French Polynesia) in complex with the Fab fragment of a highly therapeutic and neutralizing human

6 of the GI.1 P domain in complex with the Fab fragment of a human IgA monoclonal antibody (IgA 5I2) wi

7 of an immunotoxin, consisting of the F(ab')2 fragment of a monoclonal antibody against the donor MHC

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

9 in a specific pocket in the antigen-binding fragment of a therapeutic antibody such as cetuximab.

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

11 well with F-actin; aa 401-600 and aa 501-550 fragments of AbpG show the same distribution as full-len

12 Pol alpha is enriched at extending Okazaki fragments of active and stalled forks.

13 pyogenes (IdeS)- or pepsin-generated F(ab')2 fragments of all four human IgG subclasses was determine

14 ctions, co-localization images of N-terminal fragments of amelogenin and ameloblastin around the pris

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

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

17 make the virus modestly more resistant to a fragment of an antibody that blocks the normal hemagglut

18 socyanide ligand is exchanged with a nitrene fragment of an imido ligand in a series of niobium bis(i

19 Given a set of DNA fragments of an individual, it consists of determining w

20 Some fragments of ancient protein are less prone to degradati

21 Sequential treatment with the F(ab')2 fragment of anti-FcgammaRIIB mAb followed by intact anti

22 ollowed by dual enzymatic labeling using Fab fragments of anti-Dig and anti-FITC conjugated to peroxi

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

24 ic anti-immunocomplex (anti-IC) single-chain fragment of antibody variable domain (scFv) and a monocl

25 analysis demonstrated that this recombinant fragment of antibody was able to bind to an S. venezuele

26 In contrast, Fab fragments of antibody 5F10 bind the tip of the E2 B doma

27 cryo-electron density maps, we show that Fab fragments of antibody 8B10 extend radially from the vira

28 00 residues); (ii) can generate dynamic-size fragments of any length (even for the whole protein sequ

29 levels of the beta-cleaved carboxy-terminal fragment of APP (betaCTF).

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

31 The Abeta fragments of APP are the major constituent of AD-associa

32 ate longer proteinase K-resistant (PrP(res)) fragments of approximately 17-32 kDa, similar to those o

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

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

35 sed as the template for PCR amplification of fragments of at least 8 kb.

36 ciated molecular patterns, including peptide fragment of bacterial flagellin (flg22) or translation e

37 ystem with well-established roles in sensing fragments of bacterial peptidoglycan.

38 ture of a fusion between BamB and a POTRA3-5 fragment of BamA.

39 Characteristic fragments of biofilm matrix components such as proteins,

40 n to stereoselective synthesis of the C1-C12 fragment of biologically active natural product (-)-laul

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

42 e conformational space of the N-terminal 1-5 fragment of bradykinin (BK[1-5](2+)) in the gas phase by

43 The activated fragment of C3 (C3b) and factor B form the C3 proconvert

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

45 Nanometer-sized fragments of carbon in the form of multilayer graphene (

46 henylenes (or "carbon nanohoops") are cyclic fragments of carbon nanotubes that consist of n para lin

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

48 luding antibody heavy chains, the N-terminal fragment of Cfa exhibits increased expression levels rel

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

50 A noncytotoxic C-terminal fragment of Clostridium perfringens enterotoxin (cCPE) i

51 que domain opens the door for generating any fragment of collagen in its native composition and stagg

52 ected at a quaternary carbon stereocenter to fragments of comparable complexity, which are united in

53 ants in KLKB1 and ACE were associated with a fragment of complement component 3f.

54 These come in two flavors: (i) proteolytic fragments of complement proteins (C3, C4, C5) generated

55 split pair of N-terminal and central domain fragments of complexin is sufficient to activate Ca(2+)-

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

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

58 SiC) particles and metal impurities from the fragments of cutting wire mixed in ethylene glycol based

59 nt assay, we tested M65 and M30 (circulating fragments of cytokeratin-18) and their respective fracti

60 Proteolytic fragments of Dau c 1 matched its T-cell-activating regio

61 We use this core fragment of DDX3 to test the function of two recurrent m

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

63 by simultaneously deleting and inserting DNA fragments of different sizes at a common genomic locatio

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

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

66 ause they are portable and can sequence long fragments of DNA molecules without prior amplification.

67 onally characterize the AlucJHEH gene, three fragments of double-stranded RNAs (dsRNAs) were designed

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

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

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

71 Analysis with multiple fragments of each protein showed that the interaction oc

72 plasmids containing the target nucleic acid fragments of Ebola virus, and 8 CFU of Escherichia coli

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

74 We exposed fragments of eight Acropora millepora colonies (genotype

75 Small fragments of either Elmo or ITSN1 that bind GPR124 block

76 identification of analogue 3 (ELA(19-32)), a fragment of ELA that binds to APJ, activates the Galphai

77 set of Cy3-labeled nucleotides by the Klenow fragment of Escherichia coli DNA polymerase I.

78 rvature sensing and explores whether peptide fragments of even shorter length can function as curvatu

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

80 lc-ceramide (GM1), and between a recombinant fragment of family 51 carbohydrate-binding module (CBM),

81 Fragments of Fat1 accumulate in SMC mitochondria, and th

82 er it forms a complex with an RGD-containing fragment of fibronectin.

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

84 the acquisition step of adaptation, in which fragments of foreign DNA are incorporated into the host

85 In bacteria and archaea, short fragments of foreign DNA are integrated into Clustered R

86 e to foreign genetic elements by integrating fragments of foreign DNA into CRISPR (clustered regularl

87 CRISPR immunity depends on acquisition of fragments of foreign DNA into CRISPR arrays.

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

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

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

91 ies on adaptive acquisition of spacers-short fragments of foreign DNA.

92 either as acene derivatives or as molecular fragments of fullerenes and graphene nanoribbons.

93 ost of the studies have been performed using fragments of fVIII and LRP1.

94 obe the dynamics of the interaction of large fragments of Gag and various variants of protease (inclu

95 Here, using large fragments of Gag, as well as catalytically inactive and

96 Indeed, analysis of fragments of GARP from different species shows that two

97 sed let-7 levels and increased amounts of 5' fragments of glycine transfer RNAs (tRNAs).

98 The synthesis of the C1-C27 fragment of hemicalide, a marine metabolite displaying a

99 m of this work was to study the alpha137-141 fragment of hemoglobin (Thr-Ser-Lys-Tyr-Arg), a small (6

100 led binding of the inhibitors within the UP1 fragment of heterogeneous nuclear ribonucleoprotein A1,

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

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

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

104 d the identification of structurally related fragments of high ligand efficiency and with activity on

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

106 rotein (HTT), studies reveal that N-terminal fragments of HTT containing the expanded PolyQ region ca

107 Similarly, a C-terminal fragment of human eIF4G-1, eIF4G(1357-1600), which preve

108 enetically engineered to express the III7-10 fragment of human fibronectin as a membrane protein.

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

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

111 ficient protocol for the synthesis of the EF fragment of idraparinux and its C5'-epi analogue (GH uni

112 Mice injected with IgA1P (1-10 mg/kg) had Fc fragments of IgA1 in both serum and urine, associated wi

113 Further, we show that complementary fragments of IP3 R1 assemble into tetrameric structures

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

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

116 osome elucidates the organization of the six fragments of its large subunit rRNA (as opposed to a sin

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

118 sed levels of full-length JAG1 and a shorter fragment of JAG1 without affecting Jag1 messenger RNA le

119 s enables ready synthetic access to extended fragments of K30 oligosaccharides and polysaccharides.

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

121 y that allowed access to seven arabinomannan fragments of LAM (1-7).

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

123 Thick fragments of laminar crustacean cuticle are scattered wi

124 Replacing the thiazole-thiazoline fragment of largazole with a bipyridine group gave analo

125 e can successfully target genomic DNA (gDNA) fragments of length >500 bp, and it can successfully dis

126 ing potential in processing some solubilized fragments of lignin into monomer aromatic compounds.

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

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

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

130 Structural analyses of Fab fragments of mAbs 023.102 and pn132p2C05 in complex with

131 tructures of Der p 1 in complex with the Fab fragments of mAbs 5H8 or 10B9.

132 potential, the structures of antigen-binding fragments of mAbs S1-15 and A6 have been determined both

133 the curvature-sensing capabilities of seven fragments of MARCKS-ED.

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

135 at a genetic fusion of the C-terminal 19-kDa fragment of merozoite surface protein 1 (MSP119) to P. f

136 ord plasma specimens from Mozambique: 19-kDa fragment of merozoite surface protein 1 (MSP119), erythr

137 Here, we present the structure of a fragment of MICAL-1 containing the MO and the CH domains

138 was demonstrated by pull down with distinct fragments of MICAL-L2 and confocal and structured illumi

139 1-3], and they have been restricted to short fragments of mitochondrial DNA.

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

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

142 ns to IBs that are composed of an N-terminal fragment of mutant huntingtin, the causative protein of

143 Accumulation of N-terminal fragments of mutant huntingtin (mHTT) in the cytoplasm,

144 We identified a fragment of Mwh with in vivo rescue activity and that bo

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

146 Hence, this fragment of N-methylritonavir is expected to be readily

147 and nicotinamide adenine dinucleotide (NAD), fragments of NAD detected in the same or opposite polari

148 NE- and PAE-generated fragments of native and exoglycosidase-treated blood-der

149 Ectopic expression of an N-terminal fragment of NleE (NleE(34-52)) in HeLa cells showed comp

150 By overexpressing the N protein binding fragment of Nsp9 in infected Marc-145 cells, the synthes

151 roteins built from complementary polypeptide fragments of NUDT9H and NUDT9.

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

153 The intracellular fragment of ODZ1 promotes cytoskeletal remodelling of GB

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

155 strated the ability of apical and C-terminal fragments of P1 to interact.

156 tudies, we have identified TFP5, a truncated fragment of p35, the Cdk5 kinase regulatory protein, whi

157 1, Y1H screens were performed with a genomic fragment of P5CS1, containing 1.2-kB promoter and 0.8-kb

158 ional proviral expression of HIV RNA (1.3-kb fragment of p6, protease, and reverse transcriptase) and

159 Heterologously expressed fragments of PavB and PspC containing repetitive structu

160 kinase associated (PASTA) domains, and binds fragments of peptidoglycan.

161 Fab fragments of PG102, while retaining CD40 binding, did no

162 The C-terminal fragment of Pih1 contains multiple destabilization facto

163 verified using soluble N-terminal truncated fragments of PilN and PilO Cys mutants, which purified a

164 tive bioelectric dynamics in amputated trunk fragments of planaria stochastically results in a consta

165 under ROC curve = 0.96) was identified as a fragment of pleiotrophin located near the protein's C-te

166 filter deployment with residual microscopic fragments of polydioxanone suture within the caval wall

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

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

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

170 igen (HLA) Class I molecules bind to peptide fragments of proteins degraded inside the cell and displ

171 reactions of the monochloramine with peptide fragments of proteins that are associated with carbohydr

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

173 ave therefore preferred to work with peptide fragments of PrP, suggesting that these peptides might s

174 Both are fused to a fragment of Pseudomonas exotoxin A (PE38) to create immu

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

176 Sequence alignments of the crystallized fragment of PvRBP2a with other PvRBPs highlight the cons

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

178 Both Rcf3 and the C-terminal fragment of Rcf2 associate with monomeric cytochrome c o

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

180 Similar results from a fragment of RNase H demonstrate that only half of the pr

181 Among YRNAs, predominantly, fragments of RNY4 and RNY5 were detected.

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

183 with tetrapeptide ala-val-phe-ala (AVFA), a fragment of RuBisCO.

184 deposits typically consist of an N-terminal fragment of SAA1 or SAA2, here, abundant C-terminal pept

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

186 s reduce dissociation of N-terminal cleavage fragments of Scc1 (NScc1) from Smc3.

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

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

189 tional activity, but the inactive C-terminal fragment of Slit2 did not.

190 s Slit2 and Robo-1, the bioactive N-terminal fragment of Slit2 inhibited TGF-beta-induced collagen sy

191 rse components of the SMN complex, including fragments of SMN itself have contributed greatly to our

192 e find that a short palmitoylated N-terminal fragment of Sonic Hedgehog binds Patched1 and, strikingl

193 ra of H-RasGTPgammaS mixed with a functional fragment of Sos (Sos(Cat)) at a 2:1 ratio are consistent

194 cessarily undermine the ability to integrate fragments of speech dispersed across frequency and time.

195 e p35 (vAc(P35)) and a cosmid representing a fragment of Spodoptera exigua nucleopolyhedrovirus (SeMN

196 However, larger C-terminal fragments of Sr33 and MLA10 can self-associate both in v

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

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

199 to images of bodies, but it is unclear which fragments of such images drive single neurons' responses

200 ormer typically constitute accurate sequence fragments of sufficiently well-represented proteins from

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

202 s needed for the production of 3' uridylated fragments of target mRNA in vivo.

203 the crystal structure of a 1,832-amino-acid fragment of TcdA (TcdA1832), which reveals a requirement

204 promotes the clearance of an ALS associated fragments of TDP-43 and is upregulated in the surviving

205 segment is linked to a single-chain variable fragment of the 17b human monoclonal antibody recognizin

206 residue resolution a 156-residue proteolytic fragment of the androgen receptor that contains a polyQ

207 of CovRS to the stress signals Mg(2+) and a fragment of the antimicrobial peptide LL-37 result in mo

208 the internal transcribed spacer (ITS) and a fragment of the beta-tubulin gene.

209 We demonstrate that the pro-apoptotic fragment of the bone marrow kinase on chromosome X (BMX)

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

211 pothesis regarding SCA6 disease is that a CT fragment of the Cav2.1 channel, which is detected specif

212 clude that the core [Ln(eta(4) -Sb4 )3 ](3-) fragment of the crystal has three locally pi-antiaromati

213 A soluble fragment of the cytosolic domain of PAM-1 was produced i

214 and entered the nucleus; very little soluble fragment of the cytosolic domain was produced from PAM-1

215 A fragment of the DNA basic region (br) of the GCN4 bZIP t

216 milk oligosaccharides, against an N-terminal fragment of the family 51 carbohydrate-binding module, a

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

218 xposure age of Ost 65 shows that it may be a fragment of the impactor that broke up the L-chondrite p

219 f the human Janus kinase 1 (JAK1) bound to a fragment of the intracellular domain of the interferon-l

220 lectrospun membrane biofunctionalized with a fragment of the laminin beta1-chain to modulate the expr

221 ternal transcribed spacer (ITS) region and a fragment of the large subunit (LSU) of the nuclear ribos

222 present the crystal structures of an active fragment of the LegK4 protein in apo and substrate-bound

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

224 on reaction to form the iodo pyrrolizidinone fragment of the molecule is described.

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

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

227 ipped, phosphorylated upstream trisaccharide fragment of the O-PS of V. cholerae O139.

228 s, two tetrasaccharides, and a trisaccharide fragment of the O-specific antigen of Vibrio cholerae O1

229 rocytic stage vaccine candidates, the 19 kDa fragment of the P. vivax Merozoite Surface Protein 1 (Pv

230 sults suggest that the polyQ carrying the CT fragment of the P/Q-type channel is sufficient to cause

231 C and non-MeC (C) versions of a 32 bp exon 7 fragment of the p53 gene.

232 site in FH for C3b, the activation-specific fragment of the pivotal complement component, C3.

233 We provide evidence that the N-terminal AB fragment of the prodomain represents an autonomous struc

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

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

236 A 3,530-bp fragment of the rpoB gene was 98.8% similar to the S. ha

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

238 r, but we have previously described a 3.7 kb fragment of the Scn10a promoter capable of recapitulatin

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

240 and human proteins, fused to the N-terminal fragment of the Yersinia enterocolitica T3S substrate Yo

241 llographic structure of the minimal adhesive fragment of the zebrafish Pcdh19 extracellular domain.

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

243 Interestingly, isotope effects involving fragments of the anion receptor (urea, aryl ring, etc.)

244 Across a set of six single chain-Fv fragments of the anti-lymphotoxin-beta receptor antibody

245 Radiolabeled synthetic fragments of the antimicrobial peptide ubiquicidin are p

246 nternal transcribed spacer (ITS) region, and fragments of the beta-tubulin (BenA), calmodulin (CaM),

247 We also propose to name the fragments of the broken tail as 'bezoarlets'.

248 and it interacts with and generates cleavage fragments of the clogged protein.

249 erns of the cross-linker as well as backbone fragments of the connected peptides are already observed

250 de primer pairs targeting short (127-314 bp) fragments of the cytochrome c oxidase I (CO1) DNA barcod

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

252 Conserved fragments of the genes encoding beta-giardin and glutama

253 In the presence of HGT events, different fragments of the genome are the result of different evol

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

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

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

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

258 ar transporter Wza and very small amounts of fragments of the K30 capsular polysaccharide substrate r

259 of a tetrasaccharide and two pentasaccharide fragments of the Le(a)Le(x) tumor-associated carbohydrat

260 li K-12, and in EHEC they destabilize the 3' fragments of the LEE4 and LEE5 operons and promote trans

261 of CKD stage or CKD progression, were either fragments of the major circulating proteins, suggesting

262 ow that diagnostic burn patterns on eggshell fragments of the megafaunal bird Genyornis newtoni, foun

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

264 d western blot validation, we found that two fragments of the myofibrillar structural protein myomesi

265 This was accomplished by binding Fab fragments of the neutralizing antibody DV2-E104 to the v

266 on of proteins by the proteasome, generating fragments of the original sequence.

267 The receptor binds fragments of the polysaccharides in aqueous solution wit

268 , which capitalizes on de novo sequencing of fragments of the proteins present in the sample.

269 Fragments of the putative biosynthetic genes for the new

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

271 s and collect structural data on overlapping fragments of the receptor with small-angle X-ray scatter

272 on, we prepared reporter plasmids containing fragments of the SULT1C3 5'-flanking region.

273 the nuclear ribosomal DNA (rDNA), as well as fragments of the translation elongation factor 1 alpha (

274 l growth of large tumours, even if different fragments of the tumour grow sub-exponentially due to nu

275 we investigate conformational preferences of fragments of the yeast Ste2p receptor using NMR.

276 ted with S-rich particles, including organic fragments, of the sludge and amended soils.

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

278 udies reveal that a proteolytically released fragment of this collagen, termed a matricryptin, promot

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

280 isrupting the Tiam1-NMDAR interaction with a fragment of Tiam1 blocks OGD-induced Tiam1 activation bu

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

282 r expansion of NHPRTR by adding 10.1 billion fragments of tissue-specific RNA-seq data.

283 study, we investigated whether an N-terminal fragment of TLR9 could be responsible for regulation of

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

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

286 Fab fragment of TRC105, a mAb that specifically binds to CD1

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

288 tterns showed very little overlap limited to fragments of type I and III collagens as the common deno

289 of the bone resorption marker C-telopeptide fragments of type I collagen (CTX), elevated osteoclasto

290 ional intracerebroventricular infusion of Fc fragment of tyrosine kinase receptor B protein (TrkB-Fc)

291 c amyloid peptide, based on an amyloidogenic fragment of vascular endothelial growth factor receptor

292 t methodology for amplification of two large fragments of viral genome covering about 80% of the uniq

293 ted cells can incorporate viral proteins and fragments of viral RNA, being thus indistinguishable fro

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

295 These hybrid molecules join the chemical fragments of well-known antiepileptic drugs (AEDs) such

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

297 we present the crystal structure of a large fragment of WipA, WipA435.

298 were fused to complementary non-fluorescent fragments of YFP and co-expressed in 293T cells.

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

300 n which MHCII was shown to present processed fragments of zwitterionic capsular polysaccharides to T