ライフサイエンスコーパス: chimeric protein

1 filing after inducing signalling through our chimeric protein.

2 i and examined the function of the resulting chimeric protein.

3 latively weak costimulatory delivered by the chimeric protein.

4 led-coil motifs in the NH(2) terminus of the chimeric protein.

5 r, and provide approaches for targeting this chimeric protein.

6 ttempted to generate ectopic eyes with these chimeric proteins.

7 tem, rapamycin is used to heterodimerize two chimeric proteins.

8 d-type RARalpha/RXRalpha or other X-RARalpha chimeric proteins.

9 tructure-based models of UVF, EnHD, and both chimeric proteins.

10 phrinB2 and EphB4 and did not respond to the chimeric proteins.

11 eer human red blood cells that express these chimeric proteins.

12 v, and nef to encode a series of novel HIV-1 chimeric proteins.

13 human Src tyrosine kinase to create inactive chimeric proteins.

14 The chimeric proteins act on both reporter and endogenous mR

15 The chimeric proteins activate or repress the targeted mRNAs

16 The chimeric protein also enables cytokine-independent growt

17 The mutant chimeric proteins also inhibited proliferation of IFNalp

18 Henipavirus G chimeric protein analysis implicated residue 507 in the

19 Analysis of an Msh2-Msh6/Msh3 chimeric protein and mutant Msh2-Msh3 complexes showed t

20 the high-affinity binding of VCAM-1/CD106 Fc chimeric protein and promoted VCAM-1-dependent arrest to

21 part, for the higher affinity of the native chimeric protein and the lower affinity of the denatured

22 In this study, using a variety of chimeric proteins and deletion mutants, we define the fe

23 in vitro Ub binding assays using domain swap chimeric proteins and mutated domains in isolation as we

24 we have constructed a collection of C92/P98 chimeric proteins and tested their abilities, both in th

25 derstand the biochemical properties of these chimeric proteins and to establish a system to study the

26 y targeting CSP to synaptic vesicles using a chimeric protein approach.

27 etermined how targeting and stability of the chimeric proteins are affected by the length and hydroph

28 The chimeric proteins are constitutively active, stimulate o

29 Such chimeric proteins are easy to design, express, purify an

30 We show that both types of chimeric proteins are made in IAV-infected cells, genera

31 Here, using these chimeric proteins as epitope suppliers, we compared with

32 The structures of the chimeric proteins assembled into VLPs were verified immu

33 -124 of PrP, Chi3 Tg mice, which express the chimeric protein at a very low level, start developing a

34 Abrogation of Axl activation by soluble Axl chimeric protein (Axl-Fc) or small interfering RNA (siRN

35 ficacy, we designed PvRMC-CSP, a recombinant chimeric protein based on the P. vivax CSP (PvCSP).

36 While several chimeric proteins bearing residues of the M-Vpu transmem

37 subfamily members to Klotho family proteins, chimeric proteins between FGF19 subfamily members or chi

38 Using mutants of paxillin and chimeric proteins between HIC-5 and paxillin, we demonst

39 proteins between FGF19 subfamily members or chimeric proteins between Klotho family members were con

40 ivity of OATP1B3, we constructed a series of chimeric proteins between OATP1B3 and 1B1, expressed the

41 s that did not interact with S(3)-RNase, and chimeric proteins between Pi SLF(1) and Pi SLF(2) to add

42 cific regions, and used truncated Pi SLF(2), chimeric proteins between Pi SLF(2) and one of the Pi SL

43 n heat-induced desensitization, we generated chimeric proteins between TRPV1 and TRPV3, a heat-gated

44 In the chimeric proteins, both the hydrophobic core and charged

45 The VEGF-angiopoietin-1 (VA1) chimeric protein bound to both VEGF receptor-2 and Tie2

46 into a bacterial collagen-like protein, this chimeric protein bound to integrin.

47 re we developed a soluble NUDT9H model using chimeric proteins built from complementary polypeptide f

48 ally homologous when expressed as individual chimeric proteins but not when expressed in the context

49 ch allostery can evolve, we have generated a chimeric protein by joining the catalytic domain of an u

50 In particular, we design chimeric proteins by hybridizing EIC from thermophilic a

51 lar and structural domains so that the final chimeric protein can be utilized to create novel bioacti

52 The resulting chimeric proteins can adopt the [PSI+] prion state in ye

53 This simple but powerful approach, employing chimeric proteins, can reinvigorate studies of 14-3-3/ph

54 ace, and its successful use in the design of chimeric proteins capable of targeting genomic regions o

55 ssion, indicating the strong toxicity of the chimeric protein Chi3.

56 Alefacept is a chimeric protein combining CD58 immunoglobulin-like doma

57 The PIPSL gene encodes a chimeric protein combining the lipid kinase domain of PI

58 cture-function relationships by constructing chimeric proteins combining sequences from CerS2, which

59 UVF's thermostability, we built two hybrid, chimeric proteins combining the sets of buried and surfa

60 It is now evident that DSPP is a chimeric protein composed of 3 parts: dentin sialoprotei

61 In this study we used a chimeric protein composed of the 675-residue receptor-bi

62 A chimeric protein composed of the septin Cdc10 and the C-

63 re we demonstrate that FIST15, a recombinant chimeric protein composed of the T-cell-stimulatory cyto

64 Recombinant immunotoxins (RITs) are chimeric proteins composed of an Fv and a protein toxin

65 Chimeric proteins composed of domains from the two attac

66 We employed chimeric proteins composed of exogenous BH3 domains inse

67 Chimeric proteins composed of HIV Gag (p24) fused to the

68 By engineering chimeric proteins composed of Mfn1 and Mfn2, we discover

69 Using acceptor photobleaching FRET and chimeric proteins composed of MyoD, Id1, E12, E47, E12(N

70 50 partner genes and result in production of chimeric proteins composed of the ALL1 N terminus and th

71 ts leading to GDP release, we have created a chimeric protein comprised of Escherichia coli NFeoB and

72 By utilizing a knock-in mouse expressing a chimeric protein comprised of the body of Rom1 and the C

73 A contact site A (csA)-SibA chimeric protein comprising only the transmembrane and c

74 We engineered a chimeric protein consisting of GATA4 and the cell-penetr

75 85beta differ in their N-terminal sequences, chimeric proteins consisting of amino or carboxy-termina

76 steps, we performed an unbiased screen using chimeric proteins consisting of CD4 fused to the muscle

77 Recombinant chimeric proteins consisting of segments of hLf and bovi

78 the branching and cyclobutanation reactions, chimeric proteins constructed from farnesyl diphosphate

79 Through a series of chimeric protein constructions tested for their activity

80 e optical microscopy and genetic analysis of chimeric protein constructs to evaluate the binding dist

81 mation reactions are promiscuous in that the chimeric protein containing 14 repeats can readily cross

82 ocumented Pex15p traffic from the ER using a chimeric protein containing a C-terminal glycosylation a

83 A typical MocR/GabR-type regulator is a chimeric protein containing a short N-terminal helix-tur

84 AtCGL160, as well as a chimeric protein containing the amino-terminal part of A

85 A chimeric protein containing the beta-subunit of SSO0536

86 teins of Newcastle disease virus (NDV) and a chimeric protein containing the cytoplasmic and transmem

87 verexpressing in vivo a transgene encoding a chimeric protein containing the cytoplasmic domain of GP

88 could be transferred to PRMT1 by creating a chimeric protein containing the N terminus of PRMT8 fuse

89 An E1A-E6 chimeric protein containing the Ser/Thr domain of the E6

90 and undetectable at the cell surface, (ii) a chimeric protein containing the TM of ABCG1 and the cyto

91 Leu-rich repeat extensins (LRXs) are chimeric proteins containing an N-terminal Leu-rich repe

92 noic acid, was decreased in cells expressing chimeric proteins containing at least one ABCD2 moiety.

93 Like chimeric proteins containing only a single NR2A or NR2B

94 The results demonstrated that chimeric proteins containing the N-lobe or the N1.1 subd

95 teractions, the oligomeric state of purified chimeric proteins containing the Staphylococcal nuclease

96 r basis of transport inhibition, a series of chimeric proteins containing transmembrane and cytosolic

97 Chimeric proteins, containing B-finger sequences from sp

98 2-OB(Stn1) chimeras indicates that whether a chimeric protein contains the Rpa2 or Stn1 version of th

99 induced nuclear export, the human TCF4/POP-1 chimeric protein continues to function as a repressor fo

100 iption of KSHV lytic genes, and a Rad21-CTCF chimeric protein converted CTCF into an efficient transc

101 neutralized only by homologous antisera, the chimeric proteins could be neutralized by both BTV-1 and

102 In conclusion, FH-Fc chimeric proteins could serve as adjunctive treatments a

103 essing the mutant kinase B-Raf(V600E) or the chimeric protein DeltaRaf-1:ER and that MEK-ERK-sensitiv

104 Evaluation of the soluble chimeric proteins demonstrated that the meprin A5 antige

105 The analysis of chimeric proteins demonstrated that the N-terminal half

106 Chimeric proteins derived from B. subtilis AbrB and the

107 omparison to the parental m1 VacA protein, a chimeric protein (designated m2/m1) containing m2 sequen

108 Recombinant immunotoxins (RITs) are chimeric proteins designed to treat cancer.

109 l basis for receptor selectivity by studying chimeric proteins developed by interchanging loops betwe

110 Chimeric proteins driven by TAT of HIV have been exploit

111 lecules were covalently fused, the resulting chimeric protein efficiently promoted proliferation.

112 This chimeric protein elicits protective immunity, mediated b

113 We found that the chimeric protein EspA-FliCi filaments were biologically

114 ine whose oncogenic potential is driven by a chimeric protein EWS-ATF1 (Ewing's sarcoma protein-activ

115 s a pediatric bone cancer that expresses the chimeric protein EWSR1/FLI1.

116 These chimeric proteins exhibit a shift in affinities to refle

117 Mice whose red blood cells carry the chimeric proteins exhibit resistance to 10,000 times the

118 The chimeric protein exhibited decreased cell-surface expres

119 An IE62 TAD-ICP4 chimeric protein exhibited trans-activation ability (10.

120 g chemical cross-linking, we showed that the chimeric protein exists predominantly as a tetramer, med

121 munosorbent assay, the resulting recombinant chimeric proteins expressed epitopes from all three vari

122 al deficiency due to the effects of abnormal chimeric protein expression.

123 line proliferation and growth on LTR2-FABP7 chimeric protein expression.

124 core proteins, NP and M, and containing two chimeric proteins, F/F and H/G, composed of respiratory

125 -derived cell line (HEK 293-C3) to express a chimeric protein (F9CH) comprising the Gla domain of fac

126 We use a chimeric protein, FNoTNc, to investigate the molecular b

127 rehensive series of IL-36 agonist/antagonist chimeric proteins for which we measured binding to the I

128 In vitro, these chimeric proteins form amyloid fibers, with more repeats

129 The chimeric proteins form circular octamers, whereas the wi

130 Chimeric proteins formed between the Drosophila P-elemen

131 In this study, we found that a chimeric protein, formed by fusing vaccinia virus protei

132 and betac were expressed in Phoenix cells as chimeric proteins fused to enhanced cyan or yellow fluor

133 This unusual chimeric protein fuses a 70-amino acid N-terminal sequen

134 er of chromosomal translocations that create chimeric proteins, fusing the N terminus of MLL to sever

135 Chimeric proteins generated by fusing the carboxy termin

136 We have catalyzed the four reactions with chimeric proteins generated by replacing segments of a c

137 Chimeric proteins generated from the two phosphatases sh

138 e.g., from nucleases or integrases, to form chimeric proteins, genomes could be manipulated or modif

139 These chimeric proteins had similar effects on normal bone.

140 We show that the chimeric protein has mixed agonistic/antagonist properti

141 ic leukemia, but the function of the encoded chimeric protein has not yet been characterized in detai

142 d C termini of NMDA receptor subunits, these chimeric proteins have been used as a model for studying

143 hannesburg/1/66 HEF full-length protein or a chimeric protein HEF-Ecto, which consists of the HEF ect

144 yt1Aa to Ls's BinA yielding a broad-spectrum chimeric protein highly mosquitocidal to important vecto

145 Moreover, priming with the chimeric protein improved the magnitude and polyfunction

146 omains and expressed each independently as a chimeric protein in a heterologous expression system.

147 Expression of a FANCD2-Ub chimeric protein in RAD18-depleted cells enhances REV1 a

148 o overcome this bottleneck, we constructed a chimeric protein in the cyanobacterium Synechococcus elo

149 yelocytic leukemia (PML) to produce PAX5-PML chimeric protein in two patients with B-cell acute lymph

150 RNA targets bound by the chimeric protein in vivo are covalently marked with urid

151 However, a chimeric protein in which the core kinase domain of PIP5

152 he TCR constant regions and/or creation of a chimeric protein in which the human constant regions wer

153 We found that a chimeric protein in which the mispair-binding domain (MB

154 A chimeric protein in which the ScSec2-GEF domain is repla

155 This was confirmed by use of a chimeric protein in which the SH4 domain of Vac8 was swa

156 xy)-2-propylamine (ATB-BMPA) labeling of the chimeric proteins in low density microsome fractions iso

157 e examined the cleavage-secretion of ACE-CD4 chimeric proteins in mammalian cells and Pichia pastoris

158 hus potential for the production of abnormal chimeric proteins in the brains of translocation carrier

159 vely active anaplastic lymphoma kinase (ALK) chimeric proteins in the pathogenesis of anaplastic larg

160 he impact of expressing CTCFL and CTCF-CTCFL chimeric proteins in the presence or absence of endogeno

161 Investigation of the chimeric proteins in vitro reveals that repeat-expansion

162 Using chimeric proteins in which CD4 is fused to the large int

163 Previous studies of GagZip chimeric proteins in which NC was replaced with a hetero

164 We have now analyzed assembly by chimeric proteins in which nucleocapsid of human immunod

165 By assaying chimeric proteins in which portions of mouse Ro were rep

166 Using this strategy, we designed chimeric proteins in which the activation of the IFNalph

167 Characterization of chimeric proteins in which the AR and C-tail from HPV11

168 f on each protein, we constructed a panel of chimeric proteins in which the extracellular and transme

169 Comparison of chimeric proteins in which the globular head of NDV HN i

170 Using chimeric proteins in which the N- and C-terminal domains

171 In contrast, we show that chimeric proteins in which the neck region of DNGR-1 is

172 ever, several studies have demonstrated that chimeric proteins in which the nucleocapsid domain of Ga

173 ed in Cep164-depleted cells by expression of chimeric proteins in which TTBK2 is fused to the C-termi

174 dy, we generated H. pylori strains producing chimeric proteins in which VacA m1 segments of a parenta

175 foreign domain, we found that the resulting chimeric protein, in a concentration-dependent manner, t

176 ytosis and post-endocytic sorting of EGFR, a chimeric protein, in which the K63 linkage-specific deub

177 of genetic rescue experiments with CSLD-CESA chimeric proteins, in vitro biochemical reconstitution,

178 wo immunological properties: 1) it encodes a chimeric protein including peptides that may be targets

179 Chimeric proteins, including bispecific antibodies, are

180 Chimeric proteins incorporating motifs of cell-penetrati

181 We found that the chimeric protein increased the proliferation of human mo

182 rane targeting and surface expression of the chimeric protein, indicating that the BST-2 GPI anchor s

183 protein, led to nuclear accumulation of this chimeric protein, indicating that this sequence was suff

184 cting signals to direct incorporation of the chimeric protein into the virion.

185 This unique chimeric protein is composed of a 7-transmembrane domain

186 and Western blot analyses confirmed that the chimeric protein is expressed in tumor tissue, and a cel

187 the wild-type and chimeric MLL alleles, the chimeric protein is more stable.

188 ular basis for the oncogenic activity of MLL chimeric proteins is incompletely understood, it seems t

189 n to create fusion genes and their resulting chimeric proteins is supported, including inter-chromoso

190 res delivery to the PVC of either Kex2p or a chimeric protein (K-V), in which the Vps10p cytosolic ta

191 -expressing lymphoid cells stimulated with a chimeric protein linking IL-2 to the ectodomain of TGF-b

192 the LacI/GalR homologues, we have created a chimeric protein (LLhP), which comprises the LacI DNA-bi

193 s replaced with the ORF7b TMD, the resulting chimeric protein localized to the Golgi complex.

194 ried out with single islet cells adherent to chimeric proteins made of functional E-, N-, or P-cadher

195 We previously determined that these chimeric proteins maintain the [PSI+] yeast prion phenot

196 APOBEC3G/APOBEC3B chimeric proteins mapped a primary subcellular localizat

197 The PYGG chimeric protein may assist in provitamin A biofortifica

198 ionality of ABCD1/ABCD2 dimers by expressing chimeric proteins mimicking homo- or heterodimers.

199 PiSLF-like protein), and expressed GFP-fused chimeric proteins, named b-2-b and 2-b-2, in S(2) S(3) t

200 A chimeric protein (Nox2/4) consisting of the Nox2 transme

201 Using overexpression of a chimeric protein of Eve1 fused to the Gal4 activation do

202 Using chimeric proteins of GLUT5 and GLUT7, here we identified

203 howed no requirement for LTP, we constructed chimeric proteins of the two excitatory neuroligin subty

204 we compare the performance of MHETase:PETase chimeric proteins of varying linker lengths, which all e

205 the surface of red blood cells by expressing chimeric proteins of VHHs with Glycophorin A or Kell.

206 We also examined the display of chimeric proteins on the gp64null AcMNPV virion.

207 ly gated KIR3DS1(+) NK cells with KIR3DS1-Fc chimeric protein or an HLA-F-specific monoclonal antibod

208 to increase the proteomic diversity through chimeric proteins or altered regulation.

209 The chimeric protein PAX3-FOXO1, resulting from a translocat

210 esented here explain the properties of these chimeric proteins previously observed in yeast.

211 AML1-ETO is the chimeric protein product of t(8;21) in acute myeloid leu

212 AML1-ETO is the chimeric protein product of the t(8;21) in acute myeloid

213 determine whether the Nmnat1 portion of the chimeric protein provides axonal and somatic protection

214 We showed that this chimeric protein recognizes its target sequence (20 nucl

215 s lowering the critical concentration of the chimeric protein required for a nucleation reaction.

216 mycetemcomitans using truncated PhoA and Aae chimeric proteins, respectively.

217 a role for TANGO1 and TANGO1-like (TALI), a chimeric protein resulting from fusion of MIA2 and cTAGE

218 AML1-ETO and TEL-AML1 are chimeric proteins resulting from the t(8;21)(q22;q22) in

219 Further, the chimeric protein retained Msh6-like properties with resp

220 Whereas the CaNpl3 RG chimeric protein retained nearly wild-type function in S

221 We showed that neither chimeric protein retained the SI function of PiSLF(2), s

222 In the case of the F protein, analysis of chimeric proteins revealed that the signal peptide of th

223 Analysis of new chimeric proteins reveals that like T. thermophilus RNas

224 We propose that these chimeric proteins serve to equip melanocytes with novel

225 espite being transactivation-competent, this chimeric protein shows selectivity in p53 effector funct

226 h the major or minor fimbriae to the TLR4-Fc chimeric protein, signaling through TLR4 for both protei

227 The chimeric proteins, silk-elastin-like protein polymers (S

228 We found that a CD300f/Fc chimeric protein specifically binds to apoptotic/dead sp

229 We show that the proposed lambdaN-betaLac chimeric protein specifically targets its cognate RNA ap

230 te that mice expressing a soluble B7-2 Ig Fc chimeric protein spontaneously develop colitis that is d

231 simple procedure for the production of such chimeric proteins, starting from correctly folded protei

232 describe how the use of this newly developed chimeric protein strategy has allowed us to test the fun

233 Experiments with chimeric proteins suggest that the C-terminal DNA-bindin

234 Furthermore, these chimeric proteins supported 60S export even in the prese

235 The two chimeric proteins synergized, so that their co-expressio

236 We have taken advantage of a chimeric protein system to study the oligopeptide repeat

237 , the adapters LAT and SLP-76, visualized as chimeric proteins tagged with yellow fluorescent protein

238 The biosensor is based on a chimeric protein that combines the recognition and trans

239 f the quadruple mutant of strain 4243 with a chimeric protein that comprised human fH domains 6 and 7

240 d this idea by creating PAS-DHFR, a designed chimeric protein that connects a light-sensing signaling

241 d(s) mutation results in the production of a chimeric protein that contains the full-length coding se

242 these transcription factors creates a unique chimeric protein that controls a key cell-cycle and -dif

243 h the bacterial hemolysin ClyA resulted in a chimeric protein that elicited strong anti-GFP antibody

244 esponding residues from HCMV US6 generates a chimeric protein that inhibits human TAP and provides fu

245 entation by using IL-15 preassociated with a chimeric protein that is comprised of the extracellular

246 ouse model that leads to the expression of a chimeric protein that is fully human except for one amin

247 parasitic nematode, Ascaris suum, revealed a chimeric protein that is similar to a Phe-Met-Arg-Phe-am

248 c expression of alphaLNNd, a laminin/nidogen chimeric protein that provides a missing polymerization

249 Recombinant immunotoxins (RITs) are chimeric proteins that are being developed for cancer tr

250 rom Ciona intestinalis, Ci-VSP, we generated chimeric proteins that are voltage-sensitive and display

251 ce of BRD-NUT fusion oncogenes, which encode chimeric proteins that block differentiation and maintai

252 he Mixed Lineage Leukemia (MLL) gene produce chimeric proteins that cause abnormal expression of a su

253 Chimeric proteins that comprise contiguous domains of fH

254 However, analysis of chimeric proteins that contained the chaperone modules o

255 everal other non-NKCC1 homologues results in chimeric proteins that form homodimers but show little o

256 r KCNE3 C-termini with that of KCNE4 created chimeric proteins that strongly inhibited KCNQ1.

257 ve residues (HGEKL) in the ACE region of the chimeric proteins that were essential for their cleavage

258 further show, by using an allele encoding a chimeric protein, that this difference maps primarily to

259 ort that activity of nucleophosmin (NPM)/ALK chimeric protein, the dominant form of ALK expressed in

260 ociates through the PBX1 PBC-B domain of the chimeric protein to form higher-order oligomers in t(1;1

261 tentiating effect required binding of the gD chimeric protein to HVEM.

262 We construct a chimeric protein to interrogate subunit-specific contrib

263 ansmembrane (TM) and luminal tail causes the chimeric protein to lose SLN-like function.

264 wth was corrected with an inability of these chimeric proteins to form stable PD-localized complexes.

265 We used a series of deletion and chimeric proteins to identify the zinc finger domains th

266 says between sperm and recombinant Siglec-Fc chimeric proteins to measure interactions.

267 P6981 induced GFP-B-ZIP chimeric proteins to partially localize to the cytoplasm

268 Here, we used chimeric proteins to test whether DAT and SERT N and C t

269 Functional analysis of HOXA1-HOXB1 chimeric proteins uncovered a novel six-amino-acid C-ter

270 The chimeric protein was expressed in soluble form with high

271 The chimeric protein was readily incorporated into mitochond

272 lting green fluorescent protein (GFP)-tagged chimeric proteins was examined by fluorescence imaging,

273 ing a beta-lactamase (betaLa) reporter/NiV-M chimeric protein, we produced NiVLPs expressing NiV-G an

274 sed GFP reporter system and a recombinant Fc chimeric protein, we show that human FCRL6, a receptor s

275 yAsf1 C-terminal truncations and yeast-human chimeric proteins, we found that truncations at residue

276 Using a series of chimeric proteins, we identified specificity determinant

277 By analyzing ANO1-ANO6 chimeric proteins, we identify a domain in ANO6 necessar

278 Recombinant SIN viruses encoding nsP2/GFP chimeric protein were capable of growth in tissue cultur

279 ken up by mannose-6-phosphate receptors, all chimeric proteins were additionally endocytosed via mann

280 EphB2-Fc and ephrin-B2-Fc chimeric proteins were applied to adult RGC axons in vit

281 he cytoplasmic tail of PC7 were deleted, and chimeric proteins were constructed consisting of the lum

282 We checked that the chimeric proteins were correctly expressed and targeted

283 The chimeric proteins were found to be functional, as demons

284 ng of the role of gL in EBV-mediated fusion, chimeric proteins were made using rhesus lymphocryptovir

285 ies of monomeric and dimeric ebvIL-10.hIL-10 chimeric proteins were produced and characterized for re

286 glycoprotein (VSVG), we demonstrate that the chimeric proteins were successfully integrated into exos

287 wapped; NIH3T3 cells overexpressing the four chimeric proteins were tested for transformation activit

288 The chimeric proteins were variably expressed at the cell su

289 A chimeric protein West Nile virus (WNV) vaccine capable o

290 To achieve this goal we made several chimeric proteins where parts of ACAT2 were replaced by

291 However, chimeric proteins whose sequence showed divergence on th

292 parental genes PIP5K1A and PSMD4, forming a chimeric protein with a distinct cellular localization a

293 and minor fimbriae bound to a human TLR2:Fc chimeric protein with an observed K(d) of 28.9 nM and 61

294 position as the full-length protein or as a chimeric protein with its transmembrane and cytoplasmic

295 A chimeric protein with PylSn fused to the N terminus of t

296 the violet range has allowed for designing a chimeric protein with Renilla luciferase.

297 ve been seen for single transmembrane domain chimeric proteins with appended C termini of NMDA recept

298 de, PhrA, was analyzed in part by generating chimeric proteins with RapC, which targets the DNA-bindi

299 ZFNs are chimeric proteins with significant potential for the tre

300 The analysis of chimeric proteins with various N-terminal segments of hi