ライフサイエンスコーパス: engineered to express

1 cence recovery after photobleaching of cells engineered to express a beta1-GFP fusion protein indicat

2 In addition, we show that mice engineered to express a bitter taste receptor in 'sweet

3 Primary human NKT cells were engineered to express a CAR against the GD2 ganglioside

4 hase-3beta inhibitor TWS119, and genetically engineered to express a CD19-specific chimeric antigen r

5 ed therapeutically and that allogeneic cells engineered to express a chemorepellent protein would not

6 Adoptive immunotherapies composed of T cells engineered to express a chimeric antigen receptor (CAR)

7 ven single intravenous injections of T cells engineered to express a chimeric antigen receptor (CAR)

8 Human T cells engineered to express a chimeric antigen receptor (CAR)

9 n followed by autologous T cells genetically engineered to express a chimeric antigen receptor (CAR)

10 Mouse and human T cells were engineered to express a chimeric antigen receptor (CAR)

11 The adoptive transfer of autologous T cells engineered to express a chimeric antigen receptor (CAR)

12 ical trial of allogeneic T cells genetically engineered to express a chimeric antigen receptor (CAR)

13 dramatic results have been seen with T cells engineered to express a chimeric antigen receptor (CAR)

14 Adoptive transfer of T cells engineered to express a chimeric antigen receptor (CAR)

15 We used T cells engineered to express a chimeric T cell receptor that ca

16 CNiFERs are cultured cells that are engineered to express a chosen metabotropic receptor, us

17 ibit target cell Akt activity, and KS tumors engineered to express a constitutively activated Akt con

18 lpha(1A)AR stimulation using transgenic mice engineered to express a constitutively active mutant (CA

19 Adoptive transfer of T cells that are gene engineered to express a defined TCR represents a feasibl

20 owing reovirus infection, we used HeLa cells engineered to express a degradation-resistant mutant of

21 null for TGF-beta receptor II (TbetaRII) or engineered to express a dominant-negative Smad3 to atten

22 significantly reduced in S. frugiperda cells engineered to express a double-stranded RNA derived from

23 In contrast, when the cells were engineered to express a doxycycline-regulated REST/NRSF

24 In irradiated mice engineered to express a floxed p53 allele and a Nestin-C

25 oinfected with viable viruses that have been engineered to express a fluorescent reporter protein dur

26 We demonstrate that a mutation-prone virus engineered to express a foreign gene is an expedient mea

27 Furthermore, the virus can be engineered to express a foreign gene while still retaini

28 Here, we show that DENV can be genetically engineered to express a green fluorescent protein or fir

29 Adoptive transfer of T cells engineered to express a hepatitis B virus-specific (HBV-

30 n of sensory experience" in mice genetically engineered to express a human long-wavelength-sensitive

31 across cortical and limbic circuits in mice engineered to express a human loss-of-function depressio

32 e have recently shown that human CD4 T cells engineered to express a human melanoma-associated antige

33 ay "come hither" to maize pollen when it was engineered to express a maize attractant.

34 es by transplantation of primary fibroblasts engineered to express a micro-dystrophin/enhanced green

35 the slow-growing M. bovis M. bovis BCG, were engineered to express a model tumor antigen, the K(b)-re

36 lomavirus 16 E7 to knock-in mice genetically engineered to express a mutant form of pRb (pRb(DeltaLXC

37 iler's murine encephalomyelitis virus (TMEV) engineered to express a naturally occurring Haemophilus

38 Therapeutic cells engineered to express a PET reporter gene (PRG) specific

39 Importantly, T cells engineered to express a rapamycin-resistant mTOR constru

40 eport that approximately 10,000 T cells gene-engineered to express a single-chain IL-12 molecule can

41 We also demonstrate that CMFs, engineered to express a specific DR4 allele, can process

42 nce in a polyclonal immune system, mice were engineered to express a superantigen reactive to IgM of

43 eration more directly, we used MCF-10A cells engineered to express a synthetic ligand-inducible form

44 r knowledge, this is the first report of BCG engineered to express a tumor-associated antigen.

45 ced prostate cancer with T cells genetically engineered to express a tumor-reactive TCR and a dominan

46 T cells engineered to express a tumor-specific alphabeta T cell

47 ransgenic or retrovirally transduced T cells engineered to express a tumor-specific T-cell receptor.

48 HEK293 cells, engineered to express ABCG2 and fLuc, were used to scree

49 Mice engineered to express activated Ack1 exhibited a signifi

50 -231 human mammary adenocarcinoma cells were engineered to express active seprase to high levels.

51 A549 cell infection with adenovirus engineered to express AGS1/RASD1 (Ad.AGS1) inhibited log

52 B16 melanoma vaccines genetically engineered to express alphaGal epitopes (B16alphaGal) ef

53 he safety and activity of autologous T cells engineered to express an affinity-enhanced T cell recept

54 The oncolytic adenovirus ICOVIR-15K was engineered to express an EGFR-targeting BiTE (cBiTE) ant

55 Highly attenuated KBMA L. monocytogenes were engineered to express an epitope of the melanoma-associa

56 Highly attenuated KBMA L. monocytogenes were engineered to express an epitope of the melanoma-associa

57 human KRAS-dependent colon cancer cell line engineered to express an inducible KRAS-specific shRNA.

58 Ductal and acinar pancreatic cell lines were engineered to express an inducible Mist1 complementary D

59 tologous CD4(+) T cells that are genetically engineered to express an MHC class II-restricted antitum

60 mCherry monomeric red fluorescent protein engineered to express an N-terminal caspase 3 cleavage s

61 Cherry red fluorescent protein recombinantly engineered to express an N-terminal hexahistidine sequen

62 Yeast engineered to express an NR and a response element-drive

63 sing substituted peptides and DQ8 constructs engineered to express and present B:9-23 in fixed bindin

64 res, intracranial xenografts of glioma cells engineered to express Ang2 were highly invasive into adj

65 ncordantly, in human U87MG glioma xenografts engineered to express Ang2, increased expression of MT1-

66 Rodents engineered to express angiopoietin 1 (Ang-1) constitutiv

67 results suggest that lymphocytes genetically engineered to express anti-gp100 TCR may be of value in

68 results suggest that lymphocytes genetically engineered to express anti-p53 TCR may be of value for t

69 Analyses of 1c1c7/Tao variants engineered to express antisense/sense AhR constructs sug

70 ACT of T cells engineered to express artificial receptors that target c

71 more, GABARAP overexpression in CHO-K1 cells engineered to express AT(1)R increased angiotensin II bi

72 Tumor cells engineered to express B7-H3 elicit a rapid clonal expans

73 These effects were inhibited in PC3 cells engineered to express bcl2 (PC3-bcl2).

74 et genes, and mimicked the phenotype of mice engineered to express BCL6 with corepressor binding site

75 received an intravitreal transplant of MSCs engineered to express BDNF and green fluorescent protein

76 In this study, we injected VEEV or WEEV, engineered to express bioluminescent or fluorescent repo

77 Conversely, in mice engineered to express both AxD-associated mutations and

78 iruses, lacking any DNA intermediate, can be engineered to express both coding and noncoding RNAs sug

79 Mice engineered to express c-Myc in B cells (Emu-myc mice) de

80 hat pretreatment of mice for 8 h with Nissle engineered to express CAI-1 (Nissle-cqsA) greatly increa

81 Tumor cells of both types engineered to express calpain-2 antisense constructs als

82 T cells genetically engineered to express CARs can specifically recognize an

83 more, in the presence of NH(4)Cl, cell lines engineered to express cathepsin S supported infection by

84 OIR mice of hematopoietic stem cells (HSCs) engineered to express CCN1 harnessed ischemia-induced ne

85 expressing endogenous CCR4 and transfectants engineered to express CCR4 were assessed for receptor fu

86 ccurs in tissue culture cells and Drosophila engineered to express CD and UPRT.

87 therefore, we determined whether donor VSTs, engineered to express CD19.CAR, retained the characteris

88 generated HLAnull K562 cell clones that were engineered to express CD1d and costimulatory ligands.

89 one marrow progenitors that are retrovirally engineered to express Cdx4 serially replate in methylcel

90 ch approach involves the transfer of T cells engineered to express chimeric antigen receptors (CARs)

91 Similar to T-cells genetically engineered to express chimeric antigen receptors (CARS),

92 been observed following transfer of T cells engineered to express chimeric antigen receptors against

93 adoptive cell transfer therapy with T cells engineered to express chimeric antigen receptors or T-ce

94 stration of monoclonal antibodies or T cells engineered to express chimeric antigen receptors or T-ce

95 Adoptive transfer of CD8 T cells genetically engineered to express "chimeric antigen receptors" (CARs

96 (PFC) descending projection neurons in mice engineered to express Chr2 in layer V pyramidal neurons

97 Injection of a canine adenovirus (CAV-2) engineered to express Cre recombinase into the central c

98 n-defective, E1/E3 region-deleted adenovirus engineered to express CYP2B6-IRES-P450R, induced intrace

99 ld type (WT) and alpha(1)(0/0) mice and mice engineered to express diazepam-insensitive receptors (al

100 employing recombinant strains of PRV-Bartha engineered to express different reporter proteins.

101 We deafened CBA/CaJ male mice, engineered to express diphtheria toxin (DT) receptors in

102 80s of the first transgenic mice genetically engineered to express dominant oncogenes, involving inde

103 HOXA5 depletion in MCF10A cells engineered to express doxycycline-induced shHOXA5 slowed

104 rgic (mDA) neurons differentiated from hPSCs engineered to express DREADDs (designer receptors exclus

105 y ingestion of transgenic corn plant tissues engineered to express dsRNA.

106 brain cancer using a transgenic mouse model engineered to express E2F1 specifically within glial cel

107 DT40 cell lines engineered to express each of the three mammalian InsP(3

108 ator (tet-o); RCAS viruses infect only cells engineered to express ectopically the avian retroviral r

109 glucose microPET) of glioblastoma xenografts engineered to express EGFRvIII, but not their parental c

110 either transporter and sublines molecularly engineered to express either ATP7A (MeMNK) or ATP7B (MeW

111 Mice were engineered to express either cyclooxygenase-2 (COX-2) or

112 stem (CNS) was studied, using recombinant RV engineered to express either soluble TNF-alpha [SPBN-TNF

113 PIV5 was engineered to express either the RSV fusion protein (F)

114 drugs, a phenotype exacerbated in cells also engineered to express elevated levels of TbNTR or TbCPR.

115 mating, C. albicans white cells were reverse-engineered to express elevated, opaque-like levels of th

116 Human PC-3 prostate cancer cells were engineered to express enhanced green fluorescent protein

117 ularization in a human prostate cancer model engineered to express enhanced green fluorescent protein

118 Y. pestis strains engineered to express Escherichia coli LpxL are avirulen

119 with low ESRP1 expression, and PANC-1 cells engineered to express ESRP1 exhibited increased FGFR-2 I

120 ession analysis on Jurkat cells, genetically engineered to express exogenous HOX11.

121 apoptosis, Chinese hamster ovary (CHO) cells engineered to express Fc receptors were infected with re

122 CAR-deficient human dermal fibroblasts were engineered to express FcgammaR.

123 An OV engineered to express FGF2 was safe in tumor-bearing mic

124 outer membrane vesicle vaccines from mutants engineered to express fHbp variants had broad bactericid

125 and avirulent strains of Sindbis virus were engineered to express firefly luciferase, and the Xenoge

126 s using primary human PDAC cells genetically engineered to express firefly- and Gaussia luciferase, s

127 e lesion mimic background, and plant tissues engineered to express flavonoids or the avirulence gene

128 Using transgenic clonal parasite lines engineered to express fluorescent markers in combination

129 -kappaB (NF-kappaB) activity, although those engineered to express Fmod constitutively exhibited sign

130 Notably, 5HT1AR-deficient mice engineered to express functional 5HT1ARs only in DG GCs

131 mutant CCHF virus glycoproteins in CHO cells engineered to express functional or nonfunctional SKI-1.

132 sing a versatile transgenic Drosophila model engineered to express G(PA)C in tissues and cells of int

133 When the mAb heavy chains were engineered to express gag-p24, the alpha-Langerin, alpha

134 sence of soluble rhGal-9 or Raji tumor cells engineered to express Gal-9.

135 tive integrin complexes and that tumor cells engineered to express GEF-deficient GIV fail to transduc

136 tem of Deinococcus radiodurans that has been engineered to express GFP under the control of the recA

137 s and normal hematopoietic stem cells (HSCs) engineered to express Gpx3 short hairpin RNA (shRNA) wer

138 The screen employs a cell line engineered to express green fluorescent protein (GFP) in

139 ventricular assist device implantation were engineered to express green fluorescent protein (hCPCe)

140 isolated from embryonic mice transgenically engineered to express green fluorescent protein and tran

141 for clinical trials to evaluate S. gordonii engineered to express group A streptococcal M protein an

142 patient and population scales when TIPs are engineered to express >3-fold more genomic RNA than HIV

143 An S. Typhi strain engineered to express GtgE and therefore able to cleave

144 and V, the excitatory neurons in rat S1 were engineered to express halorhodopsin, a light-sensitive c

145 n between myocytes and syngeneic fibroblasts engineered to express HCN1 pacemaker channels (HCN1-fibr

146 fection with a murine cytomegalovirus (MCMV) engineered to express HEL induced extensive proliferatio

147 In cells engineered to express hemojuvelin, soluble hemojuvelin r

148 was examined in a mouse mammary tumor model engineered to express HER2 (EMT6-HER2 cells).

149 sion and a low-expressing strain genetically engineered to express high fHBP levels.

150 eplication-defective VSV can be successfully engineered to express high levels of antigenically authe

151 emonstration that once Bacillus anthracis is engineered to express high levels of SMase C, the result

152 ether human dendritic cells (DC) genetically engineered to express high levels of T-bet (i.e., DC.Tbe

153 When mAb heavy chain was engineered to express HIV Gag p24, the fusion mAb induce

154 carcinoma, and breast tumors, which were not engineered to express HMW-MAA.

155 Use of lines engineered to express HPL constitutively, in conjunction

156 Keratinocytes engineered to express HPV16 E6 or activated mutant HRAS,

157 eric virus HSV-1 17syn+/LAT2, an HSV-1 virus engineered to express HSV-2 LAT, demonstrated that this

158 In rat hepatocytes engineered to express human Cygb, Cygb-NOD activity show

159 Thus, humanized mice engineered to express human cytokines will significantly

160 dministering REGN421 to immunodeficient mice engineered to express human Dll4 inhibited the growth of

161 th of a murine colon adenocarcinoma that was engineered to express human HER2 (CT-26(HER2/neu)) in BA

162 Strikingly, ferret (but not mink) cells engineered to express human HIV-1 entry receptors suppor

163 rat strains and different tissues that were engineered to express human Hyal2 were still only poorly

164 C. elegans engineered to express human mSOD1 (G85R) in neurons deve

165 y generated humanized transgenic mouse model engineered to express human NRG1-IV, an isoform of the N

166 Conversely, HEK293 cells engineered to express human SERT and an activated form o

167 e and ICOS engagement by tumor cell vaccines engineered to express ICOS ligand enhanced antitumor imm

168 formation in vitro, and B16F melanoma cells engineered to express IGPR-1 displayed extensive angioge

169 Thus, aNSCs engineered to express IL-10 show enhanced ability to ind

170 ns with corresponding irradiated tumor cells engineered to express IL-4 or GM-CSFs, respectively, as

171 fibroblasts and human astrocytes, which are engineered to express inducible forms of neural reprogra

172 CRC lines (HCT116 and SW480) were engineered to express inducible tagged SPDEF or vector (

173 Transgenic maize engineered to express insecticidal proteins from the bac

174 NOD mice with intestinal K cells engineered to express insulin have reduced blood levels

175 ength transmembrane L1 and a secreted trimer engineered to express its extracellular domain would be

176 h induces CD4(+) and CD8(+) T-cell immunity) engineered to express Kras(G12D) (LM-Kras).

177 However, mice genetically engineered to express Kras(G12D) from its endogenous loc

178 tion of KPC mice with Listeria monocytogenes engineered to express Kras(G12D), along with depletion o

179 However, although Ba/F3 cells engineered to express leukemia-associated SHP-2 proteins

180 ty, because primary murine bone marrow cells engineered to express low amounts of BCR-ABL were substa

181 ctors from M protein, Lactococcus lactis was engineered to express M1 protein on its surface.

182 iments the tumor cells used were genetically engineered to express membrane FasL.

183 ines, consisting of MHC class I+ tumor cells engineered to express MHC class II molecules, stimulate

184 medulloblastoma cell lines (DAOY and UW228) engineered to express miR-520g, a biologically active co

185 by electroporation of synthetic DNA plasmids engineered to express modified human nAbs against multip

186 ediated events in vivo, transgenic mice were engineered to express mouse CD40 (mCD40tg) or a protein

187 ion profile of prostate adenocarcinoma cells engineered to express mt-SPOP overlaps greatly with the

188 id these problems, and miRNA clusters can be engineered to express multiple RNAi effectors, a feature

189 -3KO-M3 cells, a null background for InsP3R, engineered to express muscarinic M3 receptors.

190 Finally, Ba/F3 murine pro-B cells, engineered to express mutant ERBB2, became independent o

191 imilar observations were made with nematodes engineered to express mutant tat-activating regulatory (

192 locomotor deficit of Caenorhabditis elegans engineered to express mutTDP-43 or mutSOD1 and also prot

193 In mice engineered to express Myc and Akt1 in liver, co-expressi

194 We performed studies in mice engineered to express Myc and Akt1 in liver, which devel

195 n experiments and analysis of Fv1-null cells engineered to express natural or artificial Fv1 proteins

196 Here, we show that mouse embryo fibroblasts engineered to express Ndy1 or Ndy2 undergo immortalizati

197 It has been proposed that plants engineered to express nfsI could be used to remediate TN

198 cells stably transfected with the PTH1R and engineered to express NHERF1 under the control of tetrac

199 ry immunization (ELI) vaccine genetically re-engineered to express non-CO fragments of gag and pol fu

200 Thus, we used a mouse mutant engineered to express normal levels of SNAP-25 but only

201 Cells engineered to express only a non-phosphorylatable T1989A

202 Mice engineered to express only SPPL3 D271A in NK cells pheno

203 Here, we found that mice engineered to express only talin1(L325R) in myeloid cell

204 tem cell differentiation that can be further engineered to express other biochemical cues to control

205 thylotrophic yeast that has been genetically engineered to express over one thousand heterologous pro

206 ES cells engineered to express pancreatic and duodenal homeobox 1

207 ited proliferation of R1-11-PCFT4 HeLa cells engineered to express PCFT without the reduced folate ca

208 enhanced Id2 expression into brains of mice engineered to express platelet-derived growth factor in

209 To address this, mice were engineered to express Post Synaptic Density 95 protein (

210 ay increase the therapeutic index of T cells engineered to express powerful activation domains withou

211 tumorigenic breast cells (n = 4) genetically engineered to express PPT-I and led to anchorage-indepen

212 susceptibility in a murine model genetically engineered to express progressively decreasing levels of

213 ilar tumors composed of GeneSwitch-3T3 cells engineered to express ps20-V5-His under mifepristone reg

214 Multimeric hepatitis B core proteins engineered to express region 65-79 encoded by the DRB1*0

215 ferred to permissive feline and canine cells engineered to express rhesus and human TRIM5alpha protei

216 ferent attenuated rHPIV1 backbones were each engineered to express RSV F from three different gene po

217 is factor apoptosis ligand (TRAIL) and, when engineered to express secreted recombinant TRAIL, induce

218 eptide chimera/recombinant modular chimera), engineered to express several autologous T cell epitopes

219 xpression of SFFV gp55 in rodent fibroblasts engineered to express sf-Stk induced their transformatio

220 Cultures of agrotransformants, engineered to express sgB4 and CP subunits either transi

221 on with a recombinant -herpes virus, MHV-68, engineered to express SIINFEKL peptide, the ligand for t

222 Mice have been engineered to express similar reductions in SERT express

223 Ig gene rearrangements from transgenic mice engineered to express single copies of the unrearranged

224 extended this analysis using retrogenic mice engineered to express single TCR alpha- or beta-chains s

225 ed in non-SGI1-bearing strains of Salmonella engineered to express SO13.

226 t al demonstrated that tumor-tropic bacteria engineered to express specific cancer-related antibodies

227 in vivo, we introduced human DCIS cell lines engineered to express specific genes into a "mammary int

228 Strains were engineered to express specific gtr operons.

229 es in apoptosis were monitored in cell lines engineered to express stabilising mutations in beta cate

230 The cell line was engineered to express stably either CPG2 tethered to the

231 by mammary epithelial cells and kidney cells engineered to express SV40 early region proteins, hTERT,

232 These CAR T cells are engineered to express synthetic receptors that redirect

233 cultivation with Chinese hamster ovary cells engineered to express T-cadherin on their surface as com

234 al address the biology and safety of T cells engineered to express T-cell receptor (TCR) variants end

235 on experiments using B. pseudomallei strains engineered to express T6SS-5 in vitro show that the VgrG

236 T cells engineered to express TCRs specific for tumor Ags can dr

237 ibed a murine embryonic stem cell (ESC) line engineered to express the activated Notch 4 receptor in

238 functional characteristics of CD4(+) T cells engineered to express the alpha- and beta-chains of a hi

239 esponse to endorepellin in cells genetically engineered to express the alpha2beta1 integrin, but not

240 The encoding gene was engineered to express the central domain as residues 381

241 clostridial strain C. sporogenes genetically engineered to express the E. coli-derived cytosine deami

242 ration of a vesicular stomatitis virus (VSV) engineered to express the endogenous melanocyte antigen

243 l-arabinofuranoside ([(125)I]FIAU) to tumors engineered to express the Epstein-Barr virus thymidine k

244 We use mice engineered to express the farnesylated enhanced green fl

245 l in neurophysiological research, which were engineered to express the green fluorescent protein (GFP

246 y, influenza viruslike particles (VLPs) were engineered to express the hemagglutinin (HA) and genes f

247 Similarly, transgenic mice engineered to express the HIV protein gp120 exhibited in

248 hanced in cells lacking p53, including those engineered to express the HPV16-E6 oncoprotein or short

249 Transgenic mice engineered to express the human GLUT4 gene and promoter

250 iously, we demonstrated that transgenic mice engineered to express the human GLUT4 gene under the con

251 ld type, Arf+/-, and Arf-/- bone marrow were engineered to express the IFP.

252 on-pathogenic bacteria, has been genetically engineered to express the III7-10 fragment of human fibr

253 In human cells, engineered to express the individual TLR subtypes, 1-pho

254 ansformed mouse mammary cells that have been engineered to express the inducible oncogenic transgenes

255 examined uptake dynamics of Escherichia coli engineered to express the invasin surface receptor from

256 e optical stimulation of neurons genetically engineered to express the light-gated ion channel channe

257 ative tauopathies, transgenic (Tg) mice were engineered to express the longest human tau isoform (T40

258 found that unpolarized CD4(+)CD25(-) T cells engineered to express the MART-1(27-35) TCR selectively

259 nd adoptive transfer of monocytic cell lines engineered to express the mutant CD13 were severely impa

260 or glycogen consumption because the pfk gene engineered to express the mutant PFK (Thr-226-Ala) did n

261 kin mouse models in which endogenous Jup was engineered to express the Naxos-associated form of plako

262 /Rpr, in which the MRE-16 strain of SINV was engineered to express the proapoptotic gene reaper from

263 RIG-I) or after infection of cells that were engineered to express the reovirus sigma3 double-strande

264 in cell lines and primary bone marrow cells engineered to express the respective tyrosine kinase all

265 The yeast Saccharomyces cerevisiae was engineered to express the rho 1 subunit of the human gam

266 Complete recombinant NDV was engineered to express the SARS-CoV spike S glycoprotein,

267 MV engineered to express the sodium iodide symporter gene (

268 When engineered to express the TVA receptor for subgroup A av

269 Arabidopsis through Pseudomonas fluorescens, engineered to express the type III secretion system, als

270 0-fold when the virus was grown on FRT cells engineered to express the UL20 gene in comparison to the

271 utant as a backbone, new mutant viruses were engineered to express the wild-type (WT) V protein (+V-w

272 wild-type ARH1(+/+) cells or ARH1(-/-) cells engineered to express the wild-type ARH1 enzyme.

273 , in which a stable murine DC line XS106 was engineered to express the yellow fluorescent protein (YF

274 o validation, we produced a transgenic calf, engineered to express these tandem miRNAs.

275 ls, which possess MLG but lack MXE, might be engineered to express this Equisetum enzyme, thereby enh

276 n used to monitor tumor burden in xenografts engineered to express this marker.

277 human EGFR-mutant lung adenocarcinoma cells engineered to express this mutant PI3K.

278 MAGE-A2 and MAGE-A6) were recognized by PBLs engineered to express this TCR.

279 ted with strains of single-cycle SIV (scSIV) engineered to express three different envelope glycoprot

280 in vivo A LGR5-rainbow (LBOW) mouse line was engineered to express three different LGR5 isoforms alon

281 ivation of both human embryonic kidney cells engineered to express TLR2 (HEK-TLR2) and wild-type (WT)

282 Human T cells engineered to express TLR5L along with DMF5, a T-cell re

283 Images of xenografts engineered to express transgenic ABCG2/BCRP, as well as

284 phorylation of these kinases in 2 cell lines engineered to express TSHRs, human embryonic kidney HEK-

285 nerated during infection with vaccinia virus engineered to express TSKB20 were approximately 2.5-fold

286 Bacteria have been engineered to express tumor-necrosis-factor-alpha, hypox

287 sin mutants, but occurs prematurely in cells engineered to express two copies of myo2.

288 ation was achieved with a dual-peptide virus engineered to express two distinct peptides within the s

289 We examined the activity of human T cells engineered to express variants of a single TCR (1G4) spe

290 In studies with HEK cells engineered to express various TLRs, we show that activat

291 f-VEGF function approach with skeletal MDSCs engineered to express VEGF or soluble Flt1, a VEGF-speci

292 Transgenic corn plants engineered to express WCR dsRNAs show a significant redu

293 Using cell lines engineered to express wild-type CD33 at increased levels

294 xpress low endogenous levels of MT1-MMP were engineered to express wild-type MT1-MMP, a phosphomimeti

295 Brains of mice engineered to express wild-type or mutant PS1, or HEK293

296 bone injury, we found that MSCs genetically engineered to express Wnt-4 enhanced osteogenesis and im

297 asmodium falciparum were purified from yeast engineered to express "yeast optimized" pfcrt genes, rec

298 Cells engineered to express yneE during growth were impaired i

299 he feeder cell line was selected in G418 and engineered to express zebrafish leukemia inhibitory fact

300 ish ovarian feeder cell line (OFC3) that was engineered to express zebrafish Lif, Fgf2 and Gdnf.