ライフサイエンスコーパス: transgenic

1 OC1) and APETALA1 (AP1) were enhanced in the transgenics.

2 nce of HMP-PG to the fab1 phenotype, we used transgenic 16:0 desaturases targeted to the endoplasmic

3 L/6; RAG1(-/-) (C57BL/6); and HLA-DQ8, huCD4 transgenic Ab0 NOD mice.

4 Humanized TCR/HLA-transgenic allergy mice were treated in vivo with recomb

5 Transgenic An. gambiae overexpressing CYP6M2 or CYP6P3 s

6 el host Arabidopsis, has greatly facilitated transgenic analyses of genes important for parasitism.

7 Using transgenic and circuit-specific molecular targeting appr

8 In the present work, we combined transgenic and immunohistochemical approaches to investi

9 pe mouse backgrounds as well as in knockout, transgenic, and other types of genetically engineered mo

10 so detail how recent advances in microscopy, transgenics, and biological sensors may be used to ident

11 microgliosis are consistently observed in AD transgenic animal models devoid of such pathologies, bri

12 r across species, our data also suggest that transgenic animal models expressing human ACE2, such as

13 Our pharmacological and transgenic animal studies find that reducing polyamines

14 due to high circulating levels of IL-23, as transgenic animals and controls had similar levels of th

15 her, these changes occurred in the Abeta;tau transgenic animals at greater levels than worms harborin

16 t was validated using immunofluorescence and transgenic animals expressing NF-kappaB inducible imagin

17 ly human antibodies as biotherapeutics using transgenic animals with a notion that such mAbs bypass h

18 umanness" assessment of BCR repertoires from transgenic animals.

19 were performed on a 1 T MRI scanner using a transgenic APP/PSEN1 mouse model of Alzheimer's disease.

20 A non-transgenic approach based on RNA interference was employ

21 rmed by a cardiomyocyte-restricted (CR) Nrf2 transgenic approach in mice.

22 Unlike transgenic approaches, however, it is not facile to fore

23 reater precision than previous mutagenic and transgenic approaches.

24 equester available factor(s) from attenuated transgenic arrays, thereby preventing HLB formation and

25 innervation, we suggest that the adult K/BxN transgenic arthritic mice display a neuropathic phenotyp

26 These findings establish the id2b:gal4 transgenic as a useful tool for future studies aimed at

27 resistance function of Pm24 was validated by transgenic assay, independent mutants, and allelic assoc

28 Transgenic assays showed that both BdFTL1 and BdFTL2 cou

29 We developed transgenic B. distachyon plants expressing Tnt1 (R0) and

30 f HR since silencing of VuPOB1 expression in transgenic B301 roots lowers the frequency of HR and inc

31 dy CD4(+) T cell exhaustion, we used the TCR-transgenic B6 TEa cells that recognize a major transplan

32 eater in vitro osteoclastogenesis from Fndc5-transgenic bone marrow progenitors.

33 supply will increase the Bt toxin content in transgenic Bt rice, especially under elevated CO(2).

34 expression of the irisin precursor Fndc5 in transgenic C57BL/6J mice resulted in lower bone mass at

35 In this study, two populations of transgenic Carrizo citrange rootstocks expressing either

36 loned Sr60 also can be a useful component of transgenic cassettes including other resistance genes wi

37 Using a mouse TCR transgenic CD4(+) T cell, BthetaOM, that is specific for

38 for their ability to polarize naive OVA-TCR transgenic CD4(+) T cells.

39 brafish embryo segmentation, using the FUCCI transgenic cell-cycle-phase marker, revealed a spatial a

40 egant analysis, and in one case confirmed by transgenic complementation.

41 rmore, we conducted the so far largest fully transgenic CRISPR screen in any metazoan organism, which

42 n whether Bt corn, the most commonly planted transgenic crop worldwide, has significantly lower aflat

43 Production of hydroxy fatty acids (HFAs) in transgenic crops represents a promising strategy to meet

44 Transgenic crops that produce insecticidal proteins from

45 resistance by pests reduces the benefits of transgenic crops that produce insecticidal proteins from

46 PSPS), which confers glyphosate tolerance in transgenic crops.

47 This work lays the foundation for non-transgenic delivery of RNAi in controlling aflatoxins in

48 Our data suggest that transgenic DNA is recognized and then quickly inactivate

49 cursor protein/presenilin-1 (APP/PS-1) human transgenic double-knock-in mouse model of AD.

50 Mouse transgenic experiments from baboon and human genomic loc

51 Additionally, mouse transgenic experiments validated enhancer activity for p

52 enopus laevis photoreceptors, and found that transgenic expression of nonchain-forming P/rds generate

53 Transgenic expression of placental lactogen in beta-cell

54 We show that transgenic expression of the vitamin D receptor (VDR) on

55 argets were identified using live imaging of transgenic fish and RNA sequencing.

56 element activated expression in regenerating transgenic fish, and its genomic deletion perturbed caud

57 ental ACh signals in the olfactory center of transgenic flies in response to external stimuli includi

58 echin with epicatechin carbocation in CsANRa transgenic flower extracts formed dimeric procyanidin B1

59 s remarkably increased in CsANRa and CsMYB5b transgenic flowers.

60 ic certainty that they cannot transfer their transgenic genes to other organisms, and that they canno

61 eed, using 2-photon time-lapse imaging of SP-transgenic granule cells in mouse organotypic tissue cul

62 Transgenic, hair cell-specific expression of Tmc2b-mEGFP

63 lation were further supported by analysis of transgenic hairy roots overexpressing soybean GmWRI1b-OE

64 ouse huntingtin (Htt) gene knock-in model, a transgenic HTT sheep model, and humans.

65 rved, histologically, that nonphosphorylated transgenic human tau is enriched in synapses, whereas ph

66 Whole-brain imaging of stable transgenic id2b:gal4 larvae revealed labeling in a subse

67 LCMV-infected Il18-transgenic (Il18tg) mice developed cachexia and hyperinf

68 us-induced immunopathology, we infected Il18-transgenic (Il18tg) mice with lymphocytic choriomeningit

69 ach in wild-type and OsHOX24 over-expression transgenic in rice.

70 ype, KO (CaMKIIdelta-knockout), CaMKIIdeltaC transgenic in wild-type (TG), or KO background, and wild

71 Ectopic expression of TaRca1beta in rice transgenics indicate a direct correlation with tolerance

72 Transgenic knockdown lines of DGK2 and DGK4 confirmed th

73 In a transgenic knockin mouse (AKT-KI(+/+)) that lacked sulfh

74 immune-pathology can be illuminated through transgenic, knockout, xenotransplantation, immunological

75 died only in animal models with exogenous or transgenic labeling.

76 ulated gene promoter, we repeatedly observed transgenic larvae spontaneously expressing GFP days afte

77 ificant problem with a widely used Chat(Cre) transgenic line ensures that this map does not contain e

78 human spleen but not lung fibroblasts of the transgenic line expressing the VIR14 protein.

79 Here we utilise a transgenic line with fluorescent oenocytes to purify the

80 Recent studies have applied transgenics, lineage-tracing, and transcriptomics to hel

81 With new developments in transgenic lines and human-rodent chimeras, we anticipat

82 nable arbuscule development in B. distachyon Transgenic lines constitutively overexpressing BdRAM1 sh

83 cytokinin signaling in ARR1 gain-of-function transgenic lines is associated with increased rates of p

84 For this study, we have developed stable transgenic lines of chilli and tomato expressing CgCOM1-

85 The transgenic lines produced flowers 16 months after transf

86 e Arabidopsis thaliana ecotypes, mutants and transgenic lines to determine how control of VRN2 stabil

87 assays on leaves and fruits showed that the transgenic lines were resistant to anthracnose disease-c

88 d was incorporated to triacylglycerol in the transgenic lines without significant changes in their le

89 ling and ablating RMs populations in several transgenic lines.

90 Transgenic maize plants expressing WPGD1 and WPGD2 with

91 emogenetic inactivation method in c-fos-lacZ transgenic male and female rats.

92 ed by surgical manipulation, exogenous dyes, transgenic manipulation and phototoxicity.

93 ion and increased CatA activity in the LV of transgenic mice (CatA-TG) reduced EC-SOD protein levels

94 Here, we show that Vav1-hJAK2V617F transgenic mice (JAK2V617F+) have high BM FN content ass

95 c c-fms promoter to generate c-fms-eGFP-L10a transgenic mice (Mac(TRAP)).

96 question, we generated 4E-BP1-overexpressing transgenic mice and confirmed marked reductions in prote

97 Cardiomyocyte-specific MCUb overexpressing transgenic mice and Mcub gene-deleted (Mcub(-)(/-)) mice

98 sion in muscle progenitor cells using double-transgenic mice and myoblastic cell lines.

99 t complementary tools for cell labeling with transgenic mice and organic dyes that allow high-resolut

100 We experimentally investigated transgenic mice and performed genetic studies in a UK-ba

101 l by crossing RGS12(fl/fl) mice with CMV-Cre transgenic mice and then further induced the mice to dev

102 uorescent histone 2B fusion protein (H2B-FP) transgenic mice are important tools for tracking the mit

103 Plasma transfusion from Apom transgenic mice but not Apom knockout mice blocked fibro

104 The i.p. administration of LPS to transgenic mice carrying a human SE-coding HLA-DRB1 alle

105 Transgenic mice carrying the intronic multimerized enhan

106 d changes in PKA signaling are attenuated in transgenic mice constitutively expressing adropin and in

107 Cdx2-transgenic mice develop myelodysplastic syndrome with pr

108 despite harboring highly dysfunctional fat, transgenic mice display massive beta-cell hyperplasia, r

109 These PG-1 transgenic mice exhibited enhanced resistance to nasal b

110 We have shown that transgenic mice expressing a picornavirus RNA-dependent

111 al nuclei (LDT/SubLDT) using male and female transgenic mice expressing channelrhodopsin-(ChR2)-EYFP

112 tics of CWD prions passaged through deer and transgenic mice expressing different cervid PrP(C) polym

113 ted with cognitive dysfunction using APPSwDI transgenic mice expressing human beta-amyloid precursor

114 eceptors to activate the targeted B cells in transgenic mice expressing the germline VH of the VRC01

115 on of C/EBPbeta in human wild-type alpha-Syn transgenic mice facilitates PD pathologies and elicits m

116 from the compound mice and controls into HGF-transgenic mice further uncovered that HGF induces prost

117 Splenocytes from HLA-DQ8 transgenic mice given TIMP-GLIA nanoparticles, but not c

118 Hepatocyte-specific glypican-3 transgenic mice have decreased levels of phosphorylated

119 Although transgenic mice lacking the mitochondrial complex I acce

120 Although transgenic mice overexpressing asyn have previously been

121 In addition, transgenic mice overexpressing VDR in beta-cells were pr

122 (B6xA/J)F1 and (B6xNOD)F1 HER2 transgenic mice received Ad/E2TM after NK cell depletion

123 strategy to attenuate acute kidney injury in transgenic mice receiving contrast material.

124 In OT-II CD4(+) anti-OVA TCR transgenic mice sensitized to ovalbumin antigen, B cell

125 in the early-stage obese adipose tissue, the transgenic mice showed a healthier metabolic profile, in

126 sistance to nasal bacterial infection as the transgenic mice showed a higher survival rate (79.17% VS

127 TIMP3 transgenic mice showed compromised bone integrity as opp

128 /c mice and native virus in hACE2-expressing transgenic mice showing activity at the lowest tested do

129 ins of uninjured and olfactory bulbectomized transgenic mice that correspond to distinct stages in th

130 We generated transgenic mice that overexpressed TIMP3 or [-1A]TIMP3 d

131 Here, using K18-hACE2 transgenic mice that were originally developed for SARS

132 The exposure of LRRK2 transgenic mice to a sub-toxic dose of MPTP resulted in

133 o improve microvascular blood flow in sickle transgenic mice undergoing I/R, and we suggest how such

134 CD11b-cre transgenic mice were also used to delete Lpar1 in microg

135 o test this hypothesis, Lck-Dlx5;Lck-MyrAkt2 transgenic mice were generated.

136 itionally and selectively ablated in mature, transgenic mice where the human diphtheria toxin (DT) re

137 Transgenic mice with a knock-in mole CYP17A1 enhancer or

138 Furthermore, immunization of HLA-DR transgenic mice with a mixture of the two immunodominant

139 Immunization of HLA-DR transgenic mice with a mixture of these two immunodomina

140 Rhizolutin treatment of APP/PS1 double transgenic mice with AD significantly dissociated hippoc

141 We generated transgenic mice with expression of Ca(V)1.2 alpha(1C) su

142 targeting Sirt3 expression, we developed new transgenic mice with global Sirt3OX (Sirt3 overexpressio

143 Here, we report the generation of transgenic mice with Gq-coupled designer receptors exclu

144 n, HBV infected human liver chimeric mice or transgenic mice with integrated HBV genome.

145 med shotgun proteomics analyses of aortas of transgenic mice with macrophage-specific overexpression

146 rophic lateral sclerosis (ALS), we generated transgenic mice with neuron-specific expression of a sup

147 assessed longitudinally and spatially using transgenic mice with ubiquitously expressed Cre/ER and t

148 ic mouse variants (WT, R15L, & S59L), TDP-43 transgenic mice, FTLD-TDP patient brains, and transfecte

149 Last, aged male and female APP/PS1 transgenic mice, genetically null for the beta2 nAChR su

150 s, we used dental pulp cells from a panel of transgenic mice, in which fluorescent protein expression

151 ns and a similar demyelinating neuropathy in transgenic mice, is instead retained the ER where it act

152 Following injection to AD transgenic mice, TDP-43 induced inflammation, interacted

153 Here, using AXIN2 lineage tracing in BAC-transgenic mice, we confirm the regenerative potential o

154 n. Using a vaccine-challenge model in HLA-DR transgenic mice, we demonstrated significant alterations

155 Using a selective viral tracing method and transgenic mice, we examined the connectivity of four co

156 ers that were experimentally validated using transgenic mice, we identified a 2.9-kb regulatory eleme

157 maging of mammary cell ensembles from GCaMP6 transgenic mice, we reveal how stimulus evoked Ca(2+) os

158 vant phenotypes than those seen in Hfh4-ACE2 transgenic mice, which express human ACE2 under the cont

159 lastocysts derived from lipodystrophic A-ZIP transgenic mice, which have a genetic block in adipogene

160 skin-aging progression, we demonstrate that transgenic mice, with selective expression of CCN1 in de

161 ecomes detectable in Abeta precursor protein-transgenic mice.

162 erebellum, as was shown in Jdp2-promoter-Cre transgenic mice.

163 ed in brains of FTLD-TDP patients and TDP-43 transgenic mice.

164 FH, and CD74 in the KCNH2-3.1 overexpression transgenic mice.

165 tes using the Zona pellucida 3-Cre (Zp3-Cre) transgenic mice.

166 uction of proliferation in both CV- and R47H-transgenic mice.

167 supported by results in human (h) GRK4gamma transgenic mice.

168 ged adipocytes and increased body weights in transgenic mice.

169 6 weeks) and old (57-60 weeks) wild-type and transgenic mice.

170 on ancestor (UCA) of the human VRC26 bnAb in transgenic mice.

171 ing the Tjp1 floxed mice and Myh6(Cre/Esr1*) transgenic mice.

172 To achieve containment of transgenic microorganisms, confidence to a near-scientif

173 genetically ablated in the oncogene-induced transgenic MMTV-PymT tumor model.

174 edge, the 117VV Tg30 mouse line is the first transgenic model expressing only mutant human PrP to sho

175 d immortalized lung epithelial cells while a transgenic model featuring inducible ERBB2DeltaEx16 spec

176 We developed a transgenic model using site-directed insertion of the va

177 Subsequently, a second transgenic model was generated in which aspartic acid in

178 stereotypy, and vertical exploration in both transgenic models of hyperdopaminergia, as well as norma

179 ompound in dysregulated behaviors within the transgenic models.

180 Transgenic modulation demonstrated that GRK2 inhibition

181 This transgenic mouse also provides an inducible and reversib

182 We create the first patient inspired KCNJ2 transgenic mouse and study effects of this mutation on c

183 cular, electrophysiological, behavioral, and transgenic mouse approaches were used to characterize MC

184 The adult K/BxN transgenic mouse develops spontaneous autoimmune arthrit

185 tations in the cII gene from lambda phage in transgenic mouse embryonic fibroblasts during the transi

186 In vivo transgenic mouse experiments validate the cell type spec

187 We have generated a novel transgenic mouse expressing human asyn in LC neurons to

188 Here we report a novel transgenic mouse expressing human wild-type asyn under c

189 Using a newly generated transgenic mouse in which PSCs are specifically labeled,

190 In the second PDE4B-transgenic mouse line (TG50), markedly higher PDE4B over

191 We established a transgenic mouse line that enabled the genetic interroga

192 y used as fundamental material brains from a transgenic mouse line that expresses LacZ under the cont

193 roposed mechanism, we created a controllable transgenic mouse line that sustains cortical MET signali

194 Using a novel transgenic mouse line to model the impact of human APP (

195 With the use of a transgenic mouse line, optical clearing, and imaging tec

196 Using an MrgprC11(CreERT2) transgenic mouse line, we labeled a small subset of itch

197 ression drives tumorigenesis, we established transgenic mouse lines that ubiquitously express increas

198 ty and the formation of amyloid plaques in a transgenic mouse model (5xFAD) of early amyloid depositi

199 ntration in vivo, we developed a conditional transgenic mouse model (Flpo/Frt system) expressing bioa

200 o brain slice culture model for CWD, using a transgenic mouse model (Tg12) that expresses the elk (Ce

201 in human tau overexpressing line 66 mice, a transgenic mouse model akin to genetic variants of front

202 Using a transgenic mouse model for the sonic hedgehog (Shh) subg

203 ivery in both wild type mice and the NSG-PiZ transgenic mouse model of AAT deficiency.

204 th plaque deposition and neuronal death in a transgenic mouse model of cerebral beta-amyloidosis.

205 and autoimmune kidney disease in the Tlr7.1 transgenic mouse model of SLE.

206 Here we used a novel transgenic mouse model to compare the spatial distributi

207 We used a transgenic mouse model to show that the loss of presenta

208 This study used a cardiac-specific VCP transgenic mouse model to understand the transcriptomic

209 A transgenic mouse model with elevated skeletal muscle 2-d

210 e, we studied retroviral susceptibility in a transgenic mouse model with lifelong innate immune syste

211 In the MMTV-Delta16HER2 transgenic mouse model, oncogene transformation resulted

212 Using an IL-27 reporter transgenic mouse model, we show in this study that conve

213 Using the corresponding Plp1 transgenic mouse model, we then tested the capacity of t

214 attenuate acute colitis in a humanized IL-26 transgenic mouse model.

215 n-target/off-tumor toxicity in a human CD147 transgenic mouse model.

216 Vs, and synthesize preclinical findings from transgenic mouse models of 16p11.2 CNVs.

217 odeled acquired resistance to osimertinib in transgenic mouse models of EGFR(L858R) -induced lung ade

218 oters, and disruption of endogenous genes in transgenic mouse models of tauopathy make it difficult t

219 We utilized knockin and transgenic mouse models to evaluate the structural, func

220 ell type-specific loss- and gain-of-function transgenic mouse models to investigate the physiologic r

221 Employing skeletal muscle-specific transgenic mouse models with unbiased-omic approaches, w

222 To this end, we created two transgenic mouse models; the iMS-Nrf2(flox/flox) and iMS

223 To address this gap, here we developed a transgenic mouse overexpressing Sulf2 in hepatocytes und

224 ated with ALDH7A1 deficiency, we generated a transgenic mouse strain with constitutive genetic ablati

225 We utilized transgenic mouse strains that either constitutively expr

226 p in knowledge, we developed an H-2D(b) LoxP-transgenic mouse system using otherwise MHC class I-defi

227 Using advanced transgenic mouse technology, we show that IL-1-dependent

228 Here, we utilized novel CHCHD10 transgenic mouse variants (WT, R15L, & S59L), TDP-43 tra

229 1 channels in the cardiac pathophysiology, a transgenic mouse was generated with cardiomyocyte-specif

230 els expressing human ACE2, such as the hACE2 transgenic mouse, are also likely to be useful models fo

231 roliferative capacity in a conditional FIH-1 transgenic mouse.

232 tation: Vbeta8 TCR congenic and Valpha14 TCR transgenic NC mice.

233 Using a TCR-transgenic Nur77-GFP reporter to distinguish "antigen-sp

234 erize the path of acyl flux in wild-type and transgenic oil-accumulating tobacco leaves.

235 Transgenic overexpression of NbP3IP conferred resistance

236 We found previously that transgenic overexpression of the PP2A methylesterase, PM

237 Importantly, transgenic overexpression of TMPRSS13 in CRC cell lines

238 , expansion of the lung lymphatic network by transgenic overexpression of Vegfc in club cell secretor

239 In mice, mutant transgenic PDE3A overexpression in smooth muscle cells c

240 itive phenotype, whereas phyB-overexpression transgenic plants displayed enhanced freezing tolerance.

241 We previously generated promoter::GUS transgenic plants for all leucine-rich repeat (LRR)-RLKs

242 HFA accumulation and distribution at TAG in transgenic plants have not been well studied.

243 ich induced a strong resistance phenotype in transgenic plants upon challenge with avirulent Blumeria

244 Transgenic plants were characterized by molecular and ge

245 GRF4-GIF1 transgenic plants were fertile and without obvious devel

246 s cytokinins, which facilitates selection of transgenic plants without selectable markers.

247 es in plant leaves and generated Arabidopsis transgenic plants.

248 Control (PLM(WT)), transgenic (PLM(3SA)), ouabain-treated and hypertrophied

249 Furthermore, overexpression of MYB125 in transgenic poplar resulted in increased lignin content,

250 olignol transcript and protein abundances in transgenic Populus trichocarpa based on targeted knockdo

251 ing in vivo multiphoton calcium imaging from transgenic PUb-GCaMP6s mosquitoes, we show that Ae. aegy

252 ing strategies, showcase the past and future transgenic quail lines and foster collaborative work wit

253 In recent years, transgenic quail lines have been described.

254 trigeminal ganglia of non-protected SYMP HLA transgenic rabbits had higher frequencies of dysfunction

255 Compared to protected ASYMP HLA transgenic rabbits, the trigeminal ganglia of non-protec

256 mptomatic (ASYMP) individuals and HLA-A*0201 transgenic rabbits.

257 Here, we examined Fmr1-targeted transgenic rats (Fmr1-KO rats) as an alternative preclin

258 Add3 transgenic rats showed attenuation of proteinuria, glome

259 We used transgenic rats to study each cell type and found that c

260 om preplaque amyloid precursor protein (APP) transgenic rats were found to produce a variety of poten

261 Next, male and female transgenic rats were used to selectively label D1 or D2

262 renal vascular smooth muscle cells from Add3 transgenic rats, those from FHH rats had elevated membra

263 Liver-specific transgenic reconstitution of SULT1E1 in Sult1e1 knockout

264 histochemistry, in situ hybridization, and a transgenic reporter assay, our results demonstrate a req

265 Transgenic reporter fish demonstrated nuclear ESR activi

266 Using a transgenic reporter for RE transposition activity, we de

267 Using male D1tdTomato transgenic reporter mice, whole-cell patch-clamp electro

268 Here, we develop a transgenic reporter mouse that allows dynamic measuremen

269 dentified using numerous surface markers and transgenic reporters, but none is both universal and lin

270 Transgenic restoration of Slit-N or Slit-C does not repe

271 Their expression in transgenic rice causes ambivalent immunity: increased su

272 ry of lentiviral vectors to generate somatic-transgenic rodents to monitor signalling pathways in dis

273 olonization of drepp mutant roots as well as transgenic roots overexpressing DREPP is impaired.

274 ays on juvenile immature scions grafted onto transgenic rootstock.

275 Scnn1b transgenic (Scnn1b-Tg(+)) mice, which recapitulate cysti

276 Of these, four transgenic seedlings overexpressing previously uncharact

277 The overall protein content of the transgenic seeds was lowered by about 3% when compared t

278 mulated in higher amounts in ATP sulfurylase transgenic seeds.

279 t sites, indicates that the vast majority of transgenic sgRNA lines mediate efficient gene disruption

280 in mouse model (p = 6.0 x 10(-8)) and in the transgenic sheep model (p = 2.4 x 10(-88)).

281 rotease inhibitor was several fold higher in transgenic soybean plants when compared to the non-trans

282 oresis and immunoblot analyses revealed that transgenic soybean seeds overexpressing ATP sulfurylase

283 soybean plastid ATP sulfurylase isoform 1 in transgenic soybean without its transit peptide under the

284 Using a transgenic steroidogenesis-reporter mouse line we identi

285 ulture systems, genomes, transcriptomes, and transgenic systems available for a range of Babesia spp.

286 Adoptively transferred T cell receptor (TCR)-transgenic T cells (TCR-T cells) are not restricted by c

287 for T cells lacking SLAMF6 and expressing a transgenic TCR for gp100-melanoma antigen.

288 After doxycycline withdrawal, transgenic TDP-43(A315T) expression gradually increased

289 Constitutive expression of transgenic TDP-43(A315T) in the absence of doxycycline r

290 We generated humanized transgenic (TG) mice containing all the introns, exons,

291 d in: (i) spontaneous neuroblastomas (NB) in transgenic TH-MYCN mice; (ii) orthotopic xenografts of a

292 utaneous (NXS2 and 9464D), and a spontaneous transgenic (TH-MYCN) murine model of neuroblastoma, comp

293 ingiensis (Bt) toxins utilized in commercial transgenic traits have been reported, raising concerns o

294 Using in vivo microscopy and transgenic vascular reporters, we observed that while bc

295 enic soybean plants when compared to the non-transgenic wild-type seeds.

296 comprised of Escherichia coli (E. coli) and transgenic zebrafish embryos, we are able to design opti

297 e consequence of producing more bone, we use transgenic zebrafish in which Hh levels could be experim

298 We developed a transgenic zebrafish line that allows for cell-type-spec

299 We report a collection of 1200 transgenic zebrafish strains made with the gene-break tr

300 Furthermore, the mutants carrying the transgenic ZmNLP5 cDNA fragment significantly increased