ライフサイエンスコーパス: transgenic

1 ed genome manipulations such as knockouts or transgenics.

2 f prodelphinidins in proanthocyanidin of the transgenics.

3 ls were studied by using new T-cell receptor transgenic 1-DER mice specific for the Der p 1 allergen.

4 The analysis of transgenic 5' upstream deletion::gusA Arabidopsis lines

5 These transgenics accumulated more Cd(2+), but less Na(+) than

6 In transgenic adenocarcinoma mouse prostate model, Skp2 dep

7 sm between low- and high-grade tumors in the transgenic adenocarcinoma of mouse prostate (TRAMP) tran

8 primary tumors of the prostate cancer-prone transgenic adenocarcinoma of the mouse prostate (TRAMP)

9 describe the generation of multiple stable, transgenic Ae. aegypti strains expressing Cas9 in the ge

10 s validated these results in transgenic, non-transgenic and aged mice.

11 cal impact model, we used adoptive transfer, transgenic, and bone marrow chimera approaches to show i

12 Transgenic- and cell line-based experiments have identif

13 Middle-aged (9-11 months) transgenic animals (both male and female) displayed mild

14 Transgenic animals expressing both human proteins exhibi

15 ology compared with AD transgenic mice or AD transgenic animals with type 1 diabetes (T1D).

16 rs of neurodegeneration and neurotoxicity in transgenic animals, including analysis of both males and

17 mmation-associated neurogenesis models and a transgenic approach, we aimed to understand the cell-sou

18 Finally, genome-editing and transgenic approaches demonstrate that a highly conserve

19 dies that have utilized pharmacologic and/or transgenic approaches targeting an individual hormone/me

20 ften approached using surgical, chemical, or transgenic approaches to ablate neurons.

21 Chronic i.p. treatment of the triple transgenic (APPsw/PS1M146V/TauP301L) mice with M344, at

22 reveal its roles, we had previously produced transgenic Arabidopsis (Arabidopsis thaliana) RNA interf

23 ng an activation tag screen, we identified a transgenic Arabidopsis thaliana line with longer etiolat

24 ics and biochemical approaches, we show that transgenic BAR indeed converts two plant endogenous amin

25 ER stress markers and associated caspases in transgenic brain lysates and cells.

26 ing while monitoring cytosolic Ca(2+), and a transgenic Ca(2+) reporter mouse with Salsa6f targeted t

27 Conversely, using a transgenic caspase strategy, the intensity of cue-induce

28 nsulin resistance and steatosis formation in transgenic CCDC3 mice on high-fat diet (HFD) by reducing

29 Adoptive transfer of allospecific transgenic CD4 T cells revealed a "split tolerance" stat

30 Transgenic cell labeling showed Tac1-Pet1 soma resident

31 In the future, the established transgenic cells can be used for other gene-editing stud

32 The aim of this work was to determine if transgenic citrus plants expressing BlMGL showed increas

33 Treatment of transgenic CML mice in vivo with NIL in combination with

34 ETB deficient (ETB def) or transgenic control (TG-con) rats were used in the presen

35 ts from 2014 (n=120) and 2015 (n=120) of non-transgenic corn and their fractions (germ, pericarp, end

36 itive selection system for the generation of transgenic cotton plants with equal or higher transforma

37 ighly efficient and simple means to generate transgenic cotton plants, but also helps address many of

38 to select for transformed cells and generate transgenic cotton plants.

39 re useful for whole-body characterization of transgenic Cre mice and to detect previously unknown Cre

40 loid angiopathy (CAA) in neonatally-injected transgenic CRND8 mice.

41 Transgenic crops have revolutionized insect pest control

42 ata reported during the first two decades of transgenic crops, with each case representing the respon

43 bicide resistance genes in the production of transgenic crops.

44 lkit that will allow the rapid generation of transgenic DiCre-expressing P. falciparum lines in any g

45 Temporally controlled expression of transgenic Dmrta2 in NPCs suppresses differentiation wit

46 ed in spreading of amyloid-beta pathology in transgenic double-mutant APPSwePSEN1dE9 mice.

47 d the function of APOL1 in vivo We generated transgenic Drosophila fly lines expressing the human APO

48 Here we used transgenic Drosophila, in which the mouse OPN4 replaced

49 Here, we developed transgenic dy2J mice with muscle-specific expression of

50 this mouse with Cre drivers generated double transgenics expressing hVOS probe in GABAergic, parvalbu

51 e mutant phenotype was completely rescued by transgenic expression of AtHEMN1 Promoter and transcript

52 In beta2AR(-/-) mice, transgenic expression of beta2ARs only in airway epithel

53 The transgenic expression of enzymes can result in unintende

54 longation of transient porcine chimerism via transgenic expression of human CD47 in a primate model i

55 Through use of immunocompromised mice with transgenic expression of human GM-CSF, interleukin-3, an

56 Transgenic expression of intracellular NOTCH1 in mice wi

57 l as the plant Nicotiana benthamiana through transgenic expression of Rhodiola salidroside biosynthet

58 Transgenic expression of Salsa6f enables ratiometric ima

59 nd poorly healing cardiac ventricles using a transgenic fish model that exhibits heat-shock (HS) indu

60 As transgenic flies with either allele aged, nephrocyte fun

61 By modifying candidate SNPs in transgenic flies, we show that the largest effect is cau

62 Mice transgenic for human alphaS (line M20) injected in the h

63 We report that transgenic FOXC1 overexpression suppresses lobuloalveolo

64 st, about 90% Treg depletion obtained in BAC transgenic Foxp3.LuciDTR4 mice failed to induce complete

65 rine encephalomyelitis virus (TMEV)-infected transgenic FVB mice that express the D(b) class I molecu

66 or specificities of the OSTs in vivo using a transgenic glycoprotein reporter system and performed gl

67 Transgenic 'Greensleeves' apple trees with decreased sor

68 Both global and transgenic hCD39- and myeloid lineage CD39-overexpressin

69 sults demonstrate the usefulness of this new transgenic hepatitis B model.

70 and efficient strategy for generating stable transgenic hPSCs.

71 Transgenic Huntington's disease monkey (HD monkey) model

72 e answer this longstanding question by using transgenic Hydra expressing fluorescent proteins and a m

73 Here, we describe the generation of transgenic, inducible CRISPR-based mouse systems to engi

74 ased protein accumulation, and extracts from transgenic leaves showed higher activity on classic pero

75 recombination activating gene (Rag)2:mCherry transgenic line to identify B cell development stages in

76 ere we report the development of a zebrafish transgenic line, Tg(igfbp5a:GFP), which faithfully repor

77 Instead, the transgenic lines accumulated a range of hydroxycinnamate

78 However, no transgenic lines expressing Cas9 have been developed for

79 ow its utility by generating multiple stable transgenic lines expressing fluorescent proteins under s

80 dent copy number measurements in independent transgenic lines in these crop species.

81 ith high-chill kiwifruit Actinidia deliciosa transgenic lines overexpressing SVP2 showing suppressed

82 Here, we use transgenic lines to define the in vivo relevance of HDAC

83 such improvement was observed for the SeCspB transgenic lines under field conditions.

84 With established transgenic lines, consistent results were observed with

85 By characterizing these transgenic lines, we showed that agrp1-expressing neuron

86 n seven previously published Cre and CreERT2 transgenic lines.

87 APP(E693Q) as compared with age-matched non-transgenic littermates, and western blots showed increas

88 jections of alphaS fibrils in hemizygous M83 transgenic (M83(+/-)) mice resulted in CNS alphaS pathol

89 beetles that emerged from larval feeding on transgenic maize roots expressing dvbol dsRNA also showe

90 reviously showed that HER2(+)/PIK3CA(H1047R) transgenic mammary tumors are resistant to the HER2 anti

91 tamoxifen-inducible Cre system is a popular transgenic method for controlling the induction of recom

92 out our studies using 4 to 5 week old triple transgenic mice (Col1a1XCol2a1XCol10a1).

93 e inhibitory CREM isoform CREM-IbDeltaC-X in transgenic mice (TG) leads to spontaneous-onset AF prece

94 at insulin promoter-membrane-bound ovalbumin transgenic mice after sham or IRI procedures.

95 mias developed in Pml(C62A/C65A) mice, these transgenic mice also expressing RARalpha linked to a dim

96 In vivo sudemycin treatment of U2AF1(S34F) transgenic mice alters splicing and reverts haematopoiet

97 postmortem brains, amyloid precursor protein transgenic mice and AD cell lines.

98 4D inhibitor is able to enhance memory in AD transgenic mice and concomitantly rescues their hippocam

99 yed the Gdf5 locus for regulatory regions in transgenic mice and fine-mapped separate enhancers contr

100 n neuroblastoma growth in TH-MYCN homozygous transgenic mice and MYCN gene-amplified neuroblastoma xe

101 complex stability, and immunogenicity in A2-transgenic mice and on peripheral blood mononuclear cell

102 cells in TG of latently infected HLA-A*0201-transgenic mice and reduced recurrent ocular herpes foll

103 ic activity regulation, suggesting that CREM transgenic mice are a valuable experimental model for hu

104 ker of embryonic dSPNs and the Sox8-EGFP BAC transgenic mice are an excellent tool to study the devel

105 sponses to LPS and bacterial infection, POP2 transgenic mice are more resistant to bacterial infectio

106 sion in the cervical microenvironment of HPV-transgenic mice compared with nontransgenic mice.

107 all, this study indicates that TDP-43(A315T) transgenic mice develop key features resembling key aspe

108 However, these transgenic mice displayed normal social approach, social

109 lpha3135-145 tetramer(+) T cells in HLA-DR15 transgenic mice exhibit a conventional T-cell phenotype

110 Upon exposure to UVB irradiation, fat-1 transgenic mice exhibited a significantly reduced epider

111 nonproductive human VH rearrangements in the transgenic mice expressed shorter CDRH3 with less N addi

112 Transgenic mice expressing a dominant-negative Orai1 mut

113 jected C3a receptor-deficient mice, GFAP-C3a transgenic mice expressing biologically active C3a in th

114 We report that transgenic mice expressing endogenous levels of mutant C

115 distinct astrocyte subtypes were found using transgenic mice expressing GFP and MrgA1 receptors in as

116 We also generated transgenic mice expressing RDH10 ectopically in rod cell

117 s undergoing differentiation into oocytes in transgenic mice expressing the suicide gene, herpes simp

118 itochondria from 6-12 week old wild-type and transgenic mice in the absence of disease.

119 e to the Asp(1) site both in male and female transgenic mice in vivo and in cell lines and primary ne

120 Transgenic mice in which Tcf7l2 was selectively inactiva

121 dy, we use organotypic cultures derived from transgenic mice inducibly expressing oncogenic beta-cate

122 Moreover, a reduction in progranulin in tau transgenic mice is associated with increasing tau accumu

123 In this article, we report that transgenic mice lacking Cfh alleles exhibit delayed peri

124 Consequently, soluble gp130 fused to Fc transgenic mice lacking IL-6 trans-signaling are largely

125 We have previously shown in several AD transgenic mice lines that blocking the apoE/Abeta inter

126 By generating P301S tau transgenic mice on either a human ApoE knock-in (KI) or

127 acerbated AD-like pathology compared with AD transgenic mice or AD transgenic animals with type 1 dia

128 Transgenic mice over-expressing rabbit calpastatin (Calp

129 Here we show that clinically ill transgenic mice overexpressing hamster prion protein (Tg

130 We observed that transgenic mice overexpressing in neurons a human APP ge

131 cle of yellow fluorescent protein-expressing transgenic mice produced a 17 +/- 1% loss of dendritic s

132 , crossing the W131A mutant mice to OTII TCR transgenic mice resulted in increased negative selection

133 on of CR3 in human amyloid precursor protein-transgenic mice results in decreased, rather than increa

134 non-senescent B-cell lymphomas from Emu-Myc transgenic mice revealed substantial upregulation of an

135 In transgenic mice selectively over-expressing PGC1beta in

136 Double-transgenic mice showed 55% double labeling of periurethr

137 Transgenic mice showed less neurological deficit compare

138 in the embryonic striatum and Sox8-EGFP BAC transgenic mice specifically reveal the direct pathway a

139 This phenotype is similar to that of transgenic mice that express amyloid precursor protein (

140 p recording in spinal cord slices from adult transgenic mice that express enhanced green fluorescent

141 mmune encephalomyelitis (EAE) was induced in transgenic mice that express human CD20 on B cells.

142 measure NF-kappaB activity we used a line of transgenic mice that express the LacZ gene under the con

143 In contrast, transgenic mice that expressed KCP in the kidney, liver,

144 fects of seeded alphaS aggregation in alphaS transgenic mice through intracerebral or peripheral inje

145 We used Cre/loxP transgenic mice to conditionally target InsRs in fetally

146 lations, and oncogenic signaling, MMTV-ErbB2 transgenic mice were administered AZD4547 (2-6 mg/kg/day

147 Male FVB/N-Tg(MMTVneu)202Mul/J (Her2) transgenic mice were bred to female MNX mice having FVB/

148 lagen-induced arthritis (CIA) model and DR-1 transgenic mice were used to study the importance of LAI

149 mer that accumulates in adipose tissues from transgenic mice where FAHFAs were first discovered.

150 ation of medroxyprogesterone-treated HLA-DR4 transgenic mice with 5 x 10(5)C. trachomatis D inclusion

151 We used transgenic mice with GFP-expressing HCs, coupled with FA

152 le IL-10(eGFP) Foxp3(mRFP) reporter mice and transgenic mice with impairment in IL-10 receptor signal

153 We separately generated transgenic mice with inducible expression of proteolytic

154 esioning the LC of male and female P301S tau transgenic mice with the neurotoxin N-(2-chloroethyl)-N-

155 Chronic treatment of tau P301S and 5XFAD transgenic mice with this inhibitor reduces tau and APP

156 Eosinophils from the spleens of IL-5 transgenic mice, fluorescently labeled ex vivo, were int

157 r cells, mouse MAIT hybridoma lines, HLA-DR4-transgenic mice, MAIThighHLA-DR4+ bone marrow chimeras,

158 Using inducible Tat-expressing transgenic mice, we found that dopamine subtype 2 (D2) r

159 In female MMTV-HER2/neu transgenic mice, we found that ERalpha and ERbeta expres

160 Using a panel of preterm transgenic mice, we show that epidermis-targeted coexpre

161 Eo771/MUC1-C cells were engrafted into MUC1 transgenic mice, we showed that targeting MUC1-C associa

162 nts of the rod outer segment photocurrent in transgenic mice, which have only rod function, revealed

163 out [cKO]) when crossed with Cre recombinase transgenic mice.

164 ed or estrogen-treated nontransgenic and HPV-transgenic mice.

165 -like particles in human immunoglobulin loci transgenic mice.

166 mitochondrial and synaptic toxicities in APP transgenic mice.

167 ticulum stress in the prostate glands of ERG transgenic mice.

168 ficantly decreased fecundity of Dppa3 (R60A) transgenic mice.

169 ompared with nontransgenic controls, neither transgenic model exhibited an increase in proteinuria at

170 roteins are hyperacetylated in OVE26 mice, a transgenic model of type 1 diabetes.

171 In the present study, we show, in a quad-transgenic model, that over-expression of VEGF-A165 b al

172 e easily applied to other skeletal sites and transgenic models, and could improve our understanding o

173 a hemagglutinin as a model viral antigen and transgenic, MOG-specific B cells.

174 ion of PR3 in vivo, we generated a human PR3 transgenic mouse (hPR3Tg).

175 , tau expression was elevated in TDP-43M337V transgenic mouse brains.

176 The Emu-TCL1 transgenic mouse develops a form of leukemia that is sim

177 algorithms using single cells from Etv2-EYFP transgenic mouse embryos and reveal specific molecular p

178 vivo cerebral ischemia model, we developed a transgenic mouse expressing human CD39 (hCD39).

179 duced CNS alphaS pathology in another alphaS transgenic mouse line (M20), albeit less robustly in the

180 Furthermore, a transgenic mouse line specifically labeling SL cells sho

181 We report the development of a transgenic mouse line where Cre-recombinase-induced expr

182 Here, using a transgenic mouse line with destabilized GFP, we identifi

183 To address this hypothesis, we generated transgenic mouse lines harboring a Gata1 bacterial artif

184 al expression system, here we generated Plk1 transgenic mouse lines to examine the role of Plk1 in tu

185 ire breadth to a non-self-antigen, a TCRbeta transgenic mouse model (EF4.1) expressing a limited, yet

186 he advantages and limitations of the HLA-DR4 transgenic mouse model for evaluating human C. trachomat

187 Using a transgenic mouse model in which FlnA is selectively depl

188 V-induced skin carcinogenesis, we utilized a transgenic mouse model in which the keratin 14 promoter

189 uppress the Alzheimer's-like phenotypes in a transgenic mouse model of Abeta deposition.

190 results in suppression of tumour growth in a transgenic mouse model of breast cancer.

191 igated the impact of gammadelta T cells in a transgenic mouse model of carcinogenesis induced by HPV1

192 We used a transgenic mouse model of chronic lung disease induced b

193 vivo relevance of this pathway in our IL-15 transgenic mouse model of CTCL by showing that interfere

194 GMP signaling.SIGNIFICANCE STATEMENT In DYT1 transgenic mouse model of dystonia, PDE10A, a key enzyme

195 ilin degradation and rescued phenotypes in a transgenic mouse model of hereditary primary open-angle

196 our results show in an aggressively growing transgenic mouse model of PDAC that the coordinated acti

197 nic adenocarcinoma of mouse prostate (TRAMP) transgenic mouse model of prostate cancer.

198 In a transgenic mouse model of resectable PDAC, we investigat

199 in DIV7 cortical cultures of either from E18 transgenic mouse model or from rat E18 embryos that were

200 We showed that in a transgenic mouse model, activation of the UPR in early d

201 e therapeutic profile of CpG ODN in a triple transgenic mouse model, Tg-SwDI, with abundant vascular

202 d precursor protein (APP)/presenilin 1 (PS1) transgenic mouse model, we found that inhibition of RIPK

203 with cognitive improvements in an AD APP/PS1 transgenic mouse model.

204 t composition in the skin, we have generated transgenic mouse models for tamoxifen-inducible de novo

205 ine phosphatases Shp1 and Shp2, knockout and transgenic mouse models have revealed distinct phenotype

206 breast cancer metastasis in two conditional transgenic mouse models of PyMT-induced breast cancer.

207 METHODS AND To address the question, 2 transgenic mouse models were generated: a phospho-mimeti

208 er-induced choroidal neovascularization, and transgenic mouse models with deficient or spontaneous re

209 eam effectors Grp78/BiP and eIF2alpha in ERG transgenic mouse prostate glands indicate the presence o

210 Epithelial cells derived from ERG transgenic mouse prostates have increased prostasphere f

211 NF-kappaB signalling-deficient IkappaBDeltaN transgenic mouse rescues NKT cell development and differ

212 Transgenic mouse studies confirmed that donor islet-spec

213 Using transgenic mouse technology, we show that Shp2 is involv

214 nvolved in isotype switching, we generated a transgenic mouse that over-expressed RNase H1, an enzyme

215 we generated a doxycycline suppressible Cre transgenic mouse under the regulation of the Nkx2.5 enha

216 Expression of hCD22 on transgenic murine B cells is comparable to expression on

217 nd myeloid lineage CD39-overexpressing mice (transgenic, n=9; myeloid lineage, n=6) demonstrated sign

218 ively killed SnCs validated these results in transgenic, non-transgenic and aged mice.

219 s T1D development in NOD mice expressing the transgenic NY8.3 CD8 TCR.

220 n liver or any tissue or cell type for which transgenic or viral Cre drivers are available.

221 r CD4(+) cells from ROCK2-sufficient OVA TCR transgenic (OT-II) mice or saline i.v. 48 h before chall

222 Transgenics overexpressing PtabZIP1L showed precocious L

223 Transgenic overexpression and suppression of PtabZIP1L a

224 AHR, inflammation, and mucus production, and transgenic overexpression in WT mice exacerbates these p

225 however, most of these models have employed transgenic overexpression of alanine-expanded PABPN1.

226 pecific, conditional genetic deletion and/or transgenic overexpression of ATX established a liver pro

227 Here we report that the transgenic overexpression of GATA3 leads predominantly t

228 Intriguingly, transgenic overexpression of GCH1 in cardiomyocytes redu

229 Conversely, transgenic overexpression of miR-497 approximately 195 i

230 ML-IV patients are reportedly achlorhydric, transgenic overexpression of ML1 in mouse parietal cells

231 radation of these CYP-derived metabolites by transgenic overexpression of sEH, the protective effect

232 ene expression changes observed in mice with transgenic overexpression of the Notch intracellular dom

233 In conjunction with recently produced transgenic P. berghei parasites that express P. falcipar

234 t neurodegeneration and prolongs survival in transgenic P301S Tau mice.

235 s detected the siRNAs products in virus-free transgenic papaya tissue culture seedlings.

236 Transgenic parasite lines were generated to express the

237 i were used in growth inhibition assays with transgenic parasite lines.

238 The resulting transgenic plants (E8-SDB123) showed an increased biomas

239 We show that delayed senescence of transgenic plants and the corresponding longer stay-gree

240 1 into the soybean cultivar Williams 82, the transgenic plants exhibited enhanced resistance to F. vi

241 Conversely, transgenic plants expressing the F-box domain deletion m

242 Markets for Bt products and transgenic plants expressing their toxins are driven by

243 great challenges of transgene silencing for transgenic plants facing climate change.

244 that the increased greenness observed in the transgenic plants is due to more chlorophyll synthesis b

245 nt functions that could be produced later in transgenic plants or potentially applied exogenously to

246 o these changes remain to be identified, the transgenic plants presented here provide novel tools to

247 The resulting transgenic plants produced 2% to 3% more TAG as a compon

248 and decreased PhCAT2 expression in PAL-RNAi transgenic plants resulted in 1.6-fold increase in pheny

249 tinguish between one- and two-copy events in transgenic plants with large genomes.

250 not essential for repressing ABA response in transgenic plants, but does contribute to stronger ABA r

251 promote the expression of two transgenes in transgenic plants.

252 ed-specific accumulation of jasmonic acid in transgenic plants.

253 Cell wall components are altered in transgenic plants.

254 scale, we used high-resolution 4D imaging of transgenic quail embryos expressing fluorescent proteins

255 nd assessed their progression over time in a transgenic rat model, which allows for a finer spatial r

256 ion of EGFP in Prox1-expressing cells of the transgenic rats and allowed a convenient visualization o

257 aun02 inactivation procedure in male FosLacZ-transgenic rats to ablate selectively Fos-expressing PLC

258 We then used male FosGFP-transgenic rats to assess selective alterations of intri

259 r promoting transcriptional silencing at the transgenic RD29A promoter.

260 erexpression of full-length OsbZIP48 in rice transgenics reduced the plant height considerably.

261 tinued to work independently over a targeted transgenic reporter construct.

262 of Wt1, and used it to drive expression of a transgenic reporter in Sertoli cells.

263 In transgenic reporter mice with normal angiopoietin-Tie2 s

264 facilitate selection of promoter regions for transgenic reporters, we assembled and annotated the M.

265 ron degeneration, which can be suppressed by transgenic restoration of Zfp106 specifically in motor n

266 Transgenic rice lines overexpressing (OX) OsALMT4 releas

267 Exogenous hormone applications and transgenic rice were used to test RBSDV infectivity and

268 onally mature beta cells, recent analyses of transgenic rodent and human pancreata reveal a number of

269 Plants with transgenic roots constitutively expressing MtCLE12 requi

270 Sirt2 knockout mice, cardiac-specific SIRT2 transgenic (SIRT2-Tg) mice, and their respective litterm

271 effects arise from overexpression per se in transgenic strains.

272 , suggesting that it is highly probable that transgenic sugarcane can be successfully commercialized.

273 , suggesting that it is highly probable that transgenic sugarcane can be successfully commercialized.

274 By generating a transgenic system we exhibit that in mESCs, the pluripot

275 OT-II mice expressing a transgenic T cell receptor (TCR) with specificity for ov

276 unotherapeutic strategy using c-MPL-enhanced transgenic T cells responding to either endogenously pro

277 In this article, we show that tau-transgenic (tau-tg) mice that develop neurodegenerative

278 med by mispairing between the endogenous and transgenic TCRs, may harbor autoreactive specificities.

279 have previously demonstrated that RORgammat-transgenic (tg) C57BL/6 mice, which have Th17-biased res

280 enile beta-epithelial Na(+) channel (Scnn1b)-transgenic (Tg) mice.

281 rated a neuron-targeted Cav-1-overexpressing transgenic (Tg) mouse [synapsin-driven Cav-1 (SynCav1 Tg

282 e addressed this problem by developing a TCR-transgenic (Tg) mouse with CD4 T cells that respond to a

283 sed WISP2 in vivo, we generated an aP2-WISP2 transgenic (Tg) mouse.

284 istration of lipopolysaccharide (LPS) to HIV transgenic (Tg) rats followed by assessment of IL-1beta

285 the improvement of monoterpene production in transgenic tobacco plants.

286 ting, in less than ten months, Tomelo, a non-transgenic tomato variety resistant to the powdery milde

287 nd pollen germination and tube growth of the transgenic trees.

288 ed pollen germination and tube growth of the transgenic trees.

289 NIK transgenic Tregs competed poorly with WT Tregs in vivo a

290 ress-related parameters in SeCspA and SeCspB transgenic wheat lines indicated that these lines posses

291 fer of mycobacteria-specific (P25 CD4(+) TCR transgenic) wild-type spleen cells into sanroqueRag1(-/-

292 , ameliorated the behavioral deficits of tau transgenic worms, reduced phosphorylated and detergent-i

293 umber of abiotic stresses in E. pusillum and transgenic yeast, and its stress-resistant ability was s

294 rance and tumor growth rate in a MYCN-driven transgenic zebrafish model of neuroblastoma that arises

295 Here, we used a transgenic zebrafish model to show that Myf5 is sufficie

296 Finally, using a transgenic zebrafish model, we show that encapsulated (R

297 l consequences of this variant, we generated transgenic zebrafish models expressing wild-type or A152

298 ion of oncogenic Kras(V12) in hepatocytes of transgenic zebrafish resulted in accelerated liver tumor

299 udy, we generated a new Tg(mrc1a:egfp)(y251) transgenic zebrafish that uses a mannose receptor, C typ

300 ble and reversible HCC model - the kras(V12) transgenic zebrafish.