ライフサイエンスコーパス: Cre recombinase

1 egulation of Abl and bRaf kinases as well as Cre recombinase.

2 Mice were given tamoxifen to induce Cre recombinase.

3 optical voltage sensor under the control of Cre recombinase.

4 targeted to the early DCT using a DCT-driven Cre recombinase.

5 tantly, can be conditionally expressed using Cre recombinase.

6 ibiotic resistance genes or enzymes, such as Cre recombinase.

7 disrupted in 2 different strains of mice via cre recombinase.

8 se line with sebocyte-specific expression of Cre recombinase.

9 essing (VIP+) GABAergic interneurons express Cre recombinase.

10 modelled by confined injection of adenoviral Cre recombinase.

11 e restored to wild type by gene editing with Cre recombinase.

12 27-bp cten promoter drives the expression of Cre recombinase.

13 h cell or tissue type-specific expression of Cre recombinase.

14 etween intrinsic flexibility and function in Cre recombinase.

15 which Notch activation is induced in HSCs by Cre recombinase.

16 flwt-Smn) can be conditionally deleted using Cre recombinase.

17 gain-of-function mutation is dependent upon Cre recombinase.

18 tein gene requires the presence of exogenous Cre recombinase.

19 assay using a reporter that is activated by Cre recombinase.

20 ate light-and-chemical regulated versions of Cre recombinase.

21 ression are activated only after exposure to Cre recombinase.

22 ) mice transduced with adenovirus expressing Cre recombinase.

23 atty acid binding protein 4) promoter-driven Cre-recombinase.

24 knockout mice with expression of Mx1 or Vav Cre-recombinase.

25 the DNA specificities of orthologous Dre and Cre recombinases.

26 On exposure to cre-recombinase a stop codon is generated immediately do

27 tion of an adeno-associated virus expressing Cre recombinase (AAV-Cre) into the midbrain/pons of mice

28 nt adeno-associated viral vectors containing Cre recombinase (AAV-Cre).

29 ter fragment or by targeted integration of a Cre recombinase-activatable expression cassette driven b

30 isynaptic circuit, we constructed a panel of Cre recombinase-activated pseudorabies viruses (PRVs) th

31 ion of these lineages was only observed with Cre recombinase activation during early lung development

32 cent Tomato (Tmt) signal in cells containing Cre recombinase activity.

33 Accordingly, adenoviral Cre recombinase (AdCre)-treated LSL-Kras/Irs-1(fl/fl) (K

34 Mice with albumin promoter-driven Cre recombinase (Alb-Cre)-mediated or AAV8-mediated L-Fa

35 approach also mediated efficient delivery of Cre recombinase and Cas9:sgRNA complexes into the mouse

36 ommits suicide inside host cells by inducing Cre recombinase and deleting essential genes flanked by

37 ated viral vectors containing genes encoding Cre recombinase and green fluorescent protein were micro

38 synthetic sequence through the action of the Cre recombinase and no competition from homologous recom

39 xamine the role of PDGFR-alpha in HSCs, Lrat-Cre recombinase and Pdgfra-floxed mice were bred to gene

40 adeno-associated virus [AAV]) that expresses Cre recombinase and sgRNAs targeting Rb1, Tp53, and Rbl2

41 one oncogene (KRAS), achieved by delivering Cre recombinase and sgRNAs, which caused rapid lung tumo

42 sing adeno-associated viral vectors encoding Cre recombinase and short hairpin RNA against Crb2.

43 hod RecWay assembly, as it makes use of both Cre recombinase and the commercially available Gateway c

44 ns of two unrelated genome editing proteins, Cre recombinase and zinc-finger nucleases, under conditi

45 t (KO) mouse lines, with viral expression of Cre-recombinase and a light-activated ion channel for op

46 However, breeding with a Cre-recombinase and/or Flp-recombinase mouse is required

47 ockdown, GRK2 gene deletion (GRK2(flox/flox)/cre recombinase) and overexpression of GRK2 and its regu

48 Using bone marrow transplantation and Cre recombinase-based lineage tracing experiments, we ru

49 c markers (Sox2 and T) and tamoxifen-induced Cre recombinase-based lineage tracing to locate putative

50 Cre recombinase catalyzes the cleavage and religation of

51 letion of Pten and Grp78 mediated by Albumin-Cre-recombinase (cP(f/f)78(f/f)).

52 pha) mouse line and a gene construct driving Cre recombinase (Cre) expression in NSP cells, led to in

53 mouse strains have been developed, in which Cre recombinase (Cre) expression is driven by an RPE-spe

54 Cre recombinase (Cre) mouse driver lines in combination

55 ciated trauma or the toxicity of the chronic Cre recombinase (Cre) produced by the AAV-Cre.

56 Here, we generated knock-in mice expressing Cre recombinase (Cre) under the control of the endogenou

57 in the lung by nasal delivery of adenoviral Cre recombinase (Cre), here we show that KRAS(G12D) expr

58 In this study, we used the Cre recombinase (Cre)-loxP system under regulation of th

59 Finally, we validated that Cre recombinase (Cre)-mediated excision led to functiona

60 m by injecting an adenoviral vector encoding Cre recombinase (Cre)-regulated farnesylated green fluor

61 ogeny of mice expressing tamoxifen-inducible Cre recombinase (Cre-ERT2) under the Aicda promoter cros

62 breeding these mice with lines that express Cre-recombinase (Cre) in early embryogenesis (EIIa-Cre)

63 pulse-labeled using the tamoxifen-dependent Cre recombinase, CreER(T2), expressed from the endogenou

64 We generated mice with tamoxifen-inducible Cre recombinase (CreERT2) in the Anxa10 gene locus.

65 or 1 (Tff1) gene and the tamoxifen-inducible Cre recombinase (CreERT2)-coding sequence.

66 describe a technique based on a destabilized Cre recombinase (DD-Cre) whose activity is controlled by

67 (+) .Foxo1 (L/L) mice with lineage-specific Cre recombinase deletion of floxed FOXO1 and compared th

68 human insulin receptoropathy in mice, using Cre recombinase delivered by adeno-associated virus to k

69 hod that exploits GFP for gene manipulation, Cre recombinase dependent on GFP (CRE-DOG), a split comp

70 This strategy relies on CRE recombinase-dependent activation of an EGFP-tagged L

71 onal band of Broca cholinergic neurons using Cre recombinase-dependent adeno-associated virally media

72 Cre recombinase-dependent Ai9 reporter mice were crossed

73 Optogenetic stimulation using cre recombinase-dependent ChIEF-AAV-DJ expressed in ARC

74 ng of SOM-expressing neurons in s. oriens, a Cre recombinase-dependent construct for channelrhodopsin

75 probe within a locus designed for efficient Cre recombinase-dependent expression.

76 s nicotine reward behaviors, we engineered a Cre recombinase-dependent gene expression system to sele

77 ermine MN-enriched miRNA expression, we used Cre recombinase-dependent miRNA tagging and affinity pur

78 To address this, we used a Cre-recombinase-dependent viral vector approach to expre

79 le gene deletion system based on a dimerised Cre recombinase (diCre) to target CRK3 and elucidate its

80 PR/Cas9 to facilitate use of the dimerisable Cre-recombinase (DiCre) that is frequently used to media

81 Using male mice with Cre-recombinase directed to the oxytocin receptor gene (

82 ingly, cells targeted by tamoxifen-inducible cre recombinase driven by nestin enhancer (Nes-creER) in

83 ngineered mouse model in which expression of Cre recombinase driven by the C-type lectin domain famil

84 constitutive activation of betacatenin using cre recombinase driven by the DEAD (Asp-Glu-Ala-Asp) box

85 ating alpha7nAChR(flox) with mice expressing Cre recombinase driven by the glial acidic fibrillary pr

86 generated the Mchr1-cre mouse that expresses cre recombinase driven by the MCHR1 promoter and crossed

87 s mouse strain to transgenic mice expressing Cre recombinase driven by the megakaryocyte (MK)-specifi

88 ecific inactivation of the BBSome induced by Cre recombinase driven by the rhodopsin promoter.

89 gene was deleted using a tamoxifen-inducible Cre recombinase driven by the ubiquitously expressed ROS

90 nt marker into the VTA of male mice that had Cre-recombinase driven by OTR gene expression.

91 (IR), IGF-1 receptor (IGF1R), or both using Cre-recombinase driven by the adiponectin promoter.

92 HIF-1alpha floxed mice with mice expressing Cre-recombinase driven by the calcium/calmodulin-depende

93 Here we use Cre-recombinase driven by the CNP promoter to generate a

94 p53 and Rb were selectively abrogated using Cre-recombinase driven by the renin promoter.

95 diated by KOR on DA terminals, we utilized a Cre recombinase-driven mouse line lacking KOR in DA neur

96 These include a line for conditional Cre-recombinase-driven inactivation of the gene; a line

97 The collection of over 250 BAC Cre-recombinase driver lines produced by the GENSAT proj

98 cortex at different prenatal ages using two Cre-recombinase driver lines.

99 used two different mature RPE cell-specific Cre recombinase drivers to inactivate either Dicer1 or D

100 oral activation by tamoxifen (TAM)-inducible Cre recombinase Ela-CreERT in the submandibular gland (S

101 deno-associated virus-mediated expression of cre recombinase, eliminated cocaine-induced ERK phosphor

102 Here, through the use of Cre-recombinase-enabled, cell-specific neuron mapping te

103 Injection of Cre recombinase-encoding adenovirus (AdCre) in the ovari

104 olerant mice; and (3) Tag-activation through Cre recombinase-encoding viruses in the liver and HCC de

105 of Optopatch constructs is controlled by the Cre-recombinase enzyme.

106 ation of cKOs by local viral delivery of the Cre-recombinase enzyme.

107 pocytes prior to cold exposure, using Pdgfra-Cre recombinase estrogen receptor T2 fusion protein (Cre

108 ysis because they expressed a high amount of Cre recombinase exclusively in ameloblasts and showed de

109 expressing a tamoxifen-inducible variant of Cre recombinase expressed under control of the Npr2-prom

110 ory neurons of the postnatal forebrain using Cre recombinase expressed under the control of the alpha

111 ed mouse, and then crossed this mouse with a Cre recombinase expressing mouse driven by the human gli

112 ar Anchored Independent Labeling, to isolate Cre recombinase-expressing (Cre(+)) nuclei from the adul

113 oblasts with 2 different tamoxifen-inducible Cre recombinase-expressing gene-targeted mouse lines.

114 Using a Cre recombinase-expressing IAV, we have previously shown

115 allowed the identification of synapses from Cre recombinase-expressing or GAL4-expressing neurons in

116 neurons chemogenetically using a retrograde Cre-recombinase-expressing canine adenovirus-2 in combin

117 lidation of a transgenic mouse line in which Cre recombinase expression has been targeted to cells ex

118 ion of floxed KOR or floxed p38alpha MAPK by Cre recombinase expression in dopaminergic neurons block

119 Infected cell tagging by viral Cre recombinase expression in floxed reporter gene mice

120 rter VGLUT2 may be exploited to drive robust Cre recombinase expression in RGCs without any expressio

121 system largely depends on the specificity of Cre recombinase expression in targeted stem or progenito

122 Keratin 14-mediated Cre recombinase expression induced expression of MCPyV T

123 erate new rat strains (Cre drivers) in which Cre recombinase expression is carefully controlled tempo

124 ducible membrane-bound reporter and targeted Cre recombinase expression to a subset of glial progenit

125 bone osteocytes, no differences in Mbtps1 or cre recombinase expression were observed in cKO SOL, exp

126 After Cre recombinase expression, GsD is activated temporally

127 cells, and mature keratinocytes through OX40-Cre recombinase expression.

128 h tamoxifen-inducible smooth muscle-specific Cre recombinase expression.

129 es from transgenic mice with region-specific Cre recombinase expression.

130 hat were crossed with DAT-Cre mice, in which Cre- recombinase expression is under dopamine transporte

131 By electroporating a cre-recombinase expression vector into the cortex of E13

132 uroblast enhancers drive expression of split Cre recombinase fragments.

133 sing chemogenetics in male rats that express Cre recombinase from a Crh promoter.

134 regions, we used transgenic mice expressing Cre recombinase from the Nkx2.1 promoter to ablate loxP-

135 Here, we generated mice expressing Cre recombinase from the Robo3 locus specifically in com

136 Notably, TAxI-Cre recombinase fusion proteins induced selective recomb

137 rgeted deletion of gata3 driven by otoferlin-cre recombinase (gata3(fl/fl) otof-cre(+/-) ) in IHCs do

138 stem to excise the selectable marker and the cre recombinase genes from transgenic banana cv. 'Grande

139 enic lines expressing a controllable form of Cre recombinase have become valuable tools for manipulat

140 Using Cre recombinase, here we show that either deletion or re

141 l La allele and used it in mice that express Cre recombinase in either B cell progenitors or the fore

142 system, in conjunction with mice expressing Cre recombinase in either parvalbumin-positive, somatost

143 Male and female transgenic mice expressing Cre recombinase in FSIs allowed us to identify these spa

144 tion by Cre recombinase in mice that express Cre recombinase in GABAergic neurons.

145 validated a transgenic mouse line expressing cre recombinase in histidine decarboxylase-expressing ne

146 is used to specifically and inducibly drive Cre recombinase in ICC as a strategy to study GIST patho

147 Using mice expressing Cre recombinase in MC4R neurons, we demonstrate bidirect

148 fluorescent protein following activation by Cre recombinase in mice that express Cre recombinase in

149 ut mice with a knock-in mouse expressing the Cre recombinase in the CD45 locus.

150 We observe a broad expression of Cre recombinase in the Gfi1(Cre) mouse neonatal inner ea

151 o-associated viral (AAV) vector carrying the Cre recombinase in the hippocampus of mTORf/f mice recap

152 enomatous polyposis coli) upon expression of CRE recombinase in the liver and monitored their effects

153 ntly translated into full-length, functional Cre recombinase in the presence of nonsense suppressors

154 expression in the NAc of mice transgenic for Cre recombinase in these MSN subtypes.

155 Amhr2-Cre mice express Cre recombinase in tissues that develop into the fallopi

156 ggered by intravenous adenoviral delivery of Cre recombinase in transgenic mice expressing the hepato

157 s frequently used to drive expression of the Cre recombinase in tuft cells.

158 line was assessed on interneurons expressing Cre recombinase in vasoactive intestinal peptide (VIP) o

159 ediated delivery of functional pDNA encoding Cre recombinase in vivo to tissues in transgenic Cre-lox

160 , once the tumor is induced by activation of Cre-recombinase in a tissue-specific manner, further gen

161 ocalized infusions of adeno-associated virus Cre-recombinase in adult, targeted knock-in mice with lo

162 glutamic acid decarboxylase (GAD67-GFP), or Cre-recombinase in cells that contain glutamic acid deca

163 The Ntsr1-Cre GN220 mouse expresses Cre-recombinase in corticothalamic (CT) neurons in neoco

164 ecting adeno-associated virus that expressed Cre-recombinase in HIF-1alpha floxed mice.

165 roligins by stereotactic viral expression of Cre-recombinase in hippocampal CA1 region pyramidal neur

166 se lines (including both sexes) that express Cre-recombinase in MCs.

167 tamoxifen-inducible collagen type 2a1-driven Cre recombinase increased proliferation and beta-catenin

168 development of a transgenic mouse line where Cre-recombinase-induced expression of a mutant methionyl

169 A transgenic mouse containing a CRE-recombinase inducible CAG promoter driven CD9 protei

170 the constitutively active Eef1a1 locus in a Cre recombinase-inducible manner.

171 d in adult Mx1-cre(+)Raptor(fl/fl) mice upon cre-recombinase induction.

172 t two-hybrid method, CrY2H-seq, which uses a Cre recombinase interaction reporter to intracellularly

173 also used to deliver the biologically active Cre recombinase into a loxP-reporter T cell line.

174 oinflammation in the DR by viral delivery of Cre recombinase into interleukin (IL)-1beta(XAT) transge

175 rom lentiviral delivery of shRNAs along with Cre recombinase into lungs of Loxp-stop-Loxp-KRas mice.

176 letion of Pbx1 by retroviral transduction of Cre recombinase into Pbx2-deficient SVZ stem and progeni

177 1 or MAGL via injection of virally-delivered Cre recombinase into the MSDB of Cnr1(loxP/loxP) or Mgll

178 pproximately E11.5) we have therefore used a Cre recombinase introduced at the Ins1 locus.

179 transgenic Cre line, in which expression of Cre recombinase is controlled by a previously identified

180 Cre recombinase is mixed with a fluorophore-tagged polym

181 ne targeting using the bacteriophage-derived Cre recombinase is widely applied for functional gene st

182 Using either a keratin 5-Cre recombinase (K5-Cre) cross or an MMTV-NIC mouse, we

183 ry epithelium of an ErbB2 model coexpressing Cre recombinase led to accelerated tumor onset.

184 We identified a particular Cre-recombinase line that acts in the cortical primordiu

185 These studies combine the use of the Cre-recombinase/loxP system in mice with optogenetics to

186 In the presence of activated Cre recombinase, luciferase activity, and by proxy, HPV

187 tes in a cultured pre-B cell line as well as Cre recombinase-mediated Bcl11a(lox/lox) deletion in exp

188 This uses Cre recombinase-mediated cassette exchange to insert a c

189 Here, we used a Cre recombinase-mediated chromosome loss strategy to ind

190 Here, we show that Cre recombinase-mediated conditional deletion of Atp6ap2

191 events in preclinical mouse models requires Cre recombinase-mediated conditional gene expression in

192 n of Panx1 (Panx1 (-/-) Apoe (-/-) ) or with Cre recombinase-mediated deletion of Panx1 in endothelia

193 We show that Cre recombinase-mediated DT-A ablation selectively elimi

194 Cre recombinase-mediated excision of the stop cassette l

195 We have also used Cre recombinase-mediated expression of channelrhodopsin-

196 ducible lineage tracing to fate map, through Cre recombinase-mediated fluorescent reporter gene activ

197 By using temporal Cre recombinase-mediated gene deletion to ablate SAP exp

198 h CreMaster mice, which are characterized by Cre recombinase-mediated mast cell eradication.

199 Previous studies have demonstrated that Cre recombinase-mediated recombination can lead to combi

200 ic recombination system based on dimerizable Cre recombinase-mediated recombination in the apicomplex

201 nger needed after integration was excised by Cre recombinase-mediated recombination of lox sites.

202 eage tracings using cyclization recombinase (Cre) recombinase-mediated cell labeling represent the go

203 ion of Steroidogenic Factor-1 (SF1) to drive Cre-recombinase-mediated deletion of the brain muscle ar

204 Here, we have used Cre-recombinase-mediated genetic labeling to identify an

205 centrosome amplification can be induced by a Cre-recombinase-mediated increase in expression of Polo-

206 Cre-recombinase-mediated knockdown and overexpression of

207 Cre-recombinase-mediated Ptch1 ablation in mammary epith

208 Regulated expression of Cre recombinase mediates precise deletion of genetic ele

209 h various neurone selective, promoter-driven Cre recombinase mice resulted in GCaMP3 expression in de

210 can be controlled tissue-specifically using Cre recombinase mice.

211 26-lox-STOP-lox-miR-150 mice with WAP-driven Cre recombinase mice.

212 pment we crossed Myh9 floxed mice and Nkx2.5 cre-recombinase mice.

213 ty in mice and develop a new tissue specific Cre recombinase mouse model, we have established pCTEN-C

214 combinase (thrombopoietic deletion) or Cd11b-Cre-recombinase (myeloid deletion).

215 onsense mutation into the coding sequence of Cre recombinase (nsCre).

216 Upon activation with Cre recombinase ("on-state"), the intron is crippled and

217 anterograde tracing using mice that express Cre recombinase only in neurons producing acetylcholine,

218 A complementary DNA encoding either Cre recombinase or a tamoxifen-inducible MerCreMer chima

219 d nanoparticles with negatively supercharged Cre recombinase or anionic Cas9:single-guide (sg)RNA com

220 We characterize a previously developed split Cre recombinase (PA-Cre2.0) that is reconstituted upon l

221 of genetically encoded photoactivatable (PA) Cre recombinase, PA-Cre 3.0.

222 s of Pam (0-Cre-cKO/cKO) atrial myocytes (no Cre recombinase, PAM floxed) were transduced with Cre-GF

223 The Platelet factor 4-Cre recombinase (Pf4-Cre) transgenic mouse is the curren

224 nanoparticles (MSNs) as carriers to deliver Cre recombinase protein into maize (Zea mays) cells.

225 ify mutations in the dimerization surface of Cre recombinase (R32V, R32M and 303GVSdup) that improve

226 tegrase system in place of the bidirectional Cre recombinase reaction; and (iii) gel extraction by DN

227 o achieve constitutive HH signaling) using a Cre recombinase regulated by the lysozyme M promoter.

228 These mice were crossed with mice expressing Cre recombinase, regulated by the villin or CD11c promot

229 in postnatal testis, and a dual fluorescent Cre recombinase reporter to label FLC and ALC in vivo.

230 Stra8 (mcKO) and Zp3 (fcKO) promoter-driven Cre recombinase, respectively.

231 d disruptive sequence that can be deleted by Cre recombinase, resulting in restored IL-1R1 gene expre

232 trogradely transported AAV vector expressing Cre recombinase (Retro-Cre-GFP) into the BLA (Experiment

233 developed a recombinant JHMV that expresses Cre recombinase (rJ-Cre) and infected mice that universa

234 cells using smooth muscle protein 22-driven Cre recombinase (SMGRKO mice) and compared them with mic

235 h an adenoassociated viral vector expressing Cre recombinase specifically in hepatocytes.

236 Using the mice expressing Cre recombinase specifically in the lens epithelial cell

237 Tamoxifen (TAM) inducible Cre recombinase system is an essential tool to study gen

238 We used a tamoxifen-regulated Cre recombinase system to conditionally express the HPV

239 essing tenocytes using a tamoxifen-inducible Cre-recombinase system and caused tendon growth in adult

240 combined with a split-intein-mediated split-Cre-recombinase system in mice to isolate, characterize,

241 the potent delivery of nM concentrations of Cre recombinase, TALE- and Cas9-based transcription acti

242 mary sarcomas generated with CRISPR-Cas9 and Cre recombinase technology had similar histology, growth

243 in the current study we used CRISPR/Cas9 and Cre recombinase technology to produce mice that lack GH

244 1(CreER) mice expressing tamoxifen-inducible Cre recombinase that allow for specific manipulation of

245 nic mouse under the control of both Flp- and Cre-recombinases that is an effective tool for circuit m

246 In cells expressing Cre-recombinase, the floxed sequence is deleted, resulti

247 ce were crossed with mice transgenic for Pf4-Cre-recombinase (thrombopoietic deletion) or Cd11b-Cre-r

248 cinar cell-specific expression of knocked-in Cre recombinase through control of aquaporin 5 (Aqp5) pr

249 tability was mimicked with viral delivery of Cre recombinase to astrocytes in the LHA and rescued by

250 mbens with adeno-associated virus expressing Cre recombinase to create focal, homozygous Hdac3 deleti

251 lpha subunit and cell-specific expression of Cre recombinase to deplete PV(+) or SST(+) interneurons

252 After viral delivery of Cre recombinase to hepatocytes in vivo, GsD is expressed

253 lineage analysis has been accomplished using Cre recombinase to indelibly label a defined progenitor

254 l recombinase technology using both FlpO and Cre recombinases to generate primary sarcomas in mice wi

255 kout mouse model using progesterone receptor-Cre-recombinase to achieve Pten and Grp78 (cPten(f/f)Grp

256 We used Cre driver lines (mice expressing Cre recombinase) to comprehensively and selectively labe

257 ice with selective expression of tdTomato or cre recombinase together with optogenetics to investigat

258 ice with a retinoid acid receptor 2 promoter-Cre recombinase transgene (Rarb-cre) expressed in embryo

259 ock-out mice carrying an aP2 promoter-driven Cre recombinase transgene showed a blunted response to t

260 KD1 gene and heterozygous for an aquaporin-2-Cre recombinase transgene to achieve collecting duct-spe

261 Cell type-specific tamoxifen-inducible Cre recombinase transgenes were used to target glioblast

262 We used SMC- and EC-specific Cre recombinase transgenes with a novel floxed Eln allel

263 C transgenic mice with a tamoxifen-inducible Cre recombinase transgenic line, CAGGS-Cre-ER.

264 kout (floxed) Ptpn11 allele (Ptpn11(fl)) and Cre recombinase transgenic mice to delete Ptpn11 specifi

265 and alpha-myosin heavy-chain promoter-driven Cre recombinase transgenic mice.

266 onditional knockout [cKO]) when crossed with Cre recombinase transgenic mice.

267 t nervous system using a tamoxifen inducible Cre recombinase transgenic mouse system.

268 artifacts associated with beta-cell-specific Cre-recombinase transgenic models, raising questions abo

269 Furthermore, using different Cre-recombinase transgenic mouse strains to specifically

270 hemiparkinsonian transgenic mice expressing Cre recombinase under control of the choline acetyltrans

271 IF-1alpha floxed mice with mice that express Cre recombinase under control of the glial fibrillary ac

272 U.1) was conditionally deleted in B cells by Cre recombinase under control of the Mb1 gene in Spib (e

273 erated mice that express tamoxifen-inducible Cre recombinase under control of the Plp1 promoter and c

274 ite cells in mice, using tamoxifen-inducible Cre recombinase under control of the satellite cell-spec

275 using mice expressing a tamoxifen-dependent Cre recombinase under the control of a fibroblast-specif

276 neered the expression of tamoxifen-inducible Cre recombinase under the control of a kidney-specific p

277 yn(flox/flox) animals with mice carrying the Cre recombinase under the control of the Cd79a promoter,

278 mice with CX3CR1(CreER) mice, which express Cre recombinase under the control of the CX3C chemokine

279 mice crossed with transgenic mice expressing Cre recombinase under the control of the mouse platelet

280 virus vectors and transgenic mice expressing Cre recombinase under the D1 promoter, we also found tha

281 manipulated in knock-in mice expressing the Cre recombinase under the endogenous parvalbumin promote

282 he circadian clock gene Bmal1 and expressing Cre recombinase under the endogenous Renin promoter (Bma

283 out of Trim33 by combining floxed Trim33 and Cre recombinase under the Pax7 promoter.

284 leles floxed at exon 1 to animals expressing Cre recombinase under the pre-proglucagon promoter.

285 crossing FKRP(KD) mice with those expressing Cre recombinase under the Sox1 promoter.

286 allele using transgenic mice that expressed Cre-recombinase under control of the ubiquitous CAG prom

287 Adult transgenic mice expressing cre-recombinase under the choline acetyltransferase prom

288 e using an adeno-associated virus serotype-9 Cre recombinase vector (AAV.CBA.Cre).

289 ssociated virus 8-thyroxine-binding globulin-Cre-recombinase versus control.

290 ection of a BAAV vector encoding a bacterial Cre recombinase via canalostomy in adult mice with floxe

291 IL-22-expressing cells, a sequence encoding Cre recombinase was cloned into the Il22 locus, and IL22

292 delity lineage tracing after confirming that Cre recombinase was mesothelial specific and faithfully

293 Adenoviral Cre recombinase was used to delete RISP from isolated PA

294 ssibility that the bovine K5 promoter-driven Cre-recombinase was active early in trophoblast-lineage

295 tor cells with adenovirus expressing GFP and Cre-recombinase was successful in GRP78 ablation, and th

296 us from cells, Tre, an engineered version of Cre recombinase, was designed to target a 34-bp sequence

297 rade tropism, a canine adenovirus expressing Cre recombinase, was injected into the left intermediola

298 Using Cre recombinase we swapped a target 126-kb segment of th

299 tionally deleted using progesterone receptor Cre recombinase, which is expressed in both epithelial a

300 ing fluorescent parasite strains that inject Cre recombinase with their rhoptry proteins (Toxoplasma-