ライフサイエンスコーパス: conditional knockout

1 gesia/medication overuse headache in Dlx-DOR conditional knockouts.

2 , all of which are upregulated in Hand2 limb conditional knockouts.

3 ither individually or in combinations, using conditional knockouts.

4 or recombinases) or gene replacement (e.g., conditional knockout alleles containing exons flanked by

5 Here, we describe in vivo conditional knockout analyses of murine Ars2, which has

6 Conditional knockout analyses revealed a non-autonomous

7 Here we employed conditional knockout and modified antagonist PU.1 constr

8 Cleft palate was observed in both conditional knockout and over-expression mice, consisten

9 ctical, rapid, and economical alternative to conditional knockout and transgenic mouse models.

10 n profiles of embryonic day 14.5 (E14.5) Yap conditional knockout and YAP transgenic mouse tooth germ

11 Yap (Yap1) knockout, Yap(nestin) conditional knockout and Yap(GFAP) conditional knockout

12 models: a conditional E401K knock-in, and a conditional knockout animal.

13 We used a conditional knockout approach to investigate the roles a

14 Therefore, we used a conditional knockout approach to investigate the roles o

15 ence on Muller cell-expressed Des1 through a conditional knockout approach.

16 We show that a Tet2/Tet3 conditional knockout at early stages of B-cell developme

17 phenotype was partially rescued in the Etv2 conditional knockout background.

18 myocyte-specific deletion of Atf6 (ATF6 cKO [conditional knockout]) blunted transverse aortic constri

19 Clones bearing the conditional knockout cassette are recovered at frequenci

20 nt study we generated a B cell-specific CD83 conditional knockout (CD83 B-cKO) model.

21 us to easily and rapidly generate AID-based conditional knockout cells in a wide range of vertebrate

22 reported up to 16% efficiency in generating conditional knockout (cKO or floxed) alleles by microinj

23 the subventricular zone of both FIP200hGFAP conditional knockout (cKO) and FIP200;p53hGFAP 2cKO mice

24 Tie2-Cre-driven Hilpda conditional knockout (cKO) did not affect viability, pro

25 branchial arch mesenchyme of Yap and Taz CNC conditional knockout (CKO) embryos.

26 Mice with conditional knockout (cKO) for Scx (Scx(flx/-), Prx1Cre(

27 Here Gpr124 conditional knockout (CKO) in the endothelia of adult mi

28 ate a gene in a given tissue by generating a conditional knockout (cKO) is crucial for determining it

29 T cell development in CD2-icre HDAC3 conditional knockout (cKO) mice (HDAC3-cKO) was blocked

30 ntrol and heterozygous mice, Depdc5-Emx1-Cre conditional knockout (CKO) mice demonstrated macrocephal

31 e neuroligins, we analyzed single and triple conditional knockout (cKO) mice for all three major neur

32 ency contributes to ASD, we generated CTNNB1 conditional knockout (cKO) mice in parvalbumin interneur

33 ms associated with Parkinson's disease using conditional knockout (cKO) mice in which Ndufs4 was sele

34 Here we show that conditional knockout (cKO) mice lacking estrogen recepto

35 Germline-specific Dicer and Drosha conditional knockout (cKO) mice produce gametes (i.e. sp

36 inations of these deletions in the pleura of conditional knockout (CKO) mice, focusing on the contrib

37 We employed Myd88 conditional knockout (CKO) mice, in which Myd88 was dele

38 Cnr2 gene in midbrain DA neurons of DAT-Cnr2 conditional knockout (cKO) mice.

39 we generated two lines of Cre-mediated Tspo conditional knockout (cKO) mice.

40 In this study, by using a conditional knockout (cKO) model with selective IL-6 rec

41 tinal vascular disease, we generated a Kif11 conditional knockout (CKO) mouse and investigated the co

42 to generate a region-specific astrocytic YY1 conditional knockout (cKO) mouse model.

43 ring meiotic resumption, we developed a Plk1 conditional knockout (cKO) mouse to specifically mutate

44 Using a Thy1-Nampt(-/-) projection neuron conditional knockout (cKO) mouse, we studied the impact

45 eport that loss of ROBO2 in podocytes [Robo2 conditional knockout (cKO) mouse] is protective from glo

46 Conditional knockout (cKO) of ALK3 in the uterus was obt

47 metabolomic analysis in mice with inducible conditional knockout (cKO) of BMAL1, which is critically

48 Conditional knockout (cKO) of FGFR1 in the DT (FGFR1(DT-

49 is perinatal lethal in mice, we generated a conditional knockout (cKO) of Fst in the uterus using pr

50 phenotypes of females with a Zp3-Cre-driven conditional knockout (cKO) of Smc5 demonstrated that mat

51 dy, we showed that pyramidal-neuron specific conditional knockout (cKO) of syntaxin-4 significantly r

52 A conditional knockout (cKO) of the androgen receptor gene

53 We generated mice in which conditional knockout (CKO) of the Hif1a gene encoding th

54 all interfering RNA (siRNA), lentivirus, and conditional knockout (CKO) techniques were employed to m

55 e, using tissue-specific dynamin-1 knockout [conditional knockout (cKO)] mice at a fast central synap

56 me (APC/C) ubiquitin ligase in neurons [Cdh1 conditional knockout (cKO)], disrupts dendrite arborizat

57 Adult FOXA2 conditional knockout (cKO; Ltf (iCre/+) Foxa2 (f/f) ) mi

58 l TEC-defective (resulting from FoxN1-floxed conditional knockout [cKO]) and naturally aged mouse mod

59 ele, allowing for conditional gene ablation (conditional knockout [cKO]) when crossed with Cre recomb

60 Mutagenesis experiments using a conditional knockout constructed in M. smegmatis confirm

61 yt11 in excitatory forebrain neurons using a conditional knockout did not affect life span but impair

62 Endothelial cell-selective miR-15a/16-1 conditional knockout (EC-miR-15a/16-1 cKO) mice and wild

63 poiesis and leukemogenesis, we generated Eed conditional knockout (Eed(Delta/Delta)) mice.

64 In Sox2 conditional knockout embryos, the oral epithelium failed

65 Cross-fostering and conditional knockout experiments indicated that a TNF-al

66 s of gene depletion by CRISPR-Cas9, RNAi, or conditional knockout for melanoma modeling.

67 educes the DNA manipulation needed to make a conditional knockout gene targeting vector to only two s

68 cations that have used tamoxifen to generate conditional knockouts have not reported even the minimum

69 ue to downregulation of TbIPMK expression by conditional knockout, have reduced levels of polyphospha

70 Conditional knockout in CD4+ T cells revealed Kdm6a invo

71 Here, we ablated all three Ca(V)2s using conditional knockout in cultured hippocampal neurons or

72 nt receptor, Ryk, in mice and rats by either conditional knockout in the motor cortex or monoclonal a

73 A dental epithelium-specific Irf6 conditional knockout (Irf6-cKO) mouse was generated via

74 To this end, we used conditional knockout (KO) mice lacking STIM1 in cells of

75 Analysis of Brd4 conditional knockout (KO) mice showed that BRD4 is requi

76 city of brain FAO using a pan-brain-specific conditional knockout (KO) mouse incapable of FAO due to

77 HL2 in oral mucosal barrier, we used a Grhl2 conditional knockout (KO) mouse model, which allows for

78 Conditional knockout (KO) mouse models are invaluable fo

79 surgically induced tibial fracture model in conditional knockout (KO) Nfl (Nf1(flox/flox)) mice.

80 Conditional knockout (KO) of Fat3 in brains of adult mic

81 V-Neu transgenic female mice with or without conditional knockout (KO) of Tcfap2c, the mouse homolog

82 The conditional knockout (KO) of TFR in neural progenitor ce

83 Here we showed that HuR conditional knockout (KO) Th17 cells have decreased GM-C

84 Using a conditional knockout (KO), we here demonstrate that the

85 ea, we used an Nkx2.1-Cre driver to generate conditional knockouts (KOs) in mice of leptin receptor (

86 ikewise, mice harboring liver-specific Lats2 conditional knockout (Lats2-CKO) displayed constitutive

87 cell type-specific Cre-drivers and a Gnptab conditional knockout line, we found that only astrocyte-

88 repinephrine reuptake inhibitor, observed in conditional knockout male mice supports deficient 5-HT t

89 Using Drd1-Cre mTOR-conditional knockout male mice, we combined behavioral,

90 A novel cardiac myocyte-specific Speg conditional knockout (MCM-Speg(fl/fl)) model revealed th

91 Using three conditional knockout methods at different stages of deve

92 le Cre ( UBC-Cre/ER(T2)) line crossed to Ret conditional knockout mice ( Ret(fx/fx)), Ret was deleted

93 In Cx26 conditional knockout mice (Cx26(Sox10-Cre)) the maturati

94 We generated Dnmt1 conditional knockout mice (Dnmt1(Deltaalb) ) by crossing

95 ecting tubule/collecting duct-specific Dot1l conditional knockout mice (Dot1l(AC) ), Dot1l and Edn1 d

96 1 connecting tubule/collecting duct-specific conditional knockout mice (Edn1(AC) ), under three exper

97 To this end, we used conditional knockout mice (FoxN1-Gpr177) in which TECs a

98 ng cell type-specific Myf5-cre;Lipin1(fl/fl) conditional knockout mice (Lipin1(Myf5cKO) ) shows that

99 Using conditional knockout mice (Ncr1-Cre-Gnaq(fl/fl)), we dem

100 d mice to generate ameloblast-specific Stim1 conditional knockout mice (Stim1 cKO).

101 , administration of Notch inhibitors in Fbw7 conditional knockout mice alleviated progressive bone re

102 d LATS2 kinases in NEX-Cre lineage in double conditional knockout mice also generates similar tumours

103 Surprisingly, the double conditional knockout mice also showed growth plate defec

104 Similarly, Prkch Treg-specific conditional knockout mice also showed improved viral cle

105 ity alterations were normalized in GABA-CB1R conditional knockout mice and after subchronic treatment

106 or adipogenesis in culture and in vivo Using conditional knockout mice and derived white and brown pr

107 Conditional knockout mice and transgenic mice expressing

108 Conditional knockout mice are generated using labor-inte

109 ermore, RBCs from blood-cell-specific Piezo1 conditional knockout mice are overhydrated and exhibit i

110 Sirt-1 in GVHD induction by employing Sirt-1 conditional knockout mice as well as a pharmacological S

111 s of Stx3 and -4 in fully developed MCs from conditional knockout mice by electrophysiology and EM, a

112 cultured neural stem cells derived from Cic conditional knockout mice bypassed an EGF requirement fo

113 ent tissue- and developmental stage-specific conditional knockout mice carrying Smarcb1 and/or Nf2 de

114 cantly different in the fetal brain of Foxa2 conditional knockout mice compared with control mice.

115 Here we generated conditional knockout mice deficient in various Slit and

116 Although analyses of Fgf8 conditional knockout mice did not reveal developmental p

117 p(nestin) conditional knockout and Yap(GFAP) conditional knockout mice displayed fewer neocortical as

118 elial injury, we demonstrate that myeloid AC conditional knockout mice exhibit impairment of neutroph

119 ucture-related gene expression, whereas Tsc1 conditional knockout mice exhibited changes in genes reg

120 mice, whereas hepatocyte and macrophage Bmp6 conditional knockout mice exhibited no iron phenotype.

121 Two independent Osx conditional knockout mice exhibited similar molar abnorm

122 Studying conditional knockout mice for ELKS, we find that ELKS en

123 Here, we generated double conditional knockout mice for RIM-BP1 and RIM-BP2, and a

124 We further generated germ-cell-specific, conditional knockout mice for the key histone acetyltran

125 In vivo, megakaryocyte-specific Munc18-2 conditional knockout mice had a severe hemostatic defect

126 retinal ganglion cell death, similar to Nf1 conditional knockout mice harboring a neomycin insertion

127 Osteoclast-lineage-specific Gna13 conditional knockout mice have a severe osteoporosis phe

128 nses to TLR stimulation in vitro, and alphav-conditional knockout mice have elevated antibody respons

129 We generated conditional knockout mice in which brain AMPKalpha isofo

130 retion is abolished in acute brain slices of conditional knockout mice in which Synaptotagmin-1 is re

131 To test this model, we studied conditional knockout mice in which the vast majority of

132 Conditional knockout mice lacking ADORA2B on myeloid cel

133 sence of NF186, they fail to do so in double conditional knockout mice lacking both NF186 and the par

134 ess these questions we generated a series of conditional knockout mice lacking one or both house-keep

135 induced SNS injury, while NPY injection into conditional knockout mice lacking the Y1 receptor in mac

136 in vivo replacement strategies in quadruple conditional knockout mice of all neuroligins to avoid he

137 Both whole-body (Lgr4(-/-)) and monocyte conditional knockout mice of Lgr4 (Lgr4 CKO) exhibit ost

138 In addition, Tsc1 conditional knockout mice presented severely disorganize

139 Here, we generated conditional knockout mice removing the active zone prote

140 man cells and astrocytes derived from AP-2mu conditional knockout mice revealed a significant impairm

141 cell type datasets from Nova2-cTag and Nova2 conditional knockout mice revealed differential NOVA2 re

142 Analysis of the Bmp6 conditional knockout mice revealed that liver endothelia

143 Analysis of cell-specific IL-15Ralpha conditional knockout mice revealed that macrophages and

144 Raptor conditional knockout mice showed decreased extracellular

145 stomorphometric analysis revealed that STAT5 conditional knockout mice showed reduced bone mass, with

146 dedicated to controlling the forelimb in Ryk conditional knockout mice than in controls (wild-type or

147 ifferentiation less effectively in the STAT5 conditional knockout mice than in the wild-type mice aft

148 Conditional knockout mice utilized a new iCre driven by

149 Calpain conditional knockout mice were studied in the model.

150 n2 expression, surgical transplant and novel conditional knockout mice were super-ovulated and analyz

151 Pten in hematopoietic cells by crossing Pten conditional knockout mice with a knock-in mouse expressi

152 In our current study, we crossed our Lpd conditional knockout mice with a mouse line expressing C

153 To test this hypothesis, we used conditional knockout mice with DORs deleted from forebra

154 ramatically reduced in the absence of EpCAM, conditional knockout mice with EpCAM-deficient LCs and c

155 Topical immunization of conditional knockout mice with EpCAM-deficient LCs with

156 s to externally applied proteins, we studied conditional knockout mice with EpCAM-deficient LCs.

157 We crossed Hdac3 conditional knockout mice with Mb1-Cre knockin animals t

158 ignificantly reduced in both Raptor and Tsc1 conditional knockout mice, albeit with variations in sev

159 Mixed bone marrow chimeras, conditional knockout mice, and adoptive transfer models

160 ANP fell sharply in PAM myosin heavy chain 6 conditional knockout mice, and RNA sequencing analysis i

161 In Cyp26b1 conditional knockout mice, formation of striolar/central

162 Using Munc18-1, -2, and -3 conditional knockout mice, here we deleted expression of

163 Double conditional knockout mice, in which both receptors were

164 validated in vivo in the liver of IRE1alpha conditional knockout mice, revealing broad implications

165 In Ldlr/XBP1-conditional knockout mice, serum levels of IgG, IgE, and

166 Using conditional knockout mice, they demonstrate that talin1

167 Using conditional knockout mice, we examined the electrophysio

168 Using a genetic approach with conditional knockout mice, we identified IECs as the dom

169 Here, using dual conditional knockout mice, we show that genetic redundan

170 Using BMDC from wild type and conditional knockout mice, we show that neuropilin-1 (NR

171 es synaptic and behavioral deficits in Mecp2 conditional knockout mice, whereas about 12-fold decreas

172 reading depression model of migraine aura in conditional knockout mice.

173 pment, we generated forebrain-specific Foxp1 conditional knockout mice.

174 Arl13b expression in the kidneys from Sec10 conditional knockout mice.

175 significant functional recovery even in Ryk conditional knockout mice.

176 of these genes have been found in the GCs of conditional knockout mice.

177 hich was up-regulated in cDC2s and pDCs from conditional knockout mice.

178 n into the iNKT cell lineage in CD4-cre NKAP conditional knockout mice.

179 n partially rescues the tooth arrest in Sox2 conditional knockout mice.

180 ones were detected in the periphery of Foxn1 conditional knockout mice.

181 generating different tissue-specific Wnt10a conditional knockout mice.

182 velopmental role, Dbx1 hypothalamic-specific conditional-knockout mice display attenuated responses t

183 these CDK10 germline mutations, we generated conditional-knockout mice.

184 dress this question, we produced triple cKO (conditional knockout) mice that allow ablating all neure

185 equires a great amount of effort to create a conditional knockout model for each individual gene of i

186 address this, the authors generated a unique conditional knockout model involving the major CLP gene,

187 anism of alpha6-associated apoptosis using a conditional knockout model of alpha6 in murine BCR-ABL1+

188 We also demonstrated in a conditional knockout model of dendritic cell (DC) deplet

189 brain, we have generated a new beta-catenin conditional knockout mouse (beta-cat cKO) with targeted

190 Using a Chrnb4-cre; Dicer(flox/flox) conditional knockout mouse (Dicer CKO) to delete Dicer1

191 reduced in CHARGE patient-derived iPSCs and conditional knockout mouse brains.

192 re, we address this question by generating a conditional knockout mouse for Dpy30, which is a common

193 ptors (V1R) in dominance behavior by using a conditional knockout mouse for G protein subunit Galphai

194 differentiation and remyelination, we used a conditional knockout mouse for VGCCs in OPCs.

195 ferentiation and development by generating a conditional knockout mouse in which the protein is deple

196 n the formation of new discs, we generated a conditional knockout mouse lacking its essential ArpC3 s

197 Using a conditional knockout mouse line, we report that loss of

198 Here, by utilizing a conditional knockout mouse line, we report that PDGFRbet

199 development, we generated and analyzed three conditional knockout mouse lines, in which the essential

200 f Prdm16 in adult HSCs, we generated a novel conditional knockout mouse model and deleted Prdm16 in a

201 Here, we generate a brain specific conditional knockout mouse model deficient for Pogz, an

202 Thus, the Ezh2 conditional knockout mouse model may be useful to explor

203 le of inducing inflammaging, we used a Foxn1 conditional knockout mouse model that induces accelerate

204 We created a Ewsr1 conditional knockout mouse model to deplete EWSR1 before

205 In this study, we used a conditional knockout mouse model to investigate the role

206 circumvent this problem, we have used a WASH conditional knockout mouse model to investigate the role

207 of Rbfox1 in muscle function, we developed a conditional knockout mouse model to specifically delete

208 Here, using a newly developed paxillin conditional knockout mouse model with targeted ablation

209 sing a temporally controlled neuron-specific conditional knockout mouse model, recapitulated cellular

210 l role in B cell development by generating a conditional knockout mouse model.

211 g requires ARF for CRPC growth in Pten/Trp53 conditional knockout mouse model.

212 Tissues from PKP2 heterozygous and DP conditional knockout mouse models also exhibit elevated

213 The combination of conditional knockout mouse models and viral vector-media

214 Using different Smad4 conditional knockout mouse models, we disrupted canonica

215 By using conditional knockout mouse models, we investigated the s

216 ent using Wnt5a(-/-) and Nestin-Cre mediated conditional knockout mouse models.

217 t growth in both early- and later-stage Pkd1 conditional knockout mouse models.

218 lusively in GC B cells by crossing the Gna13 conditional knockout mouse strain with the GC-specific A

219 Using two conditional knockout mouse strains and derived cells, we

220 cell differentiation and function, an Ikaros conditional knockout mouse was developed such that Ikaro

221 formed normally after depletion of OCT2 in a conditional knockout mouse, but their proliferation is r

222 ur studies using an N-cadherin lens-specific conditional knockout mouse, N-cad(Deltalens), show that

223 ofiling and single-cell transcriptomics of a conditional knockout mouse, we demonstrate that Kat2a co

224 We previously generated an Ikbkap/Elp1 conditional-knockout mouse model that recapitulates the

225 mimicking the phenotype of Fz5/Fz8 compound conditional knockout mutants.

226 e model of pancreatic adenocarcinoma-whereas conditional knockout of another RCP cargo, alpha5 integr

227 Conditional knockout of apiAT5-3 results in transcriptio

228 generated a mouse model with kidney-specific conditional knockout of Arl13b Deletion of Arl13b in the

229 Strikingly, developmentally early conditional knockout of cerebellin-1 only modestly impai

230 Conditional knockout of Chd4 promotes recruitment of the

231 rofiling of genome architecture reveals that conditional knockout of Chd4 strengthens interactions am

232 Here, we combined a conditional knockout of Coronin 1C with a genetically en

233 Conditional knockout of Des1 expression, as shown by tis

234 We establish an oocyte-specific conditional knockout of Exosc10 in mice using CRISPR/Cas

235 We found that conditional knockout of Grp in sensory neurons results i

236 We used mice with conditional knockout of Hif1alpha (Hif1alpha(chon)) with

237 Conditional knockout of host WNT5A significantly reduced

238 Importantly, using mice carrying conditional knockout of Ifngr1 gene in different myeloid

239 Conditional knockout of its mammalian homolog Piezo1 in

240 an osteogenic tumor mouse model based on the conditional knockout of liver kinase b1 (Lkb1; also know

241 Conditional knockout of miR-17~92 in keratinocytes as we

242 We generated a new conditional knockout of MR in myofibers and quantified c

243 The conditional knockout of MYPT1 or the knock-in mutation T

244 The conditional knockout of MYPT1 or the knockin mutation T8

245 roduced a marked synaptic phenotype, whereas conditional knockout of neuroligin-3 during early develo

246 Indeed, conditional knockout of neuroligin-3 during late develop

247 Therefore, using HBC-specific conditional knockout of Notch receptors and overexpressi

248 trate that smooth muscle cell (SMC)-specific conditional knockout of Oct4 in Apoe(-/-) mice resulted

249 Conditional knockout of OPC Wntless resulted in diminish

250 ignant mouse model of pancreatic cancer with conditional knockout of p120 catenin (Ctnnd1).

251 Conditional knockout of p75NTR in single PV neurons in v

252 Conditional knockout of PDGFB in platelets demonstrates

253 erage is significantly impaired in mice with conditional knockout of PDGFB in platelets.

254 Moreover, conditional knockout of PKM2 in myeloid cells protects m

255 in mice, which was reduced by smooth muscle conditional knockout of Plk1.

256 rom female mice with dendritic cell-specific conditional knockout of Prdm1 (CKO mice) altered the pre

257 Conditional knockout of REST (repressor element 1-silenc

258 ched in the quiescent and inactive HSCs, and conditional knockout of Sel1L in hematopoietic tissues d

259 ines and in murine leukemia generated from a conditional knockout of Setd2.

260 Conditional knockout of Shank3 in the ACC was sufficient

261 We report that conditional knockout of Shp2 alleles in the ErbB2 BC mod

262 Conditional knockout of TAK1 in microglial/infiltrated m

263 fected by TDG knockdown, and adult mice with conditional knockout of Tdg are viable.

264 In this study, we generated a conditional knockout of the alpha isoform of the catalyt

265 Here, we report that in vivo knockdown or conditional knockout of the autism-linked ubiquitin liga

266 Here, we report that conditional knockout of the chromatin remodeling enzyme

267 ping granule neurons (Sync-TRAP) showed that conditional knockout of the core NuRD subunit Chd4 impai

268 We show that conditional knockout of the key ciliary trafficking gene

269 We found that conditional knockout of the mouse homeobox genes En1 and

270 Conditional knockout of the mouse homolog of TFAP2C, Tcf

271 ing in macrophages causes hypertension using conditional knockout of the myeloid vitamin D receptor i

272 ed the functional impairments resulting from conditional knockout of the ubiquitin-conjugating E2 enz

273 in CeA neurons, we performed region-specific conditional knockout of these genes and assessed the eff

274 Conditional knockout of TRF2 in post-mitotic immature ne

275 We generated mice with muscle-specific conditional knockout of Trim33 by combining floxed Trim3

276 Here, we show that conditional knockout of Ttbk2 in adult mice results in d

277 sr3 conditional knockouts, we found that the conditional knockout of Vangl2 in the hippocampus 1 week

278 We find that conditional knockout of Wls by Shh-Cre leads to defectiv

279 physiology and animal behavior by generating conditional knockouts of Atg7 in either dSPNs or iSPNs.

280 Using novel cell-type- and region-specific conditional knockouts of the GABAA receptor alpha2 subun

281 We generated Oprm1 conditional knockout (Oprm1-cKO) mice in which MOR expre

282 Ldlr knockout mice transplanted with XBP1-conditional knockout (or wild-type control littermate) b

283 macological Cdk5 inhibition, brain-wide Cdk5 conditional knockout, or viral-mediated dorsolateral str

284 We developed and dynamically characterized a conditional knockout Prss8(fl/fl), p-Villin-Cre(+) mouse

285 Finally, myofibroblast-restricted OASIS conditional knockouts resulted in resistance to kidney f

286 he ependymal cell layer does not form in the conditional knockout, revealing an unrecognized role of

287 Oocyte-specific Gdf9-iCre conditional knockout (Setd1b(Gdf9) cKO) ovaries develop

288 Further, CD4-specific conditional knockouts showed that 2B4 functions on CD4(+

289 all interfering RNA-treated DCs, or DCs from conditional knockout (Sirt1(f/f)-CD11c-Cre(+)) mice show

290 veolar epithelial cell (AECII)-specific TERT conditional knockout (SPC-Tert cKO) mice by crossing flo

291 Using conditional knockout strategies of CD28, we previously d

292 transcriptional factor, RBP-Jkappa, using a conditional knockout strategy in the mice delayed PDL ma

293 We used a conditional knockout strategy to specifically ablate FOX

294 Conditional knockout studies demonstrate a major role fo

295 ody VDR(-/-) mice, intestinal epithelial VDR conditional knockout (VDR(DeltaIEC)) mice, and cultured

296 undant function of Smad2 and Smad3, a double-conditional knockout was generated using progesterone re

297 In contrast to Celsr3 conditional knockouts, we found that the conditional kno

298 Using conditional knockouts, we show that PPARgamma signaling

299 (X-box binding protein-1) floxed mice (XBP1-conditional knockout), with antibody-mediated depletion

300 In this study, we generated the conditional knockout Wnt coreceptor low-density lipoprot