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1 n the bloodstream form of the parasite via a conditional knockout.
2 , all of which are upregulated in Hand2 limb conditional knockouts.
3 ither individually or in combinations, using conditional knockouts.
4 f Wnt proteins in this process, we created a conditional knockout allele of the Wnt cargo receptor Ev
5  or recombinases) or gene replacement (e.g., conditional knockout alleles containing exons flanked by
6 ribution to retinal development we generated conditional knockout alleles of DNA methyltransferase 1
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                                              Conditional knockout and overexpression of G9a within th
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 e its role in female reproduction by using a conditional knockout approach in mice.
14                               Here, we use a conditional knockout approach to inactivate within the n
15                         Therefore, we used a conditional knockout approach to investigate the roles o
16                                      Using a conditional knockout approach, we confirmed that DLK is
17                                Here, using a conditional knockout approach, we show that protein kina
18 F1 in endothelial cells was examined using a conditional knockout approach.
19                     We show that a Tet2/Tet3 conditional knockout at early stages of B-cell developme
20  phenotype was partially rescued in the Etv2 conditional knockout background.
21                           Clones bearing the conditional knockout cassette are recovered at frequenci
22 nt study we generated a B cell-specific CD83 conditional knockout (CD83 B-cKO) model.
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         T cell development in CD2-icre HDAC3 conditional knockout (cKO) mice (HDAC3-cKO) was blocked
29 ced proliferation in naive T cells from Egr2 conditional knockout (CKO) mice and decreased production
30                          We generated Drosha conditional knockout (cKO) mice by crossing VSMC-specifi
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 ophysiological approach to analyze nicastrin conditional knockout (cKO) mice in the hippocampal Schaf
34 ms associated with Parkinson's disease using conditional knockout (cKO) mice in which Ndufs4 was sele
35                            Here we show that conditional knockout (cKO) mice lacking estrogen recepto
36                           Here, we generated conditional knockout (cKO) mice of neuroligin-2 (Nlgn2),
37           Germline-specific Dicer and Drosha conditional knockout (cKO) mice produce gametes (i.e. sp
38 o address these questions, we generated Lgi1 conditional knockout (cKO) mice using a set of universal
39  functions and artificial decidualization in conditional knockout (cKO) mice, absence of uterine ALK5
40                            We employed Myd88 conditional knockout (CKO) mice, in which Myd88 was dele
41  we generated two lines of Cre-mediated Tspo conditional knockout (cKO) mice.
42 l stem cells isolated from GFAP-CreER-Notch1 conditional knockout (cKO) mice.
43 Cnr2 gene in midbrain DA neurons of DAT-Cnr2 conditional knockout (cKO) mice.
44                                              Conditional knockout (cKO) of ALK3 in the uterus was obt
45 role of BLIMP1 in innate immunity, we used a conditional knockout (CKO) of Blimp1 in myeloid cells an
46  metabolomic analysis in mice with inducible conditional knockout (cKO) of BMAL1, which is critically
47                              By generating a conditional knockout (cKO) of Dicer1 in the proximal par
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 g mice successfully generated progeny with a conditional knockout (CKO) of Notch1 in collagen I-expre
51  phenotypes of females with a Zp3-Cre-driven conditional knockout (cKO) of Smc5 demonstrated that mat
52                                            A conditional knockout (cKO) of the androgen receptor gene
53                                      Using a conditional knockout (cKO) strategy in mice, we sought t
54 e, using tissue-specific dynamin-1 knockout [conditional knockout (cKO)] mice at a fast central synap
55 me (APC/C) ubiquitin ligase in neurons [Cdh1 conditional knockout (cKO)], disrupts dendrite arborizat
56                                      Using a conditional-knockout (cKO) mouse model, we report that l
57 l TEC-defective (resulting from FoxN1-floxed conditional knockout [cKO]) and naturally aged mouse mod
58 ele, allowing for conditional gene ablation (conditional knockout [cKO]) when crossed with Cre recomb
59                     The B cell-specific ELL2 conditional knockouts (cKOs; ell2(loxp/loxp) CD19(cre/+)
60 defective in explants from the Bmp4/7 double conditional knockout (dCKO; Mef2c-Cre;Bmp4/7(f/f)) and m
61 poiesis and leukemogenesis, we generated Eed conditional knockout (Eed(Delta/Delta)) mice.
62                      Snail1 loss-of-function conditional knockout embryos further display upregulated
63 fferentiation, to generate Gata4Gata6 double conditional knockout embryos.
64                             Tregs from Itgb8 conditional knockouts exhibited normal suppressor functi
65                          Cross-fostering and conditional knockout experiments indicated that a TNF-al
66 educes the DNA manipulation needed to make a conditional knockout gene targeting vector to only two s
67 cations that have used tamoxifen to generate conditional knockouts have not reported even the minimum
68 ue to downregulation of TbIPMK expression by conditional knockout, have reduced levels of polyphospha
69 nt receptor, Ryk, in mice and rats by either conditional knockout in the motor cortex or monoclonal a
70            A dental epithelium-specific Irf6 conditional knockout (Irf6-cKO) mouse was generated via
71 G20/MADD in beta-cell function, we generated conditional knockout (KMA1ko) mice.
72                         To this end, we used conditional knockout (KO) mice lacking STIM1 in cells of
73 izes FVIII, we developed a Cre/lox-dependent conditional knockout (KO) model in which exons 17 and 18
74 an and colleagues characterize Shp1 and Shp2 conditional knockout (KO) murine models, underscoring th
75  surgically induced tibial fracture model in conditional knockout (KO) Nfl (Nf1(flox/flox)) mice.
76 V-Neu transgenic female mice with or without conditional knockout (KO) of Tcfap2c, the mouse homolog
77                                          The conditional knockout (KO) of TFR in neural progenitor ce
78                      Here we showed that HuR conditional knockout (KO) Th17 cells have decreased GM-C
79 ea, we used an Nkx2.1-Cre driver to generate conditional knockouts (KOs) in mice of leptin receptor (
80 ikewise, mice harboring liver-specific Lats2 conditional knockout (Lats2-CKO) displayed constitutive
81  inactivation of Tak1 in Trim33:Smad4 double conditional knockouts leads to the palatal phenotypes wh
82        A novel cardiac myocyte-specific Speg conditional knockout (MCM-Speg(fl/fl)) model revealed th
83                                      In Cx26 conditional knockout mice (Cx26(Sox10-Cre)) the maturati
84                           We generated Dnmt1 conditional knockout mice (Dnmt1(Deltaalb) ) by crossing
85                         To this end, we used conditional knockout mice (FoxN1-Gpr177) in which TECs a
86 , administration of Notch inhibitors in Fbw7 conditional knockout mice alleviated progressive bone re
87                     Surprisingly, the double conditional knockout mice also showed growth plate defec
88 n vitro organoid cultures derived from Snai1 conditional knockout mice also undergo apoptosis when Sn
89 ity alterations were normalized in GABA-CB1R conditional knockout mice and after subchronic treatment
90                                  Here we use conditional knockout mice and an acute adenovirus-mediat
91 or adipogenesis in culture and in vivo Using conditional knockout mice and derived white and brown pr
92 tasis using acute hippocampal slices from PS conditional knockout mice and primary cultured postnatal
93                                              Conditional knockout mice and transgenic mice expressing
94                                              Conditional knockout mice are generated using labor-inte
95 ermore, RBCs from blood-cell-specific Piezo1 conditional knockout mice are overhydrated and exhibit i
96                           Here, we have used conditional knockout mice as well as the differentiation
97  lung contusion was significantly reduced in conditional knockout mice at all the time points, when c
98  cultured neural stem cells derived from Cic conditional knockout mice bypassed an EGF requirement fo
99 ent tissue- and developmental stage-specific conditional knockout mice carrying Smarcb1 and/or Nf2 de
100 mic populations are similar in CD4-cre HDAC3 conditional knockout mice compared with wild-type mice,
101                            Here we generated conditional knockout mice deficient in various Slit and
102          EC-specific Snail1 loss-of-function conditional knockout mice die in utero with defects in v
103 p(nestin) conditional knockout and Yap(GFAP) conditional knockout mice displayed fewer neocortical as
104                                CD4-cre HDAC3 conditional knockout mice do not have a defect in intrat
105 elial injury, we demonstrate that myeloid AC conditional knockout mice exhibit impairment of neutroph
106 ucture-related gene expression, whereas Tsc1 conditional knockout mice exhibited changes in genes reg
107 mice, whereas hepatocyte and macrophage Bmp6 conditional knockout mice exhibited no iron phenotype.
108                          Two independent Osx conditional knockout mice exhibited similar molar abnorm
109                                     Studying conditional knockout mice for ELKS, we find that ELKS en
110 fic gradient of HDAC-activity using compound conditional knockout mice for Hdac1 and Hdac2.
111                    Here, we generated double conditional knockout mice for RIM-BP1 and RIM-BP2, and a
112  retinal ganglion cell death, similar to Nf1 conditional knockout mice harboring a neomycin insertion
113            Osteoclast-lineage-specific Gna13 conditional knockout mice have a severe osteoporosis phe
114 nses to TLR stimulation in vitro, and alphav-conditional knockout mice have elevated antibody respons
115                                              Conditional knockout mice in which Shc is deleted from e
116 , spatial memory, and metabolic functions of conditional knockout mice in which the inactivation of t
117                             Bone marrow from conditional knockout mice lacking Adam10 in the myeloid
118                                              Conditional knockout mice lacking ADORA2B on myeloid cel
119                             Here we generate conditional knockout mice lacking Arf6 in neurons, oligo
120 sence of NF186, they fail to do so in double conditional knockout mice lacking both NF186 and the par
121 induced SNS injury, while NPY injection into conditional knockout mice lacking the Y1 receptor in mac
122     Both whole-body (Lgr4(-/-)) and monocyte conditional knockout mice of Lgr4 (Lgr4 CKO) exhibit ost
123                            In addition, Tsc1 conditional knockout mice presented severely disorganize
124                           Here, we generated conditional knockout mice removing the active zone prote
125 iciency in CMFs in fibroblast-specific MyD88 conditional knockout mice resulted in a strong increase
126                         Analysis of the Bmp6 conditional knockout mice revealed that liver endothelia
127        Analysis of cell-specific IL-15Ralpha conditional knockout mice revealed that macrophages and
128                                       Raptor conditional knockout mice showed decreased extracellular
129 stomorphometric analysis revealed that STAT5 conditional knockout mice showed reduced bone mass, with
130                       However, both lines of conditional knockout mice suffer from progressive hind l
131 dedicated to controlling the forelimb in Ryk conditional knockout mice than in controls (wild-type or
132 ifferentiation less effectively in the STAT5 conditional knockout mice than in the wild-type mice aft
133 proprioception to twitching in newborn ErbB2 conditional knockout mice that lack muscle spindles and
134       Using newly generated constitutive and conditional knockout mice that target all neurexin-3alph
135                           We generated Lman1 conditional knockout mice to characterize the FVIII secr
136                                              Conditional knockout mice utilized a new iCre driven by
137                                        SOAT2 conditional knockout mice were bred with LDLr(-/-) mice
138                                              Conditional knockout mice were generated to characterize
139 lls from the hypoxia-inducible factor-1alpha conditional knockout mice were isolated and evaluated fo
140                                      Calpain conditional knockout mice were studied in the model.
141 n2 expression, surgical transplant and novel conditional knockout mice were super-ovulated and analyz
142 Pten in hematopoietic cells by crossing Pten conditional knockout mice with a knock-in mouse expressi
143     In our current study, we crossed our Lpd conditional knockout mice with a mouse line expressing C
144 ramatically reduced in the absence of EpCAM, conditional knockout mice with EpCAM-deficient LCs and c
145                      Topical immunization of conditional knockout mice with EpCAM-deficient LCs with
146 s to externally applied proteins, we studied conditional knockout mice with EpCAM-deficient LCs.
147                             We crossed Hdac3 conditional knockout mice with Mb1-Cre knockin animals t
148                       Previously, we created conditional knockout mice with Treg-specific deletion of
149 ignificantly reduced in both Raptor and Tsc1 conditional knockout mice, albeit with variations in sev
150                  Mixed bone marrow chimeras, conditional knockout mice, and adoptive transfer models
151 glion neuronal cultures are absent in Piezo2 conditional knockout mice, and ex vivo skin nerve prepar
152  circumvent this problem, we generated RIPK1 conditional knockout mice, and show that mice lacking RI
153                                       Double conditional knockout mice, in which both receptors were
154                                 Nse-Cre Pten conditional knockout mice, in which Pten is ablated in g
155                              In CD4-cre NKAP conditional knockout mice, invariant natural killer T ce
156                              In CD4-cre NKAP conditional knockout mice, NKAP-deficient RTEs fail to c
157                                 In Ldlr/XBP1-conditional knockout mice, serum levels of IgG, IgE, and
158                                           In conditional knockout mice, temporal axons display no maj
159                                        Using conditional knockout mice, we examined the electrophysio
160                      Using CNIH-2 and CNIH-3 conditional knockout mice, we find a profound reduction
161                                        Using conditional knockout mice, we found that Gli3 deficiency
162                                        Using conditional knockout mice, we found that T cells lacking
163                Using a genetic approach with conditional knockout mice, we identified IECs as the dom
164                                        Using conditional knockout mice, we show here that Nedd4-1 and
165                                        Using conditional knockout mice, we show here that Rac1 and Cd
166                                    Employing conditional knockout mice, we show that depletion of ADA
167                             Here, using dual conditional knockout mice, we show that genetic redundan
168                Using BMDC from wild type and conditional knockout mice, we show that neuropilin-1 (NR
169 n into the iNKT cell lineage in CD4-cre NKAP conditional knockout mice.
170 n partially rescues the tooth arrest in Sox2 conditional knockout mice.
171 ones were detected in the periphery of Foxn1 conditional knockout mice.
172 e role of RFX in hearing, we generate Rfx1/3 conditional knockout mice.
173 ell-specific hypoxia-inducible factor-1alpha conditional knockout mice.
174 gative regulation of Nrf2 by Hrd1 using Hrd1 conditional knockout mice.
175 .3(+) T cell expansion in Id2 and Id3 double conditional knockout mice.
176  chemoattractant, was significantly lower in conditional knockout mice.
177 this question, we created Treg-specific Cd28 conditional knockout mice.
178 pment, we generated forebrain-specific Foxp1 conditional knockout mice.
179  Arl13b expression in the kidneys from Sec10 conditional knockout mice.
180  significant functional recovery even in Ryk conditional knockout mice.
181 of these genes have been found in the GCs of conditional knockout mice.
182 hich was up-regulated in cDC2s and pDCs from conditional knockout mice.
183 velopmental role, Dbx1 hypothalamic-specific conditional-knockout mice display attenuated responses t
184 these CDK10 germline mutations, we generated conditional-knockout mice.
185                              The Setd1a-cKO (conditional knockout) mice exhibited an enlarged spleen
186 dress this question, we produced triple cKO (conditional knockout) mice that allow ablating all neure
187 address this, the authors generated a unique conditional knockout model involving the major CLP gene,
188                    We also demonstrated in a conditional knockout model of dendritic cell (DC) deplet
189                                              Conditional knockout models have shown that neural Pten
190       Cre-mediated depletion of Spartan from conditional knockout mouse embryonic fibroblasts results
191                          We demonstrate that conditional knockout mouse embryos lacking Jun in Isl1-e
192  Here we demonstrate using isogenic pairs of conditional knockout mouse ESCs, that Snail1 exerts Wnt-
193 re, we address this question by generating a conditional knockout mouse for Dpy30, which is a common
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                                      Using a conditional knockout mouse line, we report that loss of
197                         Here, by utilizing a conditional knockout mouse line, we report that PDGFRbet
198 development, we generated and analyzed three conditional knockout mouse lines, in which the essential
199         Targeted disruption of Dot1l using a conditional knockout mouse model inhibited leukemogenesi
200 le of inducing inflammaging, we used a Foxn1 conditional knockout mouse model that induces accelerate
201 of Rbfox1 in muscle function, we developed a conditional knockout mouse model to specifically delete
202 could suppress EAC development, we created a conditional knockout mouse model using progesterone rece
203                              By using a RhoA conditional knockout mouse model, we show that RhoA defi
204 l role in B cell development by generating a conditional knockout mouse model.
205 examine lincRNA-p21 function, we generated a conditional knockout mouse model.
206 ted the role of p14 in mouse DCs/LCs using a conditional knockout mouse model.
207        Tissues from PKP2 heterozygous and DP conditional knockout mouse models also exhibit elevated
208 ity, we generated tissue-specific Ugt1 locus conditional knockout mouse models and examined the role
209                                              Conditional knockout mouse models have revealed tissue s
210                         Recent studies using conditional knockout mouse models have unveiled a major
211  function of SRSF2 in hematopoiesis by using conditional knockout mouse models.
212 ent using Wnt5a(-/-) and Nestin-Cre mediated conditional knockout mouse models.
213 t growth in both early- and later-stage Pkd1 conditional knockout mouse models.
214 lusively in GC B cells by crossing the Gna13 conditional knockout mouse strain with the GC-specific A
215                                    Using two conditional knockout mouse strains and derived cells, we
216 formed normally after depletion of OCT2 in a conditional knockout mouse, but their proliferation is r
217 ur studies using an N-cadherin lens-specific conditional knockout mouse, N-cad(Deltalens), show that
218 Using fibroblast lines derived from an Arpc2 conditional knockout mouse, we established matched-pair
219       We previously generated an Ikbkap/Elp1 conditional-knockout mouse model that recapitulates the
220  mimicking the phenotype of Fz5/Fz8 compound conditional knockout mutants.
221                                              Conditional knockout of ankyrins in oligodendrocytes dis
222 e model of pancreatic adenocarcinoma-whereas conditional knockout of another RCP cargo, alpha5 integr
223 generated a mouse model with kidney-specific conditional knockout of Arl13b Deletion of Arl13b in the
224 lized Atg5(f/f);Aqp5-Cre mice which harbor a conditional knockout of Atg5, in salivary acinar cells.
225                                    Moreover, conditional knockout of beta-neurexins in CA1-region neu
226 d at much lower levels than alpha-neurexins, conditional knockout of beta-neurexins with continued ex
227                                 Importantly, conditional knockout of both Hif-1alpha and Hif-2alpha p
228 plasticity and in remote memory recall using conditional knockout of Cdc42.
229                               We report that conditional knockout of Cdh1, the key regulatory subunit
230 l striatum- or D1 dopamine receptor-specific conditional knockout of Cdk5, or ventral striatum infusi
231            Strikingly, developmentally early conditional knockout of cerebellin-1 only modestly impai
232                                              Conditional knockout of cyclin A2 or the SHH proliferati
233  Moreover, behavioral studies in mice with a conditional knockout of Deaf1 in the brain showed memory
234                                              Conditional knockout of either protein results in reduce
235             Previous studies revealed that a conditional knockout of essential member(s) of autophagy
236             Our previous studies showed that conditional knockout of FIP200 significantly suppressed
237                                 In contrast, conditional knockout of HDAC3 in neurons of the forebrai
238 e we report that mice with a T-cell-specific conditional knockout of HGK (T-HGK cKO) develop systemic
239                            We used mice with conditional knockout of Hif1alpha (Hif1alpha(chon)) with
240 s starvation-induced autophagy in larvae and conditional knockout of HTT in the mouse CNS causes char
241                               We showed that conditional knockout of Id2 alone is sufficient to promo
242 o this end, we generated a mouse strain with conditional knockout of IKKalpha in CD4 cells (Ikkalpha(
243 ocyte (MK)-specific Pf4 promoter permits the conditional knockout of Itga2 in the MK/platelet lineage
244                                 SMC-specific conditional knockout of Kruppel-like factor 4 (Klf4) res
245                                          The conditional knockout of MYPT1 or the knock-in mutation T
246                                          The conditional knockout of MYPT1 or the knockin mutation T8
247 roduced a marked synaptic phenotype, whereas conditional knockout of neuroligin-3 during early develo
248                                      Indeed, conditional knockout of neuroligin-3 during late develop
249                Therefore, using HBC-specific conditional knockout of Notch receptors and overexpressi
250 trate that smooth muscle cell (SMC)-specific conditional knockout of Oct4 in Apoe(-/-) mice resulted
251 ignant mouse model of pancreatic cancer with conditional knockout of p120 catenin (Ctnnd1).
252 mouse kidneys compared with mice with single conditional knockout of Pkd1.
253                                    Moreover, conditional knockout of PKM2 in myeloid cells protects m
254                                              Conditional knockout of PPARgamma in APCs using Cd11c-Cr
255 rom female mice with dendritic cell-specific conditional knockout of Prdm1 (CKO mice) altered the pre
256                                      Through conditional knockout of Prox1 from skeletal muscle, we d
257  phenotype is independently recapitulated by conditional knockout of Rbpj, a core Notch pathway compo
258                                              Conditional knockout of REST (repressor element 1-silenc
259                                              Conditional knockout of Runx1 in MECs by MMTV-Cre led to
260 ines and in murine leukemia generated from a conditional knockout of Setd2.
261                    Here, we demonstrate that conditional knockout of Snai1 in the intestinal epitheli
262                           Interestingly, the conditional knockout of Tgfbr2 in mouse prostatic fibrob
263                In this study, we generated a conditional knockout of the alpha isoform of the catalyt
264    Here, we report that in vivo knockdown or conditional knockout of the autism-linked ubiquitin liga
265 ts production, and created a muscle-specific conditional knockout of the class III phosphatidylinosit
266 ping granule neurons (Sync-TRAP) showed that conditional knockout of the core NuRD subunit Chd4 impai
267 tion of the NuRD complex by in vivo RNAi and conditional knockout of the core NuRD subunit Chd4 profo
268                                              Conditional knockout of the de novo Dnmt isoform, Dnmt3a
269                                              Conditional knockout of the mouse homolog of TFAP2C, Tcf
270                                              Conditional knockout of the vitamin D receptor in myeloi
271                                              Conditional knockout of TRF2 in post-mitotic immature ne
272 sr3 conditional knockouts, we found that the conditional knockout of Vangl2 in the hippocampus 1 week
273                                    Inducible conditional knockout of Wt1 in endothelial, haematopoiet
274 sed the mechanism of TRF1 action using mouse conditional knockouts of BLM, TRF1, TPP1, and Rap1 in co
275                                       Double conditional knockouts of Pkd1 and Sirt1 demonstrated del
276   Using novel cell-type- and region-specific conditional knockouts of the GABAA receptor alpha2 subun
277 dy, we used reporters, lineage analysis, and conditional knockout or activation of the Wnt/beta-caten
278 s)) which we refer to as floxed alpha7 nAChR conditional knockout or alpha7nAChR(flox).
279    Ldlr knockout mice transplanted with XBP1-conditional knockout (or wild-type control littermate) b
280 macological Cdk5 inhibition, brain-wide Cdk5 conditional knockout, or viral-mediated dorsolateral str
281 ed by Cre-mediated recombination, yielding a conditional knockout/reporter strategy suitable for mosa
282                    Oocyte-specific Gdf9-iCre conditional knockout (Setd1b(Gdf9) cKO) ovaries develop
283             Biochemical phenotyping of TbCDS conditional knockout showed drastically altered lipid me
284                                    The TbCDS conditional knockout showed morphological changes includ
285                        Further, CD4-specific conditional knockouts showed that 2B4 functions on CD4(+
286 all interfering RNA-treated DCs, or DCs from conditional knockout (Sirt1(f/f)-CD11c-Cre(+)) mice show
287                                        Using conditional knockout strategies of CD28, we previously d
288                                    We used a conditional knockout strategy to specifically ablate FOX
289                                              Conditional knockout studies demonstrate a major role fo
290                           We found that Tbx1 conditional knockout (Tbx1(cKO)) mice featured microdont
291 ed constitutive KOR knockouts (KOR(-/-)) and conditional knockouts that lack KORs in DA-containing ne
292                 Ablation of TbMCU in RNAi or conditional knockout trypanosomes reduces mitochondrial
293                               Smad1/5 double conditional knockout tumors, as well as human JGCTs, are
294 on of ccRCC, we generated a novel mouse Vhlh conditional knockout, using Hoxb7-driven Cre that is spe
295 ody VDR(-/-) mice, intestinal epithelial VDR conditional knockout (VDR(DeltaIEC)) mice, and cultured
296 role of WASH in T cells, we generated a WASH conditional knockout (WASHout) mouse model.
297                  Using a Blimp1-Cre germline conditional knockout, we discovered that Prmt5 has no ma
298                        In contrast to Celsr3 conditional knockouts, we found that the conditional kno
299                                        Using conditional knockouts, we show that PPARgamma signaling
300  (X-box binding protein-1) floxed mice (XBP1-conditional knockout), with antibody-mediated depletion

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