ライフサイエンスコーパス: ablate

1 e maintained at control levels when Cx36 was ablated.

2 olds at which phenotype and transmission are ablated.

3 the CaMKII phosphorylation site on RyR2 was ablated.

4 vantage in nuclear layers where neurons were ablated.

5 ll-length Pol was mitochondrial localization ablated.

6 d to alanine, the binding of D1D2 to LRP1 is ablated.

7 0 cells of each population were individually ablated.

8 riatum or hippocampus where CK2alpha is also ablated.

9 the CaMKII site on ryanodine receptor 2 was ablated.

10 this structure as a guide, we systematically ablated a series of proposed intermolecular interactions

11 d by nerve injury or inflammation in mice by ablating a group of adult spinal neurons defined by deve

12 Here, we examine this issue by conditionally ablating a key transcription factor Forkhead box C1 (FOX

13 In spite of both variants ablating a portion of the catalytic core and dimer-inter

14 for maintaining the sAHP when hippocalcin is ablated, a condition that likely impairs PIP2 generation

15 es, deplete presynaptic Ca(2+) channels, and ablate active zone complexes, as analyzed by electron mi

16 une evasion strategy that shows broad immune-ablating activity, we have identified a novel anti-infla

17 The clinical VT was successfully ablated acutely in all patients.

18 ll-mediated antitumor immunity.Significance: Ablating adenosine signaling is found to promote natural

19 %), 67 (89.3%), and 69 (92%) were completely ablated after one, two, and three IRE procedures, respec

20 us and replicon assays using phosphorylation-ablated alanine mutants of these sites showed that Ser-2

21 e cKO (conditional knockout) mice that allow ablating all neurexin expression in mice.

22 se oocytes to create the Zurich-3 (ZH3) Prnp-ablated allele on a pure C57BL/6J genetic background.

23 loride concentration late during development ablates alpha1beta glycinergic synapses but spares GABAe

24 al ablation volume and the percentage of the ablated amygdalohippocampal complex between seizure-free

25 ation of a less stable, more dynamic species ablate amyloid formation by increasing the energy barrie

26 organ cadherin levels compared to the Mmp20 ablated and WT mice and, instead of predominantly locati

27 enetically induced lymphoma Gal-1 expression ablated antibody-dependent lymphoma phagocytosis in vitr

28 of depths; the nail material adjacent to the ablated area was rendered porous in appearance presumabl

29 at day 2 showed small white densities in the ablated areas, which appeared to be small intraepithelia

30 itor cells that co-express Sox2 and Bmi1 are ablated, as we observed that ageing in mice started with

31 but not frequency, was reduced when SCs were ablated at E15.5, suggesting that postsynaptic alteratio

32 rates uncontrolled toxic levels of cAMP that ablates bactericidal capacities of phagocytes.

33 Mutating the bulge sequence to 5'-ACCCC-3' ablates base stacking in the loop and globally reorients

34 DeltaDC mice in which DCs are constitutively ablated because of expression of the diphtheria toxin al

35 rons or descending serotonergic neurons were ablated before hyperalgesic priming, IL-6- and carrageen

36 We find that ablating beta-CTT causes elevated rates of chromosome lo

37 Inhibition of miR-200b in Mdr2(-/-) ablates biliary proliferation, liver fibrosis, and angio

38 Multiple approaches to ablate biofilms on failing implants have been proposed a

39 Further, we show that ablating BLA neurons that project to NAc disrupts extinc

40 Pharmacological attempts to ablate BoNT/A intoxication have sought to either nullify

41 0-fold higher than the IC50 were required to ablate both ADP-ribosylation and XRCC1 chromatin binding

42 d a thymidine kinase/ganciclovir paradigm to ablate both dividing NG2(+) cell populations to determin

43 ) and Wnt1(Cre2SOR) drivers to conditionally ablate both Yap and Taz in the CNC of mice.

44 thograde coupling was previously shown to be ablated by a glycine for glutamate substitution at RyR1

45 The effect of CO2/HCO3(-) was ablated by connexin43 inhibition or knockdown.

46 ts in increased telomere fusions, which were ablated by Ctip knockdown.

47 ells even when its CD4 binding site had been ablated by deletion of a highly conserved aspartic acid

48 orms part of a secondary lineage that can be ablated by larval HU application.

49 senescence in H9C2 myoblasts, the effect was ablated by MIF replenishment.

50 the beta2-AR agonist formoterol, and was not ablated by mTOR inhibition.

51 ent even after its CD4 binding site had been ablated by mutagenesis.

52 rs during mitosis and cytokinesis and can be ablated by SETD2 deletion, which causes mitotic spindle

53 Importantly, all of these associations were ablated by the PAK inhibitor IPA3, suggesting that PAK1

54 ls and increased ROS productions, which were ablated by XMJ in concentration-dependent manner.

55 PTT serves as a minimally invasive method to ablate cancer cells.

56 Functional analysis reveals these mutations ablate canonical TGFbeta Smad signalling, which is local

57 Here, we find that ablating CDKL5 expression specifically from forebrain gl

58 urons may skew neuronal regeneration towards ablated cell types.

59 ed oxidative stress and senescence in ZDHHC3-ablated cells.

60 ion, attenuating scar-forming astrocytes, or ablating chronic astrocytic scars all failed to result i

61 io) to receive either RFA (entire BE segment ablated circumferentially) or a sham endoscopic procedur

62 activation are bidirectionally modulated by ablating CK2 in D1- or D2-positive projection neurons, i

63 e transporter gene (DAT) promoter control to ablate Cnr2 gene in midbrain DA neurons of DAT-Cnr2 cond

64 ins, using a series of mutants that alter or ablate CTTs in budding yeast.

65 We now show that Deltaafkp80(-) null mutants ablated d-Arap modifications of LPG as predicted, wherea

66 with substitution of all tryptophan residues ablating dimerization and self-renewal function complete

67 augments, but a reduction of KIT expression ablates DNMT1 transcription by STAT3 pathway leading to

68 xpressing doxycycline-inducible DOT1L shRNA, ablating DOT1L expression with doxycycline significantly

69 ed glycogen synthase activity was completely ablated during hyperinsulinemic hypoglycemia, and catech

70 demonstrate a new approach for noninvasively ablating each of these pathways and testing their necess

71 While ablating either RIPK1 or RelA in liver parenchymal cells

72 However, while IAPs are derepressed in Dnmt1-ablated embryos and embryonic stem cells (ESCs), these E

73 We ablated endogenous Crk and CrkL from cultured fibroblast

74 ective ER downregulators (SERDs) are able to ablate ER and thus, theoretically, to prevent survival o

75 Setdb1 ablated ES cells exhibit severe growth inhibition, which

76 ell as those in which P2RY12 was genetically ablated, exhibited significantly diminished movement of

77 ed L-type channel clustering at granules and ablated fast exocytosis.

78 e level of exposure to males for control and ablated females and tested for interacting effects on fe

79 However, mNSC-ablated females maintained significantly increased lifes

80 espan extension and relative fitness of mNSC-ablated females were maximized under intermediate exposu

81 When these neurons are ablated, fish failed to rotate their eyes following eith

82 tensin receptor 1 (Ntsr1) cre-driver mice to ablate floxed Cacna1a in layer VI pyramidal neurons, whi

83 To test this hypothesis, we ablated Fn1 in the neural crest (NC), a population of mu

84 In mice, mutant Ad5 vectors that are ablated for FX-binding become detargeted from hepatocyte

85 In mice selectively ablated for histone deacetylase 3 (HDAC3) in skin kerati

86 we report that tribbles homologue 2 (TRIB2) ablates forkhead box O activation and disrupts the p53/M

87 Ablating fractionated electrograms (117+/-18 ms; 44+/-13

88 mice, in which the Gad1 gene is genetically ablated from 50% of cortical and hippocampal interneuro

89 ggest that there is overall reduced, but not ablated, functionality of TMEM260 and that attenuation o

90 ts is limited by a lack of technologies that ablate gene function within specific mononuclear phagocy

91 s target DNA, RNA or protein to reduce or to ablate gene function.

92 tip and water spray was able to effectively ablate >/=95% of biofilm on all types of tested titanium

93 e engineered DNA DSB in fibroblasts that had ablated H2ax did produce clonal, stable GCRs, including

94 1A recruitment to chromatin and subsequently ablates H3K4me3 at adjacent promoters.

95 nd (223)Ra are used to image, alleviate, and ablate harmful cancerous legions with good specificity v

96 this location, we manipulated native loci to ablate hCDC14A phosphatase activity (hCDC14A(PD)) in unt

97 we used a murine genetic in vivo approach to ablate Hes1 in pancreatic progenitor cells (Ptf1a(+/Cre)

98 Importantly, knockout of Nlrp3 ablated HFD-induced insulin resistance and inflammation

99 hat regulate stable HSPC engraftment into an ablated host.

100 ivity, as Foxa3(-/-) HSC fails to repopulate ablated hosts efficiently, implicating for the first tim

101 ial proliferation, which can be abolished by ablating IL-1 signaling or depleting its major cellular

102 the systemic effect of IL-17 by genetically ablating Il-17 in the C57BL/6.NOD-Aec1Aec2, spontaneous

103 Pseudo-reentrant carousels were incorrectly ablated in 5 cases having been misinterpreted as LR.

104 TgPEPCKnet can also be ablated in a glycolysis-deficient mutant, while TgPEPCKm

105 were markedly reduced when dystroglycan was ablated in adult mice, suggesting a role for dystroglyca

106 hermore, such DNs are abrogated when RTN3 is ablated in aging and AD mouse models.

107 ssion of neuronal differentiation markers is ablated in both KIF1Bbeta-deficient mouse neuroblasts an

108 x); Osx-Cre mice, in which the Smpd3 gene is ablated in both late-stage chondrocytes and osteoblasts,

109 at leukocyte rolling on P- and L-selectin is ablated in cells lacking O-glycans, with N-glycan trunca

110 , in response to inflammasome activation, is ablated in FABP4/aP2(-/-) macrophages, as well as in FAB

111 the eye caused CNV, irrespectively if it was ablated in newborn or 3-week-old mice.

112 re.Socs3 (f/f) mice, in which SOCS3 has been ablated in osteocytes, have high trabecular bone volume

113 ectopically expressing SOX10, and is nearly ablated in Schwann cells by impairing SOX10 function.

114 The HDC/HA/HR axis was ablated in sham and BDL Kit(W-sh) mice.

115 In addition, in mice selectively ablated in skin keratinocytes for either nuclear recepto

116 When Foxc1 was specifically ablated in skin, sweat glands appeared mature, but the m

117 epair was severely perturbed when Ptpn11 was ablated in stem cells due to a deficit in stem cell prol

118 cell recovery when miR-205 is conditionally ablated in TECs.

119 ecifically, SOX9 induction was significantly ablated in the absence of ROCR, and overexpression of SO

120 In contrast, mice in which SHP2 was ablated in the Col10alpha1-Cre-expressing cells appeared

121 homologs 1 and 2 (Ezh1/2) are conditionally ablated in the embryonic epidermal progenitors that give

122 rating a novel mouse model in which PTH1R is ablated in the limb mesenchyme using Prx1Cre transgenic

123 balpha at these sites was lost when HNF6 was ablated in the liver.

124 nterestingly, STAT2 degradation activity was ablated in the NS2 ubiquitin mutant rRSV.

125 h both BMP1 and TLL1 have been conditionally ablated, including malformed periodontal ligament (PDL)

126 DD05, or DD06) should affect locomotion when ablated individually.

127 We report that, after a chemical lesion that ablates inner retinal neurons, regenerated retinal bipol

128 pDC depletion ablated interferon production and increased viral load;

129 All of the drugs ablated intraepidermal nerve fibers and produced axonopa

130 uperficial, to be visualized immediately and ablated irreversibly.

131 electively in the forebrain and to inducibly ablate it in adult mice.

132 rosome activities, we used genome editing to ablate it.

133 We identify mutations in Spy1 that ablate its ability to activate Cdk2 and to proliferate c

134 acetylation of an ApiAP2 DNA-binding domain ablates its DNA-binding propensity.

135 vhs carrying the point mutation D215N, which ablates its endoribonuclease activity, to disrupt SG for

136 itution of any canonical HS binding residues ablated Ivt-mediated transduction by AAV2-based vectors.

137 ervations, we used CRISPR/Cas9 technology to ablate Kindlin-2 expression in human MDA-MB-231 and muri

138 as(G12D)p53(L/L) pancreatic cancer models to ablate KLF10 expression and determine the impact of KLF1

139 complex was formed by the reaction of laser-ablated La atoms with acetylene molecules in a molecular

140 enous over-sprouting observed in radial glia-ablated larvae, and sFlt1 overexpression rescues it.

141 of Nrg1 (types I and II) were conditionally ablated, leaving the type III Nrg1 intact.

142 udy tachycardia activation in the previously ablated left atrium.

143 vity and blood glucose concentrations, while ablating LepRb in PAG neurons augmented glucose mobiliza

144 effectiveness was evident in 66 of 67 (98%) ablated lesions on the first contrast material-enhanced

145 es 393-396 from GII.17.2015 into GII.17.1978 ablated ligand binding and altered antigenicity, definin

146 NA) strands and used synonymous mutations to ablate m(6)A on both strands of the hemagglutinin (HA) s

147 elicited through tail stimulation [5-7] and ablating M-cells abolishes short-latency tail-elicited s

148 ical composition was determined spotwise, by ablating material from various surface locations on a 4

149 ek post-I/R in cardiomyocyte-restricted GRK2 ablated mice (also post-I/R) still demonstrated signific

150 depressed ventricular function in the Gata4-ablated mice (mutant) after injury.

151 itional skeletal myofiber-specific VEGF gene-ablated mice (VEGF(HSA-/-) ) by providing VEGF(HSA-/-) a

152 ineage neurons preserved in VT3(Lbx1)-neuron-ablated mice is largely sufficient to mediate morphine-s

153 The iBAT-ablated mice showed higher oxygen consumption and decrea

154 ays in the cold, both sham controls and iBAT-ablated mice stopped shivering and resumed routine physi

155 The iBAT-ablated mice were able to maintain optimal body temperat

156 By selectively ablating microglia in the spinal cord using a saporin-co

157 rated a mouse model in which we specifically ablated Mig-6 in uterine epithelial cells using Sprr2f-c

158 Recently, studies in eosinophil-ablated mouse strains have revealed an expanded repertoi

159 Furthermore, unlike mPDE, phospho-ablated mPDE-T309A protein exhibited impaired cell wall

160 ts, to block MEK activity and simultaneously ablate MPNSTs.

161 Mice expressing phospho-ablated MyBP-C displayed cardiac hypertrophy and prevent

162 Klf15) loss-of-function strategy was used to ablate nephrocytes and then heart function and the hemol

163 Ablating neuroblasts with hydroxyurea (HU) prior to onse

164 gical, chemical, or transgenic approaches to ablate neurons.

165 Here, we extend upon these findings by ablating newly generated cells after the epileptogenic i

166 To resolve this conflict, we ablated NF-kappaB essential modulator (NEMO) and IkappaB

167 erentiation, we used a Neurog3-Cre allele to ablate Nkx2.2, one of the earliest and most broadly expr

168 Third, we demonstrate that neither ablating nor inhibiting the mushroom body (MB), a known

169 Mice ablated of MMC9 induction failed to develop intestinal m

170 The authors tagged and ablated only regions displaying electrogram dispersion d

171 ptor MyD88, or transcription factor IRF7 was ablated or pDCs were depleted.

172 In seedlings, ablating or overexpressing PGX3 affects both cotyledon s

173 , and desired changes can be made to modify, ablate, or excise target genes.

174 s atmosphere is unlikely to be substantially ablated over the lifetime of its star.

175 in osteoclastogenesis and bone resorption by ablating p38alpha MAPK in LysM+monocytes.

176 This truncated Ig exclusion (TIE) checkpoint ablates PC clones with DeltaV-kappaLCs production and ex

177 ion as well as treatment with SFK inhibitors ablate pDC (but not conventional DC) responses both in v

178 the variation of the cross-section of laser-ablated PDMS channel; (2) the volume of PeT chamber; and

179 the micro wells in HF-etched glass and laser-ablated PDMS.

180 , mice were treated with diphtheria toxin to ablate peri-insult generated newborn granule cells, whic

181 regional genetic sympathectomy: BRAINSPAReDT ablates peripheral but not central catecholaminergic neu

182 -brain barrier, which limits its utility for ablating peripheral cells using Cre drivers that are als

183 Ablating phosphorylation of Ku70 leads to the sustained

184 141 to 160 in full-length Pol did not fully ablate Pol's mitochondrial localization, suggesting that

185 cytotoxicity by a S. cerevisiae mutant with ablated post-transfer editing activity when supplemented

186 cordingly, agonist treatment in Hepa-1 cells ablates potent ER stress-driven Fgf21 expression, and pr

187 by small interfering RNA (siRNA) completely ablated progesterone conversion in both steroidogenic mo

188 dy used a novel transgenic mouse paradigm to ablate proliferating NG2(+) cells after SCI to better un

189 epletion before infectious challenge did not ablate protection.

190 te that many common nonsense variants do not ablate protein production from their host genes.

191 frame shift mutation in SKAP (KNSTRN), both ablating protein expression.

192 Moreover, the model shows how attempts to ablate PSs in the viral RNA sequence may result in redun

193 lains why recent experiments that attempt to ablate putative PSs may not see an effect on packaging.

194 Moreover, the mutations ablated receptor-mediated activation of serum response f

195 Disruption of this patch ablated recognition of CD1d by the NKT cell TCR but not

196 However, intravitreal delivery of HS-ablated recombinant AAV2 (rAAV2) led to a 300-fold decre

197 ce leads to defective neuronal migration and ablates Reelin stimulation of hippocampal long-term pote

198 ining the time evolution of the shape of the ablated region.

199 We used genetic approaches to ablate regulator of G-protein signaling 7 (RGS7) both gl

200 wer and accompanied by larger deletions that ablated residual expression from the endogenous OTC gene

201 We genetically ablated SCs during development and after NMJ formation t

202 Ablating SCs at E8.5 (i.e., prior nerve arrival at the c

203 lantation cyclophosphamide after a chimerism-ablating secondary recipient lymphocyte infusion.

204 procedure in male FosLacZ-transgenic rats to ablate selectively Fos-expressing PLC neurons that were

205 ed in vivo: in K310R mutant mice and in mice ablated selectively for nuclear receptor corepressor 1 (

206 ent of channel closed-state inactivation and ablates sensitivity to depalmitoylation.

207 ,7-dihydroxytryptamine known to specifically ablate serotonin-neurons markedly decrease serotonin-imm

208 ts in which this ParG temporal regulation is ablated show partition deficient phenotypes as a result

209 To approach this question, we ablated SHP2 in collagen 2alpha1(Col2alpha1)-Cre- and co

210 To do so, we laser-ablate single k-fibers at different spindle locations an

211 Ca(2+)-ATPase assays showed that sAnk1 ablated SLN's inhibition of SERCA1 activity.

212 alcification was blunted in VSMC-specific AR-ablated (SM-ARKO) VSMCs compared to WT.

213 However, H-FIRE generally ablates smaller volumes of tissue than IRE.

214 onionizing physical energy based modality to ablate solid tumors with high power, or increase local p

215 stabilizing substitution markedly reduced or ablated soluble CD4 (sCD4) induction of non-NAb epitopes

216 ptor potential (TRP) channels to activate or ablate specific neuronal populations using the chemical

217 When canonical NF-kappaB signaling was ablated specifically in mature B cells, the differentiat

218 Here, we genetically ablated Stat3 in the tumor epithelia of the inducible Py

219 impaired protective CD8 T cell responses and ablated sterile protection.

220 While the PheRS-editing ablated strain grew 50% slower and displayed a 27-fold i

221 due to roughness and the TiO2 layers on the ablated surface during fabrication.

222 se, which is similar to that observed in Eda-ablated Tabby mice.

223 enome-editing strategies to either repair or ablate target genes, with emphasis on their applications

224 linically relevant parameters can be used to ablate target tissues in a non-tumor-bearing large-anima

225 refore explored the metabolic consequence of ablating TBC1D1 in both resting and contracting skeletal

226 In this study, we specifically ablated Tcf1 long isoforms in mice (p45(-/-)mice) to abr

227 In this study, we specifically ablated Tcf1 long isoforms in mice, while retaining expr

228 Ablating Tcf7 in Runx3-deficient CD8(+) TEFF cells preve

229 further identify a Tdp2 active site SNP that ablates Tdp2 Mg(2+) binding and catalytic activity, impa

230 bition of TGF-beta receptor I using SB431542 ablated TGF-beta-induced migration and invasion.

231 regulation of the pro-growth signal CDK2 and ablated TGFbeta-induced EMT.

232 We found that ablating Th17 cells by knocking out Stat3 in CD4(+) T ce

233 oncept, we engineered the vaccine DEKnull to ablate the dominant Bc epitope to partially overcome str

234 ficient in TgDHODH activity were designed to ablate the enzyme activity.

235 t al. (2017) used CRISPR/Cas9 to genetically ablate the OCT4 gene in human preimplantation embryos an

236 dult specific inhibition of tPA activity can ablate the ocular dominance shift in Lynx1 KO mice.

237 d cancer patients undergoing treatments that ablate the ovaries.

238 s, inhibition of SRC and PKCdelta completely ablated the ability of MDA-7/IL-24 to reduce the Bcl-x(L

239 hat disrupted the pTRS1 interaction with PKR ablated the ability of pTRS1 to antagonize PKR activatio

240 otein in vitro, this modification completely ablated the activity of LLO, and this inhibitory effect

241 e of pancreatic ductal adenocarcinoma (PDAC) ablated the development of salivary biomarker profile.

242 r a C3/C4 dorsal column SCI that bilaterally ablated the dorsal corticospinal tract (CST) containing

243 dismutase and catalase mimetic EUK-134 also ablated the effects of hypoxia on BKCa channel currents

244 nt, and blocking IL-5 with a neutralizing Ab ablated the IL-33-induced EoM expansion.

245 e addition of calcium to the motility assays ablated the impact of phosphorylation on maximal sliding

246 with an IFNAR-neutralizing antibody after MI ablated the interferon response and improved left ventri

247 Using a conditional targeting approach, we ablated the major CLP gene Irf6 only in the late embryon

248 Raising growth temperature to 37 degrees ablated the positive influence of some mutations on the

249 ree independent inhibitors of Hsp70 function ablated the protective effects of NAC, suggesting that N

250 In this study, we ablated the TGF-beta type 1 receptor (also termed activi

251 We conditionally ablated the tuberous sclerosis complex 1 (Tsc1) gene, an

252 Deletion of hepatocyte VEGF markedly ablates the 'off-drug'-induced metastasis.

253 drugs (DREADDs)-mediated synaptic silencing ablates the food intake and body weight reduction follow

254 g, we ectopically induced endogenous Xist by ablating the antisense repressor Tsix in mice.

255 Ablating the catalytic activity of FKBP65 or LH2 did not

256 Rescuing proliferation by ablating the cell cycle negative regulator p27 (also kno

257 Aicardi-Goutieres syndrome demonstrate that ablating the cyclic GMP-AMP synthase gene abolishes the

258 By genetically ablating the cytoskeletal regulators Rac1 or Cdc42 in th

259 Thus, by ablating the downstream transcription factors of the alt

260 Ablating the essential clock gene Bmal1 specifically in

261 Ablating the expression of Charon prevents Relish from t

262 Here, we report evidence that ablating the growth regulatory kinase Erk5 can increase

263 nalling pathway downregulated by genetically ablating the median neurosecretory cells (mNSC).

264 Taken together, our study demonstrated that ablating the NLRP3 gene significantly reduced neuroinfla

265 at the collected particles were continuously ablated; the time for complete ablation of 193 ng of suc

266 plement receptor 3-expressing phagocytes and ablates their bactericidal capacities by catalyzing unre

267 ficient to maintain adult NSC quiescence and ablating them leads to NSC activation and subsequent dep

268 in receptor expression system to selectively ablate these cells from the epileptic mouse brain.

269 nterfering RNA, TGF-beta, and IL-6 treatment ablated these proresolution effects in primary human mac

270 of mitogen-activated kinase kinase 1 or FGFR ablated these responses.

271 Ablating these neurons in adults had little effect on pr

272 Genetically ablating these neurons in juveniles disrupted their abil

273 Anti-IgE (omalizumab) treatment ablated this anaphylactic response.

274 ncreased ETC activity, co-treatment with HKL ablated this response and vastly enhanced the rate of ap

275 GFP) mice in which Tregs can be specifically ablated through administration of diphtheria toxin, we d

276 Cells are naturally and cleanly ablated through apoptosis due to the terminal activation

277 om gross tissue examination of the region of ablated tissue after MR imaging.

278 The radius of ablated tissue increased from approximately 5 mm at 150

279 sonance imaging and histological staining of ablated tissue were subsequently performed as a part of

280 on-induced tissue changes for characterizing ablated tissue.

281 le gadoteridol accumulates around and within ablated tissue.

282 Ablated tissues exhibited progressive fibrosis and chron

283 o dobutamine, whereas expression of phosphor-ablated TnI alone had little effect on the acceleration

284 Cre) to target the mandibular epithelium, we ablated transcription factor Islet1, resulting in a dist

285 Thus, there is a need for a mechanism to ablate transferred T cells after tumor eradication is co

286 he broad use of these inhibitors as tools to ablate tumor-associated macrophages that enable malignan

287 ZDHHC3-ablated tumors also showed enhanced recruitment of innat

288 In 13 (33%; 95% CI: 18, 47) of 40 completely ablated tumors, intrahepatic tumor recurrence was observ

289 nt with rapamycin or inhibition of HIF1alpha ablates UBE2O-dependent tumor biology.

290 cm; mean SUVmax, 22.7; range, 9.5-77.1) were ablated using radiofrequency (n = 16) or microwave (n =

291 Patients were ablated using single-tip ablation with conventional or s

292 oyed an inducible mouse KO that specifically ablates Utx in satellite cells (SCs) and demonstrated th

293 (HSA-/-) ) by providing VEGF(HSA-/-) and non-ablated (VEGF(f/f) ) littermates with running wheels for

294 r-generated periodic gratings were virtually ablated via a computational process based on a two-step

295 ns of many antidepressants at SERT have been ablated via knock-in substitution (SERT Met172) without

296 ISPR technology in SaOs2 cells significantly ablated vitamin D mediated inhibition of calcification.

297 rdia (FAT) is extremely difficult to map and ablate when it is difficult to induce and nonsustained.

298 These effects were ablated with selective siRNA silencing of these proteins

299 Ablating Wnt signaling in the bulge cells causes them to

300 r loss of both proteins to greatly reduce or ablate XRCC1 chromatin binding following H2O2 treatment.