ライフサイエンスコーパス: be ablated

1 base pair in the hairpin (otherwise priming is ablated).

2 l, or even cure, if all sites of disease can be ablated.

3 om patients with HGD, all areas of BE should be ablated.

4 enic mouse in which FAP-expressing cells can be ablated.

5 y, as well as the adenosine transporter, can be ablated.

6 potential in vivo of shL5 cells was found to be ablated.

7 opment, which is partially rescued when PTEN is ablated.

8 e gene cabeza (caz), the fly homolog of FUS, is ablated.

9 cell receptor-activated tyrosine kinase Lck is ablated.

10 ouse strains in which the eosinophil lineage is ablated.

11 to inhibit tRNA gene transcription when p53 is ablated.

12 ated to alanine, the binding of D1D2 to LRP1 is ablated.

13 munodeficiency patients where TACI signaling is ablated.

14 insensitive mutant SIK is introduced or LKB1 is ablated.

15 ersists even when recurrent inputs from LMAN are ablated.

16 lt mice whose agouti-related peptide neurons are ablated.

17 rotects against starvation when AgRP neurons are ablated.

18 resholds at which phenotype and transmission are ablated.

19 ody extremities, including ear and forepaws, was ablated.

20 osomes, we constructed a mutant in which NES was ablated.

21 ti-IL-17A mAb, the anti-tumor effect of APCP was ablated.

22 hich the CaMKII site on ryanodine receptor 2 was ablated.

23 were maintained at control levels when Cx36 was ablated.

24 hich the CaMKII phosphorylation site on RyR2 was ablated.

25 s with other mouse models in which Dicer has been ablated.

26 the binding sites of TFs whose activity has been ablated.

27 nts' lives different regions of the neuraxis were ablated.

28 in-repeat region with or without KASH domain were ablated.

29 rf tumor-suppressor gene and the gammac gene were ablated.

30 ding leucine of AT1aR, binding and signaling were ablated.

31 ve advantage in nuclear layers where neurons were ablated.

32 tachycardias/premature ventricular complexes were ablated.

33 When the hem is ablated a necessary balance is perturbed, and cerebra

34 al for maintaining the sAHP when hippocalcin is ablated, a condition that likely impairs PIP2 generat

35 was normal during embryonic development but was ablated after birth (alphaMHC-Cre x GRK2 fl/fl) or o

36 as preserved in mice lacking lymphocytes and was ablated after depletion of eosinophils or treatment

37 grown in 11 rats, but only one of the tumors was ablated after intravenous administration of (99m)Tc-

38 n II or thapsigargin-induced store depletion is ablated, although the mechanisms are not understood.

39 red" MGN, in which normal auditory afferents are ablated and novel retinal inputs innervate the MGN.

40 Large volumes of tissue may be ablated and large vessels coagulated with multiple-an

41 ination with rapamycin, mTOR kinase activity is ablated and apoptosis induced.

42 s result, transcription of full-length corin is ablated and W(sh) mice develop symptoms of cardiomega

43 ly induced when UCP1-dependent thermogenesis is ablated, and creatine reduction in Ucp1-deficient mic

44 IL-4Ralpha(-/-) mice, residual eosinophilia was ablated, and susceptibility to chronic adult Brugia

45 s were ablated, intermediate if some sources were ablated, and lowest if no sources were ablated (p <

46 ogenitor cells that co-express Sox2 and Bmi1 are ablated, as we observed that ageing in mice started

47 ng from the ostium of the left ventricle may be ablated at the base of the aortic cusps.

48 ty of patients with atrial fibrillation will be ablated at the time of their mitral valve surgery.

49 Phosphorylated dynein was ablated at kinetochores after inhibiting Plk1 with a

50 ude, but not frequency, was reduced when SCs were ablated at E15.5, suggesting that postsynaptic alte

51 In addition, 18 of the low-risk patients were ablated based on patient/parental decision.

52 ich the expression of full-length SH protein was ablated because it provided a modest selective advan

53 e neurons or descending serotonergic neurons were ablated before hyperalgesic priming, IL-6- and carr

54 When Kupffer cells were ablated before the onset of bacteremia, there was a

55 isted when BM-resident dendritic cells (DCs) were ablated but failed when all phagocytic cells were d

56 F was absent in 80.3% of patients if sources were ablated but in only 18.2% of patients if sources we

57 rt failure, where ISO-induced nuclear import is ablated, but G(q)-agonist mediated export is preserve

58 CMs observed in mef2ca;mef2cb double mutants are ablated by a morpholino capable of knocking down oth

59 However, when melanocyte stem cells (MSCs) are ablated by early treatment with the erbB3 inhibitor

60 As expected, RNA foci are ablated by RNase treatment.

61 es in liver and plasma F2-isoprostanes could be ablated by 1-aminobenztriazole, implicating the PB-in

62 Orthograde coupling was previously shown to be ablated by a glycine for glutamate substitution at Ry

63 his restraint of innate immune signaling can be ablated by inhibition of proteasome function.

64 , forms part of a secondary lineage that can be ablated by larval HU application.

65 ontains innervation and AF triggers that can be ablated by retrograde ethanol infusion.

66 ccurs during mitosis and cytokinesis and can be ablated by SETD2 deletion, which causes mitotic spind

67 of CHD1 and Mediator from cell extracts can be ablated by shRNA knockdown of a specific Mediator sub

68 ary cells even when its CD4 binding site had been ablated by deletion of a highly conserved aspartic

69 ompetent even after its CD4 binding site had been ablated by mutagenesis.

70 use model in which the V2a interneurons have been ablated by targeted expression of diphtheria toxin

71 d to be dependent on its enzymatic activity, being ablated by mutation of its phosphatase domain and

72 ulum stress, and that this modulatory effect is ablated by 37W and 607F.

73 e hypoxic extension of replicative life span is ablated by a dominant negative HIF.

74 th cyclooxygenase-2 (COX-2) upregulation and is ablated by COX-2 inhibitors.

75 l3 in HEK293T cells in which Cul3 expression is ablated by either siRNA or by CRISPR-Cas9 genome edit

76 onstrate that neuronal TRKB trophic function is ablated by MMP9-mediated degradation in the diabetic

77 regulation of the expression of these genes is ablated by p63 small interfering RNA as well.

78 In contrast, IL-1beta secretion is ablated by potassium, scavenging mitochondrial ROS, a

79 lation and monoubiquitylation of H2AX, which is ablated by siRNA suppression of MDC1.

80 on, is selectively denervated of LC input or is ablated by the cell-specific neurotoxin ibotenic acid

81 [Ca2+]i) transient in endothelial cells that was ablated by a combination of superoxide dismutase and

82 cular ejection fraction, 58+/-10%), only AFL was ablated by achieving bidirectional isthmus conductio

83 Rats in which the sympathoadrenal axis was ablated by adrenal medullectomy showed normal durati

84 associated with elevations in the microbiota was ablated by antibiotic pretreatment and correlated wi

85 appaB pathway in the presence of VP16, which was ablated by Bay11, suggesting that AAV transduction a

86 in response to histamine in vitro, but this was ablated by blockade of H1R but not H2R.

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

88 he p53 pathway in MRT cells, and sensitivity was ablated by CRISPR-Cas9-mediated inactivation of TP53

89 A small amount of sample material was ablated by focusing 266 nm laser light onto a spot.

90 nic mutant derivative in which Chk1 function was ablated by gene targeting.

91 The latter was ablated by inhibition of MEK, but not p38, confirmin

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

93 IL-10 promoter activity was ablated by mutating two nonpolymorphic binding sites

94 This NO-induced inhibition was ablated by mutation of the Cys-273 site.

95 dent down-regulation of GluR1 AMPAR currents was ablated by overexpression of SAP97-I2I5 (which does

96 This effect was ablated by pharmacological and genetic inhibition of

97 d to prevent apoptosis when endogenous SfIAP was ablated by RNA silencing.

98 Human cells in which RNF4 expression was ablated by siRNA or chicken DT40 cells with a homozy

99 This effect was ablated by the mutation H267A in the beta subunit.

100 ized hES-RPE showed enhanced survival, which was ablated by the presence of anti-PEDF antibody.

101 izer induction: the primary dorsal organizer was ablated by UV irradiation, and a new organizer was i

102 Both of these effects were ablated by a F170S substitution in the HPIV1 C prot

103 Both effects were ablated by angiotensin II type 1a (AT(1a)) receptor

104 results in increased telomere fusions, which were ablated by Ctip knockdown.

105 d VV-induced CD4 T-cell IFN-gamma production were ablated by cyclosporine A, which inhibits signaling

106 tic cellular lineages, second wave follicles were ablated by diptheria toxin treatment of Lgr5-DTR-EG

107 ICC-IM responses to EFS were ablated by inhibiting Ca(2+) stores with cyclopiazo

108 and most of the perifovea of the treated eye were ablated by laser photocoagulation at the start of t

109 e fovea and most of the perifovea in one eye were ablated by laser photocoagulation.

110 Importantly, these effects of FGF2 were ablated by PD173074, a small molecule inhibitor of

111 ced P-S6 levels by Western blot, and effects were ablated by pretreatment of cells with mTOR-specific

112 but was abolished if either ORF45 or RSK1/2 were ablated by siRNA, a pattern that is correlated with

113 While GEPCOT NICs were ablated by temozolomide, pre-GEPCOT cells survived

114 d luciferase activity, whereas these effects were ablated by the mutation of the seed region of the m

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

116 of the assays was confirmed, as the signals were ablated by the Scurfy mutation of the FoxP3 gene.

117 Aortic aneurysms in these LDS mice were ablated by treatment with the Ang II type 1 (AT1) r

118 eedlelike cryoprobes were placed and lesions were ablated by using real-time MR imaging for intraproc

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

120 but not if both germ line and somatic gonad were ablated, by a precursor of the DAF-12 ligand, dafac

121 lation of Spry1, Pten, and Pdcd4 when miR-21 was ablated coincided with reduced phosphorylation of ER

122 or wild-type explants in which HS expression was ablated could extend axons in response to netrin-1.

123 Transgenic mice in which CX3CR1 signaling was ablated (CX3CR1(GFP/GFP)/CX3CR1(-/-)) and preserved

124 receptor mice in which CD11b-positive cells were ablated, decreased tumor cell survival without alte

125 AF sources were ablated directly in 100% of FIRM cases and coincide

126 misregulation, and Aurora A(S361*) activity is ablated due to loss of structural integrity.

127 F/YF)) in which the PI3K binding site in Cbl is ablated due to the mutation in the regulatory tyrosin

128 nt was severely disrupted when Lhx2 function was ablated during embryonic development.

129 n which the Nr4a1 superenhancer E2 subdomain is ablated (E2 (-/-) mice).

130 lly affected when radial glial primary cilia were ablated earlier in development.

131 e synapse formation in mutants in which TrkB is ablated either in presynaptic or in both presynaptic

132 imprinted control region when transcription is ablated, establishing a connection between transcript

133 Embryos in which Ovol2 is ablated exhibit lethality by E10.5, prior to which th

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

135 When successive steps in folate biosynthesis were ablated, folE (lacking pterins and folates) and fol

136 regions with an interval confidence level >7 were ablated followed by pulmonary vein isolation (PVI).

137 CFAE sites with continuous electric activity were ablated followed by PVI.

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

139 advantageous in creating animal models that are ablated for specific cells and in other targeted cel

140 s were predominantly men (68%); the majority were ablated for the first time (71%); left atrium was 4

141 In LAAPPI the analytes are ablated from water-rich solid samples or from aqueou

142 g from the left ventricular summit (LVS) can be ablated from the great cardiac vein and remote endoca

143 ents have been reported in whom VT could not be ablated from the right or left ventricular endocardiu

144 her the nsp2 protein antagonist function can be ablated from the virus, we introduced point mutations

145 mouse model in which androgen receptor (AR) is ablated from approximately 75% of adult Leydig stem c

146 absence of Pax3, the enteric nervous system is ablated from its inception.

147 Mice in which the Ttf1 gene was ablated from differentiated neurons grew normally an

148 When PMNs were ablated from mice, DeltayopM Y. pestis grew as well

149 When Wnt and Eda were intact but Shh was ablated, germ induction and subsequent duct formatio

150 Flies in which Leuc or Lkr neurons are ablated have defects identical to those of leucokini

151 dominant and GC functionality and phenotype are ablated, i.e., EBV infection is not consistent with

152 rtantly, the anticancer effects of the drugs are ablated if CLU expression is blunted by RNA interfer

153 developmental timepoint at which podocalyxin is ablated (immature vs. mature podocytes) has a profoun

154 e report that LPS-mediated Ca2+ oscillations are ablated in ECs deficient in Nox2, Stim1, and type II

155 SF and neutrophilia, whereas these responses are ablated in G-CSF- or TLR2-deficient mice.

156 al TRPC3 channels; intriguingly, these cells are ablated in moonwalker mice by 1 month of age.

157 not apoptosis, all three of these processes are ablated in p53(3KR/3KR) cells.

158 and Ago2, but not either Ago1 or Ago2 alone, are ablated in the skin, the global expression of microR

159 TgPEPCKnet can also be ablated in a glycolysis-deficient mutant, while TgPEP

160 ich replicating osteoblast lineage cells can be ablated in an inducible manner using ganciclovir (GCV

161 g a mouse model in which the T1IFNR gene can be ablated in vivo, specifically in cardiomyocytes.

162 Dmp1Cre.Socs3 (f/f) mice, in which SOCS3 has been ablated in osteocytes, have high trabecular bone vo

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

164 xoviruses and arenaviruses, where resistance is ablated in animals depleted of microbiota.

165 pression of neuronal differentiation markers is ablated in both KIF1Bbeta-deficient mouse neuroblasts

166 flox); Osx-Cre mice, in which the Smpd3 gene is ablated in both late-stage chondrocytes and osteoblas

167 )17-dependent autoimmunity occurs when STAT3 is ablated in CD4 cells.

168 Prion protein-mediated zinc uptake is ablated in cells expressing familial associated mutan

169 that leukocyte rolling on P- and L-selectin is ablated in cells lacking O-glycans, with N-glycan tru

170 Moreover, when the Smad4 gene is ablated in combination with its DNA binding cofactor

171 Post-anoxia MEND is ablated in DHHC5-deficient hearts, inhibited by cyclo

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

173 ten conditional knockout mice, in which Pten is ablated in granule cells of the dentate gyrus and pyr

174 equires functional Foxq1 as their expression is ablated in hair follicles of satin mice.

175 e developed a model in which SHIP expression is ablated in HSCs while they are resident in a SHIP-com

176 a mouse neuronal model of TSC in which Tsc1 is ablated in most neurons during cortical development.

177 rated and studied a mouse model in which S1P is ablated in postnatal chondrocytes.

178 Concordantly, reovirus infection is ablated in primary cortical neurons derived from NgR1

179 ly increased in rho0 cells but this increase is ablated in rho0 rsb1Delta cells.

180 ur with high penetrance in mice in which Nf1 is ablated in Schwann cells in the context of a heterozy

181 knock-out model in which the Miz1 POZ domain is ablated in Schwann cells.

182 enerating a novel mouse model in which PTH1R is ablated in the limb mesenchyme using Prx1Cre transgen

183 we generated mice in which Ikbkap expression is ablated in the peripheral nervous system and identify

184 This response is ablated in Tlr4(-/-) mice or when co-administered wit

185 The VLPO was ablated in 25 rats by bilateral local injection of o

186 When NgR2 was ablated in AD transgenic mice expressing Swedish APP

187 and were markedly reduced when dystroglycan was ablated in adult mice, suggesting a role for dystrog

188 Moreover, activation of MAPK pathway was ablated in APRIL-stimulated XID cells.

189 atRA signaling was ablated in beta-cells by overexpressing a dominant-n

190 e desensitizing effect of McTnT1-44 on pCa50 was ablated in beta-Tm fibres.

191 Fbeta receptor TGFbetaRI (encoded by Tgfbr1) was ablated in cartilage.

192 rate-docking site of the PDK1 protein kinase was ablated in Cre-expressing tissues in a way that prev

193 within the peritoneal cavity, a pattern that was ablated in CXCR3-deficient mice.

194 MCC expression was ablated in each case, enabling oncogenic beta-cateni

195 assay confirmed that de novo heme synthesis was ablated in FC knock-out parasites.

196 This subset was ablated in huLangerin-DTA mice, resulting in reduced

197 of C. pneumoniae to increase the ATP content was ablated in macrophages deficient in expression of ei

198 noid-mediated long-term depression (eCB-LTD) was ablated in mBACtgDyrk1a mice.

199 ansfer into Rag1(-/-) hosts, but this effect was ablated in mice that lacked fully functional B cells

200 o the skin following cutaneous OVA challenge was ablated in mice that lacked lymph nodes.

201 I(h) was ablated in most large neurons in HCN1(-/-) mice.

202 the sole E2 SUMO-conjugating enzyme, Ube2i, was ablated in mouse oocytes beginning in primordial fol

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

204 Increased IFN-induced gene expression was ablated in NOD.IFNAR1(-/-) islets.

205 e generation were p53-dependent; this effect was ablated in p53-null cells.

206 Megakaryocyte and platelet FAK expression was ablated in Pf4-Cre/FAK-floxed mice without affecting

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

208 le repair was severely perturbed when Ptpn11 was ablated in stem cells due to a deficit in stem cell

209 In contrast, mice in which SHP2 was ablated in the Col10alpha1-Cre-expressing cells appe

210 Mouse embryos were generated in which Hnf4a was ablated in the epithelial cells of the fetal colon b

211 ptor-mediated ERK activation, a pathway that was ablated in the l/l mouse through a mutation of the t

212 v-erbalpha at these sites was lost when HNF6 was ablated in the liver.

213 ation and visualization system, the gap area was ablated in the MR scanner.

214 Interestingly, STAT2 degradation activity was ablated in the NS2 ubiquitin mutant rRSV.

215 K (Thr-172) and ACC (Ser-79), but the effect was ablated in the S399A mutant.

216 l LC patterning in neonates, but not when LC were ablated in adults and replaced by bone marrow-deriv

217 Vdelta2 T cells were ablated in blood and tissue from CD patients receiv

218 These therapeutic effects were ablated in both CD4(+)- and CD8(+)-depleted mice an

219 These responses to flagellin were ablated in DCs from NLRC4(-/-) mice but not Toll-li

220 The cardioprotective effects of metformin were ablated in mice lacking functional AMPK or eNOS.

221 These increases were ablated in MyD88-/- mice, and NF-kappaB p65 was pho

222 n of innate immunity in that these responses were ablated in MyD88-deficient mice and that flagellin

223 ptotic effects of IL-11 on DCs, whereas they were ablated in Stat1(-/-) cultures.

224 MyoD expressing cells were ablated in the epiblast by labeling them with the G

225 the ASE chemosensory neurons (ASEL and ASER) are ablated, indicating that this pair has a dominant ro

226 covered in which expression of M2-1 and M2-2 was ablated individually or together [rdeltaM2-1, rdelta

227 Freedom from AF was highest if all sources were ablated, intermediate if some sources were ablated,

228 ouse strains in which the eosinophil lineage is ablated, large numbers of T. spiralis larvae are kill

229 /-) mice, and mice in which IL-12 production was ablated only from CD8alpha(+) DCs failed to control

230 increased AP duration by 67% only when Kv2.1 is ablated or inhibited and enhanced GSIS by 2.7-fold.

231 he discriminatory salivary biomarker profile was ablated or disrupted.

232 adaptor MyD88, or transcription factor IRF7 was ablated or pDCs were depleted.

233 ent RFA every 3 months until all areas of BE were ablated or cancer developed.

234 in embryos where specific founder cells have been ablated, or where zygotic transcription has been in

235 urces were ablated, and lowest if no sources were ablated (p < 0.001).

236 ic CD8 T cells was impaired when CD4 T cells were ablated prior to infection but not at 4 days postin

237 on of GSK-3beta by phosphorylation at Ser(9) was ablated providing a molecular basis for these findin

238 When cells are ablated rather than wounded, Rho GTPase activation a

239 late Sp1 interactions with the CDK4 promoter was ablated, rendering the CDK4 promoter unresponsive to

240 F-beta1 injection into mice in which MKs had been ablated restored HSC quiescence, and conditional de

241 e vesicular glutamate transporter 2 (VGLUT2) is ablated selectively from DRG neurons.

242 onal Nurr1 gene-targeted mice in which Nurr1 is ablated selectively in mature DA neurons by treatment

243 g by engineering mice in which the Jnk1 gene was ablated selectively in adipose tissue.

244 tants in which this ParG temporal regulation is ablated show partition deficient phenotypes as a resu

245 randomly chosen obstacles in a regular array is ablated; single-file diffusion in pores; transient an

246 are increased in mice in which MHC class II is ablated specifically in LC suggesting that direct cog

247 ally null mice, in which expression of CTIP2 was ablated specifically in epidermal keratinocytes, sug

248 When canonical NF-kappaB signaling was ablated specifically in mature B cells, the differen

249 Therefore, we generated mice in which Snf5 was ablated specifically in nestin-positive and/or glial

250 ction in the prostate, the Frs2alpha alleles were ablated specifically in the prostatic epithelial pr

251 When both NM II-C and II-B are ablated the B-C-/B-C- cardiac myocytes show major de

252 When 2d and 4d were ablated the embryo developed into a rounded cell ma

253 erm line, endoderm or mesoderm founder cells are ablated, the remaining cells do not alter their clea

254 Thus, when FANCJ binding to BRCA1 is ablated, the molecular mechanism chosen for the repai

255 yD88 in DCs, the early IL-12 response by DCs was ablated, the IFN-gamma response by natural killer ce

256 e critical for protection: when PMNs in mice were ablated, the mice lost all ability to be protected

257 venting PKD are limited because PC2 function is ablated throughout the cell in existing model systems

258 f the larval heart to serotonin when the CNS was ablated, thus suggesting a direct neural input.

259 gradation in ADAMTS-4/5-double-knockout mice was ablated, to a level comparable with that in ADAMTS-5

260 When the gene encoding 4E-BP1 was ablated together with Mtor, marked improvements were

261 ation, we find that when IFN-gamma signaling is ablated, type I IFNs drive inflammation, resulting in

262 tion in this model and the activity of IL-13 was ablated under conditions leading to expression of th

263 on of MLC (serine 19) through a pathway that was ablated under conditions that blocked CD36 ligation

264 nged activation of MAPK (p38 and ERK1/2) and was ablated under MAPK inhibition.

265 arvin mutant in which the G3BP2-binding site is ablated, unlike that of wild-type alpha-parvin, in al

266 ges in transcription and locus repositioning are ablated upon transformation with v-Abl, which render

267 acellular parasitism observed in TP-null ECs was ablated upon restoration of TP expression.

268 ane positions, micrometer-diameter pores can be ablated upstream of desired cellular targets.

269 Ets-1 and Runx2 protein expression in CT26 was ablated using antisense oligonucleotides and resulte

270 -4.6 cm; mean SUVmax, 22.7; range, 9.5-77.1) were ablated using radiofrequency (n = 16) or microwave

271 Patients were ablated using single-tip ablation with conventional

272 actions of many antidepressants at SERT have been ablated via knock-in substitution (SERT Met172) wit

273 the roof of the CS, and 1 nodoventricular AP was ablated via a transseptal approach near the CS os.

274 The microbiota was ablated via germ-free or antibiotic approaches.

275 When these neurons are ablated, we found that the behavioral response is sh

276 adult mice in which hippocampal neurogenesis was ablated, we found specific impairments in spatial di

277 Using mice in which cone photoreceptors were ablated, we found that rods signal through cones at

278 for the BH3-only molecules Bim and Puma had been ablated were studied on a high-fat diet.

279 rs or transgenic mice wherein the JNK-1 gene was ablated were subjected to 5 or 20 min of ischemia fo

280 However, beta(2)AR-Nedd4 interaction is ablated when beta-arrestin2 expression is knocked dow

281 yeast Aha-type co-chaperones to act in vivo is ablated when the N terminal NxNNWHW motif is removed.

282 Similarly, long-term survival induced by DST was ablated when HO-1 activity was blocked by zinc proto

283 in mTORC2 activity in Gpat1(-/-) hepatocytes was ablated when rictor was knocked down.

284 In addition, we demonstrate that degradation was ablated when the proteasome was inhibited, whereas a

285 ll adhesion molecules and leukocyte adhesion were ablated when disrupting sympathetic nerves, demonst

286 es to guide treatment so lesions of interest are ablated whereas sparing surrounding healthy tissues,

287 cannot proceed when proliferating IA6+ cells are ablated with Mitomycin C, and injection of a single

288 ell as the increased activity of TAp63gamma, is ablated with the expression of a ubiquitin-deficient

289 t not in cytosol/nonraft membrane fractions, was ablated with cyclodextrin.

290 Rather, the tumor vasculature was ablated with high-dose intratumoral IFN-beta, and co

291 Phosphorylation of this Akt subspecies was ablated with methyl-beta-cyclodextrin, a cholesterol

292 which the expression of endogenous perforin was ablated with miR30-based short hairpin (sh) RNAs.

293 The tumor in each animal was ablated with RF (1-cm active size ablation catheter,

294 Porcine corneas were ablated with a free-electron laser tuned to 2.77 or

295 Rabbit corneas were ablated with an excimer laser and were observed and

296 he course of the study: the last 13 patients were ablated with enhanced software.

297 Seventy-three patients were ablated with MN and 72 with a standard manual appro

298 he acute phase of the disease when microglia were ablated with PLX5622, whereas other cytokines (eg,

299 d 164 with ICM, presenting with sustained VT were ablated with radiofrequency catheter ablation.

300 These effects were ablated with selective siRNA silencing of these pro