ライフサイエンスコーパス: (be|was|were|is|are) incapable of *ing

1 ician takes action that a nonphysician would be incapable of performing.

2 helial venules (HEVs), whereas naive T cells were incapable of sticking.

3 despite the fact that the ferrocenium cation is incapable of oxidizing [1](+).

4 A poliovirus (PV) mutant (termed GG), which is incapable of producing 3AB, VPg, and 3CD proteins due

5 ues or polar residues that become buried yet are incapable of forming a new hydrogen bond.

6 with anti-CD20 during Pneumocystis infection are incapable of mounting a protective immune response w

7 ted in GPR54 KOs and that such animals would be incapable of showing a compensatory rise in LH secret

8 Moreover, we show that HIV gp120 is incapable of binding a fully oxidized, monomeric 2dCD

9 that, although the modified RS-O(-) fragment is incapable of forming a pi bond with the Fe(III) cente

10 ry of 1:1, resulting in DNP-ATP-proCsp9 that is incapable of forming a productive Apoptosome with Apa

11 site and an active-site variant (D44N) that is incapable of forming a strong zinc ligand.

12 hereas others suggest that estrogen not only is incapable of providing a benefit, but actually can be

13 re conserved in CRS2, yet expression of CRS2 is incapable of rescuing a pth(ts)E.coli strain.

14 xes destabilized the WT NRS-Ad3' complex; it was incapable of forming a B complex on a native gel.

15 g in a spontaneously unfolded structure that was incapable of forming a homodimer with itself or a he

16 Furthermore, FLT3-ITD-Y589/591F was incapable of inducing a myeloproliferative phenotype

17 Additionally, LegC3 was incapable of inhibiting a defined synthetic model of

18 on- or binding-incompetent beta(2a) subunits were incapable of entering a CaMKII-dependent high-activ

19 inment at photopic intensities at which they were incapable of supporting a visually guided behavior.

20 s, which express SVCT2 at the mRNA level and were incapable of transporting AA, showed a predominance

21 First, we found that beta-catenin null cells were incapable of undergoing acinar to ductal metaplasia

22 spectrin-actin binding domain peptides that were incapable of binding actin had no deleterious effec

23 Irf9 -/- B cells were incapable of being activated through TLR7, and Stat

24 The K403 acetylated G6PD is incapable of forming active dimers and displays a com

25 hat, in the absence of cognate antigen, they were incapable of sustaining active migration.

26 production in the mouse fibroblasts, but it is incapable of stimulating adiponectin expression in th

27 Current subunit vaccines are incapable of inducing Ag-specific CD8(+) T cell cyto

28 ed, whereas a mutant nematode torsin protein was incapable of ameliorating aggregate formation.

29 igens and shared self-antigens but generally are incapable of provoking an effective immune response,

30 nts, even if sequestered within the nucleus, are incapable of transactivating an IgH reporter gene.

31 (E)-induced GnRH/LH surge and thus E should be incapable of inducing an LH surge in the absence of G

32 of the identified mutants, denoted hydEF-1, is incapable of assembling an active [Fe] hydrogenase.

33 trast to A416P, either A420P or A425P mutant was incapable of interacting and regulating cellular Src

34 Cells lacking p42 were incapable of growing and forming colonies whereas c

35 In vitro, homozygous ld/ld erythrocytes were incapable of binding ankyrin, but contrary to all p

36 ing the Wnt signaling pathway in SW480 cells is incapable of inducing apoptosis in these cells, confi

37 Similarly, AG879, a selective ErbB2 TKI, was incapable of inducing apoptosis in FET6alphaS26X cel

38 Furthermore, CII (256-276, N(263), D(266)) was incapable of preventing arthritis in DR1 IL-4(-/-) m

39 uracil-DNA glycosylase activity and, hence, was incapable of acting as a uracil-processing DNA repai

40 Both viruses were incapable of replicating at vertebrate-typical temp

41 -catalytic interface, the B subunit seems to be incapable of binding ATP, which is a marked differenc

42 embrane flippase at a rate equivalent to PS, is incapable of activating Atp8a1 activity.

43 strated basal ATPase activity, but PC lipids were incapable of stimulating ATPase activity highlighti

44 in four out of 10 patients CD4+CD25+ T cells were incapable of suppressing autologous CD4+CD25- T-cel

45 Mutant CaMKIV proteins that are incapable of developing autonomous activity within a

46 SCID or Rag(-/-) mice were incapable of resolving B. hermsii infection, indica

47 lung and spleen, while susceptible C3H mice were incapable of limiting bacteria growth, especially i

48 -independent defense mechanisms, macrophages are incapable of restricting BCG growth and of confining

49 lication of an HSV-1 mutant, Delta68H, which is incapable of binding beclin-1.

50 s based on sodium bisulfite treatment of DNA are incapable of distinguishing between the two modified

51 Although the kinetics studies are incapable of distinguishing between these possibilit

52 However, this kind of MB is incapable of differentiating between heparin and OSCS

53 methods to measure formaldehyde-induced DPCs were incapable of discriminating between endogenous and

54 regulatory state mimicking high cell density are incapable of producing biofilms.

55 genes, results in a null mutant strain that is incapable of establishing bloodstream infection in vi

56 Lamprey is incapable of elongating C22 substrates.

57 native cTnC with a mutant cTnC (DM-TnC) that is incapable of binding Ca(2+).

58 M, we have determined that a CaM mutant that is incapable of binding calcium binds to RyR1 at the apo

59 Egr2-deficient mast cells were incapable of directing CD4(+) T cell migration via

60 s, in multiple cancer types in which ABT-737 is incapable of causing cell death, ABT-737 may have add

61 e cholesterol crystal phase, and cholesterol is incapable of displacing ceramide from the bilayer pha

62 the GluN1 ligand-binding domain (LBD), which is incapable of triggering channel gating.

63 mplex by appearance on chromogenic agar, and were incapable of forming chlamydospores.

64 d cdc37-S14A or cdc37-S14,17A overexpression was incapable of protecting cka2-13 mutants on media con

65 replaced by an inactive form (iCORM-3) that is incapable of liberating CO.

66 erestingly, an inactive form of CORM-A1 that is incapable of releasing CO failed to promote both vaso

67 Substrates that are incapable of forming compact secondary structure (du

68 Obese white adipose tissue is hypoxic but is incapable of inducing compensatory angiogenesis.

69 pth and slow relaxation time and, therefore, are incapable of ensuring complex inter-pulse dynamics a

70 l-DNA-oligonucleotides of opposite chirality are incapable of forming contiguous Watson-Crick base pa

71 tivates barbed end capping by CP and why V-1 is incapable of uncapping CP-capped actin filaments, the

72 tive N-methylated analogue has been shown to be incapable of causing CXCR4 internalization.

73 ects of 5-aza was dissociated, CHOP ablation was incapable of modulating cytotoxicity; however, neutr

74 waves incident to a highly scattering medium are incapable of penetrating deep into the medium due to

75 trate, and so following fertilization, sperm were incapable of stimulating Delta 90 cyclin B1 degrada

76 aled that bare doped silicon microelectrodes are incapable of resolving different grades of attached

77 ApoB20.1H was incapable of binding dimyristoylphosphatidylcholine

78 ver, many culture-expanded therapeutic cells are incapable of targeting diseased tissues following sy

79 MpPR-1i lacks the conserved CAP tetrad and is incapable of binding divalent cations.

80 versible binding in the DNA minor groove but are incapable of inducing DNA damage.

81 207A/G208A; AA), in which the mutant ERalpha is incapable of binding DNA and can signal only through

82 previously that encephalitogenic CD4 T cells are incapable of inducing EAE when B cells are the sole

83 Mammalian sperm are incapable of fertilizing eggs immediately after ejac

84 M5eta or TRIM5theta show that these isoforms are incapable of restricting either HIV type 1 (HIV-1) o

85 Interestingly, the mutant that was incapable of expressing either type 1 or P fimbriae

86 The p53(R267W+R283H) and p53(E258D) were incapable of transactivating either promoter or ind

87 gen invasion assays, Bmp2 mutant endothelium is incapable of undergoing EMT, and addition of BMP2 pro

88 Whereas Wnt5a, Dkk2C, or both together were incapable of stimulating endogenous canonical signa

89 activating Rap1 provides evidence that Rap1 is incapable of regulating ERKs.

90 tant of B. bronchiseptica defective for hurP was incapable of regulating expression of BhuR in a heme

91 We show that macrophages are incapable of phagocytosing Exserohilum Despite a lac

92 etal-oxide-semiconductor (CMOS) counterparts are incapable of capturing fast dynamical processes with

93 nal requirement for early flagellar assembly is incapable of repressing FlbD in a class II flagellar

94 As a result, these cilia are incapable of generating fluid flow.

95 ctural similarity, however, BchL is found to be incapable of substituting for the Fe protein in a nit

96 averaged boundary shear stress and therefore is incapable of accounting for the fluctuating forces en

97 However, cycloreversion of this diolate is incapable of accounting for the observed catalytic tu

98 to ring flexibility or partial rotation but are incapable of undergoing free rotation.

99 ytes isolated from mouse preantral follicles are incapable of recovering from an experimentally induc

100 e and its mammalian homolog were reported to be incapable of deglycosylating full-length glycoprotein

101 otassium channel alpha-subunit, Kv8.2, which is incapable of forming functional channels on its own.

102 d Asp-AT-PLP-AFPA complex revealed that GabR is incapable of facilitating further steps of the transa

103 take action for future needs: other animals are incapable of anticipating future needs, and any futu

104 iotensin II peptide (SII-angiotensin), which are incapable of activating G proteins, to isolate the t

105 ning its ability to interact with E-protein, is incapable of inducing GABAergic (Pax2)- and suppressi

106 Indeed Cdc42-deficient mice are incapable of forming germinal centers or generating

107 ly uses thioredoxin as an electron donor and is incapable of using glutathione for this function.

108 We also show that ANGPTL4-inactivated LPL was incapable of binding GPIHBP1.

109 All mutants assessed were incapable of producing H2O2 and were not cytotoxic

110 ast, NOS2(-/-) mice, but not Phox(-/-) mice, were incapable of controlling H37Rv infection and died e

111 Tregs, in contrast, are incapable of mediating harmful reactions.

112 thin the short gH cytoplasmic tail, 824L gH, is incapable of executing hemifusion despite normal cell

113 a donor intestine-derived immune system and is incapable of rejecting his engrafted organs.

114 In contrast, bacterial RecA is incapable of catalyzing homologous pairing with a chr

115 However, EP T cells were incapable of controlling HSV-1 infection ex vivo an

116 firming earlier studies, the E6 and E7 genes were incapable of immortalizing human fibroblasts but di

117 markedly attenuated in IgE(-/-) animals that are incapable of producing IgE in response to A. fumigat

118 xpression and that Ei in homozygous DKO mice is incapable of triggering Igkappa gene transcription.

119 s taken at day 3, when they lack FcgammaRII, were incapable of preventing immunoreceptor tyrosine-bas

120 Many plants are incapable of flowering in inductive daylengths durin

121 ners (approximately 200 residues) appears to be incapable of existing in a context other than immedia

122 In addition, the msrA mutant was incapable of growing in hamsters and exhibited hyper

123 Strikingly, R. australis infection was incapable of promoting increased expression of MHC-I

124 Yet, the method is incapable of providing information about specific pro

125 )17 cells in vivo, IL-23 has been thought to be incapable of driving initial differentiation.

126 ulate fractions enriched for Axl1p or Ste23p are incapable of cleaving insulin, suggesting that the f

127 However, mutant Cx26 was incapable of inducing intercellular coupling in vitr

128 nced shedding of noninfectious particles and are incapable of antagonizing interferon (IFN) effective

129 inally differentiated effector phenotype and were incapable of transitioning into a memory state.

130 R1-deficient hematopoietic stem cells (HSCs) were incapable of reconstituting irradiated recipients a

131 Given this new evidence, we assert that BAT is incapable of operating its depository in the spirit o

132 Mutant p53 protein is incapable of transactivating its downstream target ge

133 ctated by the polar orientation of KOPS, and is incapable of recognizing KOPS while translocating alo

134 All embC alleles that were incapable of complementing LAM production in M. sme

135 ld-type FPR or a mutant form, DeltaST, which is incapable of undergoing ligand-stimulated phosphoryla

136 Moreover, the less toxic oligomer is incapable of disrupting lipid bilayers, in contrast t

137 technique for all traumatic brain injury, it is incapable of providing long-term prognostic informati

138 H. pylori mutants lacking either GGT or VacA are incapable of preventing LPS-induced DC maturation an

139 5LO(-/-) mice were incapable of producing LTs.

140 ansdifferentiation, the myofibroblastic HSCs are incapable of expressing many MMPs; however, the majo

141 severely altered in gametocyte development, are incapable of producing mature-stage gametocytes, and

142 Mutant podocytes were incapable of synthesizing mature miRNA, as revealed

143 ium binding-deficient form of the C2C domain is incapable of stimulating membrane fusion, further und

144 n at concentrations of 10 and 20 microM, but was incapable of blocking Met activation.

145 tained with free virus, infected MDMs or DCs were incapable of transferring MeV to HAE when applied t

146 t in the synthesis of the bba64 gene product was incapable of infecting mice via tick bite even thoug

147 the phosphorylation-mimicking mutant, S381E, was incapable of bundling microfilaments, it retains the

148 owever, even the most effective combinations were incapable of generating more than 65% of any partic

149 The attenuated 10-del ZIKV was incapable of infecting mosquitoes after oral feeding

150 The ospC mutant was incapable of infecting MyD88-deficient mice, suggest

151 ting in formation of fewer sporozoites which were incapable of infecting naive mice or hepatocytes in

152 Although humans are incapable of synthesizing Neu5Gc due to an inactivat

153 These isoforms are incapable of activating neural cell-specific splicin

154 Accordingly, neutrophils from this patient were incapable of producing neutrophil extracellular tra

155 HHV8 vFLIP is incapable of activating NF-kappaB in cells deficient

156 previously characterized ABINs, mouse ABIN-3 was incapable of inhibiting NF-kappaB activation by proi

157 urface and presents no lipid or a lipid that is incapable of mediating NKT cell selection and/or is r

158 C(2) receptor for VIP and PACAP (Vipr2(-/-)) are incapable of sustaining normal circadian rhythms of

159 tween attP and attB, the S. aurantiaca cells were incapable of building normal fruiting bodies but fo

160 ry organic aerosol (SOA) particle production was incapable of being observed.

161 th in-frame deletions of either arrA or arrB are incapable of growing on As(V), yet both are able to

162 at, unlike the isogenic wild-type parent, it is incapable of propagating on certain groEL mutant host

163 22) monomers, bending them into a shape that is incapable of forming ordered beta-sheets or fibrils.

164 5B when expressed in the hypodermis, but 5B is incapable of carrying out SM chemoattraction.

165 Proline derivatives that are incapable of forming oxazolidinones exhibit no rate

166 In diverse animal taxa, eggs and embryos are incapable of transporting oxygen by convection.

167 olase-dead RelMtb mutant, RelMtb(H80A), that is incapable of hydrolyzing (p)ppGpp but still able to s

168 tained at normal levels, neurofascin 155 low is incapable of preserving paranodal structure, thus ind

169 Hira mutant oocytes are incapable of developing parthenogenetically, indicat

170 duces apoptosis; however, coexpressing HoxA9 is incapable of rescuing Pbx-mediated apoptosis.

171 C) as alternatives to PCBs, the two isolates are incapable of dechlorinating PCBs.

172 y was selective for free ADMA and L-NMMA and was incapable of hydrolyzing peptide incorporated methyl

173 lacking both permeases, DeltafpuBDeltafatCD, was incapable of using petrobactin as an iron source and

174 Animals are incapable of synthesizing phenylalanine and must pri

175 an be blocked by a Src mutant (SrcS17A) that is incapable of being phosphorylated and activated by PK

176 Sulfolobus knockout strains that are incapable of forming pili proved to be deficient in

177 Although PrP-EGFP was incapable of sustaining prion infection in Tg(PrP-EG

178 recruited to the BID promoter and hence p53 is incapable of upregulating pro-apoptotic BID in hypoxi

179 , deficient-in-replication flaviviruses that are incapable of developing productive, spreading infect

180 Unlike WT H. pylori, ureB mutants were incapable of conferring protection against allergen

181 econdary expansion and effector function but are incapable of providing protective immunity.

182 s finding marks the first time a CcP variant is incapable of forming protein cross-links and confirms

183 lt of translation inhibition, as lamotrigine was incapable of perturbing protein synthesis in vivo or

184 ly long chain lengths of csaB bacilli, which are incapable of binding proteins with SLH-domains to SC

185 dema factor, individually or in combination, are incapable of lysing red blood cells.

186 h lacks the first 40 amino residues of muNS, is incapable of restoring reovirus growth in the complem

187 espiratory fate in otherwise wild-type mice, is incapable of promoting respiratory fate in the absenc

188 In contrast, they are incapable of suppressing responses directed against

189 bypass Rhb1p's requirement for growth, they are incapable of suppressing Rhb1p's requirement for res

190 ded an alphaT* subunit (alphaT*(R238E)) that was incapable of undergoing rhodopsin-dependent nucleoti

191 ells are no longer pluripotent, because they are incapable of giving rise to primitive endoderm and h

192 IA protein that assembles constitutively and is incapable of binding RLC still displays strong locali

193 whole organisms, but it has been thought to be incapable of targeting RNA.

194 Notably, an E. coli rnhA mutant, which is incapable of producing RNase H and thus harbors incre

195 al quantum number n = 3, they have proven to be incapable of handling Rydberg states having quantum n

196 en recognized in a rare gastrinoma, where it was incapable of binding secretin or signaling, and poss

197 e mutant version was completely inactive and was incapable of undergoing self-cleavage to generate th

198 AP-1 sites similar to wild-type Zta, but it was incapable of binding several degenerate Zta sites, i

199 that the INCENP-bound, centromeric HP1alpha is incapable of recruiting Sgo1.

200 H. influenzae is incapable of synthesizing sialic acid and is dependen

201 made equivalent levels of IL-12, yet PP pDCs were incapable of producing significant levels of type I

202 rg(-/-) mice lacking both DAP12 and FcRgamma were incapable of sustaining slow neutrophil rolling on

203 Smads using a mutant type I receptor, which is incapable of activating Smads but still retains the k

204 r, current liquid-metal-based strain sensors are incapable of resolving small pressure changes in the

205 L2 oncoprotein lacks the splicing domain and is incapable of altering splice-site selection despite r

206 Most measurement approaches, however, are incapable of assessing stiffness in the presence of

207 e to bind substrate similar to wild type but was incapable of releasing substrate during its transfer

208 hat chlorobiphenyl vancomycin analogues that are incapable of binding substrates nevertheless inhibit

209 horyl oxygens, whereas solvents such as DMSO are incapable of forming such bonds.

210 Existing sequence association tests are incapable of identifying such marker sets or individ

211 optic nerve, a CNS pathway long believed to be incapable of supporting such growth.

212 hiroptical response of a molecular monolayer is incapable of inducing such a large chiroptical effect

213 PPh3)2, AuCl, AuCl(PPh3), CuI, and Cu2(OTf)2 were incapable of catalyzing such additions.

214 the nitrite-reducing activities of the cell are incapable of reducing sulfite at a rate sufficient t

215 MogA was incapable of activating sulfite oxidase expressed in

216 GS alone is incapable of starting synthesis of a glycogen particl

217 In contrast, NK cells are incapable of destroying T-cell blasts infected with

218 Muc5ac-deficient mice were incapable of expelling T. muris from the intestine

219 required HIF-1alpha, but its presence alone was incapable of inducing target gene expression under n

220 t hTERT that retained catalytic activity but was incapable of maintaining telomere length.

221 ection of IFN-deficient STAT1(-/-) mice that are incapable of generating Th1 CD4(+) cells.

222 rtantly, DCs generated from Ifnar1(-/-) mice were incapable of initiating Th2 responses in vivo These

223 Consistent with this, centrally injected SCF was incapable of increasing thalamic mast cell populatio

224 The fact that many of these promoters are incapable of driving the synthesis of a meaningful p

225 Furthermore, cells lacking both Rb and Lin37 are incapable of exiting the cell cycle.

226 judicious use of ventilatory modalities that are incapable of meeting the ventilatory demands of the

227 The HAP1-A12 cells are incapable of producing the c-subunit, but they prese

228 quently emerge in chronically infected hosts are incapable of producing the IFN-gamma protein.

229 at the helicase-dead mutant recq4 transgenes are incapable of rescuing the null mutation, demonstrati

230 osed surfaces of cross-linked viruses should be incapable of accessing the target cell surface and me

231 Light-excited AppA was found to be incapable of forming the AppA-PpsR(2) antirepressor c

232 ion in the absence of cAMP, the F435W mutant is incapable of adopting the fully extended and active c

233 ) Escherichia coli K12 MG1655 DeltamotA that is incapable of encoding the motor torque generator for

234 This criterion, however, is incapable of explaining the three-dimensional polymod

235 The alpha3 collagenous domain is incapable of incorporating the alpha5 chain, resultin

236 nkyrin-B, a closely related ankyrin isoform, is incapable of preserving the lateral membrane followin

237 of the S4 segment within the voltage sensor is incapable of producing the observed gating charge val

238 ted C horizontal lineO activation, while [B] is incapable of promoting the same transformation.

239 ion-defective mutant of SpRheb (SpRheb-SVIA) is incapable of restoring the normal cell cycle profile

240 deletion mutant of V. cholerae strain N16961 is incapable of surviving the passage through the infant

241 Y54F is incapable of transcribing the weak tRNA(Cys) promoter

242 p2d/d as in control mice, the uterine stroma is incapable of undergoing the decidual reaction to supp

243 The mutant was incapable of avoiding the anti-microbial effect of I

244 This chimeric transgene was incapable of correcting the morphological pathology

245 g the polyamines spermidine and spermine and was incapable of recovering the acetylated polyamine N(1

246 xpression of 5 HOXA13-upregulated genes; but was incapable of repressing the expression of Ngef and C

247 retrieved the grape from an experimenter who was incapable of seeing the grape rather than an experim

248 The oxidized BDBA was incapable of triggering the aggregation of citrate-c

249 rd Nanopore reads, because existing packages were incapable of assembling the long read lengths (5-50

250 ruses induced a high level of type I IFN and were incapable of causing the spread of infection.

251 ed, and the recruited inflammatory monocytes were incapable of killing the T. gondii parasites.

252 s that the exercise countermeasures employed were incapable of providing the high intensity needed to

253 ient in components of the Nalp3 inflammasome were incapable of secreting the proinflammatory cytokine

254 ere we report that geriatric satellite cells are incapable of maintaining their normal quiescent stat

255 bone marrow long-term repopulating cells, it is incapable of mediating their transformation.

256 t) and exogenous (community) viruses, and to be incapable of controlling them as quickly and effectiv

257 legs are too slow to generate waves, should be incapable of propelling themselves along the surface.

258 could enforce synchrony on subclusters that were incapable of synchronizing themselves.

259 nable to localize to cell-ECM adhesion sites is incapable of exerting these effects.

260 In contrast, c-MYC is incapable of maintaining these tumors in the absence

261 valent site is changed subtly and the enzyme is incapable of binding thiophosphate.

262 redox center, C489S, C490S, and C489S/C490S, are incapable of reducing thioredoxin and can only be re

263 difficulties, and studies with older infants are incapable of resolving this issue.

264 with deletions of the gene for NADPH oxidase were incapable of expressing this early oxygen-dependent

265 dal inputs when presented individually, they were incapable of synthesizing this information.

266 st prominently the D129G CaM mutation, which was incapable of stimulating Thr(286) autophosphorylatio

267 once formed during transcription, appear to be incapable of interconverting through unfolding and re

268 at position 229 (m229), the latter of which is incapable of signaling through TLR5.

269 We also find that the TTR amyloid is incapable of binding thyroxine as monitored by either

270 3 did not have comparable effects, and tmRNA was incapable of attacking TnaC-tRNA(2)(Pro) in stalled

271 r than the size of solvated electrolyte ions are incapable of contributing to charge storage.

272 EpiSCs are incapable of contributing to chimerism, indicating t

273 eta receptor 1 (IFNAR-deficient mice), which are incapable of responding to type I IFNs, were substan

274 The phosphorylation-induced DLC1 monomer is incapable of binding to its substrate Bim.

275 e or mutated CD28 in its cytosolic tail that is incapable of binding to Lck, phosphoinositide 3-kinas

276 2-R86K, an SH2-deficient mutant of Grb2 that is incapable of binding to PLD2, failed to induce an enh

277 is locked into an extended conformation that is incapable of transitioning to a compressed filament.

278 D71A mutant receptor, which binds ligand but is incapable of transitioning to an active state, failed

279 ILK-binding competent LIM5-deletion mutant, was incapable of localizing to cell-ECM contact sites, s

280 fference in the motif and lacks the C target are incapable of editing tobacco psbE C214 substrates, i

281 binding that are unable to localize to PC-HC are incapable of stimulating transcription from reporter

282 Additionally, exogenously introduced p53 was incapable of activating transcription from p53 respo

283 These mutants were incapable of inhibiting transcription and downregul

284 protein traps the ribosome in a complex that is incapable of initiating translation.

285 ne (A795P) enhances NF-kappaB activation but is incapable of mediating TRIF-dependent IFN response fa

286 mice, CD8+ T cells lack NKG2D expression and are incapable of mounting tumor-specific responses.

287 p100 D(b)-restricted peptide, hgp100(25-33), were incapable of rejecting tumors.

288 c cells (BMDC) isolated from MyD88(-/-) mice were incapable of producing two important Th1 instructiv

289 rom higher-eukaryotes, including Drosophila, are incapable of binding uracil.

290 led that RAGE-binding AGEs free of endotoxin were incapable of inducing vascular cell adhesion molecu

291 Because the vector is incapable of synthesizing viral proteins, a short cou

292 null mice cannot fertilize eggs in vitro and are incapable of fusing with eggs that lack zona pelluci

293 Significantly, RhoA-T37A mutant, known to be incapable of interacting with many well-known Rho eff

294 the U2AF(35) RS domain and, therefore, might be incapable of interacting with SR proteins.

295 Further, we show that human NKG2D is incapable of associating with DAP12 and provide evide

296 d bone resorption, as does VCL(P878A), which is incapable of interacting with Arp2/3.

297 sion of a dominant-negative form of Cas that is incapable of interacting with Crk inhibits Bmx-induce

298 ode a noncytopathic VEEV capsid protein that is incapable of interfering with the innate immune respo

299 gative p53 or in heterozygous p53 knockouts, is incapable of synergizing with Ha-ras to induce bladde

300 hat other chaperones, such as ClpB and ClpX, were incapable of activating WT pi.