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1 of 99mTc-HYNIC-IgG in normal human subjects is nearly identical to 111In-DTPA-IgG.

2 Furthermore, these isolates are nearly identical to a 2007 isolate from Honduras and

3 sequent isolation of its cDNA revealed it to be nearly identical to a bovine protein expressed in the

4 f the putative terminator were determined to be nearly identical to a region in the M type 1 genome a

5 cant 9 bp long DNA consensus sequence, which is nearly identical to a consensus derived from several

6 Unexpectedly, the ACAA tetraloop structure is nearly identical to a known tetraloop fold, previousl

7 At intervals of more than three megabases it is nearly identical to a map built in Europeans.

8 It is nearly identical to a recently reported human JNKK2 a

9 arboxyl-terminal portion of the ENT2 protein was nearly identical to a smaller protein in the GenBank

10 ha4beta2 nAChRs formed from subunits with M1 were nearly identical to affinities of alpha4beta2 nAChR

11 aerobactin genes and an integrase gene that was nearly identical to an int gene found in Escherichia

12 inst CFH domains 19 and 20 (CFH19-20), which are nearly identical to CFHR1 domains 4 and 5 (CFHR14-5)

13 T-452 genomes are composed by two parts that are nearly identical to corresponding regions in ST-24 (

14 ia water, whereas delta(2)H of essential AAs was nearly identical to delta(2)H in diet.

15 sociated Cyclospora-like organisms (Cyc-bab) are nearly identical to each other and are distinct from

16 moter-Binding Factor-1 and 2), respectively, are nearly identical to each other and are similar to th

17 Spectral parameters of these mutants are nearly identical to each other and to the wild type

18 ne, the spectra of YbSi(n)(-) and EuSi(n)(-) are nearly identical to each other, while in the other t

19 ream from each of the two human Calpha genes are nearly identical to each other.

20 array and the dye film deposited on glass to be nearly identical to each other.

21 rmer effects on peripheral nerve development were nearly identical to effects obtained with injected

22 almonella phage P22, while other early genes are nearly identical to Escherichia coli phages lambda a

23 FeLIX is nearly identical to FeLV-B envelope sequences that en

24 revealed the presence of a gene, fhaS, that is nearly identical to fhaB, the FHA structural gene.

25 the coding region and the gene organization were nearly identical to human.

26 in a region of the downstream promoter that is nearly identical to its mouse homologue.

27 the fission yeast Schizosaccharomyces pombe, is nearly identical to its sister element, Tf1, in its r

28 At the DNA level kdpA and kdpC are nearly identical to kdpB and encode pilin proteins t

29 new crystalline material, MOF-5(O(h)), that is nearly identical to MOF-5 but has an octahedral morph

30 rientation selectivity of mouse simple cells is nearly identical to monocular orientation selectivity

31 nucleotide sequence of the COA-1 transcript was nearly identical to multiple expressed sequence tag

32 These phenotypes are nearly identical to mutations in dynein heavy chain

33 The structure of the SHY protein is nearly identical to other extracellular matrix glycop

34 ecay kinetics, and zolpidem sensitivity that were nearly identical to our earlier findings in culture

35 om western gorillas comprised parasites that were nearly identical to P. falciparum.

36 nce results in embryos with a phenotype that is nearly identical to par-3, par-6, and pkc-3 mutants,

37 DAP-1 is nearly identical to PIC1, a protein that interacts wi

38 Recombinant native ATIII was nearly identical to plasma-purified ATIII, whereas K

39 ure of the V60N mutant has been obtained and is nearly identical to prior crystal structures of IFABP

40 or Nup 62; K(m) = 0.5 microM for UDP-GlcNAc) are nearly identical to purified mammalian OGT.

41 ar from those reported for NHE1 and NHE2 but were nearly identical to reported values for NHE3.

42 lative abundance of intestinal AFGP isoforms are nearly identical to serum AFGPs.

43 O) (cartilage-specific knockout) mutant mice are nearly identical to Smad1/5(CKO);Smad8(-/-) mutants,

44 of the SMN2 gene, the coding region of which is nearly identical to SMN1, except that a point mutatio

45 copy number of SMN2, a duplicated gene that is nearly identical to SMN1.

46 indicated that human and mouse HK-1 peptides were nearly identical to SP in their overall activity pr

47 nal spectra of the unphotolyzed E181Q mutant are nearly identical to spectra of the native pigment, s

48 educed amino acid sequence of the SH protein was nearly identical to subgroup A and subgroup B refere

49 ay bind SRE BP in vitro with affinities that are nearly identical to that of the wild-type SRE, where

50 e diamide-oxidized protein was determined to be nearly identical to that obtained in the absence of d

51 Chain packing in the G(o) phase was found to be nearly identical to that of the orthorhombic phase of

52 ility toward acid and urea denaturation that is nearly identical to that characterizing wild-type (WT

53 free energy of activation for opacification is nearly identical to that for the displacement of apo

54 gh the phenotype of the mutation at codon 38 is nearly identical to that for the wild-type virus, our

55 tal structure shows that the engineered site is nearly identical to that found in APX.

56 re indicated by the observed chemical shifts is nearly identical to that found in carbonmonoxy-holomy

57 ts primarily of a parallel beta-helix, which is nearly identical to that found in the pectin/pectate

58 A revealed that the actual binding interface is nearly identical to that in the computational design

59 entially cleaves an amino acid sequence that is nearly identical to that in the middle of the alpha-c

60 e of [Bmim+] [PF6(-)] in the presence of CO2 is nearly identical to that in the neat ionic liquid (IL

61 rasitized, the ensuing inflammatory response is nearly identical to that observed in the native heart

62 portion of the myr 6 cDNA sequence from rat is nearly identical to that of a previously published pu

63 of C1-RasGRP exhibits a folding pattern that is nearly identical to that of C1b-PKCdelta and is compr

64 The paracaspase domain adopts a fold that is nearly identical to that of classic caspases and homo

65 at are not surface-dependent, fXSt. Louis II is nearly identical to that of fXWT.

66 eveals that the base-pairing mode of Fm7dG:C is nearly identical to that of G:C, and Fm7dG does not i

67 he metabolic profile of the Zaprinast effect is nearly identical to that of inhibitors of the mitocho

68 The sequence of delta LF mRNA is nearly identical to that of LF mRNA; however, at the

69 Although the exon/intron structure of Nurr1 is nearly identical to that of Nur77, Nurr1 possesses an

70 The fibroadenoma MED12 mutation spectrum is nearly identical to that of previously reported MED12

71 bulk modulus of the 48 atom % solid solution is nearly identical to that of pure ReB2.

72 Its homeodomain is nearly identical to that of Rx/Rax, a transcription f

73 of 20 amino acids and a total sequence that is nearly identical to that of the 64-kDa cell surface p

74 of the antigen combining site in the complex is nearly identical to that of the complexed form of the

75 the case of K118N, the twist of the monomer is nearly identical to that of the F-actin protomer, and

76 ucture of the Mrf-2 ARID in complex with DNA is nearly identical to that of the free protein.

77 ructure of the photodissociated intermediate is nearly identical to that of the ground state NiTPP, s

78 nickel atoms, the structure of the apoenzyme is nearly identical to that of the holoenzyme, suggestin

79 t the long unique region (LUR) of the genome is nearly identical to that of the previously sequenced

80 an extensive DNase I protection pattern that is nearly identical to that of the ternary complex of TF

81 the dependency on number of experiments used is nearly identical to that present in microarrays, sugg

82 bone tertiary structure of the E200K variant is nearly identical to that reported for the wild-type h

83 the engineered EF site of the 94/98E variant is nearly identical to that within the CD site, suggesti

84 The overall risk of noncutaneous cancer was nearly identical to that expected in general populat

85 e alkylation specificity at equivalent doses was nearly identical to that found for the previously re

86 n of laminin-332 by degranulated neutrophils was nearly identical to that generated with NE alone.

87 ce risk ratio of BAV in HLHS families (8.05) was nearly identical to that in BAV families (8.77).

88 ted in a jejunal and duodenal phenotype that was nearly identical to that in the ileum after deletion

89 II activity in the treated hemophilia A mice was nearly identical to that in wild-type mice through 5

90 otic gene expression induced by TNF in vitro was nearly identical to that induced by LPS in vivo, as

91 cells, the pattern of luciferase expression was nearly identical to that observed for the different

92 genomic arrangement of the Se femA/B complex was nearly identical to that observed in Sa.

93 these SCID mice showed that their pathology was nearly identical to that observed in the original Ta

94 8 unique sequences, the most common of which was nearly identical to that of M. avium strains.

95 ed dose-dependent candidacidal activity that was nearly identical to that of native Hst5 purified fro

96 hibited by GsMTx4, and although the off rate was nearly identical to that of outside-out patches, dif

97 The EPR spectrum of (Rbr(ox))(mv) was nearly identical to that of the as-isolated or chemi

98 2.7 x 10(-13)), which had an odds ratio that was nearly identical to that of the curated case-control

99 wo samples that were sequenced, the 16S rDNA was nearly identical to that of the granulocytic Ehrlich

100 The performance of the HRM-based MAA was nearly identical to that of the MAA that included CD

101 second protein revealed that its N terminus was nearly identical to that of the MOMP and also had ho

102 he regiospecificity of toluene hydroxylation was nearly identical to that of the natural isoform, wit

103 The hamster sequence was nearly identical to that of the recently reported hu

104 its ability to form discoidal lipoproteins, was nearly identical to that of the wild type protein.

105 ctivation-specific complement fragment, C3d, was nearly identical to that of the wild-type FH19-20:C3

106 us harbored viral genome at a frequency that was nearly identical to that of wild-type gammaHV68; how

107 motor stimulation produced by 10 mg/kg 4-MMC was nearly identical to that produced by 1 mg/kg d-metha

108 of parasitemia in NOS2-/- x p47phox-/- mice was nearly identical to that seen in normal control mice

109 dimer, and the UV-visible absorption spectra were nearly identical to that of Isf.

110 A-RS7 displayed biodistribution results that were nearly identical to that of the (88)Y analog in a p

111 es of four murine frizzled homologs, Mfz3-7, were nearly identical to that of Wnt-5a and Wnt-10b.

112 in temperature and the reduction in activity were nearly identical to that reported in Experiment 2,

113 8]) promoter contains sequence elements that are nearly identical to the alpha-SNAP([Peking/PI 548402

114 channels, alpha1G, H, and I, whose currents are nearly identical to the biophysical properties of na

115 mentally determined X-ray and NMR structures are nearly identical to the computational design models.

116 nd the hydrogen-bond networks in particular, are nearly identical to the design models, and the netwo

117 These orientations are nearly identical to the dipole and quadrupole orient

118 protein complexes per microtubule attachment are nearly identical to the numbers in a budding yeast k

119 d)-2.3H(2)O.CH(3)OH (O-O(average) = 2.857 A) are nearly identical to the O-O distance observed in the

120 orrelate to predicted structural motifs, but are nearly identical to the positive ions generated from

121 ries in the complete K-12 genome sequence, 4 are nearly identical to the sequences of E. coli J96 enc

122 These sequences are nearly identical to the two human fibrinogen glycope

123 maintained breast cancer cell phenotypes to be nearly identical to the cultures on commercial polyst

124 in Florida for about a century was found to be nearly identical to the genomic sequence of a mild is

125 PCA on the compressed data is shown to be nearly identical to the same analysis on the original

126 -mm section thickness protocol were found to be nearly identical to the transverse image for all sets

127 The psMTX sequence is nearly identical to the 3' part of exon 2 through exo

128 t analysis indicate that the betaE11 antigen is nearly identical to the 4F2 heavy chain antigen, a ce

129 handed rotation angle of 56.5 degrees, which is nearly identical to the 60 degree angle in the soluti

130 The active site of DAHPS(Tm) is nearly identical to the active sites of the other two

131 This structure is nearly identical to the antiparallel junction formed

132 tion is strongly affected by (GT)(4) binding is nearly identical to the assembly domain defined previ

133 scillation period (4.10 +/- 0.02 nt/protein) is nearly identical to the binding site size obtained at

134 uels (a No-Biofuel scenario) the carbon sink is nearly identical to the case with biofuels, but emiss

135 palindrome sequence (CATGTGn(5)GGCGTG) that is nearly identical to the CHO-RE of the l-type pyruvate

136 Conformer T- is nearly identical to the conformation seen in the X-ra

137 the distribution of inter-cluster distances is nearly identical to the distribution of inter-hot spo

138 the sequence of OC-derived hexapeptide (HP) is nearly identical to the E2 region of the oxytocin rec

139 This phenotype is nearly identical to the effect of injection of either

140 mation of FHA2 both at neutral and at low pH is nearly identical to the final low-pH conformation of

141 This factor is nearly identical to the human protein, contains multi

142 The structure is nearly identical to the MCP structures of the eukaryo

143 centrations of monovalent ions, a state that is nearly identical to the native folded state in the pr

144 tion, while the sequence-dependent structure is nearly identical to the native Holliday junction of d

145 scillation period (4.05 +/- 0.02 bp/protein) is nearly identical to the occluded binding site size ob

146 normal axis determined in the present study is nearly identical to the orientation of the nitroxide

147 tructures reveal that recombinant fibrinogen is nearly identical to the plasma protein but with minor

148 ce encodes a protein of 495 amino acids that is nearly identical to the previously reported protein s

149 of the 3.8-kb genomic fragment of HHV-6A(GS) is nearly identical to the published sequence of HHV-6A

150 ately n-dTn, with an intrinsic rigidity that is nearly identical to the rigidity of the corresponding

151 ter rate of mutational decay of male fitness is nearly identical to the same ratio in Drosophila.

152 This KCNQ2/KCNQ3 motif is nearly identical to the sequence on NaV alpha subunit

153 parison with that of NO-Fe(II)BlmDNAb, which is nearly identical to the spectrum of NO-Fe(II)Blm.

154 One of the overlapping spectra is nearly identical to the spectrum of wild type, and is

155 rate limiting with an actin dependence that is nearly identical to the steady-state ATPase parameter

156 emagglutinin complex in the presence of EDTA is nearly identical to the structure of the complex crys

157 bstituted with alanine (P6A), an antagonist, is nearly identical to the structure with wild-type Tax

158 rcuit current (J(sc)) of the PBHJ solar cell is nearly identical to the sum of those of the individua

159 Our ML estimate of the time to the WGD is nearly identical to the time to the speciation event

160 Since the IP3 receptor in Xenopus oocytes is nearly identical to the type I receptor of mammalian

161 onstruct three ancestral dynamins: The first is nearly identical to the ubiquitous mitochondrial divi

162 d polytetrahydrofuran (pTHF) MW distribution is nearly identical to the unreacted pTHF material.

163 of HGD--namely Glu107 to Ala (E107A), which is nearly identical to the wild type in structure, stabi

164 activity and DNA binding of the K142A enzyme is nearly identical to the WT enzyme.

165 E 47 and a linear range of 0.3-2ng/ml, which was nearly identical to the best heterologous competitiv

166 m in association with human macular XBP that was nearly identical to the CD spectrum induced by GSTP1

167 tative catalytic motif within the GDE domain was nearly identical to the corresponding domain of GDPD

168 trol of the Xenopus rhodopsin gene promoter, was nearly identical to the endogenous rhodopsin.

169 hs due to CVD (SMR = 1.02, 95% CI = 0.9-1.6) was nearly identical to the expected number.

170 in each experiment, and the sensor response was nearly identical to the frequency change during atta

171 s observed immediately after the laser pulse was nearly identical to the one-electron-reduced form of

172 rsus PCI on 12-month angina frequency scores was nearly identical to the overall benefit in the inten

173 type of mice lacking both endogenous opioids was nearly identical to the phenotype of mice mutant for

174 The DNA sequence of the p28 gene was nearly identical to the previously reported sequence

175 This value was nearly identical to the product of the joint probabi

176 the pathway the protein took as it unfolded was nearly identical to the subsequent refolding pathway

177 D estimated from the wormlike chain modeling was nearly identical to the value measured using isother

178 genes contained 3'-untranslated regions that were nearly identical to the 3'-untranslated regions of

179 rd uptake value ratio (1.20) thresholds that were nearly identical to the a priori distribution volum

180 Basmati-like accessions were nearly identical to the ancestral Japonica haplotyp

181 host lysis, integration, and DNA replication were nearly identical to the corresponding genes in phiE

182 The M. spretus-derived env substitutions were nearly identical to the corresponding regions in pr

183 ough molecular and morphogenetic stages that were nearly identical to the developing antrum of the mo

184 ucine in the carboxyl-terminal position, and were nearly identical to the leader sequence-derived pep

185 ulated apoptosis through endogenous Galpha12 were nearly identical to the mechanisms identified in QL

186 The rates of patient-reported global benefit were nearly identical to the pain response rates and did

187 of the ROC criterion values, and most levels were nearly identical to the prospective group means aft

188 uence analysis demonstrated that these cDNAs were nearly identical to the published sequences for CYP

189 The sites of oxaliplatin adducts were nearly identical to the sites of cisplatin adducts

190 Both physical and arithmetic mixtures were nearly identical to the spectrum for wild-type KatG

191 72 from Colombia, and B354 from California), were nearly identical to the T30 sequence.

192 nces of human alpha 1- and beta 2-syntrophin are nearly identical to their homologues in mouse, sugge

193 by these enzymes toward TFV amidate prodrugs are nearly identical to their preferences displayed agai

194 Five subtypes were nearly identical to their tissue-of-origin counterp

195 s rise per turn and helical twist per dimer, are nearly identical to this DNA conformation, allowing

196 ta and yields hospital quality measures that are nearly identical to those based on the true data.

197 s of European ancestry within our EHR cohort are nearly identical to those derived from a genome-wide

198 s in response to changes in the environment, are nearly identical to those in chickens.

199 o acids that comprise the HTH motifs of ExsA are nearly identical to those in LcrF/VirF, the activato

200 These enzymes and genes in B. cereus are nearly identical to those in the very closely relate

201 of genes' expression inferred from the model are nearly identical to those measured in embryos costai

202 These UV Raman spectral changes are nearly identical to those observed for the rhodopsin

203 tional potential (mEJP) decay to values that are nearly identical to those observed in DGluRIIA mutan

204 on tests for C. trachomatis on urine samples are nearly identical to those obtained on samples collec

205 These values are nearly identical to those obtained with the wild-typ

206 gth and reactivity toward triphenylphosphine are nearly identical to those of (mes)3Ir=O, the osmium

207 ects with surface properties and orbits that are nearly identical to those of 2003 EL61.

208 , resulting in CDR3alpha loop sequences that are nearly identical to those of canonical TCRs.

209 s an experimental pI and molecular mass that are nearly identical to those of dSCP2.

210 and magnetic circular dichroism spectra that are nearly identical to those of ferrous-O2 cytochrome P

211 opic features of the type 1 Cu site of Fet3p are nearly identical to those of fungal laccase, indicat

212 structure and organization of the human gene are nearly identical to those of its mouse counterpart.

213 m the putative source or (ii) sequences that are nearly identical to those of laboratory strains.

214 es of tamoxifen-HDACi conjugates (Tam-HDACi) are nearly identical to those of tamoxifen.

215 overall folding and active site architecture are nearly identical to those of the analogous complex c

216 ters and the pH-rate profile of both enzymes are nearly identical to those of the mature protease.

217 l-2-(4-methyl-imidazole-1-yl)-phenol radical are nearly identical to those of the natural abundance (

218 ision, immunity, Nin region, and lysis genes are nearly identical to those of the short-tailed Salmon

219 Asn3+ motif-bearing V alpha chain sequences are nearly identical to those utilized by the BP-specifi

220 X from China, Egypt, and India were found to be nearly identical to those of historical viruses isola

221 res within the cIAP2 5' UTR were observed to be nearly identical to those required for ribosome shunt

222 The structure of the catalytic domain is nearly identical to those of most other polymerase fa

223 structure and composition of these particles was nearly identical to those of first-generation Ad vec

224 whereas the C-terminal half of this protein was nearly identical to those of previously characterize

225 ulated by using the true FISP cine MR images were nearly identical to those at autopsy (R = 0.82, sta

226 ties determined using changes in ATP and ADP were nearly identical to those determined using previous

227 sequences from this potential source patient were nearly identical to those from cases (97.8%-98.5% s

228 de-isolation MS/MS, and quantitative results were nearly identical to those from LC-MS/MS.

229 d genotypic mapping by PCR gave results that were nearly identical to those from phenotypic mapping.

230 OI estimates from the RE plot and the bcSUVR were nearly identical to those from the Logan plot with

231 A-positive pathogenic E. coli strains tested were nearly identical to those in S. dysenteriae, indica

232 ations after a second injection of PPS14-C3d were nearly identical to those induced by secondary immu

233 nd their inferred evolutionary relationships were nearly identical to those inferred on the basis of

234 mes measured in Fm and Fm' (with NPQ) states were nearly identical to those obtained from the control

235 xhibited by histiocytic sarcoma-bearing mice were nearly identical to those of animals in which leuke

236 Several OP sequences were nearly identical to those of cultivated chemolithot

237 n both Ca(2+)-free and Ca(2+)-bound myr-Frq1 were nearly identical to those of free myristate in solu

238 of factor Xa by both of the genetic variants were nearly identical to those of recombinant native ATI

239 d CD spectra of these subunit-type complexes were nearly identical to those of subunit complexes form

240 from jaw rotations of 0.7 degrees or larger were nearly identical to those of the standard.

241 response to antigen-receptor signaling that were nearly identical to those seen in vav-/- cells.

242 rall treatment outcomes for the BWS patients were nearly identical to those without BWS, with overall

243 gly, p53 forms a tetramer on the BAX-RE that is nearly identical to what has been reported on other R

244 ethionine decarboxylase (AdoMetDC) depletion was nearly identical to what was observed in cells treat

245 se-associated mutants, A30P, A53T, and E46K, are nearly identical to wild-type alphaS, but oligomeriz

246 tation and emission spectra for this protein are nearly identical to wild-type GFP.

247 onformation of the G202A mutant was found to be nearly identical to wild-type, G alpha(i1)(G202A) x G

248 k(cat)/K(M) in the range 15 to 35 degrees C, is nearly identical to wild-type and close to half that

249 e complex with arginine, nitrate, and MgADP, was nearly identical to wild type.

250 d collagen synthesis in MIP-1alpha(-/-) mice was nearly identical to wild-type controls.

251 he inactivation-deficient hH1 mutant, hH1Q3, was nearly identical to wild-type hH1 V(a), both before

252 Ag ([4-hydroxy-3-nitrophenyl]acetyl hapten) were nearly identical to wild-type littermate controls.

253 ties of TS:C43A and TS:C210A mutant proteins were nearly identical to wild-type TS, while TS:C180A an

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