ライフサイエンスコーパス: nuclear fraction

1 ized predominantly in the cytosol and in the nuclear fraction.

2 is confirmed the identity of Gbeta(5) in the nuclear fraction.

3 ctor VIIa, tissue factor is not found in the nuclear fraction.

4 but not Ggamma(2/3) immunoreactivity in the nuclear fraction.

5 gradation or they reside in a unique soluble nuclear fraction.

6 ctivities are localized predominantly in the nuclear fraction.

7 in membrane, and 10% was associated with the nuclear fraction.

8 ed mutant pre-U2 RNA was not observed in the nuclear fraction.

9 In addition, PLDgamma was detected in the nuclear fraction.

10 owest-mobility forms are associated with the nuclear fraction.

11 levels of the DNA-PK and its activity in the nuclear fraction.

12 ns IE-1 and IE-2 were present in the soluble nuclear fraction.

13 esent in only trace amounts in the cartilage nuclear fraction.

14 he cytoplasmic fraction but decreased in the nuclear fraction.

15 4 months, and are predominantly found in the nuclear fraction.

16 gnificantly increased AP-2beta levels in the nuclear fraction.

17 PII) isolated from either the cytoplasmic or nuclear fraction.

18 ted Gli-1/2 or Twist-1 protein levels in the nuclear fraction.

19 in HSV-infected cells, especially in a crude nuclear fraction.

20 and nitration were significantly elevated in nuclear fraction.

21 rom canonical snoRNAs found in the insoluble nuclear fraction.

22 tain a 75 kDa CT-2 reactive peptide in their nuclear fraction.

23 , MaoB, and cytochrome b(5)) were in the non-nuclear fraction.

24 ation and localizes predominantly to the non-nuclear fraction.

25 of Zta or its association with the insoluble nuclear fraction.

26 trated endogenous apelin receptor species in nuclear fractions.

27 lular level in cytosolic, mitochondrial, and nuclear fractions.

28 I PKA (CalphaRIIbeta) in the particulate and nuclear fractions.

29 lk of specific estradiol binding is found in nuclear fractions.

30 noreactivity in the membrane, cytosolic, and nuclear fractions.

31 distributed in both the cytoplasmic and the nuclear fractions.

32 ed cells cPLA(2) mass shifts from cytosol to nuclear fractions.

33 e site-inhibited factor VIIa associates with nuclear fractions.

34 epletion-induced association of cPLA(2) with nuclear fractions.

35 oluble fraction but also in the membrane and nuclear fractions.

36 sistant analogs progressively accumulated in nuclear fractions.

37 ins for Phd and CRX in retinal cytosolic and nuclear fractions.

38 activated PKCdelta from the nuclear and non-nuclear fractions.

39 nscripts are almost entirely concentrated in nuclear fractions.

40 of FAC protein was reproducibly detected in nuclear fractions.

41 of the Mcl-1 protein seems to be located in nuclear fractions.

42 ed in both the membrane/cytoskeletal and the nuclear fractions.

43 s were decreased both in the cytoplasmic and nuclear fractions.

44 beta-catenin levels in both cytoplasmic and nuclear fractions.

45 associates with let-7 primary transcripts in nuclear fractions.

46 in sarcoplasmic reticulum (SR)/membrane and nuclear fractions.

47 d ATF6 with a coordinate increase of ATF6 in nuclear fractions.

48 of beta-catenin from membrane to cytoplasmic/nuclear fractions.

49 Furthermore, the p75 ICD was localized in nuclear fractions.

50 -miRNAs are enriched in chromatin-associated nuclear fractions.

51 0 kDa polypeptide in mitochondria but not in nuclear fractions.

52 BV-2 cells is enriched in mitochondrial and nuclear fractions.

53 t analysis of medium and the cytoplasmic and nuclear fractions.

54 rylated proteins in cytosolic, membrane, and nuclear fractions.

55 y further confirmed the presence of Grb14 in nuclear fractions.

56 ly in cytosolic but not in mitochondrial and nuclear fractions.

57 pase substrates DFF-45, lamin A, and PARP in nuclear fractions.

58 J-domain protein enriched in microsomal and nuclear fractions.

59 d (cytosolic) fraction, and a tightly bound (nuclear) fraction.

60 the protein could be detected mainly in the nuclear fraction 4 h after viral reactivation in Akata c

61 hat the c-fos protein level increased in the nuclear fraction after a 6-hour exposure to light, but w

62 s were determined to be the strongest in the nuclear fraction after DNA damage, which suggested forma

63 ikewise, expression of CXCR4 was detected in nuclear fractions among several prostate cancer cell lin

64 tribution of cyclooxygenase-2 (COX-2) in the nuclear fraction and approximately 10% in the cytosolic

65 enous PP-IX accumulated predominantly in the nuclear fraction and caused nuclear shape deformation an

66 PMA treatment increased RFX1 in the nuclear fraction and decreased it in the cytosol without

67 hondria) removes co-expressed Bcl-2 from the nuclear fraction and reverses its effect on transcriptio

68 of STAT1 and STAT3 from the cytosolic to the nuclear fraction and with an increase in STAT1 and STAT3

69 Both Dicer and Ago2 were detected in the nuclear fraction, and reduction of Dicer altered the str

70 Env (P70(env)) was found exclusively in the nuclear fraction, and size of its polypeptide backbone w

71 ter macrophages, localize in the cytosol and nuclear fractions, and induce apoptosis.

72 of linear viral DNA in both cytoplasmic and nuclear fractions, and there were no significant differe

73 ene glycol-based buffers and highly enriched nuclear fractions are obtained using Percoll density gra

74 s, cyclin E and cdk2 were exclusively in the nuclear fraction, associated with one another.

75 and full-length HIV-1 cDNA was found in the nuclear fraction at all time points.

76 ed from whole cells and from cytoplasmic and nuclear fractions at different times postinfection.

77 that the association of the protein with the nuclear fraction becomes labile as S phase progresses.

78 tant protein was detected in cytoplasmic and nuclear fractions but did not affect cell growth.

79 An antibody to IRS-1 immunoprecipitates from nuclear fractions (but not from cytosolic fractions) the

80 PKC immunoreactivity was observed in a crude nuclear fraction, but PKC-delta and -zeta were found in

81 RII) of PKA were present in the precartilage nuclear fraction, but were undetectable or present in on

82 H activity was subnormal in both cytosol and nuclear fractions, but its protein expression and nitrat

83 he first 2 h of infection but shifted to the nuclear fraction by 6 h postinfection.

84 uded markers to control for contamination of nuclear fractions by cytoplasmic proteins.

85 l characteristics of CREB were determined in nuclear fractions by means of Western blot and cyclic ad

86 DEX), or RU486 was measured in cytosolic and nuclear fractions by western blotting and laser confocal

87 In contrast, PR in the nuclear fraction consisted of complexes containing hsp90

88 ays (EMSAs) demonstrated that mesangial cell nuclear fractions contain a multimeric protein complex t

89 uclein oligomer, whereas the cytoplasmic and nuclear fractions contained both the oligomer and the mo

90 jority of labeled TFO was recovered from the nuclear fraction containing genomic DNA.

91 This nuclear fraction contains nascent transcripts and RNA un

92 Da activity partitions preferentially to the nuclear fraction during isolation.

93 then lysed, cPLA(2) remains associated with nuclear fractions even if the homogenate [Ca(2+)] is mar

94 5 activity, and Western blot analysis of the nuclear fraction extract for p50.

95 y was used to screen partially purified HeLa nuclear fractions for their ability to stimulate (CTG)(n

96 s of an active form of CaN and NFATc4 in the nuclear fraction from the cortex of patients with AD.

97 IF-2alpha protein expression was detected in nuclear fractions from adipose and muscle, increasing ap

98 domyosarcoma cells but was not detectable in nuclear fractions from colon carcinoma HEK293 or IMR90 c

99 of activated STAT1 alpha from cytoplasmic or nuclear fractions from IFN gamma-treated adult myocytes

100 revealed low enzyme activity against NAA in nuclear fractions from normal rats.

101 scale proteomics analysis of cytoplasmic and nuclear fractions from normal versus regenerating mouse

102 stern blots showed increased FGF2 protein in nuclear fractions from osteoblasts of Hyp mice.

103 Coimmunoprecipitation studies from nuclear fractions, gel-shift assays, and transient trans

104 ta42 as follows: (i) biochemical analysis of nuclear fractions; (ii) detection of biotin-labeled Abet

105 VEGF enriched ETS-1 in the nuclear fraction in a dose-dependent manner.

106 ion of helicase activity was observed in the nuclear fraction in AD IPL.

107 n of the p65 subunit from the cytoplasmic to nuclear fraction in Npr1-/- mice.

108 zation, but endogenous C3G is a component of nuclear fractions in a variety of cell types.

109 calized in perinuclear mitochondria, ER, and nuclear fractions in CMs, and FYN expression negatively

110 ch is detected specifically in cytosolic and nuclear fractions in SCA6 patients, is associated with t

111 exhibited greater association with isolated nuclear fractions in subjects with mild cognitive impair

112 anscriptomic approaches applied to different nuclear fractions, including mammalian native elongating

113 Enriched nuclear fractions may be used in "run-on" assays to meas

114 l/L TGF-beta, which was 2-fold higher in the nuclear fraction; mRNA levels were unaffected.

115 nsity (NARPP-50), and one was located in the nuclear fraction (NARPP-21).

116 phorylated 5-lipoxygenase accumulates in the nuclear fraction, not with the membrane or cytosolic fra

117 ne glycosylase activity were observed in the nuclear fraction of AD hippocampal and parahippocampal g

118 h translation-like features operating in the nuclear fraction of cells prevents the expression of pot

119 ulated in response to nonsense codons in the nuclear fraction of cells.

120 s of PTC-bearing TCR-beta transcripts in the nuclear fraction of cells.

121 ects retention of PTC(+) TCRbeta mRNA in the nuclear fraction of cells.

122 but with thermal stress p28 relocated to the nuclear fraction of cellular proteins.

123 FZA-B is found predominantly in the nuclear fraction of COS cells expressing an FZA-B transg

124 o such reduction is observed in RNA from the nuclear fraction of DM cell lines.

125 aphy, phosphopeptides were enriched from the nuclear fraction of HeLa cell lysate.

126 The protein is detected in the nuclear fraction of HeLa cell lysates on Western blots a

127 ncubation of apo-10'-lycopenal with the post-nuclear fraction of hepatic homogenates of ferrets resul

128 ive nuclear factor kappaB (NF-kappaB) in the nuclear fraction of hepatocytes, suggesting that CIH ind

129 t analysis of DNA isolated from the enriched nuclear fraction of infected cells and by a semiquantita

130 GFR-1alpha but not FGFR-1beta isoform in the nuclear fraction of L6 myoblast transfectants suggests t

131 At 6 hours, NF-kappaB p65 was increased in nuclear fraction of lactate-treated compared with contro

132 The nuclear fraction of lipin-1b is increased when CTDNEP1 a

133 cal results: Little ZO-1 was detected in the nuclear fraction of lysates of serum-starved cells, but

134 s (PTCs) can cause the decay of mRNAs in the nuclear fraction of mammalian cells.

135 oximately 66 kDa protein present only in the nuclear fraction of MC3T3E1 osteoblasts.

136 mor cells examined, was most abundant in the nuclear fraction of MCF-7 breast cancer cells.

137 show that geometric constraints altered the nuclear fraction of myocardin-related transcription fact

138 t WASP is present in the cytoplasmic but not nuclear fraction of normal human peripheral blood mononu

139 MTS-p53-290 cells demonstrated that only the nuclear fraction of p53 controlled cellular proliferatio

140 CHL1 show that CHL1 is predominantly in the nuclear fraction of S.

141 sociation and revealed a digitonin-insoluble nuclear fraction of S100A2, which was confirmed by immun

142 is accompanied by the phosphorylation of the nuclear fraction of ScHxk2 at serine 15 and the transloc

143 RP2 as shown by an increase in NFATc3 in the nuclear fraction of SFRP2-treated endothelial cells.

144 depressed TCR-beta mature mRNA levels in the nuclear fraction of stably transfected cells.

145 at the loss of a high-affinity AEBS from the nuclear fraction of the 289/TAM6 cell line correlates wi

146 The nuclear fraction of the endogenous FRG1 is localized in

147 mTc glucarate localized predominantly in the nuclear fraction of the infarct, with lesser extents in

148 red in similar amounts and entirely from the nuclear fraction of these transiently transfected cells.

149 ut not Ggamma(2) supported expression in the nuclear fraction of transfected wild-type Gbeta(5).

150 unofluorescence assay and was present in the nuclear fraction of unsynchronized cells by immunoblot.

151 ajority of BRCA1 protein is localized to the nuclear fraction of untreated MCF10A cells.

152 ion between WTX and TRIM28 suggests that the nuclear fraction of WTX plays a role in epigenetic silen

153 thyroid hormone receptor (TRbeta1 or TR) in nuclear fractions of 293T cells, resulting in serine pho

154 Activated MAPK was present in nuclear fractions of all T(4)-treated cells and co-immun

155 sing ionophore, readily dissociates from the nuclear fractions of ATP-replete cells upon reduction of

156 hole-cell lysates, microsomal fractions, and nuclear fractions of both cell lines by competing [3H]TA

157 D1 polypeptides are found exclusively in the nuclear fractions of both G1- and S-phase cells.

158 gh the full-length FGF-1 was detected in the nuclear fractions of both NIH/3T3 and NR33 cells, its ha

159 ds were also observed in the cytoplasmic and nuclear fractions of cells.

160 ates ERK1 and ERK2 in cytosolic and purified nuclear fractions of INS-1 cells and more of each is fou

161 g Hu proteins are present in cytoplasmic and nuclear fractions of N cells and one of them, HuD, binds

162 of internalized bFGF within cytoplasmic and nuclear fractions of native and HSPG-deficient VSMC show

163 icant amounts of bFGF were only found in the nuclear fractions of native cells.

164 protein levels of 3 transcription factors in nuclear fractions of postmortem samples from cerebellar

165 rum-starved cells, but ZO-1 was found in the nuclear fractions of rabbit corneal and 293T fibroblasts

166 NK-1R pre-mRNA species were enriched in the nuclear fractions of spinal cord samples, and in the ste

167 p53 is functionally activated in nuclear fractions of the ipsilateral LGN at 5 days postl

168 p65 subunit of nuclear factor kappaB in the nuclear fractions of these T cells.

169 Aly, TAP, Upf3X and Upf2 are detected in the nuclear fraction on CBP80-bound but not eIF4E-bound mRNA

170 the levels of PTC-bearing transcripts in the nuclear fraction prepared by two independent methods.

171 in, a biotinylated FGFR-1 is detected in the nuclear fraction prepared from FGF-2-treated, but not un

172 minimal presence in the inclusion-containing nuclear fractions prepared from Chlamydia-infected cells

173 Using isolated cytosolic and nuclear fractions prepared from rapid-autopsy postmortem

174 f endogenous p53 and HDM2 occurs in isolated nuclear fractions prepared from these recovering cells.

175 which lack SR proteins) required SRp40 and a nuclear fraction previously found to be required for ASF

176 ein originally identified from the insoluble nuclear fraction, referred to as the nuclear matrix.

177 mmunoreactivity with the capsid/tegument and nuclear fractions, respectively.

178 Immunoanalysis of nuclear fractions revealed that the enzyme was retained

179 ited basal levels of phosphorylated c-Jun in nuclear fractions, revealing that active c-Jun is presen

180 increase of the active form of Notch1 in the nuclear fraction, suggesting a novel intracellular mecha

181 titutes several percent of the enzyme in the nuclear fraction, suggesting that the distribution of th

182 s of all five tRNAs were present only in the nuclear fraction, suggesting that the mature tRNAs repre

183 alpha protein in both the cytosolic and the nuclear fractions, suggesting an increase in nuclear upt

184 r Nrf-2 levels in vitro, particularly in the nuclear fraction, than chondrocytes exposed to normal gl

185 ed between the cytosolic, mitochondrial, and nuclear fractions, the novel MGL activity expressed by B

186 an induced the mobilization of CHOP from the nuclear fractions to phagocytic vesicles.

187 onse is a dramatic partitioning shift in the nuclear fraction-to-cytoplasmic fraction mRNA ratio that

188 37 mutant particles were associated with the nuclear fraction, unlike wild-type particles, which were

189 FLAG-tagged Zta was purified from a nuclear fraction using FLAG antibody immunopurification

190 Factor VIIa associated with the nuclear fraction was intact and functionally active.

191 nt leukotriene A(4) hydrolase in the soluble nuclear fraction was substantiated by two different cell

192 strated that the increase in beta-catenin in nuclear fractions was accompanied by an even larger incr

193 tion of dsRNase from rat liver cytosolic and nuclear fractions was effected.

194 In the same nuclear fraction, we determined the catalytic activity o

195 py autoradiography, and SDS-PAGE analysis of nuclear fractions, we show that the heregulin-beta1(1-24

196 Nuclear fractions were immunoprecipitated and the result

197 Mononuclear cells (MNCs) were separated, and nuclear fractions were isolated.

198 ed the active form of Notch1 receptor in the nuclear fraction, whereas DDR1 knockdown cells show litt

199 d Delta BH4) were predominantly found in the nuclear fraction, whereas the non-active forms (Delta TM

200 The bulk of HsORC5p is in an insoluble nuclear fraction, whereas the other known human ORC subu

201 was associated with increased P-STAT3 in the nuclear fraction, which remained elevated at 22 h after

202 and decreased prolyl hydroxylase domain 2 in nuclear fractions, which denotes increased transcription

203 apid PKC-delta translocation to membrane and nuclear fractions, which was transient with CCK.

204 mutant was not expressed in the HEK-293 cell nuclear fraction with either co-transfectant.

205 Incubation of nuclear fractions with recombinant caspase-3 and caspase

206 y 75% of the radioactivity localizes in the "nuclear" fraction with a concentration of 0.3 pmol/mg DN