ライフサイエンスコーパス: methylcellulose

1 t hematopoietic progenitor cell replating in methylcellulose.

2 ed the growth of myeloid progenitor cells in methylcellulose.

3 silica capillaries coated with hydroxypropyl methylcellulose.

4 lyethylene glycol, polyvinylpyrrolidone, and methylcellulose.

5 limit of approximately 300 turnovers even in methylcellulose.

6 e identical set of cells after suspension in methylcellulose.

7 lived, and displayed clonogenic potential in methylcellulose.

8 medium and also potentiated penetration into methylcellulose.

9 Thimerosal had no effect on penetration into methylcellulose.

10 sion, and increased mammosphere formation in methylcellulose.

11 lonogenic hematopoietic progenitor assays in methylcellulose.

12 y small granulocyte and monocyte colonies in methylcellulose.

13 gomir abrogates their replating potential in methylcellulose.

14 blocks anchorage-independent cell growth in methylcellulose.

15 with 0.1% peptide in PBS with or without 2% methylcellulose.

16 her vehicle (control, 0.5% w/v hydroxypropyl-methylcellulose 0.1% w/v polysorbate-80; n = 9), 88 mg(

17 trabeculectomy was followed by injection of methylcellulose 2% into the anterior chamber.

18 These compounds were soluble in 0.5% methylcellulose/2% Tween-80 in water (MC/T) for oral adm

19 e sugar), psyllium (a fermentable fiber), or methylcellulose (a nonfermentable fiber).

20 e mod(-) actin only moves in the presence of methylcellulose, a viscosity-enhancing agent, where it m

21 PS-b-PEG), moderately negative hydroxypropyl methylcellulose acetate succinate (HPMCAS), highly negat

22 system of 70 % itraconazole in hydroxypropyl methylcellulose acetate succinate (HPMCAS).

23 inistered perorally and CT enteroclysis with methylcellulose administered through a nasojejunal tube,

24 simvastatin in methylcellulose (SIM/MCL) or methylcellulose alone (MCL).

25 ts following keratinocyte differentiation in methylcellulose also showed a reduction in downstream ca

26 (n = 4), or vehicle (0.5% w/v hydroxypropyl-methylcellulose and 0.1% w/v polysorbate 80; Control, n

27 e effect of edible coatings of hydroxypropyl methylcellulose and beeswax in concentrations of 10, 20,

28 e effect of edible coatings of hydroxypropyl methylcellulose and beeswax in concentrations of 10, 20,

29 BFU-E from peripheral blood were cultured in methylcellulose and BFU-E-derived colonies were harveste

30 numeration of colony-forming units (CFUs) in methylcellulose and cobblestone area-forming cell (CAFC)

31 tion in the percentage of CFU-G that form in methylcellulose and of granulocytes that develop in liqu

32 Methylcellulose and rigid intraocular lenses were genera

33 d textured pea protein with 1, 2, or 4 % w/w methylcellulose and spiked with menthone, model beef fla

34 s observed between 4 and 8 h of culturing in methylcellulose and was maintained for up to 24 h.

35 on of apoptosis, loss of colony formation in methylcellulose, and anti-AML activity in vivo.

36 ur delivery vehicles: artificial tears, PBS, methylcellulose, and aquaphor cream.

37 uding CD34(+) cells, colony-forming units in methylcellulose, and long-term culture-initiating cells)

38 reduced by extract dilution, by addition of methylcellulose, and paradoxically by addition of excess

39 ease formulation incorporating hydroxypropyl methylcellulose as a matrix system to target extended re

40 ) and the tannins determination method (with methylcellulose as a precipitant).

41 throid progenitor cells, we developed clonal methylcellulose assays by using recombinant zebrafish er

42 In methylcellulose assays, osteoblasts stimulate the develo

43 Utilizing Tpo in clonal methylcellulose assays, we describe for the first time t

44 nicity of CB33 human lymphoblastoid cells in methylcellulose assays.

45 The use of methylcellulose avoids artifacts of conventional negativ

46 In methylcellulose-based colony-forming assays, ABT-869 had

47 In short- and long-term methylcellulose-based culture, aortic cells generated a

48 xhibited the same propensity to variegate in methylcellulose-based cultures, suggesting that the deci

49 groups to receive 0.05 ml of a hydroxypropyl methylcellulose-based dispersive OVD to which had been a

50 pi-off CXL using 10 minutes of hydroxypropyl methylcellulose-based riboflavin soaking before 10 minut

51 We find that a methylcellulose-based semisolid medium containing Matrig

52 noparticles in a hydrophilic support medium (methylcellulose) before introducing heavy metal stains f

53 hylcellulose or ethylcellulose/hydroxypropyl methylcellulose biopolymers (as oleogelators), sunflower

54 ogel made using ethylcellulose/hydroxypropyl methylcellulose biopolymers contained lower saturation l

55 ing dramatically reduced colony formation in methylcellulose but had only modest effects in liquid cu

56 Commercially available hydroxypropyl methylcellulose capsules are employed as a fast, safe, a

57 en induced to differentiate by suspension in methylcellulose, cells maintaining genomes with mutation

58 umin, and polysaccharides, i.e. alginate and methylcellulose), charge character and polysaccharide co

59 We observed a complete absence of methylcellulose colonies, indicating absence of hematopo

60 nes to TEL-PDGFRB-mediated transformation in methylcellulose colony and murine bone marrow transducti

61 Methylcellulose colony assays at days 180 and 300 reveal

62 efractory to transformation by TEL-PDGFRB in methylcellulose colony assays.

63 progenitors have previously been defined by methylcellulose colony-forming units and by limiting dil

64 This study examined how methylcellulose concentration affects in vivo aroma rele

65 decrease in aroma intensity with increasing methylcellulose concentration observed in this study.

66 dness, chewiness, and dryness increased with methylcellulose concentration, while juiciness, fattines

67 astication was not significantly affected by methylcellulose concentration.

68 ma release was not significantly affected by methylcellulose concentration.

69 sity significantly decreased with increasing methylcellulose concentration.

70 nto the RAG(-/-) background or when grown in methylcellulose containing interleukin-7.

71 assaying for colony-forming cells (CFCs) in methylcellulose containing toxic doses of aerolysin (1 x

72 i, HOK-16B, and BaP-T cells during growth in methylcellulose-containing medium, a condition that indu

73 s response to the same procedure, the use of methylcellulose could be very promising.

74 us leukemia inhibitory factor in an in vitro methylcellulose culture assay, supporting a role for TIA

75 red in suspension for 7 days and replated in methylcellulose culture for measurement of colony-formin

76 the number of colonies formed in subsequent methylcellulose culture fourfold.

77 named based on their ability to generate in methylcellulose culture large colonies of erythroid cell

78 orted and plated as single cells per well in methylcellulose culture medium containing early acting g

79 rouracil (5-FU)-treated mice in the two-step methylcellulose culture we reported previously.

80 acquired the ability to serially replate in methylcellulose culture, a property crucially dependent

81 Elastase inhibited CFU-GM in methylcellulose culture.

82 C57BL/6-Ly-5.1 mice was examined by means of methylcellulose culture.

83 c progenitor cells that can form colonies in methylcellulose culture.

84 ells and karyotypes of the colonies grown in methylcellulose culture.

85 d karyotype studies of the colonies grown in methylcellulose culture.

86 colony-forming cells (CFC) was enumerated in methylcellulose culture.

87 k sac and embryo proper cells were plated in methylcellulose cultures and treated with selected hemat

88 nsfectants formed erythromyeloid colonies in methylcellulose cultures in the absence of added hematop

89 Methylcellulose cultures of BM cells from Fac-/- and Fac

90 When ritonavir was added to methylcellulose cultures of bone marrow cells from HIV-i

91 d to SCF + erythropoietin (Epo)-supplemented methylcellulose cultures potently enhanced the formation

92 rrow progenitors yielded smaller colonies in methylcellulose cultures than did wild-type, PU.1(+/-) o

93 iferation of myeloid colony-forming cells in methylcellulose cultures upon serial replating, whereas

94 l displayed Epo hypersensitivity in in vitro methylcellulose cultures, as indicated by more numerous

95 affected individual was observed in in vitro methylcellulose cultures, as indicated by more numerous

96 formed growth factor-independent colonies in methylcellulose cultures, but the myeloproliferative dis

97 gineered to express Cdx4 serially replate in methylcellulose cultures, grow in liquid culture, and ge

98 ed hematopoietic progenitors when added into methylcellulose cultures.

99 CFU-GEMM and burst-forming unit-erythroid in methylcellulose cultures.

100 ophage colony-stimulating factor (GM-CSF) in methylcellulose cultures.

101 tle myeloid potential in vivo, as well as in methylcellulose cultures.

102 at contain all three lineages when plated in methylcellulose cultures.

103 d into a vehicle-treated control group (0.5% methylcellulose daily for 2 d [5 rats] or 7 d [4 rats])

104 Using FTIR, we found that methylcellulose decreased the strength of hydrogen bond

105 ent with 0.1% RC-2 in PBS with or without 2% methylcellulose did not.

106 oic membrane (CAM) assay was performed using methylcellulose discs containing bFGF with or without TI

107 A recent prospective comparison of methylcellulose double-contrast barium enteroclysis to c

108 sis depicts mucosal details better than does methylcellulose double-contrast enteroclysis because of

109 um enteroclysis took a back seat to biphasic methylcellulose double-contrast enteroclysis in the inve

110 h-frozen rat spines and a system of carboxyl methylcellulose embedding, cryofilm, and polytetrafluoro

111 Methylcellulose embedment provides effective electron im

112 which incorporates HoxD3 plasmid DNA into a methylcellulose film that is placed on wounds created on

113 The distribution of CuO nanoparticles in the methylcellulose film was uniform.

114 We investigated the possibility of using methylcellulose films modified with CuO nanoparticles fo

115 We found that methylcellulose films modified with CuO nanoparticles in

116 All the methylcellulose films were characterized for bioactivity

117 In methylcellulose, FL significantly increased colony forma

118 le-stranded DNA fragmentation after being in methylcellulose for 18 to 24 hours, which contrasts with

119 Keratinocytes suspended in methylcellulose for 24 h underwent approximately 1000-fo

120 inocytes in semisolid medium containing 1.6% methylcellulose for 24 h was sufficient for the activati

121 In addition, methylcellulose-formulated AcGP64-FIV transduced mouse n

122 ith the following protocols: 1) injection of methylcellulose gel alone, subcutaneously over the calva

123 njections of 0.5 mg simvastatin in 30 microl methylcellulose gel and contralateral gel alone (n=3) or

124 ateral gel alone (n=3) or 2.0 mg simvastatin/methylcellulose gel and contralateral gel alone (n=4).

125 0.1, 0.5, 1.0, 1.5, or 2.2 mg simvastatin in methylcellulose gel in a polylactic acid membrane (SIM)

126 Topical injection of simvastatin in methylcellulose gel was shown to stimulate bone growth a

127 ntralateral mandible side was implanted with methylcellulose gel/polylactic acid membrane alone (GEL)

128 Bone marrow aspirations cultured in methylcellulose generated colonies identified by PCR to

129 Tablets of paracetamol and hyproxypropyl methylcellulose (HPMC) and 50:50 mixes of the two were p

130 Sato' using edible coatings of hydroxypropyl methylcellulose (HPMC) and beeswax (BW) at concentration

131 a hydrogel matrix composed of hydroxypropyl methylcellulose (HPMC) and polyvinylpyrrolidone (PVP) an

132 (CMC)-gelatin-CMC-sucrose, or hydroxypropyl methylcellulose (HPMC) and polyvinylpyrrolidone (PVP) so

133 By using hydroxypropyl methylcellulose (HPMC) as a thickening agent, subjects c

134 n as core and either pectin or hydroxypropyl methylcellulose (HPMC) as shell polymers.

135 ether the nonfermentable fiber hydroxypropyl methylcellulose (HPMC) could alter the intestinal microb

136 a solution of 2.5% EP in 0.2% hydroxypropyl methylcellulose (HPMC) every 90 minutes during the cours

137 -linked by 0.1% riboflavin in hydroxylpropyl methylcellulose (HPMC) instillation for 10 minutes follo

138 Methylcellulose (MC), hydroxypropyl methylcellulose (HPMC), carboxymethyl cellulose (CMC) an

139 matic review was conducted for hydroxypropyl methylcellulose (HPMC), pectin and chitosan in Pubmed, E

140 available nasal sprays-low pH hydroxypropyl methylcellulose (HPMC-NS), iota-carrageenan (Carr-NS), n

141 gy 3 (SH3) and delivering the protein from a methylcellulose hydrogel modified with SH3 binding pepti

142 of miR-203 were induced to differentiate in methylcellulose, impaired genome amplification was obser

143 locyte-macrophage and macrophage colonies in methylcellulose in response to other growth factors.

144 the untransfected 32D parental cell line in methylcellulose in the presence of IL3-conditioned mediu

145 d subsequently to a viscoelastic solution of methylcellulose in water.

146 the severity of colitis in SPF mice, whereas methylcellulose increased severity.

147 Suspension of KCs in methylcellulose induced p12 expression.

148 els of cellular transcription factors during methylcellulose-induced differentiation of W12 (20863) c

149 Calcium and methylcellulose-induced differentiation was delayed in E

150 ion but also resulted in delayed calcium and methylcellulose-induced keratinocyte differentiation.

151 s modestly more actomyosin interactions, and methylcellulose inhibited diffusion to sustain the compl

152 , the mean IOP was 18.2+/-0.45 mm Hg without methylcellulose injection and 18.3+/-0.77 mm Hg in the c

153 stopathological findings in group 1 (without methylcellulose injection) showed the subscleral spaces

154 the control eyes, and 9.8+/-0.84 mm Hg with methylcellulose injection, 18.25+/-0.7 mm Hg in the cont

155 rentiation of HPV genome-containing cells by methylcellulose is insufficient to induce cleavage.

156 rging cells in a liquid medium containing 1% methylcellulose, M. xanthus TFP-driven motility was indu

157 Although the methylcellulose matrix used in these assays does not pro

158 line ritonavir in an amorphous hydroxypropyl methylcellulose matrix with a high signal-to-noise ratio

159 Methylcellulose may have antihealing properties that ser

160 Biodegradable and antioxidant films based on methylcellulose (MC) and alpha-tocopherol nanocapsule su

161 o, we differentiated mouse BM progenitors in methylcellulose (MC) hydrogels tuned to mimic BM stiffne

162 Methylcellulose (MC) polymer was used to prepare the edi

163 using in poly(dimethylsiloxane) (PDMS) using methylcellulose (MC) to reduce electroosmosis and peak d

164 Methylcellulose (MC), hydroxypropyl methylcellulose (HPM

165 Then, utilizing thermo-responsivity of methylcellulose (MC), we developed a cytocompatible cast

166 ants were grown in nonadherent conditions in methylcellulose (MC)-containing medium, and the signalin

167 cluded in the study. Experimental [PR/RP+SIM/methylcellulose (MCL); n = 27] and control (PR/RP+MCL; n

168 -1+c-kit+ fetal liver cells were cultured in methylcellulose media with interleukin (IL)-2, IL-7, IL-

169 lls or when CD34(+) cells were cocultured in methylcellulose medium in a transwell above a stromal la

170 When CD34(+) cells were cultured in methylcellulose medium supplemented with cytokines at co

171 efinitive erythroid lineages--when plated in methylcellulose medium supplemented with hematopoietic g

172 tiation in an assay conducted with semisolid methylcellulose medium, and the PY motifs were critical

173 In contrast, penetration into methylcellulose (mimicking penetration into cervical muc

174 on scheme to Carraguard (n=3103) or placebo (methylcellulose [n=3099]), were instructed to use one ap

175 eroclysis because of the "washout" effect of methylcellulose on superficial mucosal features.

176 ct of the addition of non-reducing sugars or methylcellulose on the matrix physical properties and ra

177 also for particles moving in the presence of methylcellulose or excess skeletal muscle actin.

178 e found that an additional component such as methylcellulose or fascin is required for actin bundle f

179 lasts and endothelial cells when cultured in methylcellulose or matrigel.

180 randomised to over-encapsulated mebeverine, methylcellulose or placebo for 6 weeks and to 1 of 3 web

181 onent of mucus, but not by similarly viscous methylcellulose or simple sugars.

182 ral gavage with either vehicle control (0.5% methylcellulose) or 10 or 30 mg/kg EDP-305.

183 on containing three parts water and one part methylcellulose over a 30-minute period.

184 andard plate incorporation assay followed by methylcellulose overlay and treat-and-wash assays, using

185 Adherent methylcellulose patches formulated to locally release al

186 (MDR-1) vector, and by a quantitative GM-CFU methylcellulose plating assay.

187 to the cold embedding in a new hydroxypropyl methylcellulose/polyvinylpyrrolidone-enriched hydrogel a

188 -term culture-initiating cells (LTC-ICs) and methylcellulose replating assays.

189 aning and placement of 2.2-mg simvastatin in methylcellulose (SIM/MCL) or methylcellulose alone (MCL)

190 crotubules from the surface was prevented by methylcellulose so that continuous trajectories of micro

191 yed very similar swimming characteristics in methylcellulose solutions as in water.

192 ss speeds in different concentrations of the methylcellulose solutions.

193 rformance of achiral planar microswimmers in methylcellulose solutions.

194 cal macromolecules (bovine serum albumin and methylcellulose), soot, natural coastal sediments, and S

195 index increased with an increasing ratio of methylcellulose, suggesting that the water uptake capaci

196 y compared to wt controls upon re-plating in methylcellulose supplemented with interleukin-3.

197 ifferentiation of NOKs-Akata cells by either methylcellulose suspension or organotypic culture induce

198 After 18 hours in methylcellulose suspension, apoptosis was detected in Ha

199 lginate system (CAS; YBP=85.8%) or caseinate methylcellulose system (CMCS; YBP=74%).

200 s two-phase system (ATPS) using an ovalbumin-methylcellulose system (OMCS) in comparison to ATPS with

201 Use of the methylcellulose system to induce epithelial differentiat

202 In contrast, in group 2 (injected with methylcellulose), the subscleral space appeared fenestra

203 teracted with starch in a unique mode, while methylcellulose, the additive with the highest Tg, incre

204 c strength conditions and in the presence of methylcellulose, the DNEQ and delta-DSE actins moved in

205 irus with RC-2 or applying the peptide in 2% methylcellulose to the cornea before viral infection sig

206 d after being suspended in semisolid medium (methylcellulose) using flow cytometry to detect TUNEL-po

207 % rosuvastatin (RSV) gel incorporated into a methylcellulose vehicle for its controlled release into

208 The methylcellulose was allowed to pass through the trabecul

209 on culture and erythroid colony formation in methylcellulose was isolated.

210 suspension of cells in a semisolid medium of methylcellulose, we found that the URR of HPV31 was indu

211 Hydrogels based on alginate and methylcellulose were developed as a colorimetric indicat

212 ase, and the numbers of colonies observed in methylcellulose were similar to those produced by fresh

213 /E100A actins ceased even in the presence of methylcellulose, while I341A actin (deficient in strong

214 When cultured in methylcellulose with appropriate cytokines, AA4.1+/Fc ga

215 mononuclear cells were cultured directly in methylcellulose with growth factors.

216 When cultured in methylcellulose with IL-7 +/- CXCL12, Fak-deleted pro-B

217 Day 14 fetal thymocytes cultured in methylcellulose with interleukin-7 (IL-7), IL-15, and st

218 cells (HSCs) in vitro, ESCs were cultured in methylcellulose with stem cell factor, interleukin (IL)-

219 eatment of cells induced to differentiate in methylcellulose with the DNA synthesis inhibitor cytosin

220 lls were cultured for 1 day with and then in methylcellulose without estradiol.

221 ene therapy vectors (nonviral or viral) in a methylcellulose/xanthan gum-based foam formulation subst