ライフサイエンスコーパス: methylcellulose

1 t hematopoietic progenitor cell replating in methylcellulose.

2 silica capillaries coated with hydroxypropyl methylcellulose.

3 lyethylene glycol, polyvinylpyrrolidone, and methylcellulose.

4 limit of approximately 300 turnovers even in methylcellulose.

5 e identical set of cells after suspension in methylcellulose.

6 lived, and displayed clonogenic potential in methylcellulose.

7 medium and also potentiated penetration into methylcellulose.

8 Thimerosal had no effect on penetration into methylcellulose.

9 sion, and increased mammosphere formation in methylcellulose.

10 lonogenic hematopoietic progenitor assays in methylcellulose.

11 y small granulocyte and monocyte colonies in methylcellulose.

12 gomir abrogates their replating potential in methylcellulose.

13 blocks anchorage-independent cell growth in methylcellulose.

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

15 ed the growth of myeloid progenitor cells in 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 inistered perorally and CT enteroclysis with methylcellulose administered through a nasojejunal tube,

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

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

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

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

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

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

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

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

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

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

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

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

34 In methylcellulose assays, osteoblasts stimulate the develo

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

36 nicity of CB33 human lymphoblastoid cells in methylcellulose assays.

37 The use of methylcellulose avoids artifacts of conventional negativ

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

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

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

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

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

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

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

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

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

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

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

49 Methylcellulose colony assays at days 180 and 300 reveal

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

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

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

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

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

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

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

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

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

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

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

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

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

63 Elastase inhibited CFU-GM in methylcellulose culture.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

80 ed hematopoietic progenitors when added into methylcellulose cultures.

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

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

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

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

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

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

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

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

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

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

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

92 Methylcellulose embedment provides effective electron im

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

94 In methylcellulose, FL significantly increased colony forma

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

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

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

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

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

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

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

102 0.1, 0.5, 1.0, 1.5, or 2.2 mg simvastatin in methylcellulose gel in a polylactic acid membrane (SIM)

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

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

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

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

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

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

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

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

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

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

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

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

115 Suspension of KCs in methylcellulose induced p12 expression.

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

117 Calcium and methylcellulose-induced differentiation was delayed in E

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

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

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

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

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

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

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

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

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

127 Methylcellulose may have antihealing properties that ser

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

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

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

131 Methylcellulose (MC), hydroxypropyl methylcellulose (HPM

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

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

134 -1+c-kit+ fetal liver cells were cultured in methylcellulose media with interleukin (IL)-2, IL-7, IL-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

149 Adherent methylcellulose patches formulated to locally release al

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

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

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

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

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

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

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

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

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

159 Use of the methylcellulose system to induce epithelial differentiat

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

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

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

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

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

165 % rosuvastatin (RSV) gel incorporated into a methylcellulose vehicle for its controlled release into

166 The methylcellulose was allowed to pass through the trabecul

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

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

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

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

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

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

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

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

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

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

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