ライフサイエンスコーパス: suspension culture

1 ts-growth on solid agar medium and in liquid suspension culture.

2 he observed cytokinesis defect when grown in suspension culture.

3 CSF greatly reduced apoptosis in response to suspension culture.

4 a or on tissue culture dishes rather than in suspension culture.

5 y 2-3 h after keratinocytes were placed into suspension culture.

6 pressing Drosophila melanogaster S2 cells in suspension culture.

7 velopmental delays and decreased clumping in suspension culture.

8 PK phosphorylation during the early phase of suspension culture.

9 mary and immortalized human keratinocytes in suspension culture.

10 nce of caspase activation at later stages of suspension culture.

11 to other cell types that are able to grow in suspension culture.

12 n is phosphorylated in live amoebas grown in suspension culture.

13 pe when attempting to undergo cytokinesis in suspension culture.

14 unit-spleen (CFU-S) during 14 days of liquid suspension culture.

15 e, and cell-type-specific gene expression in suspension culture.

16 tor on Flt3low cells was not detected during suspension culture.

17 o the production of extremely small cells in suspension culture.

18 extent comparable to that observed in forced suspension culture.

19 pport the proliferation of enriched cells in suspension culture.

20 ietic cells during in vitro transductions in suspension culture.

21 ony growth nor CFU-Meg nuclear maturation in suspension culture.

22 whose products transformed CiE1 cells into a suspension culture.

23 nant human thrombopoietin (rhTpo), in liquid suspension culture.

24 rent selection and is adaptable for scalable suspension culture.

25 2% to 3% O(2) on fibronectin, compared with suspension culture.

26 cherichia coli and in tobacco cells grown in suspension culture.

27 dhered to fibronectin compared with cells in suspension culture.

28 ectin versus cells selected in a traditional suspension culture.

29 erved in cells selected with mitoxantrone in suspension culture.

30 fetal thymic organ cultures fail to do so in suspension culture.

31 cancers of both SCLC and NSCLC type grew as suspension cultures.

32 hondria from both pea leaves and Arabidopsis suspension cultures.

33 ntially glycosylated in two different carrot suspension cultures.

34 lls and in exponentially growing tomato cell suspension cultures.

35 lls or populations of cells from Arabidopsis suspension cultures.

36 olated microsomes from tobacco stems or cell suspension cultures.

37 ink organs, phloem cells, and mannitol-grown suspension cultures.

38 okinin addition to cytokinin-starved soybean suspension cultures.

39 C numbers from secondary colony formation in suspension cultures.

40 ce, that are distinct from those observed in suspension cultures.

41 more relevant fashion than the commonly used suspension cultures.

42 r, and analyzed in colony-forming assays and suspension cultures.

43 fferentiation of TEs in Arabidopsis thaliana suspension cultures.

44 in a prior study of mitochondrial editing in suspension cultures.

45 pressed CYCD3;1 in Arabidopsis thaliana cell suspension cultures.

46 s observed experimentally in a heterotrophic suspension culture; (2) that approximately only 15% of t

47 umulation was detectable in Arabidopsis cell-suspension cultures 3 to 5 h after inoculation with Coch

48 In suspension cultures, a reduction in topoisomerase IIbeta

49 In contrast, addition of GM-CSF to the suspension culture abrogated neither B-cell potential no

50 s were capable of growing in shake flasks as suspension cultures, achieving maximum concentration of

51 pneumoniae grown to mid-logarithmic phase in suspension culture adhered to cultured primary respirato

52 We have employed suspension cultured aequorin-transformed tobacco cells t

53 e expressed at detectable levels in the cell suspension culture, allowing us to present a unified mod

54 low-shear environment of optimized rotation suspension culture allows both eukaryotic and prokaryoti

55 n addition, switching cells from adherent to suspension culture also activates the AhR, representing

56 ed an average of six additional doublings in suspension culture and erythroid colony formation in met

57 ew of the transcriptional profile of a plant suspension culture and identify a refined set of 1082 ce

58 glucosaminyltransferase I-negative) cells in suspension culture and overexpress the candidate protein

59 rmal keratinocytes were unable to survive in suspension culture and rapidly became apoptotic.

60 liminated the ability of F4 cells to grow in suspension culture and retarded the growth of F4 cells i

61 were also capable of forming mammospheres in suspension culture and subsequent formation of 3D organo

62 e myeloid leukemia (AML) blasts in long-term suspension culture and the survival of leukemic stem cel

63 evels were also examined in Arabidopsis cell suspension culture and were found to be differentially c

64 agent was added to Arabidopsis thaliana cell suspension cultures and determined to induce programmed

65 rative advantage in both cytokine-stimulated suspension cultures and stromal coculture.

66 t using a cDNA library from embryogenic rice suspension cultures and the plant transcriptional activa

67 this activity was purified from Arabidopsis suspension cultures and the resulting 50 kDa polypeptide

68 an keratinocytes induced to differentiate in suspension culture, and assayed the growth capacity of t

69 ogenous galectin-3 reduced cyst formation in suspension culture, and mice-null mutant for galectin-3

70 uently used tobacco bright yellow (BY)2 cell suspension culture, and that cell cycle synchronisation

71 f the eight UGTs in Medicago organs and cell suspension cultures, and comparison of these patterns wi

72 e stiffness distribution in the cell wall of suspension-cultured Arabidopsis thaliana as a model of p

73 (125)I-labeled AtPep1 analog interacted with suspension-cultured Arabidopsis with a K(d) of 0.25 nM,

74 For example, when plant cells grown in suspension culture are challenged with fungal elicitors,

75 The upstream processes for suspension cultures are amenable for automation and are

76 biosynthesize 6a-hydroxymaackiain, when cell suspension cultures are fed 6a-hydroxymaackiain, they ac

77 Plant cell suspension cultures are invaluable models for the study

78 ne expression patterns in the senescent cell suspension cultures are more similar to those for dark-i

79 Synchronized suspension cultures are powerful tools in plant cell-cyc

80 C12F LMP transfectants to differentiate in a suspension culture assay.

81 fat pad tumors or are grown in end-over-end suspension culture assemble a characteristic, multi-glob

82 nstrated partial resistance to NVP-AEW541 in suspension cultures, become much more sensitive followin

83 The peptides were active in a petunia suspension culture bioassay at nanomolar concentrations,

84 18% in power output compared to conventional suspension culture BPV device was observed.

85 In suspension culture, Brk suppression increased the rate o

86 ) UCB SP cells did not proliferate in simple suspension cultures but did differentiate into natural k

87 5 as well as the as-1-type element in a cell suspension culture, but not with whole seedlings.

88 in-cell structures is extensively studied in suspension cultures, but remains poorly understood in su

89 cells from Arabidopsis, soybean, and carrot suspension cultures, but was low or not detectable in a

90 show in this study that signals provided in suspension culture by nonagonist peptide/MHC complexes o

91 Finally, we observed that in suspension cultures, C. perfringens induces aggregation

92 endent processes in Dictyostelium (growth in suspension culture, capping of Con A receptors, and deve

93 HPLC method to characterize amine titers in suspension cultured carrot (Daucas carota L.) cells and

94 leaves that causes a pH increase of soybean suspension-cultured cell media within 10 min at low nano

95 rms (replicons) was equivalent between wheat suspension culture cells and embryos, GUS reporter gene

96 -immunopurified with AtMSI4 from A. thaliana suspension culture cells and identified by liquid chroma

97 e promoter (Pv) or the CaMV 35S promoter, to suspension culture cells and immature zygotic embryos of

98 MFP1 is located in plastids in both suspension culture cells and leaves and is attached to t

99 tosis and cytokinesis in living tobacco BY-2 suspension culture cells by means of a green fluorescent

100 hase and G1-phase populations of Arabidopsis suspension culture cells compared to those in S-phase.

101 o be expressed in all major plant organs and suspension culture cells of Arabidopsis.

102 did not exhibit polar attachment to tobacco suspension culture cells or to tomato roots; it was also

103 reporter gene constructs in bombarded maize suspension culture cells was used to examine the role of

104 sed in tobacco (Nicotiana tabacum L. cv BY2) suspension culture cells, and the resulting proteins did

105 RNA polymerase II purified from Arabidopsis suspension culture cells, and this subunit has a stoichi

106 resent throughout the wild-type plant and in suspension culture cells, but in very low amounts, sugge

107 e of these genes is expressed in Arabidopsis suspension culture cells, but only one of the encoded po

108 fication, and with carrot (Daucus carota L.) suspension culture cells, eEF1A was the only protein tha

109 However, in contrast with suspension culture cells, no changes in leaf transcript

110 ified to homogeneity from SA-treated tobacco suspension culture cells.

111 tobacco (Nicotiana tabacum) Bright Yellow-2 suspension culture cells.

112 no or very much reduced attachment to carrot suspension culture cells.

113 abidopsis thaliana ecotype Landsberg erecta) suspension culture cells.

114 ng the various stages of the growth cycle in suspension culture cells.

115 vestigated only in isolated mitochondria and suspension culture cells.

116 en investigated during the early response of suspension cultured cells of French bean to fungal elici

117 ce receptor (SR160) from plasma membranes of suspension cultured cells of Lycopersicon peruvianum is

118 sient expression assay using maize endosperm suspension cultured cells.

119 s highly expressed in developing flowers and suspension cultured cells.

120 ile the DcAGP1 transcript is abundant in the suspension-culture cells from which the AGP was obtained

121 alinization of the culture medium of tobacco suspension-cultured cells and a concomitant activation o

122 hree new peptides cause an alkalinization of suspension-cultured cells and induce the synthesis of de

123 defense responses in both tomato leaves and suspension-cultured cells and that the only region of pr

124 LeAGP-1 was isolated from tomato suspension-cultured cells and verified to be an AGP by p

125 m and at the nuclear pore complex of tobacco suspension-cultured cells are modified by O-linked oligo

126 Nevertheless, suspension-cultured cells can be habituated to grow in h

127 generated from rapidly dividing embryogenic suspension-cultured cells co-cultivated with Agrobacteri

128 a cross-reacting protein in the membranes of suspension-cultured cells comigrates with both the nativ

129 alkalinization response to AtPep1 by tobacco suspension-cultured cells expressing the At1g73080 trans

130 ed to the endomembrane system of Arabidopsis suspension-cultured cells following sucrose density grad

131 oteinase activity was gradually increased in suspension-cultured cells following the bacterial infect

132 From these results we conclude that BY2 suspension-cultured cells have the necessary components

133 e apoplastic oxidative burst demonstrated by suspension-cultured cells in response to fungal elicitor

134 n kinase and alkalinization of the medium of suspension-cultured cells in response to systemin and ca

135 ed in roots of alfalfa after defoliation, in suspension-cultured cells incubated in sucrose-rich or -

136 ion studies with tobacco (Nicotiana tabacum) suspension-cultured cells indicate that interaction betw

137 investigations of subcellular fractions from suspension-cultured cells of "Paul's Scarlet" rose (Rosa

138 ed radioactive orthophosphate to pulse-label suspension-cultured cells of Arabidopsis in conjunction

139 he presence of sialylated glycoconjugates in suspension-cultured cells of Arabidopsis thaliana and su

140 r showed complex changes in elicitor-treated suspension-cultured cells of French bean.

141 that the initiation of defense signaling in suspension-cultured cells of Lycopersicon peruvianum by

142 th under conditions of phosphate limitation, suspension-cultured cells of tomato (Lycopersicon escule

143 Treatment of tobacco suspension-cultured cells or isolated bovine tubulin wit

144 ion and the generation of reactive oxygen in suspension-cultured cells paralleled the binding activit

145 ellow 2 (BY2) tobacco (Nicotiana tabacum L.) suspension-cultured cells possess an expansin-mediated a

146 tobacco (Nicotiana tabacum) Bright Yellow 2 suspension-cultured cells revealed the presence of sever

147 specifically to plasma membranes of tobacco suspension-cultured cells that expressed the tomato BRI1

148 e early responses of Lycopersicon peruvianum suspension-cultured cells to the polypeptide wound signa

149 bacco (Nicotiana tabacum L.) protoplasts and suspension-cultured cells treated with the cellulose syn

150 Binding of [(3)H]RH-4032 in tobacco suspension-cultured cells was shown to be saturable and

151 Treatment of suspension-cultured cells with methyl jasmonate increase

152 In this study with Arabidopsis suspension-cultured cells, combined in vivo and in vitro

153 e SR160 receptor gene, expresses the gene in suspension-cultured cells, evidenced by mRNA and protein

154 ize LeAGP-1 in tomato to the cell surface of suspension-cultured cells, maturing metaxylem elements i

155 common components in Lycopersicon peruvianum suspension-cultured cells.

156 stress and pathogen responses of leaves and suspension-cultured cells.

157 rty of the native protein when isolated from suspension-cultured cells.

158 e effect on its activity in tomato plants or suspension-cultured cells.

159 nization response in Lycopersicon esculentum suspension-cultured cells.

160 tems: Arabidopsis roots and maize (Zea mays) suspension-cultured cells.

161 e the physiological receptor for systemin in suspension-cultured cells.

162 d RNA concentration are highest in roots and suspension-cultured cells.

163 co (Nicotiana tabacum L.) cv Bright Yellow 2 suspension-cultured cells.

164 One of these is highly expressed in suspension-cultured cells.

165 ep1 receptor from the surface of Arabidopsis suspension-cultured cells.

166 observed in mature-stage rice organs and in suspension-cultured cells.

167 In suspension culture, clathrin-minus cells failed to divid

168 with fewer nonadherent hepatocytes in rocked suspension culture compared to a traditional rotational

169 d for TRAIL-R2 (DR5) and TRAIL after 24 h of suspension culture compared with cells in monolayer cult

170 vels increased in TNBC cells grown in forced suspension culture compared with those in attached condi

171 clopamine-treated ovarian cancer cells under suspension culture conditions drastically lost their abi

172 Moreover, A(-)/A(-) embryoid bodies grown in suspension culture constantly shed cells.

173 lus from which highly totipotent embryogenic suspension cultures could be established.

174 ent or evodevo), their exponential growth in suspension cultures could compete with the lithography t

175 Cell suspension cultures derived from the antisense alfalfa p

176 hosphorylated focal adhesion kinase, whereas suspension cultures did not.

177 In accordance, KRP6-overexpressing suspension cultures displayed accelerated entry into mit

178 to form self-renewing "pancreatospheres" in suspension culture, even when plated at clonal density.

179 by the model are highly consistent with our suspension culture experiments as well as previous repor

180 ed transgenic tobacco lines and derived cell suspension cultures expressing c-myc-tagged Cf-4.

181 Growth in suspension cultures favors fast-growing organisms, where

182 pts were also detected in M. truncatula cell suspension cultures following phosphate starvation.

183 These data documented that suspension culture for 2 weeks of enriched adult human b

184 r cells (lin-c-kit+Sca-1(+)) grown in liquid suspension culture for 28 days.

185 pable of preserving primitive progenitors in suspension culture for prolonged periods.

186 ns the possibility of using Arabidopsis cell suspension cultures for high-throughput analysis.

187 n bone marrow stromal cells (hMSCs) grown in suspension culture gave rise to spheres of neural progen

188 Here we demonstrate that Arabidopsis suspension cultures generate elevated levels of NO in re

189 it sensitized cells to cell death induced by suspension culture, glucose depletion, and unfolding pro

190 a corresponding reduction in clonogenic and suspension culture growth.

191 ucrose starvation-induced senescence in cell suspension cultures, has shown not only similarities but

192 dies of C. albicans have been carried out in suspension cultures; however, the medical impact of C. a

193 uding impaired growth and multinucleation in suspension culture, impaired development, and alteration

194 -up of production yield was achieved through suspension culture in a bioreactor, which enabled the pr

195 Caspase-8 was cleaved during exposure to suspension culture in four CRC lines, and cell death was

196 owed longer survival or autonomous growth in suspension culture in the absence of IL-3, as well as IL

197 bolism of (13)C9-phenylalanine in wheat cell suspension cultures in the presence of the mycotoxin deo

198 A3D8 impaired the viability of CLL cells in suspension cultures, in stroma contact models, and in vi

199 pharmacological inhibition of OGA suppressed suspension culture-induced apoptosis and increased IKKal

200 Cell numbers in the suspension cultures initiated with Flt3high cells were m

201 icrogravity (LSMMG) under optimized rotation suspension culture is a novel environmental signal that

202 We now demonstrate that suspension culture is not required and that cell-specifi

203 The availability of embryogenic suspension cultures is considered to have important impl

204 d terminal differentiation were inhibited in suspension-cultured keratinocytes by preventing the rise

205 rapidly, reversibly, and saturably bound to suspension-cultured L. peruvianum cells with a K(d) of 0

206 ces rapid alkalinization of media containing suspension-cultured Lycopersicon peruvianum cells.

207 cells can be rapidly sampled directly from a suspension culture, MACS bypasses the need for sample pr

208 mEmBP-1, a bZIP transcription activator, in suspension-cultured maize endosperm cells resulted in a

209 gene is regulated by sugar concentration in suspension-cultured maize endosperm cells, and the regio

210 intron resulted in high-level expression in suspension-cultured maize endosperm cells.

211 a key feature for any metabolomic study with suspension cultured mammalian cells and provides confide

212 tabolite profiling of industrially important suspension-cultured mammalian cells is being increasingl

213 lly relevant amounts of key metabolites from suspension-cultured mammalian cells.

214 because preventing cell attachment by forced suspension culture markedly reduced NFkappaB signaling a

215 a suggest that abrogation of TGF-beta during suspension culture may allow enhanced survival or even e

216 d by subjecting large volumes of conditioned suspension culture medium to heparin-AF Toyopearl affini

217 and tested for their abilities to alkalinize suspension culture medium, with synthetic SnHypSys I dem

218 thermore, we demonstrate the accumulation of suspension cultured MK cells as a 4N population correlat

219 e develop the recently described Arabidopsis suspension culture MM2d as a transcript profiling platfo

220 The first stage involves suspension culture of hESC colonies at 3% O(2), where th

221 -xL protein was down-regulated during forced suspension culture of keratinocytes, concurrent with lar

222 nal levels by sugars in a heterotrophic cell suspension culture of maize.

223 In serum-free suspension cultures of CD34+ cells, elastase completely

224 Human megakaryocytes were isolated from suspension cultures of cord blood and adult bone marrow

225 Dynamic suspension cultures of GO-PEI/RNA complexes-treated cell

226 ceptor rhodopsin has been expressed by using suspension cultures of HEK293S cells in defined media th

227 eas 4.1 transcripts processed in nondividing suspension cultures of HMEC strongly included this exon.

228 The other approach utilizes suspension cultures of invertebrate cells.

229 Suspension cultures of L-33(+) cells in serum-free mediu

230 colony-forming unit-spleen (CFU-S) in liquid suspension cultures of lin- c-kit+ Sca-1+ murine hematop

231 on of progenitors in vitro during 2 weeks in suspension cultures of mononuclear cells or of CD34+ cel

232 , changes in Ca2+ metabolism were studied in suspension cultures of mouse keratinocytes.

233 In 10-day suspension cultures of normal or CML CD34+ cells supplem

234 Suspension cultures of NPCs derived from human iPSCs or

235 phosphorylated/activated in adherent but not suspension cultures of PTEN-positive CWR-R1 cells.

236 synthase genes (PKS1, PKS2, PKS3) from cell suspension cultures of raspberry (Rubus idaeus L. cv. Ro

237 50-100 cells were prepared from established suspension cultures of rice cell lines.

238 sponse to heparanase was also inefficient in suspension cultures of several cell lines, suggesting a

239 s been purified to apparent homogeneity from suspension cultures of the maize (Zea mays) callus line.

240 rp, was found during seed germination and in suspension cultures of the transplastomic plants.

241 ndrocyte cultures was induced by transfer to suspension culture on poly-(2-hydroxyethyl-methacrylate)

242 cleate human platelets, either maintained in suspension culture or captured in microdrops, give rise

243 when nuclear extracts from embryogenic rice suspension cultures or maize embryos were incubated with

244 was measured in vitro in monolayer culture, suspension culture, or soft agar, and in vivo in tumor x

245 mbrane reporter protein expressed in tobacco suspension culture protoplasts whose traffic was assesse

246 tly expressed in tobacco (Nicotiana tabacum) suspension-culture protoplasts, a truncated form lacking

247 inant protein in tobacco (Nicotiana tabacum) suspension-cultured protoplasts gave an active RNase of

248 ression of FAK in U-251MG cells in aggregate suspension culture reduced the amount of p120RasGAP comp

249 oduct metabolome of Medicago truncatula cell suspension cultures responding to yeast elicitor (YE) or

250 nocytes or those induced to differentiate by suspension culture revealed that C/EBPbeta-deficient ker

251 acid, a phosphatase inhibitor, in rice cell suspension cultures revealed that the dephosphorylation

252 The issues of adapting cells to suspension culture, shear sensitivity and oxygen supply

253 However, cell suspension cultures showed that GDF-5 might act at these

254 plasma membrane-enriched fractions from both suspension-cultured soybean cells and root tissue.

255 ressed in most plant tissues examined and in suspension-cultured soybean cells.

256 In contrast, cell numbers in the suspension cultures started with Flt3low cells did not i

257 myelomonocytic cell lines upon transfer into suspension cultures supplemented with interleukin-3 and

258 opolygalacturonase treatment of the walls of suspension-cultured sycamore cells and etiolated pea ste

259 ith cells from one mouse liver in a rotating suspension culture system for up to 24 h, and the metabo

260 stimulation of production of progenitors in suspension culture than other early-acting factors, such

261 We have recently described Arabidopsis cell suspension cultures that can be effectively synchronised

262 In suspension culture, the combination of ML and SF increas

263 In suspension culture, the enhancement of cell expansion by

264 Finally, we determine that in suspension cultures, the Scrib-betaPIX-PAK2 complex func

265 ic progenitor cells (HPCs) induced in liquid suspension culture to unilineage differentiation/maturat

266 erpenes, upon exposure of M. truncatula cell suspension cultures to methyl jasmonate.

267 characterized in vivo import system, namely, suspension-cultured tobacco (Bright Yellow) BY-2 cells.

268 (CAT) proteins were expressed transiently in suspension-cultured tobacco (Nicotiana tabaccum L.) cv B

269 an be used to induce a uniform population of suspension-cultured tobacco (Nicotiana tabacum cv BY-2)

270 on was further analyzed during the growth of suspension-cultured tobacco BY-2 cells.

271 ctivity for [(3)H]NAE 14:0 was identified in suspension-cultured tobacco cells and in microsomes from

272 A basic, 51 kDa protein was purified from suspension-cultured tomato and shown to inhibit the hydr

273 accumulation of ACC synthase transcripts in suspension-cultured tomato cells after the addition of a

274 s induced in Camptotheca leaf discs and cell suspension cultures treated with fungal elicitor or meth

275 ury-2 (fl2) mutant and soybean (Glycine max) suspension cultures treated with tunicamycin (Tm) to inv

276 nes during cell death in an Arabidopsis cell suspension culture using a cDNA microarray.

277 In suspension cultures, VEGF stimulation was unable to acti

278 Breast carcinoma cell survival in suspension culture was examined when Brk protein levels

279 The persistence of CD34 expression in suspension culture was inversely correlated with the ini

280 Cell survival in monolayer and in suspension culture was measured using fluorescent labels

281 phenylpropanoid pathway in Pinus taeda cell suspension cultures was carried out using quantitative r

282 ells expressing PLCbetaCT, but not growth in suspension culture, was markedly reduced, indicating tha

283 etabolomic profiling of TNBC cells in forced suspension culture, we identified a molecular pathway cr

284 roteosome inhibitors, or when cells from the suspension cultures were allowed reattachment.

285 ons between Novikoff hepatoma cells grown in suspension cultures were carried out and correlated with

286 -to-U editing events reported in A. thaliana suspension cultures were not observed in rosette leaves.

287 , stems, roots, flowers, seed pods, and cell suspension cultures were obtained.

288 Suspension cultures were used to confirm phytase express

289 in vivo plants, in vitro shoots, callus, and suspension cultures) were investigated for the first tim

290 rated from CD34+lin-Flt3high cells in liquid suspension culture, whereas cells generated from CD34+li

291 o conferred survival to endothelial cells in suspension culture, whereas stimulation with VEGF did no

292 down promoted MDA-MB-231 cell aggregation in suspension culture, which could be prevented by MMP9 ove

293 mice that received human cells transduced in suspension culture with FL, but none of the 10 mice that

294 eived human cells transduced on stroma or in suspension culture with IL-3, IL-6, SCF, and FL, but not

295 nt of primitive hematopoietic progenitors in suspension culture with purified hyacinth FRIL alone is

296 isolated chondrocytes in serum-free alginate-suspension culture with the alpha5-blocking antibody res

297 stained with PKH26 on day 0 and incubated in suspension culture with TPO or with IL-6 and FL for 7 da

298 Treatment of pine cell suspension cultures with the general elicitor chitosan i

299 The ES cell line D3 forms embryoid bodies in suspension culture without addition of retinoic acid and

300 mice that received human cells transduced in suspension culture without FL We conclude that FLT3 liga