ライフサイエンスコーパス: callus

1 mprovement of angiogenesis in the COX-2(-/-) callus.

2 MMP-9 expression in the COX-2(-/-) fracture callus.

3 was regenerated from independently selected callus.

4 teral branches and a reduced ability to form callus.

5 ion is linearly related to the strain in the callus.

6 hondrocytes, and osteoblasts of the fracture callus.

7 n of the transcription factor LEAFY (LFY) in callus.

8 don, whereas the abaxial side evolves into a callus.

9 evels of ACT7 protein than did the wild-type callus.

10 nt in the nuclei of cotyledons and endosperm callus.

11 as been transformed into Black Mexican Sweet callus.

12 y and polyamines were measured in transgenic callus.

13 y microprojectile bombardment of embryogenic callus.

14 oot meristems and organ primordia but not in callus.

15 ranging from 7% to 150% of wild-type hNP 588 callus.

16 t TBI induces the formation of a more robust callus.

17 , and indica rice (Oryza sativa var. indica) callus.

18 e TGF-beta1 protein levels in mouse fracture callus.

19 crophages, predominated in the maturing hard callus.

20 s, stems, flowers, roots and seeds) and from callus.

21 r DH sites detected in both the seedling and callus, 31% displayed significantly different levels of

22 ), lesser toe deformities (60.0%), corns and calluses (58.2%), bunions (37.1%), and signs of fungal i

23 In the knot callus, a high density of defects originate within 1mm o

24 al. (2014) show that muscle and the fracture callus actively position fractured neonatal bone fragmen

25 cells were localized throughout the healing callus after fracture.

26 (1.7-3.7 micromol g(-1) fresh weight in the callus and 0.6-2.0 micromol g(-1) fresh weight in the le

27 healing results in reduction of the fracture callus and a delay in conversion of cartilage to bone.

28 nges were detected between total embryogenic callus and callus enriched for transition stage somatic

29 erate for a limited time as undifferentiated callus and do not show the massive deposition of ectopic

30 The presence of DC8 activity in carrot callus and endosperm is consistent with the notion that

31 ilage-to-bone transformation in the fracture callus and for undisturbed bone healing.

32 n microprojectile bombardment of embryogenic callus and hygromycin selection.

33 MARs on transgene expression levels in maize callus and in transformed maize plants.

34 omplex II ratio differs by factor 37 between callus and leaf, indicating drastic differences in elect

35 r, the amount of mannitol accumulated in the callus and mature fifth leaf (1.7-3.7 micromol g(-1) fre

36 The aim of this study was to measure callus and plasma amino acid concentrations in patients

37 sativa, the technique has been initiated in callus and shoots, but has not been optimized ever since

38 Analyses of callus and untransformed plants regenerated from callus

39 high in mature shoots, but extremely low in callus and young shoots; in E. arvense strobili, it was

40 e embryos, sugarcane (Saccharum officinarum) callus, and indica rice (Oryza sativa var. indica) callu

41 varieties (in vivo plants, in vitro shoots, callus, and suspension cultures) were investigated for t

42 cular invasion of the hypertrophic cartilage callus, and that Mmp9(-/-) mice have non-unions and dela

43 th patient-derived keratinocytes and patient callus; and (3) demonstrate that repeated siRNA treatmen

44 e use of ultrasound in the evaluation of the callus are rare and this could be a method equivalent to

45 ) newly formed bone density (NFBD); 3) total callus area (TCA); 4) osteoclast number (ON) in the call

46 We report that hyperkeratotic calluses arising in the glabrous skin of individuals wit

47 m which embryos develop and from the abaxial callus at five time points over the course of the 4 week

48 c sequence restored their ability to produce callus at rates similar to those of wild-type plants, co

49 increased amount of trabecular bone in MULTI calluses at 21 days post-injury.

50 heir biological activities in the P. lunatus callus bioassay, indicating that there may be similariti

51 er in vitro and ex vitro culture conditions (callus biomass, shoot production, and ex vitro survival)

52 parental rDNA expression in root, flower and callus, but not in leaf where D-genome rDNA dominance wa

53 ng to the formation of shoots, new roots, or callus by transferring to the appropriate organ inductio

54 The RNAi suppression of CsMYBF1 in citrus callus caused a down-regulation of many phenylpropanoid

55 A callus cDNA library from the maize inbred Mp708 was scre

56 GUS) expression cassette was introduced into callus cells via tungsten microparticles, and stable tra

57 ian strands were detected in any Arabidopsis callus cells, strands were present in leaf epidermal cel

58 obacco (Nicotiana tabacum) and Ginkgo biloba callus cells.

59 Membranes from one callus clone expressed m1 MAChR at the level of 2.0-2.5

60 ssue in response to hormones, and the mutant callus contained at least two to three times lower level

61 The callus culture for stem and leaf explants was initiated

62 Dedifferentiation in callus culture resulted in an increase of the terminal r

63 rentiation, dedifferentiation, and long-term callus culture were consistent among genotypes.

64 putrescine and these metabolites in tobacco callus cultured in vitro.

65 lation in wheat seedlings, crown tissue, and callus cultures after transfer from control (25 degrees

66 ast, no obvious differences could be seen in callus cultures between the transgene and vector control

67 Long-term callus cultures had very long telomeres.

68 f ASA1 mRNA and protein were also similar in callus cultures of mutant and wild type, although the le

69 nts with anticancer properties from in vitro callus cultures of stems and leaves of SM.

70 mbined with the observation that Arabidopsis callus cultures overexpressing CKI1 exhibit a "cytokinin

71 Undifferentiated callus cultures regenerated from the transgenic plants w

72 ts, regenerated from immature embryo derived callus cultures were normal, fertile, and transmitted th

73 However, the mutant seedlings and callus cultures will grow in tissue culture in the dark,

74 to a naturally occurring phenomenon whereby callus cultures, upon continued passage, lose their requ

75 eaves were examined with those of respective callus cultures.

76 the measurements of length and width of the callus demonstrated that the differences between results

77 we isolated a population of early periosteum-callus-derived mesenchymal stem cells (PCDSCs) from the

78 m preparation of the plant cell materials to callus development is approximately 5 weeks.

79 During callus development, a significant negative correlation w

80 ologous silencing in in vitro cultured wheat callus differ from that in differentiated organs, given

81 owing and/or differentiating cells including callus, emerging leaves, and meristem regions.

82 etected between total embryogenic callus and callus enriched for transition stage somatic embryos.

83 ful efforts at regenerating plants from seed callus, establishing a transient transformation system,

84 at Mmp9(-/-) mice generate a large cartilage callus even when fractured bones are stabilized, which i

85 In this study, extracts of the mutant callus exhibited higher AS activity than wild-type callu

86 When larvae were reared on callus expressing the proteinase, their growth was inhib

87 Stem and leaf callus extracts exerted cytotoxic effects towards CCRF-C

88 tion and genome editing, friable embryogenic callus (FEC).

89 efficacy of ultrasound in the evaluation of callus formation after fractures of long bones in childr

90 of ultrasound with radiographs in imaging of callus formation after fractures of long bones in childr

91 chondrocytes leads to a prolonged cartilage callus formation and a delayed osteogenesis initiation a

92 d in a near 50% reduction in periosteal bone callus formation at the cortical bone junction as determ

93 ive actin gene, did not significantly affect callus formation from leaf or root tissue.

94 development program is a common mechanism in callus formation from multiple organs.

95 mental defects of the QK mutant and promoted callus formation in A2QK, but not in A2Wt, after heat tr

96 , this peptide growth factor, which promotes callus formation in culture, is proteolytically cleaved

97 Furthermore, callus formation in roots, cotyledons, and petals is blo

98 ans such as petals, which clearly shows that callus formation is not a simple reprogramming process b

99 -) mice, as evidenced by restoration of bony callus formation on day 14, a near complete reversal of

100 Overexpression of ESR1 cannot induce callus formation or root formation, suggesting that its

101 Endogenous callus formation precedes specification of postembryonic

102 Callus formation was completely abolished when macrophag

103 rly anabolic progression during endochondral callus formation were investigated.

104 SC sheet-wrapped allografts showed more bony callus formation when compared to allograft alone groups

105 their osteogenic ability and subsequent bony callus formation, and could be used to induce cartilagin

106 n, and could be used to induce cartilaginous callus formation.

107 erentiation, matrix production, and ultimate callus formation.

108 onfirming that the ACT7 gene is required for callus formation.

109 cells with rooting competence that resembles callus formation.

110 ulating factor-1 significantly enhanced soft callus formation.

111 oted anabolic mechanisms during endochondral callus formation.

112 ad to a nonunion as a result of insufficient callus formation.

113 /-) animals and was accompanied by increased callus formation.

114 genous cytokinin in both root-elongation and callus-formation assays.

115 tion of MSC sheets, results showed more bony callus formed between allograft and host bone ends in bo

116 een RNA isolated from intact bone to that of callus from post-fracture (PF) days 3, 5, 7, and 10 as a

117 nducing the formation of friable embryogenic callus from which highly totipotent embryogenic suspensi

118 ean polar moment of inertia when compared to calluses from FX mice at 21 days post-injury.

119 muCT analysis revealed calluses from MULTI mice had a greater bone and total ti

120 hin granulation tissue at the expanding soft callus front.

121 ties and flat feet, as well as for corns and calluses, fungal signs, edema, ankle joint pain, tendern

122 In callus grown on high (11.5 micromolar) alpha-naphthalene

123 re the main putrescine derivatives, while in callus grown on low (1.5 micromolar) alpha-naphthalene a

124 te that RepA can stimulate cell division and callus growth in culture, and improve maize transformati

125 s production of embryogenic calli and longer callus growth periods were required to generate these la

126 RepA increased transformation frequency and callus growth rate of high type II maize germplasm.

127 nse analysis, but sequence changes caused by callus growth, Agrobacterium incubation medium, virulenc

128 Scx-mutant mice demonstrated disrupted callus healing and asymmetry.

129 localization and gene expression, as well as callus healing response.

130 ment led to altered long bone properties and callus healing.

131 ctions showed that the area of the chondriod callus in the aged P10 MSC sheet groups was significantl

132 by dystrophic nails, painful hyperkeratotic calluses in glabrous skin, and lesions involving other e

133 t the chondro-osseous border in the fracture callus, in a region we define as the transition zone (TZ

134 us and untransformed plants regenerated from callus indicated that loss of methylation is stochastica

135 on root elongation, lateral root formation, callus induction and greening, and induction of cytokini

136 A similar DC8 activity time-course during callus induction and seed development suggests that expl

137 However, although callus induction from dgt hypocotyl explants required au

138 Reentry into cell cycle after callus induction from differentiated root segments repro

139 preincubating root explants on an auxin-rich callus induction medium (CIM) and by transferring explan

140 ss involving pre-incubation on an auxin-rich callus induction medium (CIM) during which time root exp

141 ess requiring preincubation on an auxin-rich callus induction medium.

142 Neither callus induction nor root formation was affected by ESR1

143 k, a 33 kDa cysteine proteinase was found in callus initiated from maize (Zea mays L.) resistant to f

144 ration, where a pluripotent cell mass termed callus is induced.

145 1.27+/-0.38%; stem Sal B: 0.87+/-0.20%) than callus leaf did (leaf RA: 0.28+/-0.02%; leaf Sal B: 0.07

146 d exhibited developmental defects, including callus-like floral organs and fasciated shoot apical mer

147 notype resulting in widespread production of callus-like structures in the mutant.

148 level of sucrose stimulated the formation of callus-like tissue in place of the gland under N-replete

149 an Arabidopsis mutant, tso1, which develops callus-like tissues in place of floral organs.

150 suspension cultures of the maize (Zea mays) callus line.

151 te functional transposase activity in barley callus lines stably transformed with an Ac transposase g

152 , we report that adult Krt9(-/-)mice develop calluses marked by hyperpigmentation that are exclusivel

153 taining amplifiable mRNA from human skin and callus material; (2) quantitatively distinguish the sing

154 ytes may play an essential role in cartilage callus maturation at an early stage of fracture healing.

155 ped using Arabidopsis (Arabidopsis thaliana) callus membranes.

156 stromal progenitor (f-BCSP) in the fracture callus of adult mice.

157 MYB11 was responsive to the red spots in the callus of the lip, and PeMYB12 participated in the full

158 resent observations of whirled grain in knot calluses of Populus deltoides (eastern cottonwood), and

159 l lesions as well as PPK-like hyperkeratotic calluses on Krt16(-/-) front and hind paws, which severe

160 A1 in transgenic tobacco (Nicotiana tabacum) callus or somatic soybean (Glycine max) embryos resulted

161 O1 DNA binding activity in diabetic fracture calluses (P < 0.05).

162 Callus production in this mutant requires the cytokinin

163 L Furthermore, plastid stress-induced apical callus production requires elevated plastidic reactive o

164 ed protein has high homology with an alfalfa callus protein or translationally controlled human or mo

165 ts and with the subjective assessment of the callus quality.

166 <0.01), area of NFC (P <0.01), and ON in the callus region (P <0.01).

167 area (TCA); 4) osteoclast number (ON) in the callus region; and 5) newly formed dental cementum-like

168 penetrated hyperkeratotic PC skin and normal callused regions compared with nonaffected areas, and (2

169 We demonstrate that callus resembles the tip of a root meristem, even if it

170 s campestris pv campestris)-infected plants, callus, roots, and young seedlings.

171 tion of GUS activity in light- or dark-grown callus, roots, silk, developing or mature kernels, the s

172 Bone fracture callus samples were collected and analyzed by X-ray, mic

173 d to investigate muscle unloading effects on callus shape.

174 compared to allograft alone groups, the bony callus size in aged P10 MSC sheet groups was significant

175 p (P < 0.05), which was reflected by smaller callus size.

176 Specifically, mouse bone fracture callus specimens were extracted into a single solution t

177 se chain reaction analysis for both sites at callus stage, and one DD43 homology-directed recombinati

178 Quantitative analyses revealed that callus stem extracts produced higher amount of RA and Sa

179 t pin displacement decreases as the fracture callus stiffens and that pin motion is linearly related

180 erent phenotype of pnt1 cells in embryos and callus suggest a differential requirement for GPI-anchor

181 We found 58% more DH sites in the callus than in the seedling.

182 ntly higher degree of vascularization of the callus than of the healthy periosteum.

183 ngs indicate that closed head TBI results in calluses that are larger in size and have an increased b

184 Similar to the regenerating callus, the artificial tissue undergoes intramembranous

185 ctor for 81.4 % of the baits screened for in callus tissue and T1 seedlings.

186 shoot apical meristem, and develop a mass of callus tissue at the shoot apex.

187 CUC1 was generally expressed in callus tissue during early incubation on SIM, but later

188 overexpressed, BdbZIP10 protects plants and callus tissue from oxidative stress insults, most likely

189 us act7-1 mutant plants were slow to produce callus tissue in response to hormones, and the mutant ca

190 Homozygous mutant seedlings and callus tissue produced from rescued seeds appeared norma

191 we observed no silencing in any of the wheat callus tissue tested.

192 AG was produced from plant callus tissue under sterile conditions to avoid the infl

193 Immunolabeling of callus tissue with actin subclass-specific antibodies re

194 ch lower amounts in non-green organs (roots, callus tissue).

195 itivity and enhances shoot regeneration from callus tissue, correlating with enhanced stability of th

196 Proliferation of undifferentiated callus tissue, greening, and the formation of shoot stru

197 st level of AtEBP expression was detected in callus tissue, where ocs elements are very active.

198 on of stably transformed roots directly from callus tissue.

199 LeMir is also expressed in tomato callus tissue.

200 atory and resident cells within the fracture callus tissue.

201 rsensitive (DH) sites from both seedling and callus tissues of rice (Oryza sativa).

202 ree genes causes the intermediate cell mass, callus, to be incompetent to form shoot progenitors, whe

203 Black Mexican Sweetcorn callus transformed with mir1, the gene encoding the 33-k

204 sociated with key events during soft-to-hard callus transition.

205 idization with pTACR7 probe from seedling or callus treated with ABA, salt, dehydration, or heat stre

206 In callus, two of the MAR elements (Adh1 5' MAR and ARS1) r

207 Using the Power Doppler callus vascularity was visualized and vascular resistanc

208 dels have shown that EtOH decreases fracture callus volume, diameter, and biomechanical strength.

209 Indeterminate callus was generated and maintained from the sporophytes

210 Asymmetry of Scx-mutant callus was not due to muscle unloading.

211 wth of caterpillars reared on the transgenic callus was reduced 60-80%.

212 differentially expressed in the seedling and callus were frequently associated with DH sites in both

213 mutant and wild type, although the levels in callus were higher than in leaf tissue.

214 Amino acid concentrations in plasma and callus were measured with HPLC in atrophic nonunions (n

215 g ultrasound examination measurements of the callus were performed.

216 5 compared with 149 mumol/mg; P < 0.0001) in callus were significantly lower in atrophic-nonunion pat

217 e common in men, while bunions and corns and calluses were more common in women (p < 0.001).

218 exhibited higher AS activity than wild-type callus when assayed with either glutamine or ammonium su

219 d in E. fluviatile intercalary meristems and callus (which lacked MLG).

220 AtTERT mRNA is 10-20 times more abundant in callus, which has high levels of telomerase activity, ve

221 tes ubiquitous urease activity in leaves and callus while retaining normal embryo-specific urease act

222 RI) and the degree of vascularization of the callus with a subjective radiological assessment of the