ライフサイエンスコーパス: Rosa

1 st disease was observed in the recipients of ROSA 26 BM.

2 Transplanted ROSA 26 cells can be precisely identified in recipient a

3 ere irradiated and transplanted with BM from ROSA 26 donors and their tissues (spleen, marrow, brain,

4 BM from young B6 Rosa 26 Lac Z+/+ mice was radiolabeled with 111In-oxine.

5 Studies using Rosa 26 Lac-Z (B6;129S-Gt(rosa)26Sor) (Lac-Z) mice revea

6 ROSA 26 marrow mononuclear cells (containing the beta-ge

7 l donor cells can be identified in situ, the ROSA 26 model should have many applications in transplan

8 ntation, we have developed a model using the ROSA 26 mouse.

9 phatase, under the control of the ubiquitous Rosa 26 promoter.

10 At this time, only rare ROSA 26 tissue macrophages or microglia were observed.

11 e-tracing approach in triple mice containing Rosa 26(tdTomato) (tracing marker), 2.3 Col1(GFP) (bone

12 anulocyte-macrophage colonies were of donor (ROSA 26) origin determined by beta-gal staining and by n

13 , Six3-Cre transgenic mice were crossed with ROSA-26 reporter mice, and lacZ activity was assayed.

14 ed full-length infectious HIV-1 provirus and ROSA-26-regulated enhanced yellow fluorescent protein.

15 viable cells) isolated from congeneic mice ([ROSA]26 C57BL/6J) expressing Escherichia coli beta-galac

16 attachment (att) sites in cis, within the Gt(ROSA)26Sor safe harbor locus.

17 ails of podocytes, bigenic Coll1alpha1GCE;Gt(ROSA)26Sor(tm9(CAG-tdTomato)) mice allowed podocyte labe

18 Studies using Rosa 26 Lac-Z (B6;129S-Gt(rosa)26Sor) (Lac-Z) mice revealed that fetal AF macropha

19 Genomic analysis of more than 100 Rosa accessions revealed multiple evolutionary steps lea

20 support the use of O. matudae Scheinvar cv. Rosa agro-industrial by-products as functional food ingr

21 zilian woods, similar to oak, were jequitiba rosa and cerejeira, which presented the highest contents

22 E. De Rosa and M. E. Hasselmo demonstrated that 0.25 mg/kg sco

23 cies: renowned Rosa canina L. and unexplored Rosa arvensis Huds.

24 d chromosome-level genome assemblies for two Rosa banksiae subspecies and re-sequenced an additional

25 role in cardiac morphogenesis.[Dedicated to Rosa Beddington, a pioneer in mammalian embryology].

26 The ROSA beta geo26 (ROSA26) mouse strain was produced by ra

27 C57BL/6)F1 donors, 2) bone marrow cells from ROSA BL/6 F1 (lacZ-transfected) mice, 3) rat bone marrow

28 Flowers of fragrant roses such as Rosa bourboniana are ethylene-sensitive and undergo rapi

29 evaluation of Opuntia matudae Scheinvar cv. Rosa by-products (epicarp and endocarp mucilage's), in o

30 y of the Symplicity system (Medtronic, Santa Rosa, CA, USA) at 6 months follow-up in patients with tr

31 -eluting stents (ZES) (Medtronic Inc., Santa Rosa, California) and Xience V everolimus-eluting stents

32 tents (ZES) (Medtronic Cardiovascular, Santa Rosa, California) with Xience V everolimus-eluting stent

33 roup (Guardwire System [Medtronic AVE, Santa Rosa, California] or Filterwire EX [Boston Scientific Co

34 In Rosa canina (2n = 5x = 35), the pollen and ovular parent

35 d infusions of Hibiscus sabdariffa (petals), Rosa canina (receptacles), Ginkgo biloba (leaves), Cymbo

36 rawberry-tree), Prunus spinosa (blackthorn), Rosa canina and Rosa micrantha (wild roses).

37 ulmaria, Geum urbanum, Potentilla erecta and Rosa canina are usually found in treatments.

38 puree and jam) of two Rosa species: renowned Rosa canina L. and unexplored Rosa arvensis Huds.

39 ips of the two roses species Rosa rugosa and Rosa canina, including different products, on carotenoid

40 ty of hips collected from four rose species (Rosa canina, R. corymbifera, R. micrantha, and R. semper

41 ctrometry, we first characterized GIPCs from Rosa cell culture.

42 RG-II (13-26 mum) was incubated in living Rosa cell cultures and cell-free media with and without

43 Rosa cells did not take up d-[U-(14) C]apiose; therefore

44 In conclusion, in cultured Rosa cells RG-II domains have a brief window of opportun

45 l death in chimeras that are colonized by B6-ROSA cells, but again, are never fully rescued.

46 ining of the hearts demonstrated Gsalpha and Rosa cells, exhibiting a mosaic pattern.

47 pathway operates extracellularly in cultured Rosa cells, proceeds via several novel intermediates inc

48 percentage of dying cells in FVB-GFP <--> B6-ROSA chimeras yielded an intriguing mix of both intrinsi

49 By feeding Rosa chinensis "Old Blush" flowers with pathway-specific

50 2275-derived 24-nt phasiRNA pathway in rose (Rosa chinensis).

51 uces significant anthocyanin accumulation in Rosa chinensis, alongside an increase in the expression

52 eratitis FAR (C. fasciventris, C. anonae, C. rosa) complex.

53 s model was used to assess Cre activity in a Rosa Cre-ER background and quantify Cre activity upon di

54 First, we used the ROSA Cre-reporter mice to establish the feasibility of d

55 Surprisingly, deletion of Porcn in Rosa-CreER(T2)/Porcn(Del), MX1-Cre/Porcn(Del), and Vav-C

56 We used Rosa(creERT2) IL-4Ralpha(-/lox) mice, a tamoxifen (TAM)-

57 In agreement with this, Rosa cultures whose polysaccharide biosynthetic machiner

58 wall-associated RG-II domains when added to Rosa cultures.

59 ch work was designed to assess the impact of Rosa damascena (RD) extract on protective components of

60 Rosa damascena essential oil is a high-value natural pro

61 Rosa damascena is one of the most important medicinal an

62 silver nanoparticles (AgNPs) synthesized by Rosa damascena mill L. extract to control the encapsulat

63 persensitive response, preparations of rose (Rosa damascena) cell plasma membranes, partially solubil

64 gated mitigating cold stress in damask rose (Rosa damascene Mill.) using zearalenone (ZEN: 10 uL L-1)

65 gocene), although several zircons from Santa Rosa date to the Upper Oligocene.

66 aluated in the IL-33-deficient and YetCre-13 Rosa-DTA mice.

67 three insufficiently examined Rosa species: Rosa dumalis Bechst., R. dumetorum Thuill.

68 In this study, fruits of Rosa dumalis, R. canina, and R. villosa were cultivated

69 pithelial cells from bitransgenic Krt12Cre/+/ROSA(EGFP) mice were examined by fluorescence-activated

70 es in the corneas of bitransgenic Krt12cre/+/ROSA(EGFP), Krt12Cre/+/ZEG, and Krt12Cre/+/ZAP mouse lin

71 generated in which genomic integration of a ROSA-EGFP transgene resulted in exclusive expression of

72 lectrophysiology of transgenic Cre-inducible Rosa-eGFP-L10a mice in combination with retrograde viral

73 Rosehip oil (Rosa eglanteria L.) is an important oil in the food, pha

74 In this issue of Neuron, Gasset-Rosa et al. (2017) and Grima et al. (2017) describe defe

75 In this issue of Neuron, Gasset-Rosa et al. (2019) and Mann et al. (2019) demonstrate th

76 In this issue of Immunity, De Rosa et al. elucidate an important new role for leptin i

77 tire endoderm-derived pharyngeal epithelium [Rosa et al., 2019, Sci.

78 every part of the xylem vascular tissue of a Rosa floribunda cutting, forming long-range conducting w

79 Here, using Myh11-CreER(T2) ROSA floxed STOP eYFP Apoe(-/-) mice to perform SMC line

80 d cells (ENCCs) by mating Wnt1-Cre mice with Rosa-floxed-YFP mice and investigated ENCC behavior in t

81 dTomato fluorescent proteins in Sim1(Cre/+); Rosa(floxstop26TdTom) mice.

82 The Santa Rosa fossil locality in eastern Peru produced the first

83 th BM reconstituted from either tie2/lacZ or ROSA/green fluorescent protein (GFP) mice (n = 24).

84 METHODS AND Rosa hematopoietic stem cells (lin(-), cKit(+)) were tra

85 ssociated degradation (ERAD) pathway in both Rosa hybrida and Solanum lycopersicum.

86 e deciphered spatial patterns of prickles on Rosa hybrida cv. 'Red Queen' stem.

87 apid petal senescence markedly reduces rose (Rosa hybrida) flower quality and value.

88 Here, we observed that, in rose (Rosa hybrida), biologically active CK is accumulated dur

89 Indeed, in rose (Rosa hybrida), inhibition of bud outgrowth by darkness i

90 I transcription factor in woody plant rose (Rosa hybrida), regulates local auxin biosynthesis and au

91 P2/ERF) transcription factor family in rose (Rosa hybrida), RhERF1 and RhERF4 which play a role in pe

92 f parapithecid anthropoid primate from Santa Rosa in Amazonian Peru.

93 RosA interacts with at least two sRNAs, RoxS and FsrA.

94 cate that the maximum composite age of Santa Rosa is 29.6 0.08 Ma (Lower Oligocene), although several

95 es and/or genera at both CTA-27 and at Santa Rosa is now difficult to reconcile with a >11-My age dif

96 We also found that the transcription of RosA is repressed by CcpA, the key regulator of carbon-m

97 950 +/- 50 cal BP at Arlington Canyon, Santa Rosa Island, California.

98 At site CA-SRI-512 on Santa Rosa Island, Paleocoastal peoples used such tools to cap

99 erfeit samples: a fake of the famous Gronchi Rosa, issued in 1961, and a regummed 2 cent red stamp, i

100 h several signaling pathways were activated, ROSA(KIT D816V) did not exhibit an increased, but did ex

101 ROSA(KIT D816V) may provide a valuable tool for studying

102 KIT WT) cells into an SCF-independent clone, ROSA(KIT D816V), which produced a mastocytosis-like dise

103 Moreover, NSG mice bearing ROSA(KIT D816V)-derived tumors did not show mediator-rel

104 Transfection with KIT D816V converted ROSA(KIT WT) cells into an SCF-independent clone, ROSA(K

105 cell factor (SCF) -dependent human MC line, ROSA(KIT WT), expressing a fully functional immunoglobul

106 M., Rodriguez-de la Rosa, L., Mandruzzato, G., Celaya, A.

107 s in WAP-Cre/Rosa-lox-STOP-lox-LacZ (WAP-Cre/Rosa-LacZ) female mice during pregnancy, lactation and i

108 d postnatal genetic cell fate-maps by mating ROSA-LacZ-reporter mice with mice expressing Cre-recombi

109 Here we show that the ROSA-like insertion abolishes the ability of S. aureus t

110 The ROSA-like phage represents the first description of a mo

111 The ROSA-like prophage has previously been implicated in str

112 The ROSA-like prophage promoted intracellular survival of S

113 ulcers in French patients harbor a prophage, ROSA-like, that is absent from invasive isolates from di

114 The phage, namely ROSA-like, was localized in a hotspot region PhiNM2 near

115 The Rosa-Lkb1 mice exhibited body weight reduction and died

116 Accordingly, the Rosa-Lkb1 mice had increased blood glucose levels and we

117 Finally, the Rosa-Lkb1 mice had much reduced oxygen consumption, carb

118 a26-Cre(ER): Lkb1(flox/flox) (abbreviated as Rosa-Lkb1).

119 nstitutively active MAP2K1 (p.K57N) from the Rosa locus (R26(GT-Map2k1-GFP/+)) and showed, using Tg-C

120 d to conditionally misexpress Hoxc8 from the Rosa locus using select Cre drivers, which significantly

121 RI) mutation, which has been targeted to the ROSA locus, and a Cre-ER transgene that is driven by a f

122 gh cre-lox recombinase originates in WAP-Cre/Rosa-lox-STOP-lox-LacZ (WAP-Cre/Rosa-LacZ) female mice d

123 With the exception of Rosa, mature-ripe fruits are well-colored, sweet and aro

124 Five to six-month-old Ascl1-CreERT2:ROSA mice were treated peripherally with a single dose o

125 When Mx1-Cre:ROSA mice, which were injected with poly(I:C) to label m

126 Prunus spinosa (blackthorn), Rosa canina and Rosa micrantha (wild roses).

127 tion gradient in Southern California's Santa Rosa Mountains.

128 ransgenic overexpressed Gsalpha parent and a Rosa mouse containing the LacZ reporter gene, facilitati

129 editing of loxP sites in airway epithelia of ROSA(mT/mG) mice.

130 Finally, lineage tracing using ROSA(mTmG);Wt1(CreER) mice showed that adenoviral hSCF t

131 espect to site identity and multiflora rose (Rosa multiflora) invasion, soils were collected from ben

132 d (Alliaria petiolata), and multiflora rose (Rosa multiflora).

133 effects of gain of Notch function using the Rosa(NI1C) conditional allele, which carries a constitut

134 ntrahepatic bile ducts and enlarged liver in Rosa(NICD/-)::AlbCre mice could be at least partially re

135 n cells and by overexpression of the NICD in Rosa(NICD/-)::AlbCre mice in vivo induces expression of

136 Cre; Rbpjk(f/f)), gain-of-function (Prx1Cre; Rosa-NICD(f/+)) and RBPjkappa-independent Notch gain-of-

137 and compared general Notch gain-of-function (Rosa-NICD(f/+)), RBPjkappa-deficient (Rbpjkappa(f/f)), a

138 independent Notch gain-of-function (Prx1Cre; Rosa-NICD(f/+); Rbpjk(f/f)) mice for defects in MPC prol

139 RBPjkappa-deficient Notch gain-of-function (Rosa-NICD(f/+);Rbpjkappa(f/f)) conditional mutant mice,

140 Wnt signaling was enhanced in Dmp1-Cre(+/-);Rosa(Notch) femurs.

141 Dmp1-Cre(+/-);Rosa(Notch) mice exhibited an increase in trabecular bon

142 ytes, Dmp1-Cre transgenics were crossed with Rosa(Notch) mice, where a loxP-flanked STOP cassette is

143 f NFAT expression by Notch, osteoblasts from Rosa(Notch) mice, where NICD is transcribed following ex

144 g Notch1 intracellular domain (NICD), and in Rosa(Notch) osteoblastic cells by Cre recombinase-mediat

145 NFATc1 was induced in Rosa(Notch) osteoblastic cells by transducing an adenovi

146 The effects of NICD and NFATc2 in Rosa(Notch) osteoblasts were assessed, and both proteins

147 ted expression of osteoblast gene markers in Rosa(Notch) osteoblasts, but only NICD suppressed the co

148 In Rosa(Notch) osteoblasts, Notch suppressed NFATc1 express

149 itutively active NFATc2 was overexpressed in Rosa(Notch) osteoblasts.

150 puted tomography demonstrated that BGLAP-Cre;Rosa(Notch3) and Dmp1-Cre;Rosa(Notch3) mice of both sexe

151 ted that BGLAP-Cre;Rosa(Notch3) and Dmp1-Cre;Rosa(Notch3) mice of both sexes exhibited an increase in

152 re or Dmp1-Cre transgenics were crossed with Rosa(Notch3) mice, where the NOTCH3 intracellular domain

153 decreased or could not be determined in Cre;Rosa(Notch3) mice.

154 er and void or pore area in cortical bone of Rosa(Notch3) mice.

155 apuchin (Cebus imitator) in the Sector Santa Rosa of the Area de Conservacion Guanacaste, Costa Rica.

156 ars (Carrie, Keitt, Glenn, Manzanillo, Maya, Rosa, Osteen, Tommy Atkins and Kensington Pride) grown i

157 ters of normal cells derived from the normal Rosa parent.

158 potentials of whole fruit, pulp and seeds of Rosa pimpinellifolia L. were evaluated.

159 post-transcriptional regulation by CcpA via RosA places RoxS in a key position to control central me

160 nd no tumors at the level expressed from the ROSA promoter.

161 However, the death of B6-ROSA pyramidal cells never exceeded approximately 70% of

162 Thus, normally resistant B6-ROSA pyramidal neurons demonstrated an increasing sensit

163 of Molecular Microbiology, Tilly, Bestor and Rosa redefine the roles of two lipoproteins, OspC and Vl

164 he conserved sRNA RoxS and an unstudied sRNA RosA (Regulator of sRNA A).

165 The RosA/RoxS interaction not only affects the levels of Rox

166 We studied Rosa-rtTa mice (controls) and Rosa-rtTa;TRE-short hairpi

167 eas IL-21/IL-21R signaling in Doxa-inducible ROSA-rtTA-IL-21-Tg mice expands Teffs and FoxP3(-) cells

168 We studied Rosa-rtTa mice (controls) and Rosa-rtTa;TRE-short hairpin RNA mice, which have reversi

169 to compare rosehips of the two roses species Rosa rugosa and Rosa canina, including different product

170 Rosa rugosa Thunb.

171 dical activity of rose flower extracts (from Rosa rugosa Thunb.) was expressed as Standard Activity C

172 ra), raspberry (Rubus idaeus), and rose hip (Rosa rugosa); while group 'B' quince (Cydonia oblonga),

173 MYB46 in Arabidopsis thaliana and RrMYB18 in Rosa rugosa, are induced by wounding.

174 omplished through strategic employment of La Rosa's lactone and a late-stage Mitsunobu reaction.

175 Sandstone from the Upper Triassic Santa Rosa Sandstone (Dockum Group) from northwestern Texas co

176 The Santa Rosa Sandstone was derived in large part from the eroded

177 dentified in the ethanol extract of Hibiscus rosa sinensis.

178 ue (Malva sylvestris L.), hibiscus (Hibiscus rosa-sinensis L.) and nasturtium (Tropaeolum majus L.),

179 opsis colonies on Chinese hibiscus, Hibiscus rosa-sinensis, in a field setting.

180 Xyloglucans synthesised by cultured rose (Rosa sp.) cells in "heavy" or "light" media (with [13C,2

181 successfully cultured 'Paul's Scarlet' rose (Rosa sp.) cells in boron-free medium: their wall-bound p

182 ion-cultured cells of "Paul's Scarlet" rose (Rosa sp.) have revealed extensive structural similarity

183 Several extracts of examined Rosa species demonstrated inhibition potency towards pro

184 The hips of Rosa species have gained more attention in recent years

185 Phenolic acid contents of the Rosa species increased nonlinearly depending on the harv

186 olinesterase by extracts of all investigated Rosa species was observed.

187 ips and the preserves (puree and jam) of two Rosa species: renowned Rosa canina L. and unexplored Ros

188 ee and jam) of three insufficiently examined Rosa species: Rosa dumalis Bechst., R. dumetorum Thuill.

189 ornamental trees and shrubs (e.g. Hydrangea, Rosa, Spiraea, Syringa, Viburnum), functioned as major p

190 Roses (Rosa spp.) have been cultivated for their scent since an

191 We used islets isolated from Mip-CreER; Rosa-Stop-Lox-Stop-GCamP6s mice (beta-GCamP6s) that show

192 Lineage tracing using Rosa-td tomato (Col2-Cre-ERT2) mice treated with tamoxif

193 a genetic lineage tracing the WT1(CreERT2+/-)Rosa(tdT+/-) mouse model subjected to a high-fat diet, a

194 in rat and in Wilms tumor 1 (WT1)(CreERT2/+);ROSA-tdT(+/-) mice.

195 rotein (CFP), c-Kit(wsh/wsh), and Neurog3Cre;ROSA(tdTom) mice by immunohistochemistry.

196 ECL cells in stomach tissues of NeuroD1-cre;ROSA(tdTom), tryptophan hydroxylase 1 (Tph1)-cyan fluore

197 Using Rosa-tdTomato mice, we found that Prx1- or Dermo1-labele

198 ning the NTS from male and female LepR-Cre X Rosa-tdTomato mice.

199 In the coherent Monte Rosa tectonic unit, Western Alps, considerably different

200 the ROSA26-CAG-(LoxP)tdTomato(StopLoxP)EGFP (ROSA-TG) Cre-reporter was confirmed in primary cells fol

201 g ionocyte lineage tracing (FOXI1-Cre(ERT2)::ROSA-TG), ionocyte ablation (FOXI1-KO) and ionocyte-spec

202 Methods: A novel transgenic ferret model (ROSA-TG::FOXI1-Cre(ERT2)::CFTR(L/L)) was developed to sp

203 alyses produced mean age estimates for Santa Rosa that closely approximate the maximum 29.6 0.08 Ma c

204 We show RosA to be the first confirmed RNA sponge described in a

205 Using Cre-reporter, Rosa(Tomato);Mgp-Cre mice and a new knock-in model expre

206 from mice expressing transgenic SOX17 alone (ROSA(tTa/+);Ptf1(CreERTM/+);tetO-SOX17) or along with ac

207 iploid cultivars, Rosa x hybrida cv H190 and Rosa wichurana, which have contrasting scent profiles.

208 ating population from two diploid cultivars, Rosa x hybrida cv H190 and Rosa wichurana, which have co

209 Using Cre-loxP technology (Pax7-cre/ROSA YFP mice), we expose a wide range of derivatives, i

210 In Kras(G12D)/Pdx1-Cre/Tp53/Rosa(YFP) genetically modified mice, oral administration

211 We treated AAV-TBG-Cre; Rosa(YFP) mice with diethylnitrosamine (DEN), followed b

212 iven causes recombination (AAV-TBG-Cre) into Rosa(YFP) mice.

213 g T(reg) fate-tracking Foxp3(GFP-Cre-ERT2) x ROSA(YFP) reporter mice, we demonstrated that expanded p

214 Human and mouse (Kras(G12D)/Pdx1-Cre/Tp53/Rosa(YFP)) PDAC cells were incubated with inhibitors of

215 ia toxin deleted YFP(+) cells from Foxl1-Cre;Rosa(YFP/iDTR) mice and prevented the resolution of hepa

216 Based on studies of Foxl1-Cre;Rosa(YFP/iDTR) mice, Foxl1(+) HPCs and/or their descenda

217 essing HPCs and their descendants (Foxl1-Cre;Rosa(YFP/iDTR)-inducible diphtheria toxin receptor [iDTR

218 -tracing experiments based on Sox18Cre(ERt2)/Rosa-YFP mice.

219 Lineage tracing by using Cdh5cre(ERt2)/Rosa-YFP reporter strategy demonstrated that the CD31-/l

220 NDCs were isolated from Shh-cre;ROSA:YFP mice at embryonic day 12.5 and postnatal day 0,