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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

62 950 +/- 50 cal BP at Arlington Canyon, Santa Rosa Island, California.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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