ライフサイエンスコーパス: co-inject

1 ificant itch-like behavior, though only when co-injected.

2 er with other transgenes with which they are co-injected.

3 nduce oocyte germinal vesicle breakdown when co-injected.

4 s were packaged in tyrosine mutant AAV-9 and co-injected (5 x 10(12) viral genome particles/vector/mo

5 We co-injected a promoter-less nlslacZ vector with a vector

6 By co-injecting a TALE nuclease and GFP reporter targeting

7 and offspring a/a or alpha/alpha cells were co-injected, a/alpha always exhibited a competitive adva

8 by intravenous injection without the need to co-inject an agent which increases permeability of the B

9 by von Frey filaments, which was reversed by co-injected antibody to IL-4Ra, antibodies to opioid pep

10 ed by FK-506 was significantly attenuated by co-injecting BAPTA, heparin/dantrolene (inhibitors of in

11 een to identify immunocompromised mutants by co-injecting beads and E. coli.

12 f BMP4 MO had no effect on WT hematopoiesis, co-injecting BMP4 with chd MOs significantly reduced ICM

13 reference of gregarious and solitary locusts co-injected by these two monoamines displayed the same t

14 ying CaN-inhibited synaptic potentiation, we co-injected certain agents affecting Ca2+ signaling path

15 iRGD significantly potentiates co-injected chemotherapy in KPC mice with high B5 integr

16 a-galactosidase-expressing adenoviruses were co-injected, clonal expansion of myocytes was reduced, c

17 When co-injected, Crescent and Chordin proteins greatly syner

18 nced intratumoral entry of intraperitoneally co-injected dextran to approximately 300% and doxorubici

19 east cancer mouse model, we demonstrate that co-injecting Doxil and a Zirconium-89 nanoreporter ((89)

20 subunits to form heterotrimers was tested by co-injecting either tagged or untagged G beta 1 and G ga

21 Co-injected embryos exhibited an increased microcephaly,

22 Analysis of co-injected embryos showed targeted changes in up to 33%

23 is, which was reversed by Tiam1 silencing in co-injected fibroblasts.

24 For this purpose, we co-injected GFP.RN3 mRNA and mRNA for the early Xenopus

25 progesterone, and this block is reversed by co-injecting GPRx with morpholino oligonucleotides.

26 When an integrase expression plasmid was co-injected, hFIX serum levels increased more than tenfo

27 deletion both in the presence and absence of co-injected hobo transposase, indicating a permissive st

28 Within 12 h of co-injecting immunoglobulin G from neuromyelitis optica

29 reover, when dkk3a and itgalpha6b mRNAs were co-injected into embryos, luciferase activity was up-reg

30 hown to inhibit the homing of the phage when co-injected into mice with the phage.

31 Here, we show that when co-injected into mouse tumors with an oncolytic HSV, mou

32 le to give functional nitrate transport when co-injected into oocytes.

33 itionally, 99mTc-IgG and 111In-DTPA-IgG were co-injected into six subjects and scintillation camera i

34 ing of Ran-Alexa546 plus GST-GFP-RanBP1, was co-injected into the cytoplasm of cells.

35 a double-labeling experiment in which FB was co-injected into the lumbar cord.

36 luciferase and SonoVue(R) microbubbles were co-injected intravenously in mice.

37 Co-injecting low doses of nkx2.5 and ltbp3 morpholinos r

38 ious mice blocked respiratory stimulation by co-injected LP-44, a 5-HT7 receptor agonist, but had no

39 Co-injected lysine reduced the renal accumulation of 111

40 We then co-injected (mice, intraocular) unimNPs with the glutama

41 Co-injecting morpholinos with human ABCB6 mRNA partially

42 ment did not block the suppressive effect of co-injecting mouse alpha satellite DNA with the transgen

43 yP-1 furthermore improves extravasation of a co-injected nanoparticle into the tumor tissue.

44 Co-injected oocytes displayed larger currents than mKir4

45 ulated whole-cell conductance in hCFTR-mENaC co-injected oocytes was amiloride-insensitive, indicatin

46 e capacity of iRGD to deliver conjugated and co-injected payloads is markedly suppressed when B5 inte

47 analyze the potential protective effect of co-injecting recombinant alpha(1)-microglobulin (rA1M),

48 l-mediated gene transfer into tumor cells by co-injecting s.c. in nude mice tumorigenic c-Ha-ras-tran

49 Finally, in experiment three, co-injecting SCH23390, but not its inactive enantiomer,

50 Co-injected strontium was expected to be sequestered by

51 rall morphant phenotype was also obtained by co-injecting sub-phenotypic dosages of the two morpholin

52 developmental delay, which can be rescued by co-injecting synthetic capped hoxc13a or hoxc13b message

53 rain and its isogenic a/a parent strain were co-injected, the a/a/alpha2 strain exhibited a competiti

54 Importantly, when EGCG was co-injected, the detrimental effects to the retina cause

55 hotopic murine model of pancreatic cancer by co-injecting them with cancer cells and analyzing growth

56 We co-injected these EC with MDA-MB-231 breast cancer cells

57 al use of 123I-labeled D2/D3 receptor ligand co-injected to assess both pre- and postsynaptic sites o

58 and, strikingly, when Fgf3 morpholinos were co-injected together with Fgf8 morpholinos, a significan

59 By co-injecting two GoldyTALEN pairs, inheritable deletions

60 When we co-injected UT-A1 with snapin cRNA in Xenopus oocytes, u

61 abelling a region's inputs and outputs using co-injected vectors.

62 These findings, and those from co-injecting wild-type and mutant RNAs, suggest that the

63 The mice were co-injected with 125I-dsFv labeled by the Iodo-Gen metho

64 In both cases a subset of animals were co-injected with 20 microg of DOTA-ReCCMSH(Arg(11)) to d

65 In Experiment 3, 8-OH-DPAT (8 microg) co-injected with 5,7-dihydroxytryptamine (5,7-DHT; 6 mic

66 omology directed repair in single K562 cells co-injected with a donor template along with CRISPR/Cas9

67 Sea urchin eggs were co-injected with a GST fusion protein composed of the tw

68 Flies co-injected with a non-lethal dose of Destruxin A and th

69 en injected alone, but did induce fever when co-injected with a non-pyrogenic dose (when given alone)

70 f the ubiquitously expressed COL1A gene, and co-injected with a single-stranded repair template into

71 Tumor cells can also be co-injected with additional cell types, such as fibrobla

72 When co-injected with alpha-MSH, SHU-9119 (168 pmol, i.c.v.)

73 plasmalemma only when the beta2 subunit was co-injected with alpha1-EGFP.

74 imulates dendritic cell maturation and, when co-injected with antigen in vivo, significantly enhances

75 ccelerated tumor progression in WT mice when co-injected with B16F1.

76 mors resulted when B16F0 melanoma cells were co-injected with bone marrow MSCs derived from p53-defic

77 Oocytes co-injected with both CFTR and mENaC or hENaC expressed

78 Oocytes co-injected with both G551D-CFTR and ENaC expressed an a

79 w derived-macrophages from Fgf2(LMW-/-) mice co-injected with cancer cells reduce tumour growth and e

80 regions flanking the lincRNA#1 sequence were co-injected with Cas9 as ribonucleoprotein complexes int

81 ber orientation, in tumors from cancer cells co-injected with Cav1WT pMEFs compared to cancer cells o

82 ion of Edg-8 mRNA, but only when oocytes are co-injected with chimeric G(q/i)alpha protein mRNA.

83 th Chx10/Vsx2 and Vsx1 and zebrafish embryos co-injected with chx10/Vsx2 and vsx1 morpholinos, the ch

84 Oocytes co-injected with cRNA for mKir4.2 and Kir5.1, a protein

85 ritoneal neutrophil recruitment in mice when co-injected with CXCL6 into the peritoneal cavity.

86 lpha6b mRNA and itgalpha6b knockdown embryos co-injected with dkk3a mRNA were decreased in a manner s

87 is increased in the central retina; and when co-injected with EGF at postnatal day 10, TGF(beta)inhib

88 Liquid metal co-injected with electrolyte through a microfluidic flow

89 on of this [His-133-Ser]-profilin mutant was co-injected with GP5GP5GP5, the peptide's inhibitory act

90 ional brain kinetics of (11)C-buprenorphine, co-injected with increasing doses of unlabeled buprenorp

91 ferase activities of dkk3a knockdown embryos co-injected with itgalpha6b mRNA and itgalpha6b knockdow

92 otency 160-fold higher than that when MLA is co-injected with JN403.

93 he abilities of cRNA Kv1.3 (T1(-)) fragments co-injected with Kv1.3 (T1(-)) to suppress current in Xe

94 Cavitation of MBs co-injected with liposomes into tumours expressing high

95 ther, in a mouse model transfected CAFs were co-injected with MCF7 and tumour weight and proportion w

96 Moreover, animals co-injected with melatonin and cisplatin did not display

97 However, oocytes co-injected with mesophyll mRNA and KAT1 cRNA produced I

98 distribution of systemically administered OV co-injected with microbubbles.

99 In oocytes co-injected with mRNA for GirK2 and the mGluR1a metabotr

100 the growth rate of tumors derived from cells co-injected with packaging cells producing a retrovirus

101 he half-lives of A2 mutant R471A/R484A or A2 co-injected with receptor-associated protein, a classica

102 Weakly malignant epithelial cells co-injected with senescent fibroblasts had larger and gr

103 ne expression, reporter gene constructs were co-injected with specific or non-specific siRNAs and the

104 s rescued when mRNA encoding murine CFP1 was co-injected with the antisense oligonucleotide.

105 analysis of tumors derived from tumor cells co-injected with the TIMP-2 vector producer cells reveal

106 The growth rate of tumors derived from cells co-injected with the TIMP-2 vector producer cells was si

107 nt of ligand-induced Cl- currents in oocytes co-injected with thyrotropin-releasing hormone (TRH) rec

108 vitro-activated Ms limited tumor growth when co-injected with tumor cells in the skin but not in the

109 Neu1(-/-) mice were co-injected with two scAAV2/8 vectors, expressing human

110 In oocytes co-injected with wild-type SERT and an inactive SERT mut

111 ronal differentiation in the embryo and when co-injected with Xash3, Xdbx inhibits the ability of Xas

112 By co-injecting Wnt3A expressing human mammary fibroblasts

113 xt, to precisely change the LGB sequence, we co-injected ZFNs or transcription activator-like effecto