ライフサイエンスコーパス: sublethally

1 s encoding alpha-gal A and transplanted into sublethally and lethally irradiated alpha-gal A-deficien

2 , cotransplantation of donor B6 T-reg's into sublethally conditioned BALB/c recipients supported sign

3 After losing their bundles, sublethally damaged hair cells remain in the sensory epi

4 pear to be mutually exclusive, implying that sublethally damaged hair cells repair their bundles.

5 logy and immunoreactivity similar to that of sublethally damaged hair cells.

6 Mechanistically, persister cells sublethally engage apoptotic caspases to activate DNA en

7 We observed that the sublethally exposed cultures were hardly affected, while

8 ound in the majority of analyzed organs, and sublethally infected animals developed virus-specific ne

9 Sublethally infected animals suffered increased morbidit

10 mma-producing CD8(+) T cells were reduced in sublethally infected MAT infant mice.

11 BM monocytes from uninfected or sublethally infected mice bound and internalized very fe

12 Compared to splenic T cells from sublethally infected mice, splenic T cells from lethally

13 failed to worsen in vivo vascular leakage in sublethally infected mice.

14 d organs compared to the levels in naive and sublethally infected mice.

15 tivation of the apoptotic enzymic process of sublethally injured cells.

16 distributed to the apical membrane domain of sublethally injured cells.

17 -containing peptide adhere to the surface of sublethally injured MPT cells but not to control, dextro

18 ptide reduces binding of RGD-coated beads to sublethally injured MPT cells by approximately 50%.

19 tes the repair of physiological processes in sublethally injured renal proximal tubular cells (RPTC).

20 e 1 day after kidney ischemia/reperfusion in sublethally injured tubular cells and that the protein i

21 RPTCs sublethally injured with TBHP exhibited a 50% decrease i

22 Two NHPs were sublethally inoculated by the intravenous (IV) or intrab

23 xpressing porcine GalT and transplanted into sublethally irradiated (3 Gy) GalT-/- mice.

24 Tcm, support donor chimerism (> 6 months) in sublethally irradiated (5.5Gy) mice, without GVHD sympto

25 complex (MHC) class-I incompatible marrow in sublethally irradiated (550 cGy) bm1 recipients, whereas

26 TCR-transgenic donors were transplanted into sublethally irradiated (750 cGy) Ld+ or Ld- recipients.

27 or CD28(+/+) T cells were transplanted into sublethally irradiated (750 cGy), MHC class-I incompatib

28 or CD28(+/+) T cells were transplanted into sublethally irradiated (750 cGy), MHC class-II incompati

29 raftment of C57BL/6 x 129/F2(H-2b) marrow in sublethally irradiated (800 cGy) recipients (AKR/J, H-2k

30 Unexpectedly, reconstitution of sensitized, sublethally irradiated +/+ and -/- mice with bone marrow

31 R1) were used for syngeneic transplants into sublethally irradiated adult mice.

32 effect of GCV treatment on alloengraftment, sublethally irradiated AKR mice underwent transplantatio

33 onally derived murine neurosphere cells into sublethally irradiated allogeneic hosts leads to a donor

34 However, reconstitution studies of sublethally irradiated and BM-reconstituted mice indicat

35 ecule-1 (VCAM-1) using null strains and mice sublethally irradiated and bone marrow (BM) reconstitute

36 Male mice were sublethally irradiated at 5 months of age and treated (o

37 nvestigated the role of IFN-gamma in GVHD in sublethally irradiated B6D2F1 recipients of B6 allo-HCT.

38 transfer of C57BL/6-primed lymphoid cells to sublethally irradiated BALB/c mice engrafted with C57BL/

39 CD3 and IL-2, then adoptively transferred to sublethally irradiated BALB/c or C57BL/6 recipients bear

40 Hence, even when hosts are sublethally irradiated before hematopoietic cell transpl

41 Balb/c mice were sublethally irradiated before receiving skin or vascular

42 Sublethally irradiated BNX (beige/nude/xid) mice were in

43 l-depleted BALB/c BM cells were infused into sublethally irradiated C57BL/6 mice and administered KGF

44 d by infusing lpr, gld, and B6 LN cells into sublethally irradiated CB10 mice.

45 cells from CBA/J host animals with GVHD into sublethally irradiated CBA/J recipients Depletion of Vbe

46 or mechanisms in the response to livers from sublethally irradiated donors.

47 active CD4(+) and CD8(+) TCR Tg T cells into sublethally irradiated hosts, both Tg T cells population

48 When DC-expanded Tregs were introduced into sublethally irradiated hosts, the T cells suppressed gra

49 decrease the transient GVHD morbidity in the sublethally irradiated hosts.

50 However, sublethally irradiated Hoxa-9-/- mice develop persistent

51 usion of parental lymph node (LN) cells into sublethally irradiated hybrid F1 recipients created a mu

52 erism, and early chimerism in particular, in sublethally irradiated immunodeficient and lethally irra

53 It is reported that preconditioning sublethally irradiated immunodeficient NOD/SCID (nonobes

54 Sublethally irradiated Ldlr (-/-) mice exhibited increas

55 e transfer of naive C57BL/6 splenocytes into sublethally irradiated line SV11 mice expressing the SV4

56 Herein, we demonstrate that sublethally irradiated lymphopenic mice transfused with

57 of highly purified CD4+ or CD8+ T cells into sublethally irradiated MHC class II or I disparate recip

58 not dependent on lethal irradiation, because sublethally irradiated mice all had elevated serum IgM a

59 -host reaction to promote alloengraftment in sublethally irradiated mice and provide a graft-vs-leuke

60 ing gene-1-deficient (RAG-/-) recipients, in sublethally irradiated mice naive CD8 T cells of donor o

61 However, activation of VEGFR-3 in sublethally irradiated mice resulted in significantly el

62 Reciprocal bone marrow transplantation in sublethally irradiated mice revealed that enhanced susce

63 eneic bone marrow and result in the death of sublethally irradiated mice treated with costimulation b

64 transplants can be successfully performed in sublethally irradiated mice with and without ex vivo cul

65 robust allogeneic hematopoietic chimerism in sublethally irradiated mice without subsequent GVHD by b

66 s potently increased donor BM engraftment in sublethally irradiated mice, an event occurring independ

67 ift resolution and restored efferocytosis in sublethally irradiated mice.

68 mice bearing progressive MCA205 sarcoma into sublethally irradiated mice.

69 al T cells to undergo HP after transfer into sublethally irradiated mice.

70 provided long-term B-cell reconstitution in sublethally irradiated mice.

71 a, from immunized mice efficiently protected sublethally irradiated naive mice against a subsequent t

72 istance to DEX in a xenogeneic GVHD model in sublethally irradiated NOD-scid IL2rgamma(null) mice.

73 ations of human cord blood were infused into sublethally irradiated NOD-SCID mice.

74 proliferate in the hematopoietic tissues of sublethally irradiated NOD/LtSz-scid/scid mice.

75 lls, or CD34(+) cells were transplanted into sublethally irradiated NOD/SCID mice.

76 old more human myeloid cells are produced in sublethally irradiated NOD/SCID-IL-2Receptor-gammachain-

77 within 3 weeks after being transplanted into sublethally irradiated NOD/scid-IL-2Rgammac-null mice.

78 eparated into CD34(+) cells and infused into sublethally irradiated nonobese diabetic (NOD)severe com

79 sure to vector stocks and then injected into sublethally irradiated nonobese diabetic-severe combined

80 ytic as well as myeloid/lymphoid lineages in sublethally irradiated nonobese diabetic/severe combined

81 Oral administration of ABT263 to either sublethally irradiated or normally aged mice effectively

82 eder system and in vivo after injection into sublethally irradiated Rag1(-/-) mice.

83 (KO) donor cells to reconstitute DCs/LCs in sublethally irradiated recipients and compared the resul

84 r of splenocytes from KyA-immune donors into sublethally irradiated recipients resulted in a greater

85 ) but promotes lethality in unirradiated and sublethally irradiated recipients.

86 produced inflammation when transferred into sublethally irradiated recipients.

87 logeneic T cell-depleted marrow infused into sublethally irradiated recipients.

88 ed by CD4(+) and CD8(+) T cells infused into sublethally irradiated recipients.

89 umors and bone marrow were transplanted into sublethally irradiated secondary recipients, 10 of these

90 eukemia; (2) GM-AML cells are tumorigenic in sublethally irradiated SJL/J mice but not in Swiss nu/nu

91 ative syndrome within 1 month of transfer to sublethally irradiated syngeneic recipients.

92 Moreover, sublethally irradiated TSLPR KO mice showed weaker recov

93 gen-primed B and T lymphocytes were given to sublethally irradiated wild-type mice or mice deficient

94 eloaded with MC-540 or rose bengal (RB) were sublethally irradiated with green light.

95 B cell-deficient (scid, xid, IL-7(-/-), and sublethally irradiated) hosts.

96 10(6) T-bet(-/-) lymph node (LN) cells into sublethally irradiated, major histocompatibility complex

97 Experiments using sublethally irradiated, naive rats adoptively transferre

98 5(+) cells recovered from the bone marrow of sublethally irradiated, transplanted NOD-Scid IL2Rgamma(

99 poietic stem cells (HSCs) were injected into sublethally-irradiated NOD-scid-IL2Rg-/- (NSI) mice.

100 to offset this M1-like polarization process, sublethally ischemic neurons may instead secrete a poten

101 failed to increase GVHD mortality in either sublethally or lethally irradiated animals that received

102 AG1 were compared for efficacy and safety in sublethally preconditioned Rag1(-/-) mice undergoing tra

103 ways at concentrations that are lethally and sublethally toxic to aquatic organisms.

104 In mice infected sublethally with Listeria monocytogenes, fibrin is depos