ライフサイエンスコーパス: parabiotic

1 We now formally demonstrate by parabiotic, adoptive transfer, and developmental studies

2 ously used selective combinations of normal, parabiotic, and radioablated mice to demonstrate that bl

3 Shared circulation between the parabiotic animals was confirmed by Evans blue dye injec

4 To prevent immune reaction between the parabiotic animals, all mice were bred to be Rag1(-/-).

5 mice in which remyelination was enhanced by parabiotic coupling to a younger mouse and in multiple s

6 Parabiotic experiments are still used and were recently

7 Using a blood-perfused, parabiotic, isolated rabbit heart model, 45 hearts under

8 epair by generating chimeric animals through parabiotic joining of wild-type (wt) and diabetic (db/db

9 migration of endogenous DCs to the thymus in parabiotic mice and after painting mouse skin with fluor

10 Furthermore, parabiotic mice and BM chimeras of nonirradiated recipie

11 ether with congenic bone marrow chimeras and parabiotic mice as tools to differentiate LC- and blood-

12 Experiments in normal, radioablated, and parabiotic mice document the cyclical accumulation (3-5

13 Experiments using parabiotic mice fed a high-fat diet (HFD) showed differe

14 Analysis of parabiotic mice revealed that adipose ILC1s maintained l

15 Consequently, the observations on the parabiotic mice support the notion that PXE is a metabol

16 This study was designed to test, using parabiotic mice that were joined surgically, whether ste

17 Parabiotic mice were generated surgically by joining gre

18 Parabiotic mice were made by surgically linking C3(-/-)

19 In parabiotic mice with separate organs but shared blood ci

20 In parabiotic mice with separate organs, but a shared blood

21 These kinetics were confirmed in parabiotic mice, and in cohorts of mice in whom gating w

22 We created parabiotic mice, joining ROSA26 and PeP3b animals, to st

23 Using parabiotic mice, we demonstrated that, despite their int

24 Using parabiotic mice, we determined that, after mobilization

25 Similarly, in GFP+:GFP- parabiotic mice, we found substantial chimerism of hemat

26 Using parabiotic mice, we further show that circulating CD8(+)

27 Here, by using parabiotic mice, we show that a preexisting pool of CD4

28 of blood-borne HSCs using genetically marked parabiotic mice, which are surgically conjoined and shar

29 pair of ischaemic myocardium using GFP+-GFP- parabiotic mice.

30 ocytes was determined by timed separation of parabiotic mice.

31 mice, together with bone marrow chimera and parabiotic models, we found that embryonic precursor cel

32 ertility, we established transplantation and parabiotic mouse models to assess the capacity of circul

33 ralization factor(s) in circulation, we used parabiotic pairing, ie, surgical joining of two mice, to

34 tor cells from these tissues, we established parabiotic pairings (that is, a shared circulatory syste

35 the circulation into tumors was confirmed in parabiotic pairs of COL-EGFP mice and transgenic mice de

36 Intriguingly, in parabiotic pairs of two WT mice, leptin infusion into on

37 r, leptin treatment resulted in death of the parabiotic pairs.

38 OL-EGFP(+) cells in tumors developing in the parabiotic partner lacking the fluorescent reporter.

39 ns of blood-derived monocytes from the young parabiotic partner, and preventing this recruitment part

40 Th2 cells recirculate and seed the lung of a parabiotic partner, conferring susceptibility to OVA cha

41 ocytes and progenitor cells derived from the parabiotic partner, suggesting splenic progenitor cells

42 later; 10.1% of marrow HSCs derived from the parabiotic partner.

43 old regenerating muscle of the heterochronic parabiotic partners.

44 they arise and in the gonads of the natural parabiotic partners.

45 eria: 1) inefficient (<20%) exchange between parabiotic partners; 2) gated importation by the thymus;

46 Using a blood-perfused parabiotic rabbit heart Langendorff model, myocardial ox

47 this historic study, Kurt R. Reissmann used parabiotic rats to demonstrate the functional existence

48 /ob) confirm hypotheses generated from early parabiotic studies that suggested the existence of a cir

49 Using time-lapse confocal imaging, parabiotic surgical pairing of zebrafish embryos, and bl

50 lized a combination of genetic fate mapping, parabiotic, transcriptional, and functional analyses and

51 rohemorrhage were found in the brains of the parabiotic wild-type mice.

52 g-term potentiation was markedly impaired in parabiotic wild-type mice.

53 Finally, using parabiotic zebrafish, we show that cxcr1 acts HSPC nonau