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1 ses to young and aged blood in heterochronic parabiosis.
2 sis were tissue resident, as demonstrated by parabiosis.
3 systemic IgE in circulation, as indicated by parabiosis.
4 ng surgically coupled, is less invasive than parabiosis.
5 ing that also emerge following heterochronic parabiosis.
6 he experimental aging model of heterochronic parabiosis.
7 ells, Alzheimer's disease, and heterochronic parabiosis.
8 and Abeta plaques after a 12-month period of parabiosis.
9 ads to different outcomes than heterochronic parabiosis.
10 ession patterns, genetic lineage tracing and parabiosis.
11  molecules into the brains of mice following parabiosis.
12 ges, we joined the circulation of mice using parabiosis.
13 uthful systemic milieu through heterochronic parabiosis.
14 s controls were phenotypically unaffected by parabiosis.
15 T iso-mRNA switching and was not affected by parabiosis.
16  we identify, using intravenous labeling and parabiosis, a bona-fide tissue-resident B cell populatio
17 e of circulating factors using heterochronic parabiosis, a surgical technique in which joining of ani
18 festyle interventions, such as heterochronic parabiosis, administration of 'young blood', exercise an
19 ression with age that is largely mimicked by parabiosis: aged blood reduces global gene expression, a
20          Using several approaches, including parabiosis and an evolving barcode system, we demonstrat
21                            Conversely, using parabiosis and depletion studies, we demonstrated that e
22                               However, using parabiosis and fate-mapping approaches in mice, we found
23                                        Using parabiosis and fate-mapping approaches, we confirmed tha
24        Using a combination of time-dependent parabiosis and flow cytometry techniques, we first chara
25                          We confirmed, using parabiosis and flow cytometry, that these proteins are i
26     Here we use intravascular cell labeling, parabiosis and multiplex 3D imaging to identify a popula
27  by other experimental approaches, including parabiosis and non-conditioned transfer of HSCs after bo
28                                        Using parabiosis and plasma infusion, we found that blood-born
29 change in mice and compare this process with parabiosis and plasma injections.
30 ne translation, we tested their validity via parabiosis and quantitative immunofluorescence microscop
31 youthful levels recapitulated the effects of parabiosis and reversed age-related hypertrophy, reveali
32                       Using a combination of parabiosis and serum transfer experiments, we find evide
33                   Here we used fate mapping, parabiosis and single-cell transcriptomics to demonstrat
34                                   Isochronic parabiosis and spatial transcriptomics confirmed that a
35 SF) and stem cell factor at days 17 to 20 of parabiosis and were studied 3 weeks later; 10.1% of marr
36                                           In parabiosis, animals are surgically coupled, which has se
37 he negative effects of B2M and heterochronic parabiosis are, in part, mitigated in the hippocampus of
38                We have used the technique of parabiosis, as a means of adoptive transfer, to demonstr
39                                      Using a parabiosis-based strategy, we identified and isolated ma
40              In this study, using a model of parabiosis between APPswe/PS1dE9 transgenic AD mice and
41  established a chimeric blood circulation by parabiosis between fetal chicks and quails to determine
42 in-expressing haematopoietic stem cells, and parabiosis between genetically marked mice, confirmed th
43                                Here, we used parabiosis between intact and SCN-lesioned mice to show
44                                              Parabiosis, bromodoxyuridine (BrdU) pulse-chase analysis
45 eage tracing and cell tracking, splenectomy, parabiosis, cell adoptive transfer, and functional chara
46 ell and tissue transplantation, apheresis or parabiosis.Clarifying the source of proteins in mixed bi
47                                              Parabiosis-conjoined surgery to provide a shared circula
48 iR-210 using bone marrow transplantation and parabiosis (conjoining of circulatory systems).
49 ed a naturally occurring process of vascular parabiosis coupled with intravascular microinjection of
50                     Studies of heterochronic parabiosis demonstrated that with age, the composition o
51 poietic and endothelial cell chimerism after parabiosis demonstrates that circulating cells can give
52                                          Via parabiosis during chronic hypoxia to induce miR-210 prod
53                                              Parabiosis experiments confirmed that RIPC in this latte
54                                              Parabiosis experiments demonstrate that the kidney conta
55                                 Accordingly, parabiosis experiments demonstrated that MAIT and NKT ce
56                                              Parabiosis experiments demonstrating that dendritic cell
57              By performing BrdU labeling and parabiosis experiments in adult mice, we found that circ
58                                              Parabiosis experiments indicate that impaired regenerati
59                            Chimeric mice and parabiosis experiments indicated that the main fraction
60              Bone marrow transplantation and parabiosis experiments revealed a cell-intrinsic require
61 descendants resided in the adult spleen, and parabiosis experiments showed that these cells migrated
62                                              Parabiosis experiments testing whether humoral factors f
63                                           In parabiosis experiments, splenic DCs were only partially
64 tivating gene 2 GFP reporter mice along with parabiosis experiments, we demonstrate that the vast maj
65 g lymphocytes into lymph nodes and long-term parabiosis experiments, we have found that, contrary to
66  confocal imaging, bone marrow chimeras, and parabiosis experiments, we show that meningeal B cells d
67                                      Through parabiosis experiments, we uncovered cellular states ass
68 d not circulate or emigrate from the lung in parabiosis experiments, were protected from in vivo Ab l
69           This protocol describes the use of parabiosis for efficient transplantation of skin from a
70 Here we provide evidence that mice joined by parabiosis gradually recover much physiology relevant to
71                                Heterochronic parabiosis has been used as a model to study the effects
72  animals using a surgical procedure known as parabiosis has created a wealth of information towards o
73 between mice even after prolonged joining by parabiosis have suggested that DCs are derived from self
74 e conclude that, compared with heterochronic parabiosis, heterochronic blood exchange in small animal
75           Glycemic control was unaffected by parabiosis; however, the distribution of circulating leu
76 gans and their rejuvenation in heterochronic parabiosis (HP), a classical model to study systemic agi
77 able to hemodynamic or behavioral effects of parabiosis, implicating a blood-borne factor.
78                                        Using parabiosis in combination with FAP-deficient transgenic
79              Experiments using heterochronic parabiosis, in which the circulatory systems of young an
80                   Furthermore, heterochronic parabiosis increased aged hepatocyte proliferation and r
81                                              Parabiosis may also be used, taking advantage of the sha
82  prominent role of mitochondrial function in parabiosis-mediated rejuvenation.
83                                    Following parabiosis, memory T cells rapidly equilibrated into the
84         In mice rejuvenated by heterochronic parabiosis, miR-29c-3p was the most prominent miRNA rest
85     This defect is even more pronounced in a parabiosis model that demonstrates a profound reduction
86                              Here, we used a parabiosis model that demonstrates preferential hematoge
87      In addition, we developed a tumor/wound parabiosis model to understand the ability of tumors and
88 total body irradiation, we employed a murine parabiosis model with tie-2-LacZ FvB/N mice connected to
89                Type 2 memory was analyzed by parabiosis model, flow cytometry with in vivo antibody l
90                                         In a parabiosis model, lung Mks were partially replaced over
91                                       In the parabiosis model, mice previously exposed intranasally t
92                                      Using a parabiosis model, we demonstrated that a healing wound w
93  enhanced ILC2 trafficking to the lungs in a parabiosis mouse model of tissue disruption and repopula
94            Using two-photon microscopy and a parabiosis mouse model, we observed the migration and ac
95 ty of residence proxies by integrating mouse parabiosis, multi-organ sampling, intravascular staining
96 ither exogenous or endogenous clusterin, and parabiosis of db clusterin(-/-) double-mutant to WT mice
97          We reconfirmed the lethal effect of parabiosis of db mutant on WT mice and further showed th
98                                              Parabiosis of db mutant, which overexpress leptin, to wi
99 we show, using multiple approaches including parabiosis of mice with GVHD, that GVHD is instead prima
100  research as an alternative to heterochronic parabiosis or plasma injections.
101  normally decline with age, by heterochronic parabiosis or systemic delivery of recombinant protein,
102 a youthful circulation through heterochronic parabiosis or systemic reconstitution with young haemato
103                            As a consequence, parabiosis or transfusion of monocytic cells results in
104 shared blood circulation between 2 mice (aka parabiosis) or repeated injections of young blood plasma
105 providing a shared blood circulation through parabiosis, or through repeated injections of plasma fro
106 lation, partial reprogramming, heterochronic parabiosis, pharmaceutical administration and senescent
107               Here, we used transplantation, parabiosis, plasma transfer, exercise, calorie restricti
108 ed with the stress or other aspect(s) of the parabiosis procedure.
109       While quail fetuses were unaffected by parabiosis, quail serum caused premature troponin T iso-
110                                              Parabiosis refers to the condition in which two entire l
111 equal exchange of DCs between mice joined by parabiosis reflected uneven distribution of DC precursor
112                                Heterochronic parabiosis rejuvenates the performance of old tissue ste
113 vironments, such as after transplantation or parabiosis, remains a challenge.
114                       Notably, heterochronic parabiosis restored the activation of Notch signalling a
115                                              Parabiosis revealed that SLO CD69(+) memory CD8 T cells
116                                              Parabiosis revealed that tumor-specific Trm and Tcirm co
117 ure to youthful circulation by heterochronic parabiosis reverses the aged fracture repair phenotype a
118                                        After parabiosis, secreted PCSK9 was transferred to the circul
119                            Second, combining parabiosis, single-cell analyses, and gene knockouts, we
120                                              Parabiosis studies confirm that T(RM) establishment foll
121     The use of fate-mapping technologies and parabiosis studies have provided insight into the ontoge
122                                  The initial parabiosis studies were done in 2010, and the final stud
123 factors and rekindled scientific interest in parabiosis studies.
124 dal B cells circulate freely, as revealed by parabiosis studies.
125 6/INK4A mRNA did not change in heterochronic parabiosis, suggesting the involvement of other pathways
126                              With the use of parabiosis surgery, this study shows that soluble danger
127 al proteins after exposure to young blood in parabiosis (synaptophysin P = .02; calbindin P = .02) or
128 ues was examined using adoptive transfer and parabiosis systems.
129                    Only modestly restored by parabiosis, these features are rooted in elevated cell-i
130 at the appetite suppression in WT mice after parabiosis to db mutants is the result of induced hyperl
131                                      We used parabiosis to determine whether the central nervous syst
132                                      We used parabiosis to introduce fluorescent-labeled bone marrow-
133 ve to one young mouse and transferred during parabiosis to its old partner.
134 ineage tracing, transplantation studies, and parabiosis to show that most adult cardiac fibroblasts d
135                                              Parabiosis was surgically induced at 4 weeks of age, and
136                                        Using parabiosis we report that thymic involution, declines in
137                    Here, using heterochronic parabiosis we show that blood-borne factors present in t
138 dust mite (HDM) model of allergic asthma and parabiosis, we demonstrate that Th2 Trm cells and circul
139                                        Using parabiosis, we found that amyloid-associated myeloid cel
140 injury, heterochronic adoptive transfer, and parabiosis, we found that the lung microenvironment drov
141         Using passive antibody transfers and parabiosis, we identified a restrictive blood-endothelia
142                          Using heterochronic parabiosis, we observe that young circulating factors ar
143                                      Through parabiosis, we showed that IL-15c drive local proliferat
144  set out to explain the differing effects of parabiosis with genetically diabetic (db) mice versus ad
145                                 Using murine parabiosis with novel transcriptomic technologies, we de
146 is impaired in Chrm1(--) mice and rescued by parabiosis with wild-type mice, suggesting a relay by a

 
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