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1 ing resident gp38/podoplanin(+) fibroblastic reticular cells.
2 ells, a profile associated with fibroblastic reticular cells.
3 hat gives rise exclusively to adult marginal reticular cells.
4 follicular dendritic cells, and fibroblastic reticular cells.
5 5, CCL21 and IL-6 expression in fibroblastic reticular cells.
6 derived mainly from T-cell zone fibroblastic reticular cells.
7 re than one MG nucleus can arise from single reticular cells.
8 trix components, and associated fibroblastic reticular cells.
9 ained by stromal cells, chiefly fibroblastic reticular cells.
10 lla with a mesh-like network of fibroblastic reticular cells along which immune cells migrate, and a
11 elial cells, ependymal cells, and by stromal reticular cells and follicular dendritic cells of lympho
12 xpressing host cells, including fibroblastic reticular cells and follicular dendritic cells.
13 romal organizers give rise to adult marginal reticular cells and form a dedicated stromal niche for i
14  synergistic cross-talk between fibroblastic reticular cells and interstitial flow.
15                                        Giant reticular cells and large neurons in the mesencephalic t
16 ic IL-7-Cre mice, we found that fibroblastic reticular cells and LECs strongly up-regulated IL-7 expr
17      Of the major LNSC subsets, fibroblastic reticular cells and lymphatic endothelial cells are know
18 stromal cells, which include CXCL12-abundant reticular cells and osteoblasts, results in constitutive
19 ed by lymphatic endothelial and fibroblastic reticular cells and promotes blood-lymph separation duri
20 s, uncontrolled proliferation of bone marrow reticular cells, and fibrosis of the marrow compartment.
21 +) cells, plasma cells, follicular dendritic/reticular cells, and germinal center B cell-like cells.
22 y reduced numbers of lymph node fibroblastic reticular cells at the steady state.
23 by increased TRC while UCD shows increased B-reticular cells (BRC).
24 nderpinned by specialized B cell-interacting reticular cells (BRCs).
25 icroscopy showed that SFTSV colocalized with reticular cells but did not colocalize with dendritic ce
26 ectional crosstalk with MAdCAM-1(+) marginal reticular cells by providing tumor-necrosis factor (TNF)
27                         We described labeled reticular cells by their position, morpohology, somatic
28 ined by the presence of ER-TR7+ fibroblastic reticular cells, CD21/35+ follicular dendritic cells (FD
29 ized with endothelial cells and fibroblastic reticular cells, confirming observations using a single-
30               Specifically, the fibroblastic reticular cell-derived DAMP IL-33 is increased by recipi
31 ibute to obesity, to lymph node fibroblastic reticular cell development and function.
32        Secondary lymphoid organ fibroblastic reticular cells emerged as the critical cellular source
33  follicular dendritic cells and fibroblastic reticular cells exhibited staining.
34 g cap-dependent mRNA translation in a rabbit reticular cell extract assay (RRL-IVT).
35           Specifically, CXCL13(+) follicular reticular cells form a small-world network of guidance s
36 ence of an aberrantly remodeled fibroblastic reticular cell (FRC) network expressing elevated fibrobl
37                     Loss of the fibroblastic reticular cell (FRC) network in lymphoid tissues during
38 that is 'posted' on the stromal fibroblastic reticular cell (FRC) network on which T cells traffic.
39 ing structural elements of LTs, fibroblastic reticular cell (FRC) network, not only form the architec
40 the survival factor IL-7 on the fibroblastic reticular cell (FRC) network, resulting in apoptosis and
41 loss of both TN numbers and the fibroblastic reticular cell (FRC) network.
42 at lymphotoxin signaling in the fibroblastic reticular cell (FRC) stromal subset was required for pro
43                                 Fibroblastic reticular cell (FRC) subtypes heightened the expression
44 tworks of CD45(-)gp38(+)CD31(-) fibroblastic reticular cell (FRC)-like cells.
45 tex is composed of a network of fibroblastic reticular cells (FRC) and reticular fibers linking sinus
46                                 Fibroblastic reticular cells (FRC) are immunologically specialized my
47 tional, and functional state of fibroblastic reticular cells (FRC) in human and murine DLBCL.
48  demonstrate viral targeting of fibroblastic reticular cells (FRC) in the lymphoid organs.
49 licles via conduits secreted by fibroblastic reticular cells (FRC).
50 inflammatory [i]CAF and CCL19 + fibroblastic reticular cell [FRC]-like).
51 ng caused a loss of T-cell zone fibroblastic reticular cells (FRCs) and CCL21 expression in lymphoid
52 in (PDPN) signalling in stromal fibroblastic reticular cells (FRCs) and its modulation by CLEC-2 expr
53                                 Fibroblastic reticular cells (FRCs) and lymphatic endothelial cells (
54  produced by stromal cells like fibroblastic reticular cells (FRCs) and supports adaptive immunity by
55                                 Fibroblastic reticular cells (FRCs) and their specialized collagen fi
56                                 Fibroblastic reticular cells (FRCs) are a crucial part of the stromal
57                                 Fibroblastic reticular cells (FRCs) are known to inhabit T cell-rich
58                                 Fibroblastic reticular cells (FRCs) are lymphoid stromal cells essent
59                                 Fibroblastic reticular cells (FRCs) are specialized fibroblasts of se
60                                 Fibroblastic reticular cells (FRCs) are specialized fibroblasts that
61                                 Fibroblastic reticular cells (FRCs) are specialized stromal cells tha
62                 Lymph node (LN) fibroblastic reticular cells (FRCs) define LN niches and regulate lym
63                                 Fibroblastic reticular cells (FRCs) direct the interaction and activa
64                                 Fibroblastic reticular cells (FRCs) form a cellular network that serv
65                 In lymph nodes, fibroblastic reticular cells (FRCs) form a collagen-based reticular n
66 ntly described for lymph nodes, fibroblastic reticular cells (FRCs) form a network in the T cell zone
67                                 Fibroblastic reticular cells (FRCs) form the cellular scaffold of lym
68  robust therapeutic efficacy of fibroblastic reticular cells (FRCs) in sepsis.
69                                 Fibroblastic reticular cells (FRCs) in the T cell zone of lymph nodes
70                                 Fibroblastic reticular cells (FRCs) maintain the architecture of seco
71   At the initiation of GVHD, LN fibroblastic reticular cells (FRCs) rapidly reduced expression of gen
72                      Lymph node fibroblastic reticular cells (FRCs) respond to signals from activated
73                                 Fibroblastic reticular cells (FRCs) showed enrichment for higher expr
74 1 (GREM1)-expressing lymph node fibroblastic reticular cells (FRCs) support DC homeostasis via provis
75 ytokine and chemokine-producing fibroblastic reticular cells (FRCs) supporting B and T cell survival.
76 anized in a rigid 3D network of fibroblastic reticular cells (FRCs) that are a rich cytokine source.
77                 gp38(+) stromal fibroblastic reticular cells (FRCs) that express VEGF are enriched fo
78 nic stromal cells, particularly fibroblastic reticular cells (FRCs), during experimental autoimmune e
79 LN) stromal cells, particularly fibroblastic reticular cells (FRCs), provide critical structural supp
80                                 Fibroblastic reticular cells (FRCs), through their expression of CC c
81 ttributable at least in part to fibroblastic reticular cells (FRCs), which are a major population of
82                  We report that fibroblastic reticular cells (FRCs), which reside in the T cell zone
83 nto distinctive compartments by fibroblastic reticular cells (FRCs).
84 networks containing tolerogenic fibroblastic reticular cells (FRCs).
85  and molecular cues provided by fibroblastic reticular cells (FRCs).
86 s the lymphatic vasculature and fibroblastic reticular cells (FRCs).
87                                 Fibroblastic reticular cells from secondary lymphoid organs, but not
88 endent development of VSMCs and perivascular reticular cells from the common progenitor highlighted t
89              Dendritic cells or fibroblastic reticular cells from wild-type and Ccl19-deficient mice
90        However, the mechanisms that regulate reticular cell function are not well understood.
91 terminal nucleus); noradrenergic, raphe, and reticular cell groups (e.g., locus coeruleus, dorsal rap
92 The major target cells of SFTSV appear to be reticular cells in lymphoid tissues of intestine and spl
93 articularly those ensheathed by fibroblastic reticular cells in the lymph node.
94 localized in specific midbrain and hindbrain reticular cells, including Mauthner's neuron; specific c
95 s support lymphocyte function, and targeting reticular cells is a potential strategy for controlling
96 ls and T-B cell border-enriched fibroblastic reticular cells, is developmentally required for T(FR) c
97 including endothelial cells, CXCL12-abundant reticular cells, leptin-receptor-positive stromal cells,
98                  The first, F3: fibroblastic reticular cell-like fibroblast (CCL19(+)CD74(+)HLA-DRA(+
99 CL19(+)CD74(+)HLA-DRA(+)), is a fibroblastic reticular cell-like subtype that is predicted to maintai
100                       In the thymic cortical reticular cell line, IL-1 and TNF induce a protein of th
101 s lymphotoxin-mediated Ccl19pos fibroblastic reticular cell lineage differentiation.
102  component of the CHT niche, and mature into reticular cells lining and interconnecting sinusoids.
103  types of LN SC subsets, namely fibroblastic reticular cells, lymphatic endothelial cells, and blood
104 critical mediators, and LTbetaR signaling on reticular cells mediated cell survival by modulating pod
105 ion molecules and chemokines by fibroblastic reticular cells most likely facilitates their influence
106                       Surprisingly, marginal reticular cells (MRCs) rather than FDCs expressed B cell
107 al expansion and differentiation of marginal reticular cells (MRCs), a population of lymphoid stromal
108  microscopy, we showed that the fibroblastic reticular cell network regulated naive T cell access to
109 ion of dendritic cells with the fibroblastic reticular cell network within lymph nodes and to microsc
110 ce between intersections in the fibroblastic reticular cell network, suggesting that at an intersecti
111 gely move along conduits of the fibroblastic reticular cell network, they appear to execute random wa
112 and pathological alterations of fibroblastic reticular cell networks in the draining lymph nodes.
113           Overall, we show that fibroblastic reticular cell niches control the ultimate molecular and
114 omal cells expressed markers of fibroblastic reticular cells of lymphoid organs and were readily expa
115                   Our data thus suggest that reticular cells of the B cell zone generate microenviron
116 ion, and disrupted perivascular fibroblastic reticular cell organization, the re-establishment of vas
117                    Mice lacking fibroblastic reticular cell PDPN or platelet CLEC-2 exhibited signifi
118 The peptidase inhibitor 16 (PI16)-expressing reticular cell (PI16(+) RC) subset of adult tonsils exhi
119 cells (TRC), and ACTA2-positive perivascular reticular cells (PRC) were the predominant source of inc
120 19-deficient dendritic cells or fibroblastic reticular cells produced lower amounts of type 2 cytokin
121 ed stromal subset, particularly fibroblastic reticular cell, production of cytokines and chemokines,
122                                 Fibroblastic reticular cell relaxation depended upon inhibition of co
123                                 Fibroblastic reticular cells responded rapidly to DST by transcribing
124     The reduction in lymph node fibroblastic reticular cells resulted in abnormal lymph node organiza
125   Within secondary lymphoid tissues, stromal reticular cells support lymphocyte function, and targeti
126 occurs in the lymph node, where fibroblastic reticular cells support the maintenance of naive T cells
127  lymph nodes, dendritic cells (DCs) maintain reticular cell survival in multiple compartments.
128 s into selected pairs of MG nuclei result in reticular cells that are labelled from either both nucle
129 f collagen fibers ensheathed by fibroblastic reticular cells that connects the subcapsular sinus floo
130 e identify a network of DZ CXCL12-expressing reticular cells that likely support DZ functions.
131 chment to CD4(-) lymphoid organ fibroblastic reticular cells that mediate transinfection of CD4(+) T
132  (HSCs) reside in vascular niches containing reticular cells that secrete CXCL12, a chemokine that pr
133  find the transcription profile of PP T zone reticular cells to be altered in Crohn's disease and tha
134  the inhibitory connections that go from the reticular cells to thalamic relay cells; and (3) that we
135                CXCL13+ FDCs, PDGFRA + T-zone reticular cells (TRC), and ACTA2-positive perivascular r
136  immunoregulatory properties of fibroblastic reticular cells, we reviewed the most recent advances in
137 rents in the postsynaptic thalamic relay and reticular cells were dramatically elevated, favoring reb
138                                 Fibroblastic reticular cells were flow-sorted at different timepoints
139 opulation reminiscent of the CXCL12-abundant reticular cells, which compose the BM HSPC niche.
140 nstrated that PDPN expressed on fibroblastic reticular cells, which surround HEVs, functions as an ac
141  increased numbers of recipient fibroblastic reticular cells with higher BAFF transcript levels.
142 s that the extensive network of fibroblastic reticular cells within the T cell areas helps guide T ce

 
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