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1 siological roles in endothelial function and lymphocyte homing.
2  chronic inflammation and dendritic cell and lymphocyte homing.
3 edicted to promote the overall efficiency of lymphocyte homing.
4 ode high endothelial venules does not affect lymphocyte homing.
5 synthesis of L-selectin ligands required for lymphocyte homing.
6 s in venules at sites of inflammation and in lymphocyte homing.
7 te extravasation in inflammation, and faulty lymphocyte homing.
8 our understanding of how L-selectin mediates lymphocyte homing.
9 f the existence of a biological rheostat for lymphocyte homing.
10 ion molecules in regulating inflammation and lymphocyte homing.
11 hold for the amount of L-selectin needed for lymphocyte homing.
12 s in lymphocyte rolling and is essential for lymphocyte homing.
13 icking in HEV, accounting for the diminished lymphocyte homing.
14 environment also plays a role in determining lymphocyte homing.
15 stent with a selective role for CCR4 in skin lymphocyte homing.
16 HEV-specific L-selectin ligands required for lymphocyte homing.
17 ter receptor a4beta7 on lymphocytes controls lymphocyte homing.
18  to the control of leukocyte recruitment and lymphocyte homing.
19 mutant mice displayed a severe impairment in lymphocyte homing and a compromised contact hypersensiti
20 irst direct evidence of CCR10 involvement in lymphocyte homing and accumulation in vivo, and demonstr
21 ion profiles and flow-cytometric analysis of lymphocyte homing and cell proliferation markers demonst
22 e-binding molecules involved in constitutive lymphocyte homing and chronic and acute inflammation pro
23 nt B cells and deregulated genes involved in lymphocyte homing and dissemination of human lymphomas.
24  differentiation, specifically hampering gut lymphocyte homing and IgA(+) plasma cell differentiation
25               DOCK2 plays a critical role in lymphocyte homing and immunological synapse formation by
26 mmation and therefore influences patterns of lymphocyte homing and inflammation.
27 ), a lectin-like adhesion molecule, mediates lymphocyte homing and leukocyte accumulation at sites of
28 does not appear to play an essential role in lymphocyte homing and leukocyte extravasation or in T ce
29 hat LFA-1 does not play an essential role in lymphocyte homing and leukocyte extravasation.
30       Here we identify the gene encoding the lymphocyte homing and migration protein CD44 as a target
31                                        Basal lymphocyte homing and neutrophil recruitment to inflamed
32 sulfo sialyl Lewis X in L-selectin-dependent lymphocyte homing and recruitment.
33 ouble null mice exhibited a markedly reduced lymphocyte homing and reduced lymphocyte counts as a res
34 o function of endothelial heparan sulfate in lymphocyte homing and stimulation of the immune response
35 HEV-specific L-selectin ligands required for lymphocyte homing and suggest that LSST and Core2GlcNAcT
36 attributable to a combination of blockage of lymphocyte homing and the release of thymocytes from the
37 immune system adhesion molecules involved in lymphocyte homing and the translation of those discoveri
38 sues expresses tissue-specific receptors for lymphocyte homing, and recent work utilizing phage homin
39 in, fibrotic diseases, cholestatic pruritus, lymphocyte homing, and thrombotic diseases by producing
40 eptor activities, leukocyte trafficking, and lymphocyte homing are controlled prominently but incompl
41                          Certain features of lymphocyte homing are maintained in lymphoma recruitment
42 w current thinking about the ATX/LPA axis in lymphocyte homing, as well as in models of allergic airw
43 tive gene splicing, regulates hematopoiesis, lymphocyte homing, B-lineage cell growth, and angiogenes
44                          L-selectin mediates lymphocyte homing by facilitating lymphocyte adhesion to
45                          L-selectin mediates lymphocyte homing by facilitating lymphocyte adhesion to
46                          L-selectin mediates lymphocyte homing by facilitating lymphocyte adhesion to
47                                Inhibition of lymphocyte homing by treatment with FTY720 did not impai
48             Moreover, in an in vivo model of lymphocyte homing, cells expressing only the truncated f
49  independently also from major shifts in the lymphocyte-homing chemokines, CXCL12, CXCL13, and CCL19/
50 dressin required for Peyer's patch-selective lymphocyte homing during ontogeny of the murine intestin
51 rked by up-regulation of genes that regulate lymphocyte homing, followed by quenching of genes that i
52 ial venules, specialized vessels involved in lymphocyte homing from the blood into lymph nodes and Pe
53                                    Selective lymphocyte homing from the blood into tissues is control
54 o intact mucosal immunity through effects on lymphocyte homing, IgA production, and resistance to ant
55 1 receptor internalization in HCC cells or T lymphocyte homing in immunocompetent mice.
56 ed as critical mediators of skin-specific TH lymphocyte homing in mice and humans.
57 on of 6-sulfo sLe(x) carried on N-glycans to lymphocyte homing in mice.
58  evidence for the importance of N-glycans in lymphocyte homing in mouse and indicate that this depend
59 f alpha(4)beta(7), which might contribute to lymphocyte homing in the absence of L-Sel.
60 zed alphaLbeta2-dependent adhesion in vitro, lymphocyte homing in vivo, and firm adhesion but not rol
61 at potentially regulate L-selectin-dependent lymphocyte homing in vivo.
62  contributed in vivo to O-glycan-independent lymphocyte homing in wild-type and mutant mice.
63  processes, including embryonic development, lymphocyte homing, inflammation, and cancer progression.
64 ssins encoded by Madcam1 and St6gal1 control lymphocyte homing into intestinal tissues, regulating im
65          The molecular mechanisms regulating lymphocyte homing into lymph nodes are only partly under
66 echanism of action, i.e. chemokine-dependent lymphocyte homing into secondary lymphoid organs associa
67 s and natural killer T cells, is involved in lymphocyte homing into the aortic wall and modulates the
68  of beta7-deficient mice, demonstrating that lymphocyte homing is a competitive process and that inte
69 ces reveal that the exquisite specificity of lymphocyte homing is determined by combinatorial "decisi
70                                              Lymphocyte homing is mediated by specific interaction be
71                                              Lymphocyte homing is mediated by specific interactions b
72 tion, an analogous function of VE-JAM during lymphocyte homing is plausible.
73 s article a review of the molecular basis of lymphocyte homing is presented, and mechanisms by which
74                Although the role of CCL28 in lymphocyte homing is well established, direct in vivo ev
75                                       During lymphocyte homing, L-selectin mediates the tethering and
76                  ICAM-2 is not essential for lymphocyte homing or the development of leukocytes, with
77 , Th1 cell lines and clones, we compared the lymphocyte homing patterns of a Chlamydia-specific, prot
78  is an essential regulator of hematopoiesis, lymphocyte homing, pre-B-cell growth, and angiogenesis.
79 R4, its ligand CCL17/TARC, and the cutaneous lymphocyte-homing process.
80                                         This lymphocyte "homing" process disperses the immunologic re
81                        The expression of the lymphocyte homing receptor and activation marker L-selec
82                   In this study, we examined lymphocyte homing receptor and vascular addressin expres
83  resulted in more pronounced shedding of the lymphocyte homing receptor CD62L and in increased progra
84                           MAdCAM-1 binds the lymphocyte homing receptor for Peyer's patches, the inte
85                                          The lymphocyte homing receptor integrin alpha(4)beta(7) is u
86        Functional analyses revealed that the lymphocyte homing receptor L-selectin (CD62L) is the key
87 ress enhances the function of the L-selectin lymphocyte homing receptor through an interleukin-6 (IL-
88 inally identified as the lymph node-specific lymphocyte homing receptor, L-selectin has also been sug
89         These findings suggest expression of lymphocyte homing receptors by B cells and vascular addr
90                            Identification of lymphocyte-homing receptors on L-Sel(-/-) and L-Sel(+/+)
91                     Recent reports that some lymphocyte homing-receptors are shared by the liver and
92                                     Blocking lymphocyte homing rescued bleeding, indicating that PDPN
93 ibutes to HEV-born L-selectin ligands, since lymphocyte homing retained in FucT-VII(-/-) mice is revo
94 ting lymphocytes and increased expression of lymphocyte-homing signals in the metastatic tumors.
95  for CD44 and CD62L expression for mediating lymphocyte homing, thus permitting the development of au
96 ve T and B cells and play a critical role in lymphocyte homing to appropriate zones within secondary
97 sal tissues and lungs in humans and mediates lymphocyte homing to barrier epithelia of the airways, o
98 ow unappreciated dominant role for VCAM-1 in lymphocyte homing to BM.
99 osis, enhancing surface a(4)B(7) display and lymphocyte homing to GALT.
100 le (HEV) gene that is crucial for regulating lymphocyte homing to lymph nodes (LN).
101              Although the requirements for T lymphocyte homing to lymph nodes (LNs) are well studied,
102                                              Lymphocyte homing to lymph nodes and Peyer's patches is
103                                     Notably, lymphocyte homing to lymph nodes was decreased by 30%.
104         Understanding the molecular basis of lymphocyte homing to lymphoid organs was originally a pr
105 he vascular addressins that direct selective lymphocyte homing to lymphoid organs.
106                    Their interaction directs lymphocyte homing to mucosa-associated lymphoid tissues.
107 egrin alpha4beta7 plays an important role in lymphocyte homing to mucosal lymphoid tissues and has be
108 hibit binding to MAdCAM in vitro and inhibit lymphocyte homing to murine intestines in vivo.
109 teraction of alpha4beta7 with MAdCAM inhibit lymphocyte homing to murine intestines without effecting
110 -79 anti-PNAd mAb in vivo effectively blocks lymphocyte homing to mutant PPs.
111                                              Lymphocyte homing to normal tissues and recruitment to i
112 aracterize the adhesion cascade that directs lymphocyte homing to peripheral lymph nodes (PLNs), we i
113 ne alone leads to only partial impairment of lymphocyte homing to peripheral lymph nodes and moderate
114 gh endothelial venules, considerably reduced lymphocyte homing to peripheral lymph nodes and reduced
115 a 7 integrins and L-selectin account for all lymphocyte homing to Peyer's patches, but P-selectin-dep
116 a 4 integrins, which play a critical role in lymphocyte homing to Peyer's Patches, made no significan
117  Despite this, KLF3 overexpression abolishes lymphocyte homing to Peyer's patches, much like beta7 de
118 st a novel P-selectin dependent mechanism of lymphocyte homing to Peyer's patches.
119 ion cascade that dictates the specificity of lymphocyte homing to PLNs.
120                                       During lymphocyte homing to secondary lymphoid organs and insta
121 ectin expressed on leukocytes is involved in lymphocyte homing to secondary lymphoid organs and leuko
122 kocyte adhesion molecule L-selectin mediates lymphocyte homing to secondary lymphoid organs and to ce
123 ment into the inflamed peritoneal cavity and lymphocyte homing to secondary lymphoid organs were impa
124                        During the process of lymphocyte homing to secondary lymphoid organs, such as
125 d VLA-4-mediated adhesion as well as human T lymphocyte homing to secondary lymphoid organs.
126  by which fever-range temperatures stimulate lymphocyte homing to secondary lymphoid tissues by incre
127    The role of various adhesion molecules in lymphocyte homing to the brain and in inflammatory autoi
128                These results indicate that T lymphocyte homing to the genital mucosa requires the int
129 alpha 4 beta 7 and L-selectin involvement in lymphocyte homing to the gut and to peripheral lymph nod
130  cell adhesion molecule-1 (MAdCAM-1) directs lymphocyte homing to the gut, and alpha E beta 7 mediate
131 ion to Peyer's patch venules, but suppressed lymphocyte homing to the gut, diminishing the capacity o
132 ability, reduced mucosal injury, and reduced lymphocyte homing to the gut.
133 olecule (MAdCAM-1) plays a pivotal role in T-lymphocyte homing to the gut.
134  molecule-1 (MAdCAM-1) to selectively reduce lymphocyte homing to the intestinal tract.
135  receptors may be particularly important for lymphocyte homing to the RA joint.
136           According to the current paradigm, lymphocyte homing to the small intestine requires the ex
137  (ultraviolet-induced vitamin D3) to imprint lymphocyte homing to the small intestines and T cell mig
138 mune system may be compartmentalized because lymphocyte homing to the upper respiratory tract appears
139                        The steps involved in lymphocyte homing to the white pulp cords of the spleen
140 ndothelial surfaces have been identified for lymphocyte homing to various lymphoid organs and to tiss
141 the requirement of CRAC channel function for lymphocyte homing using expression of a dominant-negativ
142                              Human and mouse lymphocyte homing was assessed, and cells were tracked w
143                                              Lymphocyte homing, which contributes to inflammation, ha
144                Mutant mice maintained robust lymphocyte homing, yet they lacked O-glycan L-selectin l

 
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