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1 ates intercellular adhesion of coelomocytes (immunocytes).
2 nd led to hypersensitive and hyperresponsive immunocytes.
3 ctions between infected epithelial cells and immunocytes.
4 oducing beta-cells are destroyed by invading immunocytes.
5 raft mucosa undergoes repopulation with host immunocytes.
6 ith aberrant regulation of keratinocytes and immunocytes.
7 ay cells have been proposed to be the sponge immunocytes.
8 relevant direction for attraction of mucosal immunocytes.
9 mitantly reduce repopulation by autoreactive immunocytes.
10 s (n = 8), did not contain such NKR positive immunocytes.
11 kin by injection of autologous blood-derived immunocytes.
12 ation of knockout mouse strains and specific immunocyte ablation techniques.
13 on in xenografts composed of human PHKCs and immunocytes abolished psoriasiform hyperplasia and infla
14 a(2+)-permeable cation channel essential for immunocyte activation, insulin secretion, and postischem
15 nological synapse," the membrane assembly of immunocyte adhesion and signaling.
16  in the distribution and function of splenic immunocytes and a significant reduction in suppressive a
17 s that direct cell- cell interaction between immunocytes and airway smooth muscle may also modulate a
18  pathologic interplay between skin cells and immunocytes and can result in disfiguring cutaneous lesi
19 sses that include inflammatory activation of immunocytes and macrophages, spillage of intracellular c
20 ow clear that molecular interactions between immunocytes and microbes are mediated largely by Toll-li
21 noid substance, can be found in invertebrate immunocytes and microglia.
22  arterial endothelial cells and invertebrate immunocytes and microglia.
23 ive resources for the 3D genome structure of immunocytes and sheds insights into the order of genome
24 lls depends on interactions with other local immunocytes and, importantly, subtypes of VAT mesenchyma
25 are hyperplastic keratinocytes, infiltrating immunocytes, and activated endothelial cells.
26 sease, continuously fed by a mixed influx of immunocytes, and thus susceptible to evolve over time in
27 ermis is mitotically active and red spherule immunocytes are highly migratory within the spine.
28             In sea urchin embryos, pigmented immunocytes are specified in vegetal epithelium, transit
29 ur current understanding of how these unique immunocytes arise, traffic to various sites, and may or
30      In addition, infected mice given primed immunocytes at 4 d.p.i. showed a significant increase in
31 ctional trafficking of lymphocytes and other immunocytes begins as soon as the vascular clamp is rele
32   Antiviral responses, neuroinflammation and immunocyte blood-brain barrier (BBB) trafficking follow
33 ated during HCV infection, and LPA activates immunocytes, but whether this contributes to immune acti
34 lerotic changes in the absence of detectable immunocytes by acting on VSMCs to potentiate growth-fact
35 nchymal cells are separated from circulating immunocytes by the endothelium, which is targeted by mic
36 cavity, the coelom, containing four types of immunocytes called coelomocytes.
37                                    Dedicated immunocyte cell surface receptors sense spatially distri
38  mammary gland to prepare for lactation, yet immunocyte changes that accompany this rapid remodeling
39 nism of treatment response in tumor spheroid/immunocyte co-cultures.
40 sults from a blockade of the infiltration of immunocytes containing beta-endorphin and the consequent
41 our NN skin samples injected with autologous immunocytes converted to psoriatic plaques.
42  in gene and chromatin structure within skin immunocytes could provide key insights into the pathogen
43  modulation of the keratinocyte phenotype by immunocyte-derived cytokines, in which induction of CDw6
44 that promise site-specific actions affecting immunocyte differentiation and proliferation are feasibl
45 that promise site-specific actions affecting immunocyte differentiation and proliferation are now fea
46 inferred from transcriptional changes during immunocyte differentiation.
47                     As well, we propose that immunocytes disperse when Sp-Eph enhances adhesion, caus
48                                              Immunocytes dynamically reprogram their gene expression
49  activation of various cell types, including immunocytes (eg, macrophages and T cells), smooth muscle
50 ion or function of Sp-Eph results in rounded immunocytes entering ectoderm but not adopting a dendrit
51 nflammation or persistent changes in mucosal immunocytes, enterochromaffin and mast cells, enteric ne
52         Various types of innate and adaptive immunocytes exert positive or negative influences at spe
53                                         Some immunocytes express proteins homologous to the Drosophil
54                                              Immunocytes express Sp-Eph and Sp-Efn is expressed throu
55 put in vivo analysis of the transcriptome of immunocytes from an invertebrate.
56                   Adoptive transfer of human immunocytes from dual treated, virus-free animals to uni
57 e the breadth and underpinning of changes in immunocyte gene expression due to genetic variation in m
58  build quantitative and predictive models of immunocyte gene regulatory networks.
59            Previous models of TF function in immunocytes had restricted each TF to a single functiona
60 The results of functional in vitro assays on immunocytes (haemocytes) of the Mediterranean mussel Myt
61            We showed imaging of infiltrating immunocytes in BLT mice that spontaneously developed a g
62 serve to inhibit the pathogenetic ability of immunocytes in psoriasis.
63 ermine the role of I kappa B-alpha deficient immunocytes in the pathogenesis of the skin disease in a
64 airway epithelium, airway smooth muscle, and immunocytes in the respiratory mucosa, suggesting potent
65  specifically in coelomocytes, which are the immunocytes in the sea urchin.
66 tocompatibility complex class II+, or CD11b+ immunocytes in the skin mesenchyme was increased, and es
67 lly, video microscopic tracing of GFP-tagged immunocytes in the skin of mouse ears reveals that motil
68                                  Circulating immunocytes including CD4(+) and CD8(+) T cells, regulat
69 iferation, we discovered that intraepidermal immunocytes, including both CD4 and CD8+ T cells, expres
70 mal keratinocytes and dermal infiltration of immunocytes, including lymphocytes.
71 lti-layered capsule, which reduced allograft immunocyte infiltrates by enhancement of apoptotic death
72                                              Immunocyte infiltration and cytotoxicity play critical r
73 d MC903-induced itch, epidermal hyperplasia, immunocyte infiltration, and resulted in lower transcrip
74                           In mosaic embryos, immunocytes insert preferentially in ectoderm expressing
75 Expressing Sp-Efn throughout embryos permits immunocyte insertion in ventral ectoderm.
76                       Injection of activated immunocytes into symptomless psoriatic skin grafts, chan
77 l role of keratinocytes in the regulation of immunocytes is poorly understood.
78 and acanthosis and introduce targeting nerve-immunocyte/KC interactions as potential psoriasis therap
79  are important in the development of several immunocyte lineages and modulating the immune response.
80 of molecularly defined neuron subsets and of immunocyte lineages remains unclear.
81 f the IFN-induced response across a range of immunocyte lineages.
82 tion, homeostasis, and communications of all immunocyte lineages.
83 nses to the main gammac cytokines across all immunocyte lineages.
84                                  As the main immunocytes lining pulmonary alveoli, alveolar macrophag
85 umor metabolic activity and tumor associated immunocytes may be a critical driver of improved clinica
86 m and host immune cells and demonstrate that immunocytes may influence the ability of C. albicans to
87 anding of how KCs communicate with microbes, immunocytes, neurons, and other cells to form an effecti
88 -alpha-syn and vasoactive intestinal peptide immunocytes or natural Tregs administered to MPTP mice a
89    SMO deficiency also substantially altered immunocyte phenotype and in vitro function.
90 nal mucosa is capable of developing a mature immunocyte population and that exposure to luminal stimu
91           Intraepithelial and lamina propria immunocyte population densities and subset distributions
92                                      Mucosal immunocyte population densities were lower in AN cysts h
93 y to develop a mucosal immune system with an immunocyte population similar to that of native small in
94  by unfavorably altering effector:suppressor immunocyte ratios and upregulating PD-1 expression on CD
95 t, we prevented treatment-induced peripheral immunocyte recruitment and, surprisingly, largely ablate
96                                              Immunocyte recruitment is a multistep, sequential engage
97                      Glial cells orchestrate immunocyte recruitment to focal areas of viral infection
98 conserved transcriptional program supporting immunocyte recruitment.
99 tation (ITx) on the basis of altered mucosal immunocytes, rejecting and rejection-free ITx allografts
100        In all but one psoriatic patient, the immunocytes required preactivation with IL-2 and superan
101                      Coculture of PHKCs with immunocytes resulted in the upregulation of RAC1-depende
102 parallel with immunophenotyping of cutaneous immunocytes revealed a distinct dichotomy in atopic derm
103                    Because they occur in the immunocyte-rich lymphoid tissues, they are easily access
104 ller cell activity was observed, and splenic immunocytes secreted copious quantities of IFN-gamma.
105 d defined novel phenotypic markers for these immunocytes (see the related article beginning on page 2
106  automated system and strategy for screening immunocyte-solid tumor interactions, enabling the discov
107         However, critical changes within key immunocyte subsets are not known.
108 ovides evidence for the presence of specific immunocyte subsets in mixed tissues.
109                      Mast cells are granular immunocytes that reside in the body's barrier tissues.
110 r lavage fluids after challenge, and splenic immunocytes that secreted IL-5 but not gamma interferon
111 driven by proinflammatory cytokines from the immunocytes, the functional role of keratinocytes in the
112 d molecular patterns (PAMPs) activate innate immunocytes through pattern recognition receptors.
113 n indirect communicator with other cutaneous immunocytes to enhance defense and potentially contribut
114 by the ability of pathogenetic blood-derived immunocytes to induce secondary activation and disordere
115 invasive labeling and subsequent tracking of immunocytes, to investigate pancreatic infiltrate dynami
116  and HBD2 in mucosal inflammation to include immunocyte trafficking and killing of microbes with the
117 immunophenotyping, microbiome profiling, and immunocyte transcriptomics in intestinal organs.
118                  The presence of NKR bearing immunocytes was also observed in 10 of 15 different biop
119                    In contrast, if activated immunocytes were exposed to 1alpha, 25-dihydroxycholecal
120 re combined immunodeficient mice, autologous immunocytes were injected into dermis, and the resultant
121 servations in which autologous blood-derived immunocytes were injected into PN skin engrafted onto SC
122 e pancreatic islets by a mixed population of immunocytes, which results in the impairment and eventua

 
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