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1 ble to effectively attach to the respiratory mucosal epithelia.
2 ll development is conserved across different mucosal epithelia.
3  translates to an overall protective role in mucosal epithelia.
4 many different diseases of the cutaneous and mucosal epithelia.
5 ctin filaments and junctional disassembly in mucosal epithelia.
6 o enhance IgG-mediated antigen uptake across mucosal epithelia.
7 BV intermittently productively replicates in mucosal epithelia.
8 molecule expressed on the apical membrane of mucosal epithelia.
9 ediates the transcytosis of HIV-1 across the mucosal epithelia.
10 and/or intracellular killing activity within mucosal epithelia.
11 fically localized in the epidermis and other mucosal epithelia.
12  recruitment of lymphocytes and monocytes to mucosal epithelia.
13 eptides that have been identified in several mucosal epithelia.
14  The gammadelta T cells are prevalent in the mucosal epithelia and are postulated to act as 'sentries
15 cytomegalovirus (CMV) infection initiates in mucosal epithelia and disseminates via leukocytes throug
16  implicate dysregulated interactions between mucosal epithelia and innate immune cells as the underly
17 ad of herpes simplex virus type 1 (HSV-1) in mucosal epithelia and neuronal tissue depends primarily
18 s available commercially may be toxic to the mucosal epithelia and none are able to provide controlle
19  the molecular interactions between PMNs and mucosal epithelia and the associated functional conseque
20 at regulate goblet cell development in other mucosal epithelia, and epithelium-specific Ets (ESE) tra
21 ective delivery in the brain, blood vessels, mucosal epithelia, and the skin.
22 regarding regulation of PMN migration across mucosal epithelia are poorly understood.
23 ingiva, and the "nonkeratinized" oral lining mucosal epithelia-are formed by intrinsically distinct k
24                      These results show that mucosal epithelia can act as a nonlymphoid reservoir for
25                                     Skin and mucosal epithelia deploy antimicrobial peptides (AMPs) t
26 en-specific dIgA and small-molecule drugs to mucosal epithelia for therapy.
27             Well-characterized mPV sera bind mucosal epithelia from the hDsg3 mice, but not mucosal t
28 n previously appreciated, with expression on mucosal epithelia from the trachea, cornea, and conjunct
29   To effectively achieve multifunctionality, mucosal epithelia have evolved unique microenvironments
30 anisms underlying disease progression on all mucosal epithelia, including those in the mouth, lungs,
31   Given that migration of neutrophils across mucosal epithelia is associated with disease symptoms an
32           The integrity of the epidermis and mucosal epithelia is highly dependent on resident self-r
33                     One notable exception in mucosal epithelia is M cells, which are specialized for
34 ltistep model for neisserial colonization of mucosal epithelia is proposed.
35              Given that PMN migration across mucosal epithelia is strongly correlated with disease sy
36 he first time segmentally distributed in the mucosal epithelia layer of the gastrointestinal tract.
37 ide distribution in close proximity with the mucosal epithelia makes them one of the first cell types
38 ression of histo-blood group antigens on the mucosal epithelia of human respiratory, genitourinary, a
39  of hUG expression are characteristic of the mucosal epithelia of many organs, hUG expression is eith
40 is virus in the basal skin epidermis and the mucosal epithelia of the digestive tract (K14 HPV49 E6/E
41 dicate how hormonally induced changes to the mucosal epithelia of the female genital tract mediate th
42 esulting in either mild recurrent lesions in mucosal epithelia or fatal encephalitis.
43 HIF-1alpha and HIF-2alpha are coexpressed in mucosal epithelia that constitute the barrier between th
44 (matrix metalloproteinase-7) is expressed by mucosal epithelia throughout the body and functions in h
45 atrix to colonize the basolateral domains of mucosal epithelia to perpetuate the infectious process.
46 ples of regional immunity are known in other mucosal epithelia, to date, no immune microenvironments
47 may be relevant in HIV transmission in other mucosal epithelia where complex microbial communities ca
48 nant and malignant disorders of squamous and mucosal epithelia, which have been associated with HPV i

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