戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ease in peripheral tissues, such as skin and mucosal epithelia.
2 ble to effectively attach to the respiratory mucosal epithelia.
3 ll development is conserved across different mucosal epithelia.
4  translates to an overall protective role in mucosal epithelia.
5 many different diseases of the cutaneous and mucosal epithelia.
6 ctin filaments and junctional disassembly in mucosal epithelia.
7 o enhance IgG-mediated antigen uptake across mucosal epithelia.
8 BV intermittently productively replicates in mucosal epithelia.
9 molecule expressed on the apical membrane of mucosal epithelia.
10 ediates the transcytosis of HIV-1 across the mucosal epithelia.
11 and/or intracellular killing activity within mucosal epithelia.
12 fically localized in the epidermis and other mucosal epithelia.
13  recruitment of lymphocytes and monocytes to mucosal epithelia.
14 eptides that have been identified in several mucosal epithelia.
15 rosmolar lubricants are toxic to the vaginal mucosal epithelia.
16 eceptor (PIGR), which is expressed mainly on mucosal epithelia.
17 ns, and it controls IgM/IgA transport across mucosal epithelia.
18 forming genus alpha, species 7, which infect mucosal epithelia.
19 paracellular penetration of both viruses via mucosal epithelia.
20  capacity of glycoprotein DMBT1 helps defend mucosal epithelia against microbes.
21  The gammadelta T cells are prevalent in the mucosal epithelia and are postulated to act as 'sentries
22 n-sensing nociceptor neurons innervating all mucosal epithelia and associating with LCs, strongly inh
23 cytomegalovirus (CMV) infection initiates in mucosal epithelia and disseminates via leukocytes throug
24  implicate dysregulated interactions between mucosal epithelia and innate immune cells as the underly
25 ad of herpes simplex virus type 1 (HSV-1) in mucosal epithelia and neuronal tissue depends primarily
26 s available commercially may be toxic to the mucosal epithelia and none are able to provide controlle
27  the molecular interactions between PMNs and mucosal epithelia and the associated functional conseque
28                          Upon replication in mucosal epithelia and transmission to nerve endings, cap
29 at regulate goblet cell development in other mucosal epithelia, and epithelium-specific Ets (ESE) tra
30 ective delivery in the brain, blood vessels, mucosal epithelia, and the skin.
31 regarding regulation of PMN migration across mucosal epithelia are poorly understood.
32 ingiva, and the "nonkeratinized" oral lining mucosal epithelia-are formed by intrinsically distinct k
33 ft cells-rare solitary chemosensory cells in mucosal epithelia-are undergoing intense scientific scru
34                      These results show that mucosal epithelia can act as a nonlymphoid reservoir for
35                                     Skin and mucosal epithelia deploy antimicrobial peptides (AMPs) t
36 en-specific dIgA and small-molecule drugs to mucosal epithelia for therapy.
37             Well-characterized mPV sera bind mucosal epithelia from the hDsg3 mice, but not mucosal t
38 n previously appreciated, with expression on mucosal epithelia from the trachea, cornea, and conjunct
39   To effectively achieve multifunctionality, mucosal epithelia have evolved unique microenvironments
40 provide a critical defence from pathogens at mucosal epithelia including the female reproductive trac
41 anisms underlying disease progression on all mucosal epithelia, including those in the mouth, lungs,
42 h-protein vaccines to deliver antigen across mucosal epithelia is a promising strategy to promote muc
43   Given that migration of neutrophils across mucosal epithelia is associated with disease symptoms an
44           The integrity of the epidermis and mucosal epithelia is highly dependent on resident self-r
45                     One notable exception in mucosal epithelia is M cells, which are specialized for
46 ltistep model for neisserial colonization of mucosal epithelia is proposed.
47              Given that PMN migration across mucosal epithelia is strongly correlated with disease sy
48 he first time segmentally distributed in the mucosal epithelia layer of the gastrointestinal tract.
49 ide distribution in close proximity with the mucosal epithelia makes them one of the first cell types
50 ression of histo-blood group antigens on the mucosal epithelia of human respiratory, genitourinary, a
51 omavirus, MmuPV1, infects both cutaneous and mucosal epithelia of laboratory mice and can be used to
52  of hUG expression are characteristic of the mucosal epithelia of many organs, hUG expression is eith
53 is virus in the basal skin epidermis and the mucosal epithelia of the digestive tract (K14 HPV49 E6/E
54 dicate how hormonally induced changes to the mucosal epithelia of the female genital tract mediate th
55 esulting in either mild recurrent lesions in mucosal epithelia or fatal encephalitis.
56 HIF-1alpha and HIF-2alpha are coexpressed in mucosal epithelia that constitute the barrier between th
57 as a key mediator of mitochondrial health in mucosal epithelia through the regulation of mitophagy an
58 (matrix metalloproteinase-7) is expressed by mucosal epithelia throughout the body and functions in h
59 atrix to colonize the basolateral domains of mucosal epithelia to perpetuate the infectious process.
60 ples of regional immunity are known in other mucosal epithelia, to date, no immune microenvironments
61 APOBEC3B expression in healthy and malignant mucosal epithelia, validating key observations with immu
62 may be relevant in HIV transmission in other mucosal epithelia where complex microbial communities ca
63 nant and malignant disorders of squamous and mucosal epithelia, which have been associated with HPV i