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1 and characterize the role of MCs in chronic allergic contact dermatitis.
2 ty (CHS) of murine skin serves as a model of allergic contact dermatitis.
3 may notably influence the course of chronic allergic contact dermatitis.
4 onfirmed the generation of skin TRM cells in allergic contact dermatitis.
5 ffects the risk of contact sensitization and allergic contact dermatitis.
6 immunological processes like irritative and allergic contact dermatitis.
7 t and cosmetics, and they are known to cause allergic contact dermatitis.
8 e a potential therapeutic avenue in treating allergic contact dermatitis.
9 and in experimental animal studies to evoke allergic contact dermatitis.
10 ated with the development of T-cell-mediated allergic contact dermatitis.
11 lesional skin of patients with psoriasis or allergic contact dermatitis.
12 CD4+ and CD8+ T cells from individuals with allergic contact dermatitis.
13 contact dermatitis and oxazolone, a model of allergic contact dermatitis.
14 f psoriasis, fixed drug eruption, atopic and allergic contact dermatitis.
15 re examined utilizing models of irritant and allergic contact dermatitis.
16 including psoriasis, atopic dermatitis, and allergic contact dermatitis.
17 f occupational skin disease are irritant and allergic contact dermatitis.
18 NAAA inhibitor, ARN077, in a mouse model of allergic contact dermatitis.
19 contact hypersensitivity, an animal model of allergic contact dermatitis, a common pruritic disorder
23 reviews the recent literature pertaining to allergic contact dermatitis (ACD) in the pediatric popul
29 (NKT cells) in cellular infiltrate of human allergic contact dermatitis (ACD) skin challenge sites.
30 xisting irritant contact dermatitis (ICD) or allergic contact dermatitis (ACD) that is sometimes clin
33 ell as irritant contact dermatitis (ICD) and allergic contact dermatitis (ACD), are common skin disea
34 nd inflammation are commonly associated with allergic contact dermatitis (ACD), it is not known if th
44 patients (n = 703) presenting with possible allergic contact dermatitis and subsequently undergoing
45 transiently compromised, such as psoriasis, allergic contact dermatitis, and blistering disorders.
46 in diseases, including psoriasis, atopic and allergic contact dermatitis, and cutaneous T-cell lympho
47 sensitizing chemicals in the development of allergic contact dermatitis, and suggest that the irrita
48 lergic background such as atopic dermatitis, allergic contact dermatitis, and urticaria are very comm
52 ich could be applicable for the treatment of allergic contact dermatitis, are still largely unknown.
53 s diagnosed with either atopic dermatitis or allergic contact dermatitis as well as in an inducible m
54 by prominent barrier abnormalities (subacute allergic contact dermatitis, atopic dermatitis), topical
55 anaphylatoxin C5a is a critical mediator of allergic contact dermatitis, bridging essential aspects
56 to Ni(++) is one of the most common forms of allergic contact dermatitis, but how the T-cell receptor
57 rin barrier defects might also predispose to allergic contact dermatitis by allowing greater penetrat
60 In the past decade, mechanisms underlying allergic contact dermatitis have been intensively invest
64 reviews the recent literature pertaining to allergic contact dermatitis in the pediatric population.
65 ct of topically applied THC on DNFB-mediated allergic contact dermatitis in wild-type and CB1/2 recep
66 s included dyskeratosis follicularis Darier, allergic contact dermatitis, infectious folliculitis, va
71 ults provide support for the hypothesis that allergic contact dermatitis is not a classic delayed typ
74 ective mechanism in those who do not develop allergic contact dermatitis is tolerance induction by re
76 reports have suggested that chemical-induced allergic contact dermatitis may not be a traditional typ
79 ne (acute irritant contact dermatitis, acute allergic contact dermatitis) or by prominent barrier abn
80 ere observed in sensory neurons of mice with allergic contact dermatitis- or dry skin-elicited itch;
81 tor-alpha agonists in models of irritant and allergic contact dermatitis produced in mouse ears by to
83 tcomes of CD39 deficiency in irritant versus allergic contact dermatitis, reflecting its diverse role
86 inflammatory responses in a mouse model for allergic contact dermatitis, the contact hypersensitivit
88 this study we use an in vivo mouse model of allergic contact dermatitis to investigate how nanoparti
89 ver, the frequency of DNCB sensitization and allergic contact dermatitis to topically applied mechlor
91 n the group using white petrolatum developed allergic contact dermatitis vs 4 patients (0.9%) in the
92 molecular and cellular mechanism underlying allergic contact dermatitis, we evaluated oxazolone-indu
93 IV hypersensitivity reactions, resulting in allergic contact dermatitis, which clinically resembles
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