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1 CD8+ T cells from individuals with allergic contact dermatitis.
2 presents select aspects of AD, psoriasis, or contact dermatitis.
3 ration of the phorbol ester-induced irritant contact dermatitis.
4 ermatitis and oxazolone, a model of allergic contact dermatitis.
5 lize to immunologically nonspecific forms of contact dermatitis.
6 is, fixed drug eruption, atopic and allergic contact dermatitis.
7 ed utilizing models of irritant and allergic contact dermatitis.
8 sulfate is a well-known inducer of irritant contact dermatitis.
9 nduced skin cancers or allergic and irritant contact dermatitis.
10 g psoriasis, atopic dermatitis, and allergic contact dermatitis.
11 ional skin disease are irritant and allergic contact dermatitis.
12 ibitor, ARN077, in a mouse model of allergic contact dermatitis.
13 acterize the role of MCs in chronic allergic contact dermatitis.
14 of murine skin serves as a model of allergic contact dermatitis.
15 bly influence the course of chronic allergic contact dermatitis.
16 igand 1 (CXCL1) in a mouse model of irritant contact dermatitis.
17 the generation of skin TRM cells in allergic contact dermatitis.
18 e risk of contact sensitization and allergic contact dermatitis.
19 tial therapeutic avenue in treating allergic contact dermatitis.
20 rs they are one of the most common causes of contact dermatitis.
21 gical processes like irritative and allergic contact dermatitis.
22 metics, and they are known to cause allergic contact dermatitis.
23 xperimental animal studies to evoke allergic contact dermatitis.
24 atory responses and pruritus associated with contact dermatitis.
25 ape-stripping test and in a disease model of contact dermatitis.
26 the development of T-cell-mediated allergic contact dermatitis.
27 are antigenic determinants in patients with contact dermatitis.
28 skin of patients with psoriasis or allergic contact dermatitis.
29 ypersensitivity, an animal model of allergic contact dermatitis, a common pruritic disorder in humans
30 studied the role of cathelicidin in allergic contact dermatitis, a model requiring dendritic cells of
31 e confirmed the major findings in irritative contact dermatitis, a second model of cutaneous inflamma
34 the recent literature pertaining to allergic contact dermatitis (ACD) in the pediatric population.
41 rritant contact dermatitis (ICD) or allergic contact dermatitis (ACD) that is sometimes clinically di
42 e evaluated the effect of OA-NO2 on allergic contact dermatitis (ACD) using an established model of c
45 mation are commonly associated with allergic contact dermatitis (ACD), it is not known if they are me
50 atitis (AD) as well as allergic and irritant contact dermatitis (ACD, ICD) are characterized by the s
51 by either inflammation alone (acute irritant contact dermatitis, acute allergic contact dermatitis) o
53 t SerpinB2(-/-) mice are more susceptible to contact dermatitis after topical application of dinitrof
59 ose association was also found with allergic contact dermatitis and increased specific IgE to Malasse
60 R agonists reduce inflammation in a model of contact dermatitis and inhibit inflammatory gene express
62 rhinitis, asthma, and/or eczema in 38.2% and contact dermatitis and other eczema in 35.9%), and menta
63 12-myristate-13-acetate, a model of irritant contact dermatitis and oxazolone, a model of allergic co
66 (n = 703) presenting with possible allergic contact dermatitis and subsequently undergoing patch tes
70 ing chemicals in the development of allergic contact dermatitis, and suggest that the irritant effect
71 o strong levels in basal cells of psoriasis, contact dermatitis, and the proliferative cells of the a
78 ed with either atopic dermatitis or allergic contact dermatitis as well as in an inducible mouse mode
79 pment of a spray to detect urushiol to avoid contact dermatitis, as well as to detect catecholamines
80 ent barrier abnormalities (subacute allergic contact dermatitis, atopic dermatitis), topical H1/2r ag
81 toxin C5a is a critical mediator of allergic contact dermatitis, bridging essential aspects of innate
82 is one of the most common forms of allergic contact dermatitis, but how the T-cell receptor (TCR) re
83 er defects might also predispose to allergic contact dermatitis by allowing greater penetration of ch
84 Atopic dermatitis (AD), psoriasis (PS), and contact dermatitis (CD) are common skin diseases, charac
87 observed seem to be in most cases 'systemic contact dermatitis' due to oral or parenteral re-exposur
89 ngredients represented in the North American Contact Dermatitis Group (NACDG) series were conducted u
93 past decade, mechanisms underlying allergic contact dermatitis have been intensively investigated by
94 tes, especially during allergic and irritant contact dermatitis, however, is less well understood.
95 Atopic dermatitis (AD), as well as irritant contact dermatitis (ICD) and allergic contact dermatitis
96 tients, there is often a coexisting irritant contact dermatitis (ICD) or allergic contact dermatitis
98 In addition, AFC inhibits in vivo allergic contact dermatitis in a mouse model utilizing sensitizat
102 ically applied THC on DNFB-mediated allergic contact dermatitis in wild-type and CB1/2 receptor-defic
104 The most represented forms of non-eczematous contact dermatitis include the erythema multiforme-like,
105 had no effect on croton oil-induced irritant contact dermatitis, indicating that morphine's effects o
106 d dyskeratosis follicularis Darier, allergic contact dermatitis, infectious folliculitis, varicella z
113 ide support for the hypothesis that allergic contact dermatitis is not a classic delayed type hyperse
117 chanism in those who do not develop allergic contact dermatitis is tolerance induction by repeated ex
118 own to cause skin rash, dermal inflammation, contact dermatitis, leucoderma, and cancer promotion.
120 ave suggested that chemical-induced allergic contact dermatitis may not be a traditional type IV hype
121 iscontinued therapy because of side effects (contact dermatitis [n = 2], nausea [n = 1], and acute pa
124 irritant contact dermatitis, acute allergic contact dermatitis) or by prominent barrier abnormalitie
125 ved in sensory neurons of mice with allergic contact dermatitis- or dry skin-elicited itch; however,
128 agonists in models of irritant and allergic contact dermatitis produced in mouse ears by topical tre
133 CD39 deficiency in irritant versus allergic contact dermatitis, reflecting its diverse roles in regu
135 or fragrances were derived from the American Contact Dermatitis Society's Contact Allergen Management
137 In a well-established model of allergic contact dermatitis, the absence of Mincle leads to a sig
138 tory responses in a mouse model for allergic contact dermatitis, the contact hypersensitivity (CHS) r
139 chlorhexidine gluconate is a known cause of contact dermatitis, the phenotypic range of this adverse
141 dy we use an in vivo mouse model of allergic contact dermatitis to investigate how nanoparticles (NPs
142 ed aluminium tubes pose a risk of developing contact dermatitis to patients sensitized to ER based on
143 frequency of DNCB sensitization and allergic contact dermatitis to topically applied mechlorethamine
146 up using white petrolatum developed allergic contact dermatitis vs 4 patients (0.9%) in the group usi
147 r and cellular mechanism underlying allergic contact dermatitis, we evaluated oxazolone-induced chang
148 osts of chlorhexidine-impregnated sponge and contact dermatitis were calculated prospectively using m
150 sensitivity reactions, resulting in allergic contact dermatitis, which clinically resembles eczema.
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