Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
The chemistry of contact allergy: why is a molecule allergenic?
|
Contact Dermatitis
|
1995
|
1.42
|
2
|
Isoeugenol is an important contact allergen: can it be safely replaced with isoeugenyl acetate?
|
Contact Dermatitis
|
1999
|
1.39
|
3
|
Presence of resin acids in "Oakmoss" patch test material: a source of misdiagnosis?
|
J Invest Dermatol
|
2000
|
1.39
|
4
|
Antitumor principles from Ginkgo biloba L.
|
Chem Pharm Bull (Tokyo)
|
1987
|
1.03
|
5
|
Allergic contact dermatitis: epidemiology, molecular mechanisms, in vitro methods and regulatory aspects. Current knowledge assembled at an international workshop at BfR, Germany.
|
Cell Mol Life Sci
|
2011
|
1.02
|
6
|
Ectopic contact dermatitis from ethyl cyanoacrylate instant adhesives.
|
Contact Dermatitis
|
1993
|
0.90
|
7
|
Further important sensitizers in patients sensitive to fragrances.
|
Contact Dermatitis
|
2002
|
0.88
|
8
|
Regulation of the contact sensitivity response to urushiol with anti-urushiol monoclonal antibody ALG 991.
|
Arch Dermatol Res
|
1999
|
0.87
|
9
|
Novel predictive assay for contact allergens using human skin explant cultures.
|
Am J Pathol
|
1996
|
0.82
|
10
|
Deodorants on the European market: quantitative chemical analysis of 21 fragrances.
|
Contact Dermatitis
|
1998
|
0.79
|
11
|
Further important sensitizers in patients sensitive to fragrances.
|
Contact Dermatitis
|
2002
|
0.78
|
12
|
ATPase and morphologic changes in Langerhans cells induced by epicutaneous application of a sensitizing dose of DNFB.
|
J Invest Dermatol
|
1989
|
0.78
|
13
|
Allergic contact dermatitis to plants: understanding the chemistry will help our diagnostic approach.
|
Actas Dermosifiliogr
|
2012
|
0.78
|
14
|
[Formation of Langerhans granules seems linked to membrane ATPase activity of epidermal Langerhans cells].
|
C R Acad Sci III
|
1985
|
0.78
|
15
|
Refinement of the relative alkylation index (RAI) model for skin sensitization and application to mouse and guinea-pig test data for alkyl alkanesulphonates.
|
Arch Dermatol Res
|
1991
|
0.78
|
16
|
Lyral is an important sensitizer in patients sensitive to fragrances.
|
Br J Dermatol
|
1999
|
0.77
|
17
|
ATPase and morphologic changes induced by UVB on Langerhans cells in guinea pigs.
|
J Invest Dermatol
|
1985
|
0.77
|
18
|
Patch testing with budesonide in serial dilutions: the significance of dose, occlusion time and reading time.
|
Contact Dermatitis
|
1999
|
0.77
|
19
|
Deodorants: a clinical provocation study in fragrance-sensitive individuals.
|
Contact Dermatitis
|
1998
|
0.77
|
20
|
Mechanism of allergic contact dermatitis from propacetamol: sensitization to activated N,N-diethylglycine.
|
Contact Dermatitis
|
1998
|
0.77
|
21
|
Synthesis and interaction studies of 13C labeled lactone derivatives with a model protein using 13C NMR.
|
Bioorg Med Chem
|
1993
|
0.76
|
22
|
Bihaptens with 5- and 6-methyl-substituted alkylcatechols and methylene lactone functional groups: tools for hapten (allergen or tolerogen)-protein interaction studies.
|
Chem Res Toxicol
|
1993
|
0.76
|
23
|
Occupational allergic contact dermatitis from ethyl cyanoacrylate.
|
Contact Dermatitis
|
1995
|
0.76
|
24
|
Sesquiterpene lactone mix is not an adequate screen for Compositae allergy.
|
Contact Dermatitis
|
1995
|
0.75
|
25
|
Structure-activity relationships for contact allergenic potential of gamma,gamma-dimethyl-gamma-butyrolactone derivatives. 1. Synthesis and electrophilic reactivity studies of alpha-(omega-substituted-alkyl)-gamma,gamma-dimethyl-gamma-butyrolacton es and correlation of skin sensitization potential and cross-sensitization patterns with structure.
|
Chem Res Toxicol
|
1994
|
0.75
|
26
|
Skin sensitization to eugenol and isoeugenol in mice: possible metabolic pathways involving ortho-quinone and quinone methide intermediates.
|
Chem Res Toxicol
|
1997
|
0.75
|
27
|
Para-phenylendiamine (PPD) 1% pet. is an important allergen in the standard series.
|
Contact Dermatitis
|
2005
|
0.75
|
28
|
Saturated analogues of poison ivy allergens. Synthesis of trans,trans- and cis,trans-3-alkyl-1,2-cyclohexanediols and sensitizing properties in allergic contact dermatitis.
|
J Med Chem
|
1986
|
0.75
|
29
|
Synthesis and photocyclization of alpha-methylene-gamma-butyrolactone-thymine heterodimers.
|
Chem Res Toxicol
|
1995
|
0.75
|
30
|
Tixocortol pivalate contact allergy in the GPMT: frequency and cross-reactivity.
|
Contact Dermatitis
|
2001
|
0.75
|
31
|
A murine in vitro model of allergic contact dermatitis to sesquiterpene alpha-methylene-gamma-butyrolactones.
|
Arch Dermatol Res
|
1992
|
0.75
|
32
|
Patch-testing with serial dilutions of tixocortol pivalate and potential cross-reactive substances.
|
Acta Derm Venereol
|
2000
|
0.75
|
33
|
Testing with corticosteroid aldehydes in corticosteroid-sensitive patients (preliminary results).
|
Contact Dermatitis
|
1998
|
0.75
|
34
|
Regulatory classification of substances oxidized to skin sensitizers on exposure to air.
|
Contact Dermatitis
|
1999
|
0.75
|
35
|
Identification of coumarin as the sensitizer in a patient sensitive to her own perfume but negative to the fragrance mix.
|
Contact Dermatitis
|
1999
|
0.75
|
36
|
Mesalazine and para-phenylenediamine allergy.
|
Contact Dermatitis
|
2004
|
0.75
|
37
|
Systemic contact dermatitis from pseudoephedrine.
|
Contact Dermatitis
|
1991
|
0.75
|
38
|
Patch testing with serial dilutions of budesonide, its R and S diastereomers, and potentially cross-reacting substances.
|
Am J Contact Dermat
|
2001
|
0.75
|
39
|
Risk assessment of dimethylfumarate residues in dwellings following contamination by treated furniture.
|
Risk Anal
|
2013
|
0.75
|
40
|
The repeated open application test: suggestions for a scale of evaluation.
|
Contact Dermatitis
|
1998
|
0.75
|
41
|
Fragrances and other materials in deodorants: search for potentially sensitizing molecules using combined GC-MS and structure activity relationship (SAR) analysis.
|
Contact Dermatitis
|
1998
|
0.75
|
42
|
Contents of fragrance allergens in children's cosmetics and cosmetic-toys.
|
Contact Dermatitis
|
1999
|
0.75
|
43
|
Sensitizing capacity of three methyl alkanesulphonates: a murine in vivo and in vitro model of allergic contact dermatitis.
|
Arch Dermatol Res
|
1990
|
0.75
|
44
|
Identification of Lilial as a fragrance sensitizer in a perfume by bioassay-guided chemical fractionation and structure-activity relationships.
|
Contact Dermatitis
|
2000
|
0.75
|
45
|
The time-dose-response relationship for elicitation of contact dermatitis in isoeugenol allergic individuals.
|
Toxicol Appl Pharmacol
|
2001
|
0.75
|
46
|
Occupational erythema-multiforme-like dermatitis from sensitization to costus resinoid, followed by flare-up and systemic contact dermatitis from beta-cyclocostunolide in a chemistry student.
|
Contact Dermatitis
|
2001
|
0.75
|
47
|
Contact allergy to topical corticosteroids and systemic contact dermatitis from prednisolone with tolerance of triamcinolone.
|
Acta Derm Venereol
|
1995
|
0.75
|
48
|
Routine patch testing with frullanolide mix: an European Environmental and Contact Dermatitis Research Group multicentre study.
|
Contact Dermatitis
|
2003
|
0.75
|
49
|
A successful murine model for contact sensitization to a sesquiterpene-alpha-methylene-gamma-butyrolactone: sensitization to alantolactone in four strains of mice.
|
J Invest Dermatol
|
1991
|
0.75
|
50
|
Structure-activity relationships for contact allergenic potential of gamma,gamma-dimethyl-gamma-butyrolactone derivatives. 2. Quantitative structure-skin sensitization relationships for alpha-substituted-alpha-methyl-gamma,gamma-dimethyl-gamma-butyrolactone s.
|
Chem Res Toxicol
|
1994
|
0.75
|
51
|
Evidence for [2 + 2] photoreaction of alpha-methylene-gamma-butyrolactones with thymine: an explanation for chronic actinic dermatitis to sesquiterpene lactones?
|
Photochem Photobiol
|
1999
|
0.75
|
52
|
'Hydrocortisone alcohol'.
|
Contact Dermatitis
|
1993
|
0.75
|
53
|
Skin sensitization to linalyl hydroperoxide: support for radical intermediates.
|
Chem Res Toxicol
|
1997
|
0.75
|
54
|
Clothing dermatitis from Naphthol AS.
|
Contact Dermatitis
|
2001
|
0.75
|
55
|
[Contact allergy to beta blockaders in eye drops: cross allergy?].
|
Ann Dermatol Venereol
|
1997
|
0.75
|
56
|
Synthesis of a water-soluble analog of 6-methyl-3-N-alkyl catechol labeled with carbon 13: NMR approach to the reactivity of poison ivy/oak sensitizers toward proteins.
|
Bioorg Med Chem Lett
|
1999
|
0.75
|