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Journal Abstract Search

158 related items for PubMed ID: 1825847

  • 1. Perfluorinated analogues of poison ivy allergens. Synthesis and skin tolerogenic activity in mice.
    Fraginals R, Schaeffer M, Stampf JL, Benezra C.
    J Med Chem; 1991 Mar; 34(3):1024-7. PubMed ID: 1825847
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  • 2. 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.
    Lepoittevin JP, Benezra C.
    J Med Chem; 1986 Feb; 29(2):287-91. PubMed ID: 2936885
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  • 7. Delayed contact sensitivity to catechols. 3. The relationship of side-chain length to sensitizing potency of catechols chemically related to the active principles of poison ivy.
    Baer H, Watkins RC, Kurtz AP, Byck JS, Dawson CR.
    J Immunol; 1967 Aug; 99(2):370-5. PubMed ID: 4226616
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  • 12. The synthesis of compounds structurally related to poison ivy Urushiol. 4,5-dimethyl-3-pentadecylcatechol.
    Byck JS, Dawson CR.
    J Org Chem; 1967 Apr; 32(4):1084-8. PubMed ID: 4227456
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  • 13. Preservation of allergic contact dermatitis to poison ivy (urushiol) in late HIV disease. The implications and relevance to immunotherapy with contact allergens.
    Smith KJ, Skelton HG, Nelson A, Wagner KF, Hackley BE.
    Dermatology; 1997 Apr; 195(2):145-9. PubMed ID: 9310722
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  • 15. Synthesis of compounds structurally related to poison ivy urushiol. 3. 3-n-Pentadecylcatechol and 3-n-alkylcatechols of varying side-chain length.
    Kurtz AP, Dawson CR.
    J Med Chem; 1971 Aug; 14(8):729-32. PubMed ID: 4107134
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  • 18. Transcriptome profiling reveals Th2 bias and identifies endogenous itch mediators in poison ivy contact dermatitis.
    Liu B, Tai Y, Liu B, Caceres AI, Yin C, Jordt SE.
    JCI Insight; 2019 Jun 11; 5(14):. PubMed ID: 31184997
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  • 20. Nonenzymic spectrophotometric determination of potential poison ivy cross-reactors.
    Quattrone AJ.
    Clin Chem; 1977 Mar 11; 23(3):571-5. PubMed ID: 138495
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