These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 138495)

  • 1. Nonenzymic spectrophotometric determination of potential poison ivy cross-reactors.
    Quattrone AJ
    Clin Chem; 1977 Mar; 23(3):571-5. PubMed ID: 138495
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Recognizing the Toxicodendrons (poison ivy, poison oak, and poison sumac).
    Guin JD; Gillis WT; Beaman JH
    J Am Acad Dermatol; 1981 Jan; 4(1):99-114. PubMed ID: 6451640
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 195(2):145-9. PubMed ID: 9310722
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Immunologic studies of poisonous Anacardiaceae: I. Production of tolerance and desensitization to poison Ivy and oak urushiols using esterified urushiol derivatives in guinea pigs.
    Watson ES; Murphy JC; Wirth PW; Waller CW; Elsohly MA
    J Invest Dermatol; 1981 Mar; 76(3):164-70. PubMed ID: 6453903
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analogues of poison ivy urushiol. Synthesis and biological activity of disubstituted n-alkylbenzenes.
    ElSohly MA; Adawadkar PD; Benigni DA; Watson ES; Little TL
    J Med Chem; 1986 May; 29(5):606-11. PubMed ID: 2939241
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Occupational poison ivy and oak dermatitis.
    Epstein WL
    Dermatol Clin; 1994 Jul; 12(3):511-6. PubMed ID: 7923948
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 5(14):. PubMed ID: 31184997
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Resorcinols and catechols: a clinical study of cross-sensitivity.
    Knight TE; Boll P; Epstein WL; Prasad AK
    Am J Contact Dermat; 1996 Sep; 7(3):138-45. PubMed ID: 8957327
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Quantitation and cloning of human urushiol specific peripheral blood T-cells: isolation of urushiol triggered suppressor T-cells.
    Kalish RS; Morimoto C
    J Invest Dermatol; 1989 Jan; 92(1):46-52. PubMed ID: 2521239
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Allergic contact dermatitis caused by Lithraea molleoides and Lithraea brasiliensis: identification and characterization of the responsible allergens.
    Alé SI; Ferreira F; González G; Epstein W
    Am J Contact Dermat; 1997 Sep; 8(3):144-9. PubMed ID: 9249282
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Studies on poison ivy. In vitro lymphocyte transformation by urushiol-protein conjugates.
    Dupuis G
    Br J Dermatol; 1979 Dec; 101(6):617-24. PubMed ID: 161173
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A study of cross-reactions between mango contact allergens and urushiol.
    Oka K; Saito F; Yasuhara T; Sugimoto A
    Contact Dermatitis; 2004; 51(5-6):292-6. PubMed ID: 15606656
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Separation and structural determination of the olefinic components of poison ivy urushiol, cardanol and cardol.
    SYMES WF; DAWSON CR
    Nature; 1953 May; 171(4358):841-2. PubMed ID: 13054743
    [No Abstract]   [Full Text] [Related]  

  • 16. The allergenic principles of poison ivy; note on the synthesis of 3-substituted catechols.
    MASON HS
    J Am Chem Soc; 1947 Sep; 69(9):2241. PubMed ID: 20262749
    [No Abstract]   [Full Text] [Related]  

  • 17. 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
    [No Abstract]   [Full Text] [Related]  

  • 18. Images in clinical medicine. The mango-poison ivy connection.
    Tucker MO; Swan CR
    N Engl J Med; 1998 Jul; 339(4):235. PubMed ID: 9673302
    [No Abstract]   [Full Text] [Related]  

  • 19. Hyposensitization to poison ivy after working in a cashew nut shell oil processing factory.
    Reginella RF; Fairfield JC; Marks JG
    Contact Dermatitis; 1989 Apr; 20(4):274-9. PubMed ID: 2526711
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The allergenic principles of poison ivy; absorption spectra of 3-n-pentadecylcatechol and related compounds.
    MASON HS
    J Am Chem Soc; 1948 Jan; 70(1):138-40. PubMed ID: 18918804
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.