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J L Stampf

Showing results (1-10 of 26) with videos related to

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Contact Dermatitis|April 1, 1984
Thin-layer chromatography study of organic dye allergensI Brandle, J L Stampf, J Foussereau
Canadian Journal of Biochemistry|March 1, 1978
Synthesis of and allergic contact dermatitis to bicyclo-[2,2,1]-heptyl-alpha-methylene-gamma-butyrolactones derived from norbornene and campheneG Schlewer, J L Stampf, C Benezra
Archives of Dermatological Research|January 1, 1988
Allergic contact dermatitis to tulips: an example of enantiospecificityC Papageorgiou, J L Stampf, C Benezra
Archives of Dermatological Research|January 1, 1982
Stereospecificity of allergic contact dermatitis (ACD) to enantiomers. Part III. experimentally induced ACD to a natural sesquiterpene dialdehyde, polygodial in guinea pigsJ L Stampf, C Benezra, Y Asakawa
Archives of Dermatological Research|January 1, 1984
Allergic contact dermatitis to laurel (Laurus nobilis L.): isolation and identification of haptensA Cheminat, J L Stampf, C Benezra
Contact Dermatitis|October 1, 1978
Animal and human sensitivity to alpha-methylene-gamma-butyrolactone derivativesJ L Stampf, G Schlewer, C Benezra
Journal of Medicinal Chemistry|September 1, 1980
Synthesis of alpha-methylene-gamma-butyrolactones: a structure-activity relationship study of their allergenic powerG Schlewer, J L Stampf, C Benezra
Molecular Immunology|August 1, 1980
Allergic contact dermatitis to alpha-methylene-gamma-butyrolactones. Preparation of alantolactone-protein conjugates and induction of contact sensitivity in the guinea pig by an alantolactone-skin protein conjugateG Dupuis, C Benezra, G Schlewer, et al.
Contact Dermatitis|January 1, 1990
Cross-reaction in allergic contact dermatitis from alpha-methylene-gamma-butyrolactones: importance of the cis or trans ring junctionM Schaeffer, P Talaga, J L Stampf, et al.
The Journal of Investigative Dermatology|May 1, 1986
Induction of tolerance to poison ivy urushiol in the guinea pig by epicutaneous application of the structural analog 5-methyl-3-n-pentadecylcatecholJ L Stampf, C Benezra, V Byers, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Contact Dermatitis|April 1, 1984
Thin-layer chromatography study of organic dye allergensI Brandle, J L Stampf, J Foussereau
Canadian Journal of Biochemistry|March 1, 1978
Synthesis of and allergic contact dermatitis to bicyclo-[2,2,1]-heptyl-alpha-methylene-gamma-butyrolactones derived from norbornene and campheneG Schlewer, J L Stampf, C Benezra
Archives of Dermatological Research|January 1, 1988
Allergic contact dermatitis to tulips: an example of enantiospecificityC Papageorgiou, J L Stampf, C Benezra
Archives of Dermatological Research|January 1, 1982
Stereospecificity of allergic contact dermatitis (ACD) to enantiomers. Part III. experimentally induced ACD to a natural sesquiterpene dialdehyde, polygodial in guinea pigsJ L Stampf, C Benezra, Y Asakawa
Archives of Dermatological Research|January 1, 1984
Allergic contact dermatitis to laurel (Laurus nobilis L.): isolation and identification of haptensA Cheminat, J L Stampf, C Benezra
Contact Dermatitis|October 1, 1978
Animal and human sensitivity to alpha-methylene-gamma-butyrolactone derivativesJ L Stampf, G Schlewer, C Benezra
Journal of Medicinal Chemistry|September 1, 1980
Synthesis of alpha-methylene-gamma-butyrolactones: a structure-activity relationship study of their allergenic powerG Schlewer, J L Stampf, C Benezra
Molecular Immunology|August 1, 1980
Allergic contact dermatitis to alpha-methylene-gamma-butyrolactones. Preparation of alantolactone-protein conjugates and induction of contact sensitivity in the guinea pig by an alantolactone-skin protein conjugateG Dupuis, C Benezra, G Schlewer, et al.
Contact Dermatitis|January 1, 1990
Cross-reaction in allergic contact dermatitis from alpha-methylene-gamma-butyrolactones: importance of the cis or trans ring junctionM Schaeffer, P Talaga, J L Stampf, et al.
The Journal of Investigative Dermatology|May 1, 1986
Induction of tolerance to poison ivy urushiol in the guinea pig by epicutaneous application of the structural analog 5-methyl-3-n-pentadecylcatecholJ L Stampf, C Benezra, V Byers, et al.
Pageof 3