Andrew M Gulick, Age 57443 Cottonwood Dr, Williamsville, NY 14221

Andrew Gulick Phones & Addresses

Amherst, NY

443 Cottonwood Dr, Williamsville, NY 14221 (716) 639-7920

Buffalo, NY

1 Pilgrim Rd, Madison, WI 53711 (608) 273-0806

443 Cottonwood Dr, Buffalo, NY 14221 (716) 861-1990

Work

Position: Professional/Technical

Education

Degree: Graduate or professional degree

Emails

Mentions for Andrew M Gulick

Andrew Gulick resumes & CV records

Resumes

Andrew Gulick Photo 28

Manager

Location:
Buffalo, NY
Work:
Fred Meyer
Manager
Education:
Portland Community College
Andrew Gulick Photo 29

Associate Professor

Location:
Buffalo, NY
Industry:
Higher Education
Work:
University at Buffalo
Associate Professor
Hauptman-Woodward Medical Research Institute
Principal Research Scientist
Education:
University of Wisconsin - Madison 1989 - 1994
Doctorates, Doctor of Philosophy, Biochemistry
Brown University 1985 - 1989

Publications & IP owners

Us Patents

Glutathione S-Transferase Isoforms

US Patent:
6136605, Oct 24, 2000
Filed:
Aug 26, 1994
Appl. No.:
8/297431
Inventors:
William E. Fahl - Madison WI
Andrew M. Gulick - Madison WI
T. Herbert Manoharan - Madison WI
Ralph B. Puchalski - La Jolla CA
Katharine Kramer - Madison WI
Wyeth W. Wasserman - Madison WI
Assignee:
Wisconsin Alumni Research Foundation - Madison WI
International Classification:
C12N 1500
C12N 1512
C07H 2104
US Classification:
435440
Abstract:
A method is described for the creation of novel isoforms of the enzyme glutathione S-transferase which have enhanced activity in host cells against specific toxic agents. The method includes site directed mutagenesis and selection with the targeted agent in the host cells. The sites of directed mutagenesis is the site of electrophile binding by the native form of the enzyme. This site has proven susceptible to manipulation without loss of enzymatic activity. Various techniques for enhancing the expression, activity, or localization of the expressed enzyme in mammalian cells are described. Genes for the mutant isoforms of the enzyme may be useful in cancer therapeutics to confer upon selected groups of cells heightened resistance to antineoplastic agents.

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