S E Kane - JoVE Visualize

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Cancer Research|April 15, 1995

Use of the stress-inducible grp78/BiP promoter in targeting high level gene expression in fibrosarcoma in vivoG Gazit, S E Kane, P Nichols, et al.

Molecular Biology of the Cell|May 22, 1998

Effect of carbohydrate position on lysosomal transport of procathepsin LR G Lingeman, D S Joy, M A Sherman, et al.

Biochemistry|July 22, 1997

Alteration of substrate specificity by mutations at the His61 position in predicted transmembrane domain 1 of human MDR1/P-glycoproteinY Taguchi, K Kino, M Morishima, et al.

Biochemistry|June 19, 1998

Involvement of carboxy-terminal amino acids in secretion of human lysosomal protease cathepsin LS S Chauhan, D Ray, S E Kane, et al.

The Biochemical Journal|September 15, 1989

Glycosylation of procathepsin L does not account for species molecular-mass differences and is not required for proteolytic activityS M Smith, S E Kane, S Gal, et al.

Gene|December 14, 1989

A new vector using the human multidrug resistance gene as a selectable marker enables overexpression of foreign genes in eukaryotic cellsS E Kane, D H Reinhard, C M Fordis, et al.

Virology|March 1, 1996

Bicistronic and two-gene retroviral vectors for using MDR1 as a selectable marker and a therapeutic geneM Z Metz, L Matsumoto, K A Winters, et al.

The Journal of Biological Chemistry|December 25, 1993

Targeted disruption of the mouse mdr1b gene reveals that steroid hormones enhance mdr gene expressionS Altuvia, W D Stein, S Goldenberg, et al.

Molecular and Cellular Biology|August 1, 1988

Use of a cloned multidrug resistance gene for coamplification and overproduction of major excreted protein, a transformation-regulated secreted acid proteaseS E Kane, B R Troen, S Gal, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 25, 1998

Desensitization and sensitization of cells to fluoropyrimidines with different antisenses directed against thymidylate synthase messenger RNAJ Ju, S E Kane, H J Lenz, et al.

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Showing results (11-20 of 29) with videos related to

Sort By:

Pageof 3

Cancer Research|April 15, 1995

Use of the stress-inducible grp78/BiP promoter in targeting high level gene expression in fibrosarcoma in vivoG Gazit, S E Kane, P Nichols, et al.

Molecular Biology of the Cell|May 22, 1998

Effect of carbohydrate position on lysosomal transport of procathepsin LR G Lingeman, D S Joy, M A Sherman, et al.

Biochemistry|July 22, 1997

Alteration of substrate specificity by mutations at the His61 position in predicted transmembrane domain 1 of human MDR1/P-glycoproteinY Taguchi, K Kino, M Morishima, et al.

Biochemistry|June 19, 1998

Involvement of carboxy-terminal amino acids in secretion of human lysosomal protease cathepsin LS S Chauhan, D Ray, S E Kane, et al.

The Biochemical Journal|September 15, 1989

Glycosylation of procathepsin L does not account for species molecular-mass differences and is not required for proteolytic activityS M Smith, S E Kane, S Gal, et al.

Gene|December 14, 1989

A new vector using the human multidrug resistance gene as a selectable marker enables overexpression of foreign genes in eukaryotic cellsS E Kane, D H Reinhard, C M Fordis, et al.

Virology|March 1, 1996

Bicistronic and two-gene retroviral vectors for using MDR1 as a selectable marker and a therapeutic geneM Z Metz, L Matsumoto, K A Winters, et al.

The Journal of Biological Chemistry|December 25, 1993

Targeted disruption of the mouse mdr1b gene reveals that steroid hormones enhance mdr gene expressionS Altuvia, W D Stein, S Goldenberg, et al.

Molecular and Cellular Biology|August 1, 1988

Use of a cloned multidrug resistance gene for coamplification and overproduction of major excreted protein, a transformation-regulated secreted acid proteaseS E Kane, B R Troen, S Gal, et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 25, 1998

Desensitization and sensitization of cells to fluoropyrimidines with different antisenses directed against thymidylate synthase messenger RNAJ Ju, S E Kane, H J Lenz, et al.

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