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C J Cooksey

Showing results (21-30 of 36) with videos related to

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Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|August 6, 2016
Quirks of dye nomenclature. 6. Malachite greenC J Cooksey
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|October 26, 2018
The red insect dyes: carminic, kermesic and laccaic acids and their derivativesC J Cooksey
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|January 4, 2015
Quirks of dye nomenclature. 4. Fuchsine: four shades of magentaC J Cooksey, A T Dronsfield
Pigment Cell Research|January 1, 1988
Initial mushroom tyrosinase-catalysed oxidation product of 4-hydroxyanisole is 4-methoxy-ortho-benzoquinoneS Naish, C J Cooksey, P A Riley
The Biochemical Journal|November 15, 1994
Oxidation of monohydric phenol substrates by tyrosinase: effect of dithiothreitol on kineticsS Naish-Byfield, C J Cooksey, P A Riley
Biochemical Pharmacology|March 15, 1990
Reaction kinetics of 4-methoxy ortho benzoquinone in relation to its mechanism of cytotoxicity: a pulse radiolysis studyE J Land, C J Cooksey, P A Riley
Pigment Cell Research|January 1, 1988
Major primary cytotoxic product of 4-hydroxyanisole oxidation by mushroom tyrosinase is 4-methoxy ortho benzoquinoneS Naish, J L Holden, C J Cooksey, et al.
Melanoma Research|December 1, 1992
Reactivity of orthoquinones involved in tyrosinase-dependent cytotoxicity: differences between alkylthio- and alkoxy-substituentsC J Cooksey, K Jimbow, E J Land, et al.
Science (New York, N.Y.)|June 24, 1983
Sucrose: a constitutive elicitor of phytoalexin synthesisC J Cooksey, P J Garratt, J S Dahiya, et al.
Anti-Cancer Drug Design|March 1, 1995
Tyrosinase-mediated cytotoxicity of 4-substituted phenols: quantitative structure-thiol-reactivity relationships of the derived o-quinonesC J Cooksey, E J Land, C A Ramsden, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|August 6, 2016
Quirks of dye nomenclature. 6. Malachite greenC J Cooksey
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|October 26, 2018
The red insect dyes: carminic, kermesic and laccaic acids and their derivativesC J Cooksey
Biotechnic & Histochemistry : Official Publication of the Biological Stain Commission|January 4, 2015
Quirks of dye nomenclature. 4. Fuchsine: four shades of magentaC J Cooksey, A T Dronsfield
Pigment Cell Research|January 1, 1988
Initial mushroom tyrosinase-catalysed oxidation product of 4-hydroxyanisole is 4-methoxy-ortho-benzoquinoneS Naish, C J Cooksey, P A Riley
The Biochemical Journal|November 15, 1994
Oxidation of monohydric phenol substrates by tyrosinase: effect of dithiothreitol on kineticsS Naish-Byfield, C J Cooksey, P A Riley
Biochemical Pharmacology|March 15, 1990
Reaction kinetics of 4-methoxy ortho benzoquinone in relation to its mechanism of cytotoxicity: a pulse radiolysis studyE J Land, C J Cooksey, P A Riley
Pigment Cell Research|January 1, 1988
Major primary cytotoxic product of 4-hydroxyanisole oxidation by mushroom tyrosinase is 4-methoxy ortho benzoquinoneS Naish, J L Holden, C J Cooksey, et al.
Melanoma Research|December 1, 1992
Reactivity of orthoquinones involved in tyrosinase-dependent cytotoxicity: differences between alkylthio- and alkoxy-substituentsC J Cooksey, K Jimbow, E J Land, et al.
Science (New York, N.Y.)|June 24, 1983
Sucrose: a constitutive elicitor of phytoalexin synthesisC J Cooksey, P J Garratt, J S Dahiya, et al.
Anti-Cancer Drug Design|March 1, 1995
Tyrosinase-mediated cytotoxicity of 4-substituted phenols: quantitative structure-thiol-reactivity relationships of the derived o-quinonesC J Cooksey, E J Land, C A Ramsden, et al.
Pageof 4