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W A Fenton

Showing results (31-40 of 57) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1993
Three independent mutations in the same exon of the PCCB gene: differences between Caucasian and Japanese propionic acidaemiaT Tahara, J P Kraus, T Ohura, et al.
Nature|February 6, 1985
Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locusR Rozen, J Fox, W A Fenton, et al.
Archives of Biochemistry and Biophysics|April 1, 1982
Purification and properties of methylmalonyl coenzyme A mutase from human liverW A Fenton, A M Hack, H F Willard, et al.
Cell|September 10, 1993
Folding in vivo of bacterial cytoplasmic proteins: role of GroELA L Horwich, K B Low, W A Fenton, et al.
Cell|October 24, 2001
GroEL/GroES-mediated folding of a protein too large to be encapsulatedT K Chaudhuri, G W Farr, W A Fenton, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990
Mutation eliminating mitochondrial leader sequence of methylmalonyl-CoA mutase causes muto methylmalonic acidemiaF D Ledley, R Jansen, S U Nham, et al.
Cell|February 14, 1986
Targeting of pre-ornithine transcarbamylase to mitochondria: definition of critical regions and residues in the leader peptideA L Horwich, F Kalousek, W A Fenton, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Targeting of nuclear-encoded proteins to the mitochondrial matrix: implications for human genetic defectsL E Rosenberg, W A Fenton, A L Horwich, et al.
Molecular and Cellular Biology|December 1, 1988
Mitochondrial import and processing of mutant human ornithine transcarbamylase precursors in cultured cellsG Isaya, W A Fenton, J P Hendrick, et al.
Cell|February 9, 1996
Characterization of the active intermediate of a GroEL-GroES-mediated protein folding reactionJ S Weissman, H S Rye, W A Fenton, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|January 1, 1993
Three independent mutations in the same exon of the PCCB gene: differences between Caucasian and Japanese propionic acidaemiaT Tahara, J P Kraus, T Ohura, et al.
Nature|February 6, 1985
Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locusR Rozen, J Fox, W A Fenton, et al.
Archives of Biochemistry and Biophysics|April 1, 1982
Purification and properties of methylmalonyl coenzyme A mutase from human liverW A Fenton, A M Hack, H F Willard, et al.
Cell|September 10, 1993
Folding in vivo of bacterial cytoplasmic proteins: role of GroELA L Horwich, K B Low, W A Fenton, et al.
Cell|October 24, 2001
GroEL/GroES-mediated folding of a protein too large to be encapsulatedT K Chaudhuri, G W Farr, W A Fenton, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1990
Mutation eliminating mitochondrial leader sequence of methylmalonyl-CoA mutase causes muto methylmalonic acidemiaF D Ledley, R Jansen, S U Nham, et al.
Cell|February 14, 1986
Targeting of pre-ornithine transcarbamylase to mitochondria: definition of critical regions and residues in the leader peptideA L Horwich, F Kalousek, W A Fenton, et al.
Annals of the New York Academy of Sciences|January 1, 1986
Targeting of nuclear-encoded proteins to the mitochondrial matrix: implications for human genetic defectsL E Rosenberg, W A Fenton, A L Horwich, et al.
Molecular and Cellular Biology|December 1, 1988
Mitochondrial import and processing of mutant human ornithine transcarbamylase precursors in cultured cellsG Isaya, W A Fenton, J P Hendrick, et al.
Cell|February 9, 1996
Characterization of the active intermediate of a GroEL-GroES-mediated protein folding reactionJ S Weissman, H S Rye, W A Fenton, et al.
Pageof 6