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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 acidaemia
T Tahara, J P Kraus, T Ohura, et al.
Nature
|
February 6, 1985
Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locus
R 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 liver
W A Fenton, A M Hack, H F Willard, et al.
Cell
|
September 10, 1993
Folding in vivo of bacterial cytoplasmic proteins: role of GroEL
A 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 encapsulated
T 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 acidemia
F 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 peptide
A 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 defects
L 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 cells
G 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 reaction
J S Weissman, H S Rye, W A Fenton, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 57) with videos related to
Sort By:
Page
of 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 acidaemia
T Tahara, J P Kraus, T Ohura, et al.
Nature
|
February 6, 1985
Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locus
R 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 liver
W A Fenton, A M Hack, H F Willard, et al.
Cell
|
September 10, 1993
Folding in vivo of bacterial cytoplasmic proteins: role of GroEL
A 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 encapsulated
T 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 acidemia
F 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 peptide
A 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 defects
L 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 cells
G 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 reaction
J S Weissman, H S Rye, W A Fenton, et al.
Page
of 6