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The Journal of Biological Chemistry
|
January 5, 1989
Expression of the yeast aspartyl protease, proteinase A. Phosphorylation and binding to the mannose 6-phosphate receptor are altered by addition of cathepsin D sequences
P L Faust, S Kornfeld
The Journal of Cell Biology
|
January 7, 1998
Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder
P L Faust, M E Hatten
Cell
|
October 19, 1990
Generation of a lysosomal enzyme targeting signal in the secretory protein pepsinogen
T J Baranski, P L Faust, S Kornfeld
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1985
Cloning and sequence analysis of cDNA for human cathepsin D
P L Faust, S Kornfeld, J M Chirgwin
The Journal of Cell Biology
|
November 1, 1987
Renin, a secretory glycoprotein, acquires phosphomannosyl residues
P L Faust, J M Chirgwin, S Kornfeld
Journal of Molecular Neuroscience : MN
|
August 2, 2001
The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction
P L Faust, H M Su, A Moser, et al.
Current Opinion in Neurobiology
|
May 6, 1998
New directions for neuronal migration
A L Pearlman, P L Faust, M E Hatten, et al.
European Journal of Biochemistry
|
September 18, 2001
Purification of brain peroxisomes and localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase
W J Kovacs, P L Faust, G A Keller, et al.
Neurology
|
April 1, 1993
Polyglucosan body disease simulating amyotrophic lateral sclerosis
T D McDonald, P L Faust, C Bruno, et al.
Journal of Inherited Metabolic Disease
|
May 4, 2005
Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain
P L Faust, D Banka, R Siriratsivawong, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
The Journal of Biological Chemistry
|
January 5, 1989
Expression of the yeast aspartyl protease, proteinase A. Phosphorylation and binding to the mannose 6-phosphate receptor are altered by addition of cathepsin D sequences
P L Faust, S Kornfeld
The Journal of Cell Biology
|
January 7, 1998
Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder
P L Faust, M E Hatten
Cell
|
October 19, 1990
Generation of a lysosomal enzyme targeting signal in the secretory protein pepsinogen
T J Baranski, P L Faust, S Kornfeld
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1985
Cloning and sequence analysis of cDNA for human cathepsin D
P L Faust, S Kornfeld, J M Chirgwin
The Journal of Cell Biology
|
November 1, 1987
Renin, a secretory glycoprotein, acquires phosphomannosyl residues
P L Faust, J M Chirgwin, S Kornfeld
Journal of Molecular Neuroscience : MN
|
August 2, 2001
The peroxisome deficient PEX2 Zellweger mouse: pathologic and biochemical correlates of lipid dysfunction
P L Faust, H M Su, A Moser, et al.
Current Opinion in Neurobiology
|
May 6, 1998
New directions for neuronal migration
A L Pearlman, P L Faust, M E Hatten, et al.
European Journal of Biochemistry
|
September 18, 2001
Purification of brain peroxisomes and localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase
W J Kovacs, P L Faust, G A Keller, et al.
Neurology
|
April 1, 1993
Polyglucosan body disease simulating amyotrophic lateral sclerosis
T D McDonald, P L Faust, C Bruno, et al.
Journal of Inherited Metabolic Disease
|
May 4, 2005
Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain
P L Faust, D Banka, R Siriratsivawong, et al.
Page
of 2