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Archives of Biochemistry and Biophysics
|
August 15, 1988
N-benzoyl-L-tyrosyl-p-aminobenzoic acid hydrolase: a metalloendopeptidase of the human intestinal microvillus membrane which degrades biologically active peptides
E E Sterchi, H Y Naim, M J Lentze, et al.
Archives of Biochemistry and Biophysics
|
December 1, 1996
Proteolytic processing of human lactase-phlorizin hydrolase is a two-step event: identification of the cleavage sites
M Wüthrich, J Grünberg, D Hahn, et al.
The Journal of Clinical Investigation
|
August 1, 1988
Sucrase-isomaltase deficiency in humans. Different mutations disrupt intracellular transport, processing, and function of an intestinal brush border enzyme
H Y Naim, J Roth, E E Sterchi, et al.
Journal of Cellular and Molecular Medicine
|
December 20, 2007
Insights into post-translational processing of beta-galactosidase in an animal model resembling late infantile human G-gangliosidosis
R Kreutzer, M Kreutzer, M J Pröpsting, et al.
Vaccine
|
March 21, 2001
Recombinant measles viruses expressing heterologous antigens of mumps and simian immunodeficiency viruses
Z Wang, L Hangartner, T I Cornu, et al.
The Journal of Biological Chemistry
|
March 13, 1999
Hierarchy of sorting signals in chimeras of intestinal lactase-phlorizin hydrolase and the influenza virus hemagglutinin
R Jacob, U Preuss, P Panzer, et al.
Journal of Virology
|
March 14, 1998
Chimeric measles viruses with a foreign envelope
P Spielhofer, T Bächi, T Fehr, et al.
The Journal of Biological Chemistry
|
April 18, 1998
Routing and processing of lactase-phlorizin hydrolase in transfected Caco-2 cells
J Ouwendijk, W J Peters, R A van de Vorstenbosch, et al.
The Journal of Pathology
|
August 10, 1999
Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation)
K P Zimmer, P le Coutre, H M Aerts, et al.
The Journal of Clinical Investigation
|
February 1, 1996
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment
J Ouwendijk, C E Moolenaar, W J Peters, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 80) with videos related to
Sort By:
Page
of 8
Archives of Biochemistry and Biophysics
|
August 15, 1988
N-benzoyl-L-tyrosyl-p-aminobenzoic acid hydrolase: a metalloendopeptidase of the human intestinal microvillus membrane which degrades biologically active peptides
E E Sterchi, H Y Naim, M J Lentze, et al.
Archives of Biochemistry and Biophysics
|
December 1, 1996
Proteolytic processing of human lactase-phlorizin hydrolase is a two-step event: identification of the cleavage sites
M Wüthrich, J Grünberg, D Hahn, et al.
The Journal of Clinical Investigation
|
August 1, 1988
Sucrase-isomaltase deficiency in humans. Different mutations disrupt intracellular transport, processing, and function of an intestinal brush border enzyme
H Y Naim, J Roth, E E Sterchi, et al.
Journal of Cellular and Molecular Medicine
|
December 20, 2007
Insights into post-translational processing of beta-galactosidase in an animal model resembling late infantile human G-gangliosidosis
R Kreutzer, M Kreutzer, M J Pröpsting, et al.
Vaccine
|
March 21, 2001
Recombinant measles viruses expressing heterologous antigens of mumps and simian immunodeficiency viruses
Z Wang, L Hangartner, T I Cornu, et al.
The Journal of Biological Chemistry
|
March 13, 1999
Hierarchy of sorting signals in chimeras of intestinal lactase-phlorizin hydrolase and the influenza virus hemagglutinin
R Jacob, U Preuss, P Panzer, et al.
Journal of Virology
|
March 14, 1998
Chimeric measles viruses with a foreign envelope
P Spielhofer, T Bächi, T Fehr, et al.
The Journal of Biological Chemistry
|
April 18, 1998
Routing and processing of lactase-phlorizin hydrolase in transfected Caco-2 cells
J Ouwendijk, W J Peters, R A van de Vorstenbosch, et al.
The Journal of Pathology
|
August 10, 1999
Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation)
K P Zimmer, P le Coutre, H M Aerts, et al.
The Journal of Clinical Investigation
|
February 1, 1996
Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment
J Ouwendijk, C E Moolenaar, W J Peters, et al.
Page
of 8