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J W Callahan

Showing results (51-60 of 72) with videos related to

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Journal of Neurochemistry|November 1, 1984
Regulation of mRNAs for three enzymes in the glial cell model C6 cell lineS Kumar, D P Weingarten, J W Callahan, et al.
Archives of Neurology|September 1, 1974
Juvenile GM1 gangliosidosis. Occurrence with absence of two beta-galactosidase componentsJ A Lowden, J W Callahan, M G Norman, et al.
FEBS Letters|January 15, 1998
Maturation and degradation of beta-galactosidase in the post-Golgi compartment are regulated by cathepsin B and a non-cysteine proteaseY Okamura-Oho, S Zhang, J W Callahan, et al.
The British Veterinary Journal|May 1, 1990
Properties of partially purified goat kidney beta-D-mannosidaseR D Pearce, J W Callahan, A Novak, et al.
Journal of Biomedical Materials Research|January 16, 1998
Macrophage phagocytosis of polyethylene particulate in vitroI Voronov, J P Santerre, A Hinek, et al.
Canadian Journal of Veterinary Research = Revue Canadienne De Recherche Veterinaire|January 1, 1990
Caprine beta-D-mannosidosis: characterization of a model lysosomal storage disorderR D Pearce, J W Callahan, P B Little, et al.
Neurology|June 1, 1981
Type 2 GM1 gangliosidosis with long survival and neuronal ceroid lipofuscinosisJ A Lowden, J W Callahan, R A Gravel, et al.
American Journal of Human Genetics|March 11, 2000
Decreased elastin deposition and high proliferation of fibroblasts from Costello syndrome are related to functional deficiency in the 67-kD elastin-binding proteinA Hinek, A C Smith, E M Cutiongco, et al.
The Journal of Biological Chemistry|January 3, 1997
Identification of Glu-268 as the catalytic nucleophile of human lysosomal beta-galactosidase precursor by mass spectrometryJ D McCarter, D L Burgoyne, S Miao, et al.
The Biochemical Journal|June 7, 2000
Characterization of beta-galactosidase mutations Asp332-->Asn and Arg148-->Ser, and a polymorphism, Ser532-->Gly, in a case of GM1 gangliosidosisS Zhang, R Bagshaw, W Hilson, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
Journal of Neurochemistry|November 1, 1984
Regulation of mRNAs for three enzymes in the glial cell model C6 cell lineS Kumar, D P Weingarten, J W Callahan, et al.
Archives of Neurology|September 1, 1974
Juvenile GM1 gangliosidosis. Occurrence with absence of two beta-galactosidase componentsJ A Lowden, J W Callahan, M G Norman, et al.
FEBS Letters|January 15, 1998
Maturation and degradation of beta-galactosidase in the post-Golgi compartment are regulated by cathepsin B and a non-cysteine proteaseY Okamura-Oho, S Zhang, J W Callahan, et al.
The British Veterinary Journal|May 1, 1990
Properties of partially purified goat kidney beta-D-mannosidaseR D Pearce, J W Callahan, A Novak, et al.
Journal of Biomedical Materials Research|January 16, 1998
Macrophage phagocytosis of polyethylene particulate in vitroI Voronov, J P Santerre, A Hinek, et al.
Canadian Journal of Veterinary Research = Revue Canadienne De Recherche Veterinaire|January 1, 1990
Caprine beta-D-mannosidosis: characterization of a model lysosomal storage disorderR D Pearce, J W Callahan, P B Little, et al.
Neurology|June 1, 1981
Type 2 GM1 gangliosidosis with long survival and neuronal ceroid lipofuscinosisJ A Lowden, J W Callahan, R A Gravel, et al.
American Journal of Human Genetics|March 11, 2000
Decreased elastin deposition and high proliferation of fibroblasts from Costello syndrome are related to functional deficiency in the 67-kD elastin-binding proteinA Hinek, A C Smith, E M Cutiongco, et al.
The Journal of Biological Chemistry|January 3, 1997
Identification of Glu-268 as the catalytic nucleophile of human lysosomal beta-galactosidase precursor by mass spectrometryJ D McCarter, D L Burgoyne, S Miao, et al.
The Biochemical Journal|June 7, 2000
Characterization of beta-galactosidase mutations Asp332-->Asn and Arg148-->Ser, and a polymorphism, Ser532-->Gly, in a case of GM1 gangliosidosisS Zhang, R Bagshaw, W Hilson, et al.
Pageof 8