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B I Brown

Showing results (11-20 of 34) with videos related to

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Archives of Pathology & Laboratory Medicine|June 1, 1983
Glycogen storage disease type IBJ J Buchino, B I Brown, D M Volk
Carbohydrate Research|March 1, 1978
Structure of the polysaccharide formed by incubating glycogen with D-[14C]glucose in the presence of the glycogen debranching enzyme [amylo-(1 linked to 6)-glucosidase-4-alpha-glucanotransferase]D H Brown, D J Sprinkle, B I Brown
Biochimica Et Biophysica Acta|November 10, 1972
Preparation and properties of the glycogen-debranching enzyme from rabbit liverR B Gordon, D H Brown, B I Brown
The Journal of Biological Chemistry|July 25, 1978
The apparent activity in vivo of the lysosomal pathway of glycogen catabolism in cultured human skin fibroblasts from patients with type III glycogen storage diseaseD H Brown, L M Waindle, B I Brown
Annals of the New York Academy of Sciences|February 9, 1973
Studies on the structure and mechanism of action of the glycogen debranching enzymes of muscle nd liverD H Brown, R B Gordon, B I Brown
Biochemistry|March 17, 1970
Studies of lysosomal alpha-glucosidase. I. Purification and properties of the rat liver enzymeP L Jeffrey, D H Brown, B I Brown
American Journal of Diseases of Children (1960)|June 1, 1985
X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardationJ P Keating, B I Brown, N H White, et al.
Metabolism: Clinical and Experimental|July 1, 1986
Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiencyM Tuchman, B I Brown, B A Burke, et al.
American Journal of Human Genetics|October 1, 1990
Definitive prenatal diagnosis for type III glycogen storage diseaseB Z Yang, J H Ding, B I Brown, et al.
American Journal of Human Genetics|December 1, 1987
Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage diseaseY T Chen, J K He, J H Ding, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Archives of Pathology & Laboratory Medicine|June 1, 1983
Glycogen storage disease type IBJ J Buchino, B I Brown, D M Volk
Carbohydrate Research|March 1, 1978
Structure of the polysaccharide formed by incubating glycogen with D-[14C]glucose in the presence of the glycogen debranching enzyme [amylo-(1 linked to 6)-glucosidase-4-alpha-glucanotransferase]D H Brown, D J Sprinkle, B I Brown
Biochimica Et Biophysica Acta|November 10, 1972
Preparation and properties of the glycogen-debranching enzyme from rabbit liverR B Gordon, D H Brown, B I Brown
The Journal of Biological Chemistry|July 25, 1978
The apparent activity in vivo of the lysosomal pathway of glycogen catabolism in cultured human skin fibroblasts from patients with type III glycogen storage diseaseD H Brown, L M Waindle, B I Brown
Annals of the New York Academy of Sciences|February 9, 1973
Studies on the structure and mechanism of action of the glycogen debranching enzymes of muscle nd liverD H Brown, R B Gordon, B I Brown
Biochemistry|March 17, 1970
Studies of lysosomal alpha-glucosidase. I. Purification and properties of the rat liver enzymeP L Jeffrey, D H Brown, B I Brown
American Journal of Diseases of Children (1960)|June 1, 1985
X-linked glycogen storage disease. A cause of hypotonia, hyperuricemia, and growth retardationJ P Keating, B I Brown, N H White, et al.
Metabolism: Clinical and Experimental|July 1, 1986
Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiencyM Tuchman, B I Brown, B A Burke, et al.
American Journal of Human Genetics|October 1, 1990
Definitive prenatal diagnosis for type III glycogen storage diseaseB Z Yang, J H Ding, B I Brown, et al.
American Journal of Human Genetics|December 1, 1987
Glycogen debranching enzyme: purification, antibody characterization, and immunoblot analyses of type III glycogen storage diseaseY T Chen, J K He, J H Ding, et al.
Pageof 4