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Archives of Biochemistry and Biophysics|May 15, 1984
Human lysosomal beta-glucosidase: kinetic characterization of the catalytic, aglycon, and hydrophobic binding sitesG A Grabowski, S Gatt, J Kruse, et al.Clinics in Perinatology|August 14, 2001
Prenatal genetic screening in the Ashkenazi Jewish populationR E Zinberg, R Kornreich, L Edelmann, et al.Pediatric Radiology|January 1, 1995
Resolution of a proximal humeral defect in type-1 Gaucher disease by enzyme replacement therapyG M Pastores, G Hermann, K Norton, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1996
Mouse uroporphyrinogen decarboxylase: cDNA cloning, expression, and mappingC Wu, W Xu, C A Kozak, et al.Clinical Genetics|May 20, 2003
Pulmonary involvement in type 1 Gaucher disease: functional and exercise findings in patients with and without clinical interstitial lung diseaseA Miller, L K Brown, G M Pastores, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1978
Central retinal artery occlusion complicating Fabry's diseaseN A Sher, W Reiff, R D Letson, et al.Genomics|April 1, 1992
Invariant exon skipping in the human alpha-galactosidase A pre-mRNA: Ag+1 to t substitution in a 5'-splice site causing Fabry diseaseH Sakuraba, C M Eng, R J Desnick, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Regional assignment of the structural gene for human alpha-L-iduronidaseE H Schuchman, K H Astrin, P Aula, et al.Journal of Molecular Biology|June 17, 1994
Crystallization and preliminary X-ray analysis of human alpha-galactosidase A complexR Murali, Y A Ioannou, R J Desnick, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 1, 1996
Bone density in Type 1 Gaucher diseaseG M Pastores, S Wallenstein, R J Desnick, et al.Pageof 40