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Neurochemical Research|May 5, 1999
Gene transfer approaches to the lysosomal storage disordersJ A Barranger, E O Rice, W P SwaneyBiochemical Medicine|April 1, 1985
Purification and characterization of bovine brain glucocerebrosidaseP U Reddy, G J Murray, J A BarrangerThe Journal of Biological Chemistry|November 15, 1985
Biosynthesis of the lysosomal enzyme glucocerebrosidaseA H Erickson, E I Ginns, J A BarrangerEuropean Journal of Biochemistry|January 15, 1986
Studies on the turnover of glucocerebrosidase in cultured rat peritoneal macrophages and normal human fibroblastsP K Das, G J Murray, J A BarrangerNaunyn-Schmiedeberg'S Archives of Pharmacology|June 1, 1982
Organomegaly and histopathology in an animal model of mucopolysaccharidosis induced by suraminS Rees, G Constantopoulos, J A Barranger, et al.Neurology|February 1, 1980
Electroencephalographic findings in Gaucher diseaseR Nishimura, N Omos-Lau, C Ajmone-Marsan, et al.Gastroenterology|January 1, 1981
LIver abnormalities in patients with Gaucher's diseaseS P James, F W Stromeyer, C Chang, et al.Biochemical and Biophysical Research Communications|July 25, 1996
Expression of human lysosomal alpha-mannosidase activity in transfected murine cells and human alpha-mannosidase deficient fibroblastsW Wang, V L Nebes, M C Schmidt, et al.Surgery, Gynecology & Obstetrics|April 1, 1987
Operative technique and results of subtotal splenectomy for Gaucher diseaseP C Guzzetta, R H Connors, J Fink, et al.Methods in Molecular Medicine|February 5, 2014
Methods for Retrovirus-Mediated Gene Transfer to CD34(+) Enriched CellsA B Bahnson, M Nimgaonkar, E D Ball, et al.Pageof 11