F S Furbish

Medicine · Health Sciences

13h-index1.4kcitations24works0.02yr avg
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Research Topics

Lysosomal Storage Disorders Research(15), Glycosylation and Glycoproteins Research(8), Carbohydrate Chemistry and Synthesis(6), Pancreatic function and diabetes(6), Glycogen Storage Diseases and Myoclonus(4)

Publications24 total

The Use of Biomarkers and Clinical Goals in the Management of Gaucher Disease
2010
Therapeutic response to intravenous infusions of glucocerebrosidase in a patient with Gaucher disease.
Proceedings of the National Academy of Sciences·1990· 370 citedOpen Access
Structure of the N-asparagine-linked oligosaccharide units of human placental beta-glucocerebrosidase.
Journal of Biological Chemistry·1984· 126 citedOpen Access
INTERACTION OF HUMAN PLACENTAL GLUCOCEREBROSIDASE WITH HEPATIC LECTINS
Elsevier eBooks·1984· 13 cited
Mutations of glucocerebrosidase: discrimination of neurologic and non-neurologic phenotypes of Gaucher disease.
Proceedings of the National Academy of Sciences·1982· 120 citedOpen Access
Enhanced macrophage uptake of synthetically glycosylated human placental beta-glucocerebrosidase.
Journal of Biological Chemistry·1982· 83 citedOpen Access
Prospects for enzyme replacement therapy in heritable metabolic disorders
1982· 1 cited
Enzyme Replacement Therapy
1982· 12 cited
Delivery of hexosaminidase A to the cerebrum after osmotic modification of the blood--brain barrier.
Proceedings of the National Academy of Sciences·1981· 83 cited
Uptake and distribution of placental glucocerebrosidase in rat hepatic cells and effects of sequential deglycosylation
Biochimica et Biophysica Acta (BBA) - General Subjects·1981· 191 cited
A new group of glucocerebrosidase isozymes found in human white blood cells
Biochemical and Biophysical Research Communications·1980· 15 cited
Fucose plays a role in the clearance and uptake of glucocerebrosidase by rat liver cells
Biochemical and Biophysical Research Communications·1980· 18 cited
Status of enzyme replacement therapy for Gaucher disease.
PubMed·1980· 16 cited
Studies of lysosomal function: I. Metabolism of some complex lipids by isolated hepatocytes and Kupffer cells
Biochemical and Biophysical Research Communications·1978· 9 cited
The uptake of agalacto‐glucocerebrosidase by rat hepatocytes and kupffer cells
FEBS Letters·1978· 31 cited
Incorporation of Exogenous Enzymes into Lysosomes
ACS symposium series·1978· 8 cited
Differential uptake of native and desialylated glucocere-brosidase by rat hepatocytes and Kupffer cells
Gastroenterology·1978
The uptake of native and desialylated glucocerebrosidase by rat hepatocytes and Kupffer cells
Biochemical and Biophysical Research Communications·1978· 93 cited
[56] Glucocerebrosidase from human placenta
Methods in enzymology on CD-ROM/Methods in enzymology·1978· 11 cited
Factors that Influence the Uptake and Turnover of Glucocerebrosidase and α-Galactosidase in Mammalian Liver
Advances in experimental medicine and biology·1978· 7 cited
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Frequent Co-authors

Roscoe O. Brady(15), John A. Barranger(7), Peter G. Pentchev(7), J. A. Barranger(7), Clifford J. Steer(4), Andrew E. Gal(4), Roscoe O. Brady(4), Gary J. Murray(3), E. Anthony Jones(3), Nancy Krett(2), Henry E. Blair(2), Joseph Shiloach(2), Edward I. Ginns(2), J. A. Barranger(2), Norman W. Barton(1), Mark D. Garfield(1), S. Takasaki(1), Akira Kobata(1), Samuel J. Pirruccello(1), Christopher Hudson Moore(1)