Enzyme replacement treatment for Tay-Sachs disease brain cells in culture utilizing concanavalin A-mediated hexosaminidase A uptake: biochemical and morphological evidence of GM2 mobilization

scientific article published on 01 January 1980

Enzyme replacement treatment for Tay-Sachs disease brain cells in culture utilizing concanavalin A-mediated hexosaminidase A uptake: biochemical and morphological evidence of GM2 mobilization is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/BF00688529
P698PubMed publication ID7376831

P2093author name stringM Adachi
D Amsterdam
S E Brooks
L Schneck
L M Hoffman
P2860cites workAlterations of astrocytic organelles in various lipidoses and allied diseasesQ48874070
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Introduction of purified hexosaminidase A into Tay-Sachs leukocytes by means of immunoglobulin-coated liposomes.Q52477095
Concanavalin A mediated uptake of enzymes by fibroblastsQ67441409
The transport of lysosomal enzymesQ67658695
Concanavalin A toxicity: histological studiesQ67870578
A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblastsQ68684301
In Vivo Toxicity of Concanavalin AQ68924026
The Tay-Sachs disease fibroblast model: failure to respond to exogenous hexosaminidase AQ69555912
In vitro correction of deficient human fibroblasts by beta-glucuronidase from different human sourcesQ69820185
Glycosphingolipids in cultured human skin fibroblasts. II. Characterization and metabolism in fibroblasts from patients with inborn errors of glycosphingolipid and mucopolysaccharide metabolismQ70445223
Protein measurement with the Folin phenol reagentQ20900776
Phosphohexosyl recognition is a general characteristic of pinocytosis of lysosomal glycosidases by human fibroblastsQ28332962
Phosphohexosyl components of a lysosomal enzyme are recognized by pinocytosis receptors on human fibroblastsQ35027280
A general method for the introduction of enzymes, by means of immunoglobulin-coated liposomes, into lysosomes of deficient cellsQ35066086
Hair-roots in screening and diagnosis of Tay-Sachs diseaseQ39419478
Lectin-mediated uptake of lysosomal hydrolases by genetically deficient human fibroblastsQ39659849
Ultrastructural alterations of tissue cultures from human fetal brain infected with the E variant of EMC virusQ39955041
Cytology, growth characteristics and cellular alterations following SV40-induced transformation of human foetal brain cells derived from a Gm2 gangliosidosis and controlQ40281154
Pinocytosis in fibroblasts. Quantitative studies in vitroQ41189675
Effect of lectins on endocytosis and secretion of lysosomal enzymes by cultures fibroblastsQ41608058
Purification and properties of human kidney-cortex hexosaminidases A and B.Q41840309
Liposomes containing Antiviral Antibody can protect Cells from Virus InfectionQ45816496
Fetal Tay-Sachs disease brain cells in culture: lack of turnover in [(14)C]glucosamine-labeled G(M2).Q48212930
Glycosphingolipids in fetal Tay-Sachs disease brain and lung culturesQ48267993
GM2 ganglioside in fetal Tay-Sachs disease brain cultures: a model system for the diseaseQ48375488
P433issue1
P921main subjectTay-Sachs diseaseQ560337
P304page(s)9-17
P577publication date1980-01-01
P1433published inActa NeuropathologicaQ343168
P1476titleEnzyme replacement treatment for Tay-Sachs disease brain cells in culture utilizing concanavalin A-mediated hexosaminidase A uptake: biochemical and morphological evidence of GM2 mobilization
P478volume50

Reverse relations

cites work (P2860)
Q41757590Biology and potential strategies for the treatment of GM2 gangliosidoses
Q34547567Characterization of a new model of GM2-gangliosidosis (Sandhoff's disease) in Korat cats
Q36370552Delivery of hexosaminidase A to the cerebrum after osmotic modification of the blood--brain barrier
Q45189355Gangliosides in SV-40-transformed cells derived from Tay-Sachs disease fetal brain
Q45869915Systemic FIV vector administration: transduction of CNS immune cells and Purkinje neurons

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