Intracellular degradation of sulforhodamine-GM1: use for a fluorescence-based characterization of GM2-gangliosidosis variants in fibroblasts and white blood cells-Reference-Cited by-同舟云学术

Intracellular degradation of sulforhodamine-GM1: use for a fluorescence-based characterization of GM2-gangliosidosis variants in fibroblasts and white blood cells

Published:1996-03 Issue:1-2 Volume:247 Page:105-120
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Agmon Vered,Khosravi Rami,Marchesini Sergio,Dinur Tama,Dagan Arie,Gatt Shimon,Navon Ruth

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

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4. Hexosaminidase A deficiency in adults;Navon;Am J Med Genet,1986

5. GM2-gangliosidosis. Hexosaminidase mutations not of Tay-Sachs type produce unusual clinical variants;Kolodny;Trends Neurosci,1983

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3. 16. Late-onset GM2 gangliosidosis and other hexosaminidase mutations among Jews;Tay-Sachs Disease;2001

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5. Intracellular degradation of fluorescent glycolipids by lysosomal enzymes and their activators;Journal of Inherited Metabolic Disease;1999-06