GM1 gangliosidoses - Wikipedia, the free encyclopedia
14 Aug 2009 ... The GM1 gangliosidoses are caused by a deficiency of beta-galactosidase, with resulting abnormal storage of acidic lipid materials in cells ...
http://en.wikipedia.org/wiki/GM1_gangliosidoses...
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OMIM - GM1-GANGLIOSIDOSIS, TYPE I
MIM #230500 · Text · Description · Clinical Features · Other Features · Biochemical Features · Molecular Genetics · Genotype/Phenotype Correlations ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230500...
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Gangliosidoses Information Page: National Institute of ...
The GM1 gangliosidoses are caused by a deficiency of beta-galactosidase. Symptoms of early infantile GM1 (the most severe subtype, with onset shortly after ...
http://www.ninds.nih.gov/disorders/gangliosidoses/Gangliosid...
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Molecular basis of GM1 gangliosidosis and Morquio disease, type B ...
GM1 gangliosidosis and Morquio B disease are distinct disorders both clinically and biochemically yet they arise from the same beta-galactosidase enzyme ...
http://www.ncbi.nlm.nih.gov/pubmed/10571006...
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Molecular Therapy - Abstract of article: 698. Gene Therapy of ...
Gene Therapy of Murine GM1 Gangliosidosis by Genetically Modified Bone Marrow Hematopoietic Progenitor Cells. Renata Sano1, Alessandra Tessitore1, ...
http://www.nature.com/mt/journal/v9/n1s/abs/mt2004822a.html...
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Brain ceramide hexosides in Tay-Sachs disease and generalized ...
In GM1-gangliosidosis, ceramide tetrahexoside is the major ceramide hexoside, while ceramide trihexoside is present only in small amount. ...
http://www.ncbi.nlm.nih.gov/pubmed/14564716...
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Canine GM1-gangliosidosis. A clinical, morphologic, histochemical ...
Diagnosis of GM1 gangliosidosis based on detection of urinary oligosaccharides with high performance liquid chromatography. Clin Chim Acta. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=18...
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GM1 gangliosidosis in adults: clinical and molecular analysis of ...
GM1 gangliosidosis in adults: clinical and molecular analysis of 16 Japanese patients. Yoshida K, Oshima A, Sakuraba H, Nakano T, Yanagisawa N, Inui K, ...
http://www.ncbi.nlm.nih.gov/pubmed/1353343...
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Quantitation of the enzymically deficient cross reacting material ...
Immunological studies of beta galactosidase in normal human liver and in GM1 gangliosidosis. Am J Hum Genet. 1974 Nov;26(6):683–691. [PubMed] ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16...
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GM1 gangliosidosis: review of clinical, molecular, and therapeutic ...
GM(1) gangliosidosis is a lysosomal storage disorder due to deficiency of the beta-galactosidase enzyme. This deficiency results in accumulation of GM(1) ...
http://www.ncbi.nlm.nih.gov/pubmed/18524657...
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