search:gm1 ganglioside相關網頁資料

      • ghr.nlm.nih.gov
        GM1 gangliosidosis is an inherited disorder that progressively destroys nerve cells (neurons) in the brain and spinal cord. Some researchers classify this condition into three major types based on the age at which signs and symptoms first appear. Although
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      • en.wikipedia.org
        Structure of GM1 ganglioside. A ganglioside is a molecule composed of a glycosphingolipid (ceramide and oligosaccharide) with one or more sialic acids ( e.g. ...
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    日期:2024-09-02
    30 Jan 2014 ... The name ganglioside was first applied by the German scientist Ernst Klenk in 1942 to ... Structural formula of ganglioside GM1 (alternative) ......
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    日期:2024-09-03
    GM1 gangliosidosis is an inherited disorder that progressively destroys nerve ... GM1 ganglioside is important for normal functioning of nerve cells in the brain....
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    日期:2024-09-06
    Ganglioside GM1 was isolated from the small intestinal mucosa of man, pig, and beef and amounted to 0.1, 2.0, and 43 nmol per g fresh weight, respectively....
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    日期:2024-09-05
    11 Dec 2014 ... GM1 gangliosidosis is an autosomal recessive lysosomal storage disorder characterized by the generalized accumulation of GM1 ganglioside, ......
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    日期:2024-09-04
    stant (KA) of the cholera toxinbinding was, for cells of all three species, about 109 liters/mol. Exogenously added GM1 ganglioside was incorporated in intestinal ......
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    日期:2024-09-03
    31 Jul 2013 ... Recently, one family of lipids known as gangliosides has emerged as a .... The current research on gangliosides, especially GM1, is very ......
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    日期:2024-09-03
    Binding and Aggregation Mechanism of Amyloid beta-Peptides onto the GM1 Ganglioside-Containing Lipid Membrane. J Phys Chem B [PubMed]. Miyazaki, Y....