search:gm1 disease相關網頁資料

- en.wikipedia.org
  
  GM1 - Wikipedia, the free encyclopedia
  
  GM1 (monosialotetrahexosylganglioside) the "prototype" ganglioside, is a member of the ganglio series of gangliosides which contain one sialic acid residue. GM1 has important physiological properties and impacts neuronal plasticity and repair mechanisms,
  
  2024-07-16
  
  瀏覽：432
- www.glycoscienceresearch.com
  
  Glycoscience Research Inc | GM1 ganglioside for Reseach and Clinical Development
  
  Please visit our website often to learn about what’s going on with the farm and with research on GM1 ganglioside. See our latest updates and let us hear from you here or on our ...
  
  2024-07-14
  
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GM1 Ganglioside Effects on Parkinson's Disease - Full Text View - ClinicalTrials.gov

日期：2024-07-14

The purpose of this trial is to examine the short term effects (24 Weeks) of GM1 on Parkinson's disease (PD) symptoms, as well as the effects of long-term treatment (120 Weeks) with GM1 on disease progression, and to examine the extent to which GM1 ......

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Ovine GM1 gangliosidosis - Glycoscience Research Inc | GM1 ganglioside for Reseach and Cl

日期：2024-07-15

Ovine GM1 gangliosidosis is an autosomal recessive, lysosomal storage disease in sheep associated with a profound deficiency of the lysosomal enzyme acid beta-galatosidase. Due to this missing enzyme GM1 ganglioside, asialo GM1 ganglioside and galactose ....

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GM1 gangliosidosis - Genetics Home Reference

日期：2024-07-15

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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GM1 gangliosidosis - Genetics Home Reference

日期：2024-07-14

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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GM1 Gangliosidosis - Medscape Reference

日期：2024-07-17

11 Dec 2014 ... GM1 gangliosidosis is an autosomal recessive lysosomal storage disorder characterized by the generalized accumulation of GM1 ganglioside, ......

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GM1 gangliosidoses - Wikipedia, the free encyclopedia

日期：2024-07-11

The GM1 gangliosidoses are caused by a deficiency of beta-galactosidase, with resulting abnormal storage of acidic lipid materials in cells of the central and peripheral nervous systems, but particularly in the nerve cells....

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GM1 Gangliosidosis - A DATABASE OF HEREDITARY OCULAR DISEASE | Hereditary Ocular Di

日期：2024-07-11

This is an autosomal recessive lysosomal storage disease secondary to a mutations in GLB1 (3p21.33). It is allelic to Morquio B disease (MPS IVB) (253010). The mutations in the beta-galactosidase-1 gene result in intracellular accumulation of GM1 ganglios...

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GM1 Gangliosidosis - Diseases & Conditions - Medscape Reference

日期：2024-07-16

GM1 Gangliosidosis. GM1 gangliosidosis is an autosomal recessive lysosomal storage disorder characterized by the generalized accumulation of GM1 ganglioside, oligosaccharides, and the mucopolysaccharide keratan sulfate (and their derivatives). ... Acid β ...

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