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Showing 1 to 2 of 2 for “"Morquio A Syndrome"”.

  1. Development of a Cellular Model for Morquio A Syndrome

    <p>Mucopolysaccharidosis IVA (MPS IVA; Morquio A), is a lysosomal storage disorder characterized by the deficiency of N-acetylgalactosamine-6-sulfatase (GALNS), resulting in the accumulation of glycosaminoglycans (GAGs) such as keratan sulfate (KS) (Northover et al., 1996) and …

    dominican Repository record for Development of a Cellular Model for Morquio A Syndrome (opens in a new tab)

  2. Analysis of Macrophage-­‐Derived Inflammatory Response in the Presence of Glycosaminoglycans: A Possible Clue on the Role of Inflammation in the Pathogenesis of Morquio A

    … Mucopolysaccharidosis IVA (MPS IVA or Morquio A syndrome) is characterized by the functional loss of the enzyme N-­‐acetylgalactosamine-­‐6-­‐ sulfatase (GALNS). The absence of GALNS leads to the chronic accumulation of the glycosaminoglycans keratan sulfate (KS) and possibly …

    dominican Repository record for Analysis of Macrophage-­‐Derived Inflammatory Response in the Presence of Glycosaminoglycans: A Possible Clue on the Role of Inflammation in the Pathogenesis of Morquio A (opens in a new tab)