1 on of sphingolipids, phospholipids, and acid mucopolysaccharides.

2 containing phospholipids, sphingolipids, and mucopolysaccharides.

3  is occupied by membrane-spanning mucins and mucopolysaccharides densely tethered to the airway surfa

4 lular matrix, resulting in cell aggregation, mucopolysaccharide deposition, and significant obstructi

5  an exosite that binds both factor X and the mucopolysaccharide, heparin.

6 analyses revealed co-deposits of Cochlin and mucopolysaccharide in human TM around Schlemm's canal, s

7 istributed throughout the lumen and the acid mucopolysaccharide localized in the central core.

8                                              Mucopolysaccharide (MPS) diseases are characterized by a

9 ally, the findings suggest that the capsular mucopolysaccharide of serogroup A strains of P. multocid

10 nt unexpected finding in a neurodegenerative mucopolysaccharide storage disease, the Sanfilippo syndr

11 erkeley, led me, rather improbably, to study mucopolysaccharide storage disorders in the intramural p

12       I have traced the path from studies of mucopolysaccharide turnover in cultured cells to the dev