Pages that link to "Q28256588"

The following pages link to A cerebrosidesulfatase from swine kidney (Q28256588):

Displaying 48 items.

• Saposin A: second cerebrosidase activator protein (Q24339463) (← links)
• Evidence for two cDNA clones encoding human GM2-activator protein (Q24527339) (← links)
• N-glycosylation is required for full enzymic activity of the murine galactosylceramide sulphotransferase (Q24534884) (← links)
• Distribution of saposin proteins (sphingolipid activator proteins) in lysosomal storage and other diseases (Q24558637) (← links)
• Characterization of a mutation in a family with saposin B deficiency: a glycosylation site defect (Q24558729) (← links)
• Nucleotide sequence of cloned cDNA for human sphingolipid activator protein 1 precursor (Q24631874) (← links)
• The protective role of prosaposin and its receptors in the nervous system (Q27014092) (← links)
• Developing therapeutic approaches for metachromatic leukodystrophy (Q28297086) (← links)
• Concentrations of an activator protein for sphingolipid hydrolysis in liver and brain samples from patients with lysosomal storage diseases (Q28366590) (← links)
• Basic findings and current developments in sphingolipidoses (Q33923858) (← links)
• Sphingolipidoses. (Q34302979) (← links)
• Biochemistry and Genetics of gangliosidoses (Q34429195) (← links)
• Genetic heterogeneity in metachromatic leukodystrophy (Q34707253) (← links)
• Biosynthesis and degradation of mammalian glycosphingolipids (Q35153204) (← links)
• Correction of sulfatide metabolism after transfer of prosaposin cDNA to cultured cells from a patient with SAP-1 deficiency (Q35195388) (← links)
• Assignment of the gene for human sphingolipid activator protein-2 (SAP-2) to chromosome 10. (Q35200397) (← links)
• Ganglioside biochemistry (Q35361488) (← links)
• Chemical studies in gargoylism (Q36061310) (← links)
• Ascorbic acid sulfate sulfohydrolase (C2 sulfatase): the modulator of cellular levels of L-ascorbic acid in rainbow trout (Q36311527) (← links)
• Immunological evidence for deficiency in an activator protein for sulfatide sulfatase in a variant form of metachromatic leukodystrophy (Q37612374) (← links)
• The immunological functions of saposins (Q37761491) (← links)
• Lysosomal lipid storage diseases (Q37866549) (← links)
• My journey into the world of sphingolipids and sphingolipidoses (Q38066410) (← links)
• Gangliosides and gangliosidoses: principles of molecular and metabolic pathogenesis. (Q38115769) (← links)
• Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidoses (Q38241614) (← links)
• The anomalous kinetics of sulphatase A. (Q38365749) (← links)
• Sulfatide content and (Na++K+)-ATPase activity of skin and gill during larval development of the chilean frog,Calyptocephalella caudiverbera (Q39300584) (← links)
• Blocks in the catabolism of sulphatides and gangliosides as a cause of human neurological diseases (Q39990023) (← links)
• Importance of splicing for prosaposin sorting (Q40979179) (← links)
• A triple-binding-domain model explains the specificity of the interaction of a sphingolipid activator protein (SAP-1) with sulphatide, GM1-ganglioside and globotriaosylceramide (Q41835537) (← links)
• Additional biochemical findings in a patient and fetal sibling with a genetic defect in the sphingolipid activator protein (SAP) precursor, prosaposin. Evidence for a deficiency in SAP-1 and for a normal lysosomal neuraminidase (Q42071359) (← links)
• Bile salt activation of cerebroside sulphate sulphohydrolase (Q42880840) (← links)
• Simplified procedure for preparation of 35S-labeled brain sulfatide (Q48510156) (← links)
• Juvenile metachromatic leucodystrophy. Case report with clinical, histopathological, ultrastructural and biochemical observations (Q48625431) (← links)
• Progressive blocking of cortical functions in the adult form of metachromatic leukodystrophy (Q52267011) (← links)
• [Clinical, light and electron microscopy findings in 4 cases of metachromatic leucodystrophy in children]. (Q54150949) (← links)
• [Glycolipids of the cell surface--biochemistry of their decomposition]. (Q64939603) (← links)
• Preparation of specific ligand for the purification of arylsulfatases by affinity chromatography (Q67833437) (← links)
• Immunocytochemical localization of sphingolipid activator protein-1, the sulfatide/GM1 ganglioside activator, to lysosomes in human liver and colon (Q70166179) (← links)
• Chance and discovery in research on the cause of infantile amaurotic idiocy (Q70804277) (← links)
• [Lipid-protein interactions: mechanisms of enzymatic glycolipid catabolism and their genetic restrictive escapes] (Q71338884) (← links)
• Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivo (Q71435387) (← links)
• Sphingolipid activator proteins in the neuronal ceroid-lipofuscinoses: an immunological study (Q71905303) (← links)
• Genetic complementation in somatic cell hybrids of cerebroside sulfatase activator deficiency and metachromatic leukodystrophy fibroblasts (Q72579615) (← links)
• Homegenizer for continuous homogenizing for the preparative extraction of cell particles (Q72661830) (← links)
• The structure and chemistry of sulfatides (Q72758266) (← links)
• Glycosphingolipid degradation and animal models of GM2-gangliosidoses (Q77202738) (← links)
• Intracellular degradation of fluorescent glycolipids by lysosomal enzymes and their activators (Q77979919) (← links)