Potier, Michel

Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis

Pshezhetsky, A. V., Richard, C., Michaud, L., Igdoura, S., Wang, S., Elsliger, M.-A., Qu, J., Leclerc, D., Gravel, R., Dallaire, L., et al. (1997) · Nature Genetics

Lysosomal Storage Disorders ResearchGlycosylation and Glycoproteins Research

Cited by 212

Association of N-Acetylgalactosamine-6-sulfate Sulfatase with the Multienzyme Lysosomal Complex of β-Galactosidase, Cathepsin A, and Neuraminidase

Pshezhetsky, A. V., & Potier, M. (1996) · Journal of Biological Chemistry

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 90

Molecular mechanism of lysosomal sialidase deficiency in galactosialidosis involves its rapid degradation

VINOGRADOVA, V. M., MICHAUD, L., MEZENTSEV, V. A., LUKONG, E. K., EL-ALFY, M., MORALES, R. C., POTIER, M., & PSHEZHETSKY, V. A. (1998) · Biochemical Journal

Lysosomal Storage Disorders ResearchGlycogen Storage Diseases and Myoclonus

Cited by 63

Direct Affinity Purification and Supramolecular Organization of Human Lysosomal Cathepsin A

Pshezhetsky, A. V., & Potier, M. (1994) · Archives of Biochemistry and Biophysics

Lysosomal Storage Disorders ResearchProtease and Inhibitor Mechanisms

Cited by 37

Human lysosomal .beta.-galactosidase-cathepsin A complex: Definition of the .beta.-galactosidase-binding interface on cathepsin A

Pshezhetsky, A. V., Elsliger, M.-A., Vinogradova, M. V., & Potier, M. (1995) · Biochemistry

Lysosomal Storage Disorders ResearchEnzyme Structure and Function

Cited by 26