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American Journal of Human Genetics|June 1, 1994
Four novel PEPD alleles causing prolidase deficiencyP Ledoux, C Scriver, P HechtmanAmerican Journal of Human Genetics|November 1, 1996
Expression and molecular analysis of mutations in prolidase deficiencyP Ledoux, C R Scriver, P HechtmanCanadian Journal of Biochemistry|April 1, 1977
Characterization of an activating factor required for hydrolysis of Gm2 ganglioside catalyzed by hexosaminidase AP HechtmanThe Biochemical Journal|March 1, 1980
Interaction of activating protein and surfactants with human liver hexosaminidase A and GM2 gangliosideP Hechtman, Z KachraPediatric Research|October 1, 1992
Prolidase deficiency in cultured human fibroblasts: biochemical pathology and iminodipeptide-enhanced growthM Dolenga, P HechtmanThe Biochemical Journal|December 1, 1977
Purification and properties of the hexosaminidase A-activating protein from human liverP Hechtman, D LeBlancThe Journal of Biological Chemistry|January 25, 1983
Purification and properties of two enzymes catalyzing galactose transfer to GM2 ganglioside from rat liver GolgiF Kaplan, P HechtmanHand Surgery & Rehabilitation|November 17, 2022
Metacarpophalangeal hyperextension in thumb basal joint osteoarthritis: Radiological study and implications for treatmentP LedouxActa Orthopaedica Belgica|January 1, 1995
[Transmission of forces at the carpal arch in hyperextension of the wrist--mathematical model]P LedouxJournal of Chromatography|April 4, 1980
High-capacity method for purification of human liver hexosaminidase B using hydrophobic chromatographyJ Hardwick, P HechtmanPageof 13