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The 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 HechtmanThe Biochemical Journal|January 15, 1984
Rat liver Golgi galactosyltransferases. Distinct enzymes for glycolipid and glycoprotein acceptor substratesF Kaplan, P HechtmanDNA and Cell Biology|October 1, 1993
Tay-Sachs disease screening and diagnosis: evolving technologiesP Hechtman, F KaplanBiochimica Et Biophysica Acta|June 20, 1997
Formation of a ternary complex between GM2 activator protein, GM2 ganglioside and hexosaminidase AF Yadao, P Hechtman, F KaplanGenetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
The GM2 gangliosidoses databases: allelic variation at the HEXA, HEXB, and GM2A gene lociP Cordeiro, P Hechtman, F KaplanJournal of Inherited Metabolic Disease|January 1, 1991
Allele-specific amplification of genomic DNA for detection of deletion mutations: identification of a French-Canadian Tay-Sachs mutationF Kaplan, B Boulay, J Bayleran, et al.Human Genetics|April 1, 1992
The French Canadian Tay-Sachs disease deletion mutation: identification of probable foundersM De Braekeleer, P Hechtman, E Andermann, et al.European Journal of Human Genetics : EJHG|May 1, 1997
A chronic GM2 gangliosidosis variant with a HEXA splicing defect: quantitation of HEXA mRNAs in normal and mutant fibroblastsM J Fernandes, P Hechtman, B Boulay, et al.Human Mutation|January 1, 1992
A glycine250--> aspartate substitution in the alpha-subunit of hexosaminidase A causes juvenile-onset Tay-Sachs disease in a Lebanese-Canadian familyI Trop, F Kaplan, C Brown, et al.Genetic Epidemiology|January 1, 1992
Specificity and sensitivity of hexosaminidase assays and DNA analysis for the detection of Tay-Sachs disease gene carriers among Ashkenazic JewsM J Fernandes, F Kaplan, C L Clow, et al.Pageof 26