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Toxicologic Pathology|January 1, 1989
The role of chemicals in the etiology of diabetes mellitusG L Wilson, S P LeDouxProgress in Nucleic Acid Research and Molecular Biology|September 14, 2001
Base excision repair of mitochondrial DNA damage in mammalian cellsS P LeDoux, G L WilsonHuman Genetics|April 1, 1992
The French Canadian Tay-Sachs disease deletion mutation: identification of probable foundersM De Braekeleer, P Hechtman, E Andermann, et al.Pediatric Research|December 1, 1988
In situ activation of human erythrocyte prolidase: potential for enzyme replacement therapy in prolidase deficiencyP Hechtman, A Richter, N Corman, et al.Pediatric Research|October 1, 1977
Red blood cell carbonic anhydrase activity in children with distal renal tubular acidosisB S Kaplan, M Mills, P Hechtman, 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.Pediatric Research|March 1, 1982
Deficiency of the hexosaminidase A activator protein in a case of GM2 gangliosidosis; variant ABP Hechtman, B A Gordon, N M Ng Ying KinHuman 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.The Journal of Hand Surgery, European Volume|June 20, 2008
A finite-element analysis of Kienbock's diseaseP Ledoux, D Lamblin, A Wuilbaut, et al.Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|January 1, 1989
Purification and characterization of activated human erythrocyte prolidaseA M Richter, G L Lancaster, F Y Choy, et al.Pageof 13