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Free Radical Biology & Medicine|August 18, 2000
Glycoxidation and lipoxidation in atherogenesisJ W Baynes, S R ThorpeGlycobiology|June 6, 1998
Human alpha-galactosidase A: characterization of the N-linked oligosaccharides on the intracellular and secreted glycoforms overexpressed by Chinese hamster ovary cellsF Matsuura, M Ohta, Y A Ioannou, et al.Genetic Testing|January 1, 1997
Arylsulfatase A pseudodeficiency: altered kinetic and heat-inactivation propertiesY Qu, J B Miller, R J Desnick, et al.Analytical Biochemistry|January 1, 1984
Synthesis of a fluorescent derivative of glucosyl ceramide for the sensitive determination of glucocerebrosidase activityT Dinur, G A Grabowski, R J Desnick, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1982
Gaucher type I (Ashkenazi) disease: a new method for heterozygote detection using a novel fluorescent natural substrateG A Grabowski, T Dinur, S Gatt, et al.American Heart Journal|June 1, 1977
Electrocardiographic and vectorcardiographic abnormalities in Fabry's diseaseJ Mehta, N Tuna, J H Moller, et al.Clinical Genetics|December 1, 1984
Interstitial deletion of the long arm of chromosome 6 [del(6) (q16q22)]: case report and review of the literatureM F Schwartz, S Kaffe, S Wallace, et al.American Journal of Human Genetics|November 1, 1984
Assignment of the structural gene encoding human aspartylglucosaminidase to the long arm of chromosome 4 (4q21----4qter)P Aula, K H Astrin, U Francke, et al.Genetics|August 1, 1985
Animal model studies of allelism: characterization of arylsulfatase B mutations in homoallelic and heteroallelic (genetic compound) homozygotes with feline mucopolysaccharidosis VIM M McGovern, N Mandell, M Haskins, et al.American Journal of Medical Genetics|August 28, 1995
Genetic mapping of the cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletionB D Gelb, E Cooper, M Shevell, et al.Pageof 40