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The Journal of Clinical Investigation|May 15, 1997
Identification and expression of acid beta-glucosidase mutations causing severe type 1 and neurologic type 2 Gaucher disease in non-Jewish patientsM E Grace, R J Desnick, G M PastoresThe Tohoku Journal of Experimental Medicine|May 1, 1983
Microautoradiographic study on the tissue localization of liposome-entrapped or unentrapped 3H-labeled beta-galactosidase injected into ratsH Onodera, G Takada, K Tada, et al.The Journal of Biological Chemistry|March 10, 1984
Human alpha-L-iduronidase. I. Purification and properties of the high uptake (higher molecular weight) and the low uptake (processed) formsE H Schuchman, N A Guzman, R J DesnickArchives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1979
The ocular manifestations in Fabry's diseaseN A Sher, R D Letson, R J DesnickThe Journal of Cell Biology|December 1, 1992
Overexpression of human alpha-galactosidase A results in its intracellular aggregation, crystallization in lysosomes, and selective secretionY A Ioannou, D F Bishop, R J DesnickGenomics|January 1, 1990
Human arylsulfatase B: MOPAC cloning, nucleotide sequence of a full-length cDNA, and regions of amino acid identity with arylsulfatases A and CE H Schuchman, C E Jackson, R J DesnickAdvances in Nephrology From the Necker Hospital|January 1, 1989
Fabry disease: molecular genetics of the inherited nephropathyR J Desnick, K H Astrin, D F BishopDiabetes|January 19, 1999
Role of oxidative stress in diabetic complications: a new perspective on an old paradigmJ W Baynes, S R ThorpeDrugs & Aging|August 1, 1996
Role of the Maillard reaction in diabetes mellitus and diseases of agingS R Thorpe, J W BaynesAmino Acids|December 9, 2003
Maillard reaction products in tissue proteins: new products and new perspectivesS R Thorpe, J W BaynesPageof 40