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M L Katz

Showing results (1-10 of 111) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1993
Hereditary ceroid-lipofuscinosis: methylated amino acids in storage body proteinsM L Katz
Advances in Experimental Medicine and Biology|January 1, 1989
Incomplete proteolysis may contribute to lipofuscin accumulation in the retinal pigment epitheliumM L Katz
Biochimica Et Biophysica Acta|December 16, 1996
Decreased plasma carnitine and trimethyl-L-lysine levels associated with lysosomal accumulation of a trimethyl-L-lysine containing protein in Batten diseaseM L Katz
Experimental Eye Research|February 1, 1992
Influence of dietary vitamin A on autofluorescence of leupeptin-induced inclusions in the retinal pigment epitheliumM L Katz, M Norberg
The American Journal of Pathology|February 1, 1991
Juvenile ceroid lipofuscinosis. Evidence for methylated lysine in neural storage body proteinM L Katz, M Rodrigues
Biochimica Et Biophysica Acta|February 14, 1992
Methylated lysine in storage body protein of sheep with hereditary ceroid-lipofuscinosisM L Katz, K O Gerhardt
American Journal of Medical Genetics|June 5, 1995
Canine hereditary ceroid-lipofuscinosis: evidence for a defect in the carnitine biosynthetic pathwayM L Katz, A N Siakotos
Mechanisms of Ageing and Development|September 29, 1995
Vitamin A incorporation into lipofuscin-like inclusions in the retinal pigment epitheliumM L Katz, C L Gao
Investigative Ophthalmology & Visual Science|November 1, 2001
Effect of Rpe65 knockout on accumulation of lipofuscin fluorophores in the retinal pigment epitheliumM L Katz, T M Redmond
Mechanisms of Ageing and Development|April 1, 1985
Senescence and the retinal pigment epithelium: alterations in basal plasma membrane morphologyM L Katz, W G Robison
Pageof 12

Showing results (1-10 of 111) with videos related to

Sort By:
Pageof 12
Journal of Inherited Metabolic Disease|January 1, 1993
Hereditary ceroid-lipofuscinosis: methylated amino acids in storage body proteinsM L Katz
Advances in Experimental Medicine and Biology|January 1, 1989
Incomplete proteolysis may contribute to lipofuscin accumulation in the retinal pigment epitheliumM L Katz
Biochimica Et Biophysica Acta|December 16, 1996
Decreased plasma carnitine and trimethyl-L-lysine levels associated with lysosomal accumulation of a trimethyl-L-lysine containing protein in Batten diseaseM L Katz
Experimental Eye Research|February 1, 1992
Influence of dietary vitamin A on autofluorescence of leupeptin-induced inclusions in the retinal pigment epitheliumM L Katz, M Norberg
The American Journal of Pathology|February 1, 1991
Juvenile ceroid lipofuscinosis. Evidence for methylated lysine in neural storage body proteinM L Katz, M Rodrigues
Biochimica Et Biophysica Acta|February 14, 1992
Methylated lysine in storage body protein of sheep with hereditary ceroid-lipofuscinosisM L Katz, K O Gerhardt
American Journal of Medical Genetics|June 5, 1995
Canine hereditary ceroid-lipofuscinosis: evidence for a defect in the carnitine biosynthetic pathwayM L Katz, A N Siakotos
Mechanisms of Ageing and Development|September 29, 1995
Vitamin A incorporation into lipofuscin-like inclusions in the retinal pigment epitheliumM L Katz, C L Gao
Investigative Ophthalmology & Visual Science|November 1, 2001
Effect of Rpe65 knockout on accumulation of lipofuscin fluorophores in the retinal pigment epitheliumM L Katz, T M Redmond
Mechanisms of Ageing and Development|April 1, 1985
Senescence and the retinal pigment epithelium: alterations in basal plasma membrane morphologyM L Katz, W G Robison
Pageof 12