Search research articles
Contact Us
Filters
Showing results (1-10 of 111) with videos related to
Page
of 12
Sort By:
Journal of Inherited Metabolic Disease
|
January 1, 1993
Hereditary ceroid-lipofuscinosis: methylated amino acids in storage body proteins
M L Katz
Advances in Experimental Medicine and Biology
|
January 1, 1989
Incomplete proteolysis may contribute to lipofuscin accumulation in the retinal pigment epithelium
M 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 disease
M L Katz
Experimental Eye Research
|
February 1, 1992
Influence of dietary vitamin A on autofluorescence of leupeptin-induced inclusions in the retinal pigment epithelium
M L Katz, M Norberg
The American Journal of Pathology
|
February 1, 1991
Juvenile ceroid lipofuscinosis. Evidence for methylated lysine in neural storage body protein
M L Katz, M Rodrigues
Biochimica Et Biophysica Acta
|
February 14, 1992
Methylated lysine in storage body protein of sheep with hereditary ceroid-lipofuscinosis
M 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 pathway
M L Katz, A N Siakotos
Mechanisms of Ageing and Development
|
September 29, 1995
Vitamin A incorporation into lipofuscin-like inclusions in the retinal pigment epithelium
M 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 epithelium
M L Katz, T M Redmond
Mechanisms of Ageing and Development
|
April 1, 1985
Senescence and the retinal pigment epithelium: alterations in basal plasma membrane morphology
M L Katz, W G Robison
Page
of 12
Search research articles
Search
Showing results (1-10 of 111) with videos related to
Sort By:
Page
of 12
Journal of Inherited Metabolic Disease
|
January 1, 1993
Hereditary ceroid-lipofuscinosis: methylated amino acids in storage body proteins
M L Katz
Advances in Experimental Medicine and Biology
|
January 1, 1989
Incomplete proteolysis may contribute to lipofuscin accumulation in the retinal pigment epithelium
M 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 disease
M L Katz
Experimental Eye Research
|
February 1, 1992
Influence of dietary vitamin A on autofluorescence of leupeptin-induced inclusions in the retinal pigment epithelium
M L Katz, M Norberg
The American Journal of Pathology
|
February 1, 1991
Juvenile ceroid lipofuscinosis. Evidence for methylated lysine in neural storage body protein
M L Katz, M Rodrigues
Biochimica Et Biophysica Acta
|
February 14, 1992
Methylated lysine in storage body protein of sheep with hereditary ceroid-lipofuscinosis
M 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 pathway
M L Katz, A N Siakotos
Mechanisms of Ageing and Development
|
September 29, 1995
Vitamin A incorporation into lipofuscin-like inclusions in the retinal pigment epithelium
M 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 epithelium
M L Katz, T M Redmond
Mechanisms of Ageing and Development
|
April 1, 1985
Senescence and the retinal pigment epithelium: alterations in basal plasma membrane morphology
M L Katz, W G Robison
Page
of 12