A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis von Katz, Martin L., Khan, Shahnawaz, Awano, Tomoyuki, Shahid, S. Adam, Siakotos, Aristotle N., Johnson, Gary S.

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Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder von Sleat, David E., Gin, Rosalie M., Sohar, Istvan, Wisniewski, Krystyna, Sklower-Brooks, Susan, Pullarkat, Raju K., Palmer, David N., Lerner, Terry J., Boustany, Rose-Mary, Uldall, Peter, Siakotos, Aristotle N., Donnelly, Robert J., Lobel, Peter

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Molecular genetics of palmitoyl-protein thioesterase deficiency in the U.S von Das, A K, Becerra, C H, Yi, W, Lu, J Y, Siakotos, A N, Wisniewski, K E, Hofmann, S L

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Acetaldehyde-modified and 4-hydroxynonenal-modified proteins in the livers of rats with alcoholic liver disease von Li, C, Nanji, AA, Siakotos, AN, Lin, RC

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Studies of renal injury III: Lipid-induced nephropathy in type II diabetes von Dominguez, Jesus H., Tang, Nianjun, Xu, Wei, Evan, Andrew P., Siakotos, Aristotle N., Agarwal, Rajiv, Walsh, James, Deeg, Mark, Pratt, Howard J., March, Keith L., Monnier, Vincent M., Weiss, Miriam F., Baynes, John W., Peterson, Richard

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Quantitative Measurement of 4-Hydroxyalkenals in Oxidized Low-Density Lipoprotein by Gas Chromatography-Mass Spectrometry von Vankuijk, F.J.G.M., Siakotos, A.N., Fong, L.G., Stephens, R.J., Thomas, D.W.

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Lysine methylation of mitochondrial ATP synthase subunit c stored in tissues of dogs with hereditary ceroid lipofuscinosis von KATZ, M. L, CHRISTIANSON, J. S, NORBURY, N. E, CHUN-LAN GAO, SIAKOTOS, A. N, KOPPANG, N

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Altered mitochondrial function in canine ceroid-lipofuscinosis von SIAKOTOS, A. N, BLAIR, P. S, SAVILL, J. D, KATZ, M. L

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Coding sequence and exon/intron organization of the canine CLN3 (batten disease) gene and its exclusion as the locus for ceroid-lipofuscinosis in english setter dogs von Shibuya, Hisashi, Liu, Po-Ching, Katz, Martin L., Siakotos, Aristotle N., Nonneman, Dan J., Johnson, Gary S.

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Low Molecular Weight Storage Material in Infantile Ceroid Lipofuscinosis (CLN1) von Dawson, G., Cho, Seongeun, Siakotos, A. N., Kilkus, J.

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Late-infantile ceroid-lipofuscinosis: lysine methylation of mitochondrial ATP synthase subunit c from lysosomal storage bodies von Katz, Martin L, Siakotos, Aristotle N, Gao, Quanyin, Freiha, Bassam, Chin, David T

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Improved Synthesis of Various Isotope Labeled 4-Hydroxyalkenals and Peroxidation Intermediates von Rees, M. S., van Kuijk, F. J.G.M., Siakotos, A. N., Mundy, B. P.

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Mitochondrial abnormalities in CLN2 and CLN3 forms of Batten disease von Dawson, G, Kilkus, J, Siakotos, A N, Singh, I

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Reduced phospholipase activity, peptide storage and the pathogenesis of canine neuronal ceroid‐lipofuscinosis von Dawson, G., Kilkus, J., Siakotos, A. N.

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Low-molecular-weight, calcium-dependent phospholipase A sub(2) genes are linked and map to homologous chromosome regions in mouse and human von Tischfield, JA, Xia, Y-R, Shih, D M, Klisak, I, Chen, J, Engle, S J, Siakotos, AN, Winstead, M V, Seilhamer, J J

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Elevated levels of neutrophil 4‐hydroxynonenal in canine neuronal ceroid‐lipofuscinosis and human immortalized lymphocytes of NCL patients von Siakotos, A. N., Kuijk, F. J. G. M., Tischfield, J. A.

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Perspective of biochemical research in the neuronal ceroid-lipofuscinosis von Rider, J. Alfred, Dawson, Glyn, Siakotos, Aristotle N.

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Quantitative analysis of phospholipids by thin‐layer chromatography and phosphorus analysis of spots von Rouser, George, Siakotos, A. N., Fleischer, Sidney

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The Discovery of a Particle Unique to Brain and Spleen Subcellular Fractions from Scrapie-infected Mice von Siakotos, A. N, Raveed, D, Longa, G

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Canine hereditary ceroid-lipofuscinosis: Evidence for a defect in the carnitine biosynthetic pathway von Katz, Martin L., Siakotos, Aristotle N.

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