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Neuromuscular Disorders : NMD|January 1, 1991
Neurological disorders due to mutations of the mitochondrial genomeM Zeviani, S DiDonatoFEBS Letters|November 12, 1990
Purification, characterization and partial amino acid sequences of carnitine palmitoyl-transferase from human liverG Finocchiaro, I Colombo, S DiDonatoThe Biochemical Journal|October 1, 1994
Divergent sequences in the 5' region of cDNA suggest alternative splicing as a mechanism for the generation of carnitine acetyltransferases with different subcellular localizationsO Corti, S DiDonato, G FinocchiaroHuman Genetics|June 1, 1995
Redefinition of the coding sequence of the MXI1 gene and identification of a polymorphic repeat in the 3' non-coding region that allows the detection of loss of heterozygosity of chromosome 10q25 in glioblastomasR Albarosa, S DiDonato, G FinocchiaroNeurology|June 1, 1979
Hepatic ketogenesis and muscle carnitine deficiencyS DiDonato, F Cornelio, G Storchi, et al.Gene|April 30, 1993
Cloning of human and rat cDNAs encoding the mitochondrial single-stranded DNA-binding protein (SSB)V Tiranti, M Rocchi, S DiDonato, et al.Neuroscience Letters|November 11, 1991
Isolation and sub-chromosomal localization of a DNA fragment of the human choline acetyltransferase geneR Cervini, M Rocchi, S DiDonato, et al.Neurology|October 1, 1991
Primary carnitine deficiency: heterozygote and intrafamilial phenotypic variationB Garavaglia, G Uziel, F Dworzak, et al.Neurology|December 1, 1979
Fatal ataxic encephalopathy and carnitine acetyltransferase deficiency: a functional defect of pyruvate oxidation?S DiDonato, M Rimoldi, A Moise, et al.Genomics|September 1, 1994
Molecular cloning of cDNAs encoding human carnitine acetyltransferase and mapping of the corresponding gene to chromosome 9q34.1O Corti, G Finocchiaro, E Rossi, et al.Pageof 5