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Proceedings of the National Academy of Sciences of the United States of America|January 15, 1991

cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferaseG Finocchiaro, F Taroni, M Rocchi, et al.

Neurology|November 1, 1993

Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patientsS DiDonato, M Zeviani, P Giovannini, et al.

Human Molecular Genetics|November 1, 1995

Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformantsV Tiranti, M Munaro, D Sandonà, et al.

Human Molecular Genetics|March 1, 1994

Mutations and polymorphisms of the gene encoding the beta-subunit of the electron transfer flavoprotein in three patients with glutaric acidemia type III Colombo, G Finocchiaro, B Garavaglia, et al.

Genomics|January 20, 1995

Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesisV Tiranti, E Rossi, A Ruiz-Carrillo, et al.

Muscle & Nerve|July 1, 1991

Carnitine in muscle, serum, and urine of nonprofessional athletes: effects of physical exercise, training, and L-carnitine administrationJ Arenas, J R Ricoy, A R Encinas, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 15, 1992

Molecular characterization of inherited carnitine palmitoyltransferase II deficiencyF Taroni, E Verderio, S Fiorucci, et al.

European Journal of Human Genetics : EJHG|January 1, 1995

Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex familiesM Eoli, M Pandolfo, A Amoroso, et al.

Human Molecular Genetics|January 1, 1995

Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutationsE Verderio, P Cavadini, L Montermini, et al.

American Journal of Human Genetics|December 1, 1990

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.

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Showing results (31-40 of 47) with videos related to

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Pageof 5

Proceedings of the National Academy of Sciences of the United States of America|January 15, 1991

cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferaseG Finocchiaro, F Taroni, M Rocchi, et al.

Neurology|November 1, 1993

Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patientsS DiDonato, M Zeviani, P Giovannini, et al.

Human Molecular Genetics|November 1, 1995

Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformantsV Tiranti, M Munaro, D Sandonà, et al.

Human Molecular Genetics|March 1, 1994

Mutations and polymorphisms of the gene encoding the beta-subunit of the electron transfer flavoprotein in three patients with glutaric acidemia type III Colombo, G Finocchiaro, B Garavaglia, et al.

Genomics|January 20, 1995

Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesisV Tiranti, E Rossi, A Ruiz-Carrillo, et al.

Muscle & Nerve|July 1, 1991

Carnitine in muscle, serum, and urine of nonprofessional athletes: effects of physical exercise, training, and L-carnitine administrationJ Arenas, J R Ricoy, A R Encinas, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 15, 1992

Molecular characterization of inherited carnitine palmitoyltransferase II deficiencyF Taroni, E Verderio, S Fiorucci, et al.

European Journal of Human Genetics : EJHG|January 1, 1995

Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex familiesM Eoli, M Pandolfo, A Amoroso, et al.

Human Molecular Genetics|January 1, 1995

Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutationsE Verderio, P Cavadini, L Montermini, et al.

American Journal of Human Genetics|December 1, 1990

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.

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