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G Finocchiaro

Showing results (61-70 of 355) with videos related to

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Minerva Pediatrica|March 1, 1991
[Metabolic myopathies]G Finocchiaro, M Zeviani, B Garavaglia, et al.
The Journal of Biological Chemistry|December 23, 1994
Expression and characterization of human and chimeric human-Paracoccus denitrificans electron transfer flavoproteinsK R Herrick, D Salazar, S I Goodman, et al.
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.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
cDNA cloning, sequence analysis, and chromosomal localization of human carnitine palmitoyltransferaseG Finocchiaro, F Taroni, M Rocchi, et al.
Neurology|October 10, 2001
High frequency of the H63D mutation of the hemochromatosis gene (HFE) in malignant gliomasF Martinez di Montemuros, D Tavazzi, E Salsano, et al.
Genomics|November 1, 1994
Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32C Gellera, E Verderio, G Floridia, et al.
Minerva Dietologica E Gastroenterologica|October 1, 1989
[The role of the intestine in the pathogenesis and treatment of multiple organ failure]A M Costantino, G Finocchiaro, A Pezzana, et al.
Genomics|August 1, 1992
Localization of the human gene for carnitine palmitoyltransferase to 1p13-p11 by nonradioactive in situ hybridizationF Minoletti, I Colombo, A L Martin, et al.
Neuroreport|January 6, 1999
Retroviral-mediated transfer of the galactocerebrosidase gene in neural progenitor cellsE Torchiana, L Lulli, E Cattaneo, 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.
Pageof 36

Showing results (61-70 of 355) with videos related to

Sort By:
Pageof 36
Minerva Pediatrica|March 1, 1991
[Metabolic myopathies]G Finocchiaro, M Zeviani, B Garavaglia, et al.
The Journal of Biological Chemistry|December 23, 1994
Expression and characterization of human and chimeric human-Paracoccus denitrificans electron transfer flavoproteinsK R Herrick, D Salazar, S I Goodman, et al.
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.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
cDNA cloning, sequence analysis, and chromosomal localization of human carnitine palmitoyltransferaseG Finocchiaro, F Taroni, M Rocchi, et al.
Neurology|October 10, 2001
High frequency of the H63D mutation of the hemochromatosis gene (HFE) in malignant gliomasF Martinez di Montemuros, D Tavazzi, E Salsano, et al.
Genomics|November 1, 1994
Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32C Gellera, E Verderio, G Floridia, et al.
Minerva Dietologica E Gastroenterologica|October 1, 1989
[The role of the intestine in the pathogenesis and treatment of multiple organ failure]A M Costantino, G Finocchiaro, A Pezzana, et al.
Genomics|August 1, 1992
Localization of the human gene for carnitine palmitoyltransferase to 1p13-p11 by nonradioactive in situ hybridizationF Minoletti, I Colombo, A L Martin, et al.
Neuroreport|January 6, 1999
Retroviral-mediated transfer of the galactocerebrosidase gene in neural progenitor cellsE Torchiana, L Lulli, E Cattaneo, 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.
Pageof 36