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P Cavadini

Showing results (1-10 of 16) with videos related to

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Current Genetics|November 1, 1993
Transcript accumulation of the GGP1 gene, encoding a yeast GPI-anchored glycoprotein, is inhibited during arrest in the G1 phase and during sporulationL Popolo, P Cavadini, M Vai, et al.
Biochimica Et Biophysica Acta|June 7, 1996
Cloning, sequencing and regulation of a cDNA encoding a small heat-shock protein from Schizosaccharomyces pombeI Orlandi, P Cavadini, L Popolo, et al.
Schweizer Archiv Fur Tierheilkunde|May 4, 2022
Inconspicuous post-mortem findings in rabbits from Switzerland naturally -infected with Rabbit Haemorrhagic -Disease Virus 2S Albini, U Hetzel, P Cavadini, et al.
Human Molecular Genetics|October 13, 2000
Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiaeP Cavadini, C Gellera, P I Patel, et al.
The Journal of Biological Chemistry|October 6, 2000
Two-step processing of human frataxin by mitochondrial processing peptidase. Precursor and intermediate forms are cleaved at different ratesP Cavadini, J Adamec, F Taroni, et al.
Yeast (Chichester, England)|March 30, 1996
Candida albicans homologue of GGP1/GAS1 gene is functional in Saccharomyces cerevisiae and contains the determinants for glycosylphosphatidylinositol attachmentM Vai, I Orlandi, P Cavadini, et al.
Nature Genetics|July 1, 1993
Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patientsF Taroni, E Verderio, F Dworzak, et al.
The Journal of Biological Chemistry|July 31, 1999
Yeast and human frataxin are processed to mature form in two sequential steps by the mitochondrial processing peptidaseS S Branda, P Cavadini, J Adamec, et al.
Pediatric Neurology|March 30, 2000
Clinical and molecular heterogeneity in very-long-chain acyl-coenzyme A dehydrogenase deficiencyR Pons, P Cavadini, S Baratta, et al.
Human Molecular Genetics|February 9, 1999
The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosisA Wong, J Yang, P Cavadini, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Current Genetics|November 1, 1993
Transcript accumulation of the GGP1 gene, encoding a yeast GPI-anchored glycoprotein, is inhibited during arrest in the G1 phase and during sporulationL Popolo, P Cavadini, M Vai, et al.
Biochimica Et Biophysica Acta|June 7, 1996
Cloning, sequencing and regulation of a cDNA encoding a small heat-shock protein from Schizosaccharomyces pombeI Orlandi, P Cavadini, L Popolo, et al.
Schweizer Archiv Fur Tierheilkunde|May 4, 2022
Inconspicuous post-mortem findings in rabbits from Switzerland naturally -infected with Rabbit Haemorrhagic -Disease Virus 2S Albini, U Hetzel, P Cavadini, et al.
Human Molecular Genetics|October 13, 2000
Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiaeP Cavadini, C Gellera, P I Patel, et al.
The Journal of Biological Chemistry|October 6, 2000
Two-step processing of human frataxin by mitochondrial processing peptidase. Precursor and intermediate forms are cleaved at different ratesP Cavadini, J Adamec, F Taroni, et al.
Yeast (Chichester, England)|March 30, 1996
Candida albicans homologue of GGP1/GAS1 gene is functional in Saccharomyces cerevisiae and contains the determinants for glycosylphosphatidylinositol attachmentM Vai, I Orlandi, P Cavadini, et al.
Nature Genetics|July 1, 1993
Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patientsF Taroni, E Verderio, F Dworzak, et al.
The Journal of Biological Chemistry|July 31, 1999
Yeast and human frataxin are processed to mature form in two sequential steps by the mitochondrial processing peptidaseS S Branda, P Cavadini, J Adamec, et al.
Pediatric Neurology|March 30, 2000
Clinical and molecular heterogeneity in very-long-chain acyl-coenzyme A dehydrogenase deficiencyR Pons, P Cavadini, S Baratta, et al.
Human Molecular Genetics|February 9, 1999
The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosisA Wong, J Yang, P Cavadini, et al.
Pageof 2