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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 sporulation
L 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 pombe
I 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 2
S Albini, U Hetzel, P Cavadini, et al.
Human Molecular Genetics
|
October 13, 2000
Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae
P 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 rates
P 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 attachment
M 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 patients
F 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 peptidase
S 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 deficiency
R 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 apoptosis
A Wong, J Yang, P Cavadini, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 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 sporulation
L 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 pombe
I 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 2
S Albini, U Hetzel, P Cavadini, et al.
Human Molecular Genetics
|
October 13, 2000
Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae
P 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 rates
P 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 attachment
M 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 patients
F 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 peptidase
S 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 deficiency
R 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 apoptosis
A Wong, J Yang, P Cavadini, et al.
Page
of 2