Patrizia Cavadini

Papers authored by Patrizia Cavadini

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2006 Patrizia Cavadini

, Giorgio Biasiotto

, Maura Poli, Sonia Levi, Rosanna Verardi, Isabella Zanella

, Manuela Derosas, Rosaria Ingrassia, Marcella Corrado, Paolo Arosio

RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload

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S. Parolini, W. Vermi, F. Gallo, F. Gentili, E. Mercenaro, Griffiths Gm, L. D. Notarangelo, E. Marcenaro, Notarangelo Ld, G. M. Griffiths, A. Moretta, S. Booth, M. Donini, M. Benassi, D. Ferrari and 6 other authors

Innate immunity defects in Hermansky-Pudlak type 2 syndrome

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2005 Gianmario Gerardi, Giorgio Biasiotto

, Paolo Santambrogio, Isabella Zanella

, Rosaria Ingrassia, Marcella Corrado, Patrizia Cavadini

, Manuela Derosas, Sonia Levi, Paolo Arosio

Recombinant human hepcidin expressed in Escherichia coli isolates as an iron containing protein

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Patrizia Cavadini

, William Vermi, Fabio Facchetti

, Stefania Fontana, Seiho Nagafuchi, Evelina Mazzolari, Anna Sediva, Veronica Marrella, Anna Villa, Alain Fischer, Luigi D. Notarangelo, Raffaele Badolato

AIRE deficiency in thymus of 2 patients with Omenn syndrome

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2004 Anna Virginia Gulino, Daniele Moratto, Silvano Sozzani, Patrizia Cavadini

, Karel Otero, Laura Tassone, Luisa Imberti, Silvia Pirovano, Lucia D. Notarangelo, Roberta Soresina, Evelina Mazzolari, David L. Nelson, Luigi D. Notarangelo, Raffaele Badolato

Altered leukocyte response to CXCL12 in patients with warts hypogammaglobulinemia, infections, myelokathexis (WHIM) syndrome

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2002 Oleksandr Gakh, Patrizia Cavadini

, Grazia Isaya

Protein import and processing reconstituted with isolated rat liver mitochondria and recombinant mitochondrial processing peptidase

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

P. Cavadini

, H. A. O'Neill, O. Benada, G. Isaya

Assembly and iron-binding properties of human frataxin, the protein dificient in Friedreich ataxia

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Oleksandr Gakh, Patrizia Cavadini

, Grazia Isaya

Mitochondrial processing peptidases

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2001 Patrizia Cavadini

, Jiri Adamec, Franco Taroni, Oleksandr Gakh, Grazia Isaya

Two-step processing of human frataxin by mitochondrial processing peptidase - Precursor and intermediate forms are cleaved at different rates

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2000 C. Gellera

, P. Cavadini

, P. I. Patel, G. Isaya

Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae

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This paper was not found in any repository, but could be made available legally by the author.

Roser Pons, Patrizia Cavadini

, Silvia Baratta, Federica Invernizzi, Eleonora Lamantea, Barbara Garavaglia

, Franco Taroni

Clinical and molecular heterogeneity in very–long-chain acyl-coenzyme a dehydrogenase deficiency

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1999 Steven S. Branda, Patrizia Cavadini

, Jiri Adamec, Frantisek Kalousek, Franco Taroni, Grazia Isaya

Yeast and Human Frataxin Are Processed to Mature Form in Two Sequential Steps by the Mitochondrial Processing Peptidase

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J. Yang, P. Cavadini

, C. Gellera

, A. Wong, B. Lonnerdal, F. Taroni, G. Cortopassi

The Friedreich’s ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis

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1998 Kaoru Wataya, Jun Akanuma, Patrizia Cavadini

, Yoko Aoki, Shigeo Kure, Federica Invernizzi, Ichiro Yoshida, Jun‐ichi-I. Kira, Franco Taroni, Yoichi Matsubara, Kuniaki Narisawa

Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: Functional analysis and association with polymorphic haplotypes and two clinical phenotypes

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1997 P. Cavadini

, C. Diblasi, S. Baratta, A. Princivalle, S. Didonato, G. Battaglia, M. Mora, F. Taroni

Expression and mitochondrial localization of frataxin, the Friedreich's ataxia gene product

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1996 J.-P. Bonnefont, F. Taroni, P. Cavadini

, C. Cepanec, M. Brivet, J.-M. Saudubray, J.-P. Leroux, F. Demaugre

Molecular analysis of carnitine palmitoyltransferase II deficiency with hepatocardiomuscular expression

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1995 E. Verderio, P. Cavadini

, L. Montermini, H. Wang, E. Lamantea, G. Finocchiaro, S. DiDonato, C. Gellera

, F. Taroni

Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations

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1994 Cinzia Gellera

, Elisabetta Verderio, Giovanna Floridia, Gaetano Finocchiaro, Laura Montermini, Patrizia Cavadini

, Orsetta Zuffardi, Franco Taroni

Assignment of the Human Carnitine Palmitoyltransferase II Gene (CPT1) to Chromosome 1p32

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1993 Franco Taroni, Elisabetta Verderio, Federica Dworzak, Patrick J. Willems, Patrizia Cavadini

, Stefano DiDonato

Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients

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E. Verderio, P. Cavadini

, M. Pandolfo, S. DiDonato, F. Taroni

Two novel sequence polymorphisms of the human carnitine palmitoyltransferase II (CPT1) gene

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Papers authored by Patrizia Cavadini