Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Andrea Biondani"'
Autor:
Edwin Wong, Carla Nester, Teresa Cavero, Alexandre Karras, Moglie Le Quintrec, Liz Lightstone, Ute Eisenberger, Maria Jose Soler, David Kavanagh, Erica Daina, Manuel Praga, Nicholas R. Medjeral-Thomas, Anja Gäckler, Clara Garcia-Carro, Andrea Biondani, Frederique Chaperon, Kenneth Kulmatycki, Julie Milojevic, Nicholas J.A. Webb, Prasanna Kumar Nidamarthy, Guido Junge, Giuseppe Remuzzi
Publikováno v:
Kidney International Reports, Vol 8, Iss 12, Pp 2754-2764 (2023)
Introduction: Complement 3 glomerulopathy (C3G) is a rare inflammatory kidney disease mediated by dysregulation of the alternative complement pathway. No targeted therapy exists for this aggressive glomerulonephritis. Efficacy, safety, tolerability,
Externí odkaz:
https://doaj.org/article/4142dfa19bbe4b318478e3240af7c53c
Autor:
Achille Iolascon, Luigia De Falco, Franck Borgese, Maria Rosaria Esposito, Rosa Anna Avvisati, Pietro Izzo, Carmelo Piscopo, Helene Guizouarn, Andrea Biondani, Antonella Pantaleo, Lucia De Franceschi
Publikováno v:
Haematologica, Vol 94, Iss 8 (2009)
Background Stomatocytoses are a group of inherited autosomal dominant hemolytic anemias and include overhydrated hereditary stomatocytosis, dehydrated hereditary stomatocytosis, hereditary cryohydrocytosis and familial pseudohyperkalemia.Design and M
Externí odkaz:
https://doaj.org/article/9cca593df5394f18b9db1fc6786766ca
Autor:
Cinzia Scambi, Lucia De Franceschi, Patrizia Guarini, Fabio Poli, Angela Siciliano, Patrizia Pattini, Andrea Biondani, Valentina La Verde, Oscar Bortolami, Francesco Turrini, Franco Carta, Ciro D'Orazio, Baroukh M Assael, Giovanni Faccini, Lisa M Bambara
Publikováno v:
PLoS ONE, Vol 4, Iss 3, p e4782 (2009)
Cystic fibrosis (CF) is one of the most common fatal autosomal recessive disorders in the Caucasian population caused by mutations of gene for the cystic fibrosis transmembrane conductance regulator (CFTR). New experimental therapeutic strategies for
Externí odkaz:
https://doaj.org/article/2538d0a6dfbd40b9ad833858e4dbdda1
Autor:
Loris Turretta, Carlo Brugnara, Lucia De Franceschi, Ari Elson, Francesco Michelangelo Turrini, Andrea Biondani, Achille Iolascon, Anna Maria Brunati, Renzo Deana, Silverio Perrotta, Carlo Laudanna, Cristina Bulato, Franco Carta
Publikováno v:
PROTEOMICS. 8:4695-4708
Protein tyrosine phosphatases (PTPs) are crucial components of cellular signal transduction pathways. We report here that red blood cells (RBCs) from mice lacking PTPe (Ptpre −/− ) exhibit abnormal morphology and increased Ca 2+ -activated-K + ch
Autor:
Andrea Biondani, Franco Turrini, Lucia De Franceschi, Franco Carta, Alessandro Matte, Alida Filippini, Yves Beuzard, Angela Siciliano
Publikováno v:
PROTEOMICS – CLINICAL APPLICATIONS. 2:706-719
Sickle cell disease (SCD) is an autosomal recessive genetic red cell disorder characterized by the production of a defective form of hemoglobin, hemoglobin-S, that is worldwide-distributed. The acute clinical manifestations of SCD are related to hemo
Autor:
Chris Lamb, Massimo Delledonne, Andrea Biondani, Annalisa Polverari, Irene Murgia, Pier Filippo Sbicego, Davide Ederle
Publikováno v:
Plant Physiology and Biochemistry. 40:605-610
The mechanisms involved in plant defense show several similar characteristics with the innate immune systems of vertebrates and invertebrates. In animals, nitric oxide (NO) cooperates with reactive oxygen intermediates (ROI) to kill tumor cells and i
Autor:
Riccardo Gavioli, Giuseppe De Santis, Enrico Fainardi, Luca Battistini, Giovanna Borsellino, Manuela Ferracin, Luisa Caniatti, Enrico Granieri, Roberto Furlan, Maria Rosaria Tola, Massimiliano Castellazzi, Barbara Zagatti, Andrea Biondani, Massimo Negrini
Altered miRNA expression in T regulatory cells in course of multiple sclerosis. OBJECTIVES: Multiple sclerosis (MS) is a chronic inflammatory response against constituents of the central nervous system. It is known that regulatory T cells (Tregs) pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f0e80213dd50b67b0fead743c4c65fc
http://hdl.handle.net/11392/1379093
http://hdl.handle.net/11392/1379093
Autor:
Pietro Izzo, Rosa Anna Avvisati, Maria Rosaria Esposito, Franck Borgese, Carmelo Piscopo, Andrea Biondani, Achille Iolascon, Luigia De Falco, Lucia De Franceschi, Hélène Guizouarn, Antonella Pantaleo
Publikováno v:
Haematologica
Haematologica, Ferrata Storti Foundation, 2009, 94 (8), pp.1049-59. ⟨10.3324/haematol.2008.002873⟩
Haematologica, Ferrata Storti Foundation, 2009, 94 (8), pp.1049-59. ⟨10.3324/haematol.2008.002873⟩
International audience; BACKGROUND: Stomatocytoses are a group of inherited autosomal dominant hemolytic anemias and include overhydrated hereditary stomatocytosis, dehydrated hereditary stomatocytosis, hereditary cryohydrocytosis and familial pseudo
Autor:
Seth L. Alper, Emma Villa-Moruzzi, Angela Siciliano, Andrea Biondani, Lucia De Franceschi, Carlo Brugnara, Giorgio Berton, Clifford A. Lowell
Publikováno v:
Pflugers Archiv : European journal of physiology. 451(6)
The K-Cl cotransport (KCC) is an electroneutral-gradient-driven-membrane transport system, which is involved in regulation of red cell volume. Although the regulatory cascade of KCC is largely unknown, a signaling pathway involving phosphatases and k
Autor:
Lucia De Franceschi, Francesco Michelangelo Turrini, Baroukh M. Assael, Fabio Poli, Lisa Maria Bambara, Angela Siciliano, Franco Carta, Giovanni Faccini, Oscar Bortolami, C. D'Orazio, Andrea Biondani, Valentina La Verde, Patrizia Guarini, Patrizia Pattini, Cinzia Scambi
Publikováno v:
PLoS ONE
PLoS ONE, Vol 4, Iss 3, p e4782 (2009)
PLoS ONE, Vol 4, Iss 3, p e4782 (2009)
Background Cystic fibrosis (CF) is one of the most common fatal autosomal recessive disorders in the Caucasian population caused by mutations of gene for the cystic fibrosis transmembrane conductance regulator (CFTR). New experimental therapeutic str