Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Ermanna Rovida"'
Autor:
Anna Cozzi, Daniel I. Orellana, Paolo Santambrogio, Alicia Rubio, Cinzia Cancellieri, Serena Giannelli, Maddalena Ripamonti, Stefano Taverna, Giulia Di Lullo, Ermanna Rovida, Maurizio Ferrari, Gian Luca Forni, Chiara Fiorillo, Vania Broccoli, Sonia Levi
Publikováno v:
Stem Cell Reports, Vol 13, Iss 5, Pp 832-846 (2019)
Summary: Neuroferritinopathy (NF) is a movement disorder caused by alterations in the L-ferritin gene that generate cytosolic free iron. NF is a unique pathophysiological model for determining the direct consequences of cell iron dysregulation. We es
Externí odkaz:
https://doaj.org/article/1a80b9ac5a774715806543d0e61b3993
Autor:
Sonia Levi, Ermanna Rovida
Publikováno v:
Neurobiology of Disease, Vol 81, Iss , Pp 134-143 (2015)
Neuroferritinopathy is a rare, late-onset, dominantly inherited movement disorder caused by mutations in L-ferritin gene. It is characterized by iron and ferritin aggregate accumulation in brain, normal or low serum ferritin levels and high variable
Externí odkaz:
https://doaj.org/article/57e9ad6d8bbc4a24803a2640d31b1f11
Publikováno v:
Cellular and Molecular Life Sciences. 78:3355-3367
Neuroferritinopathy is a rare autosomal dominant inherited movement disorder caused by alteration of the L-ferritin gene that results in the production of a ferritin molecule that is unable to properly manage iron, leading to the presence of free red
Autor:
Alicia Rubio, Serena Giannelli, Vania Broccoli, Maurizio Ferrari, Chiara Fiorillo, Daniel Orellana, Ermanna Rovida, Giulia Di Lullo, Paolo Santambrogio, Anna Cozzi, Cinzia Cancellieri, Stefano Taverna, Gian Luca Forni, Maddalena Ripamonti, Sonia Levi
Publikováno v:
Stem Cell Reports, Vol 13, Iss 5, Pp 832-846 (2019)
Stem Cell Reports
Stem Cell Reports
Summary Neuroferritinopathy (NF) is a movement disorder caused by alterations in the L-ferritin gene that generate cytosolic free iron. NF is a unique pathophysiological model for determining the direct consequences of cell iron dysregulation. We est
Autor:
Nasr Eldin Elwali, Gitana Aceto, Ahmed Elhaj, Ida Biunno, Khalid Dafaallah Awadelkarim, Chiara Carmela Spinelli, Annalisa Morgano, Elgaylani Abdalla Eltayeb, Pasquale De Blasio, Ermanna Rovida, Renato Mariani-Costantini, Dafalla Omer Abuidris
Publikováno v:
Familial Cancer. 13:437-444
Premenopausal breast cancer (BC) is one of the most common cancers of women in rural Africa and part of the disease load may be related to hereditary predisposition, including mutations in the BRCA1 gene. However, the BRCA1 mutations associated with
Publikováno v:
Proteins: Structure, Function, and Bioinformatics. 78:2679-2690
Endothelial protein C receptor (EPCR) is a CD1-like transmembrane glycoprotein with important regulatory roles in protein C (PC) pathway, enhancing PC's anticoagulant, anti-inflammatory, and antiapoptotic activities. Similarly to homologous CD1d, EPC
Autor:
José Hermida, Cristina Razzari, Sirous Zeinali, Elena M. Faioni, Pier Mannuccio Mannucci, D. Asti, Ermanna Rovida
Publikováno v:
British Journal of Haematology. 108:265-271
Two mutations in exons 3 and 9 of the protein C gene were identified by amplification and sequencing from symptomatic probands referred for venous thromboembolism and thrombophilia screening. The phenotype associated with the mutations is a type II p
Autor:
Anna Cozzi, Ermanna Rovida, Paolo Arosio, Alberto Albertini, Sonia Levi, Pauline M. Harrison, Paolo Santambrogio, Peter J. Artymiuk, Patrizia Pinto
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Ferritin is a protein of 24 subunits which assemble into a shell with 432 point symmetry. It can be denatured reversibly in acidic guanidine hydrochloride, with the formation of poorly populated renaturation intermediates. In order to increase the ac
Autor:
Luciano Milanesi, Ermanna Rovida, Gabriele Trombetti, Alessandro Orro, Pasqualina D'Ursi, Marco Moscatelli, Giulia Morra
Publikováno v:
Journal of biomolecular structure and dynamics (Online) 33 (2015): 85–92. doi:10.1080/07391102.2013.851033
info:cnr-pdr/source/autori:Pasqualina D'Ursi a*, Alessandro Orro a, Giulia Morra b, Marco Moscatelli ac, Gabriele Trombetti a, Luciano Milanesi a & Ermanna Rovida d*/titolo:Molecular dynamics and docking simulation of a natural variant of Activated Protein C with impaired protease activity: implications for integrin-mediated antiseptic function./doi:10.1080%2F07391102.2013.851033/rivista:Journal of biomolecular structure and dynamics (Online)/anno:2015/pagina_da:85/pagina_a:92/intervallo_pagine:85–92/volume:33
info:cnr-pdr/source/autori:Pasqualina D'Ursi a*, Alessandro Orro a, Giulia Morra b, Marco Moscatelli ac, Gabriele Trombetti a, Luciano Milanesi a & Ermanna Rovida d*/titolo:Molecular dynamics and docking simulation of a natural variant of Activated Protein C with impaired protease activity: implications for integrin-mediated antiseptic function./doi:10.1080%2F07391102.2013.851033/rivista:Journal of biomolecular structure and dynamics (Online)/anno:2015/pagina_da:85/pagina_a:92/intervallo_pagine:85–92/volume:33
Activated Protein C (APC) is a multifunctional serine protease, primarily known for its anticoagulant function in the coagulation system. Several studies have already elucidated its role in counteracting apoptosis and inflammation in cells, while sig