Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Raffaele Murru"'
Autor:
Eleonora Cocco, Raffaele Murru, Gianna Costa, Amit Kumar, Enrico Pieroni, Cristina Melis, Luigi Barberini, Claudia Sardu, Lorena Lorefice, Giuseppe Fenu, Jessica Frau, Giancarlo Coghe, Nicola Carboni, Maria Giovanna Marrosu
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e59790 (2013)
We performed a case-control study in 2,555 multiple sclerosis (MS) Sardinian patients and 1,365 healthy ethnically matched controls, analyzing the interactions between HLA-DRB1-DQB1 haplotypes and defining a rank of genotypes conferring a variable de
Externí odkaz:
https://doaj.org/article/377ae2525b204c589623a27a46f8f3a8
Autor:
Eleonora Cocco, Claudia Sardu, Enrico Pieroni, Maria Valentini, Raffaele Murru, Gianna Costa, Stefania Tranquilli, Jessica Frau, Giancarlo Coghe, Nicola Carboni, Matteo Floris, Paolo Contu, Maria Giovanna Marrosu
Publikováno v:
PLoS ONE, Vol 7, Iss 4, p e33972 (2012)
IntroductionGenetic predisposition to multiple sclerosis (MS) in Sardinia (Italy) has been associated with five DRB1*-DQB1* haplotypes of the human leukocyte antigen (HLA). Given the complexity of these associations, an in-depth re-analysis was perfo
Externí odkaz:
https://doaj.org/article/126a83fcf85c436e9d9781955e754d9e
Autor:
Eleonora Cocco, Alessandra Meloni, Maria Rita Murru, Daniela Corongiu, Stefania Tranquilli, Elisabetta Fadda, Raffaele Murru, Lucia Schirru, Maria Antonietta Secci, Gianna Costa, Isadora Asunis, Stefania Cuccu, Giuseppe Fenu, Lorena Lorefice, Nicola Carboni, Gioia Mura, Maria Cristina Rosatelli, Maria Giovanna Marrosu
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e41678 (2012)
Vitamin D response elements (VDREs) have been found in the promoter region of the MS-associated allele HLA-DRB1*15:01, suggesting that with low vitamin D availability VDREs are incapable of inducing *15:01 expression allowing in early life autoreacti
Externí odkaz:
https://doaj.org/article/681972ee6990452aa896122b232f7594
Autor:
Pina Ziranu, Valentina Aimola, Andrea Pretta, Marco Dubois, Raffaele Murru, Nicole Liscia, Flaviana Cau, Mara Persano, Giulia Deias, Enrico Palmas, Francesco Loi, Marco Migliari, Valeria Pusceddu, Marco Puzzoni, Eleonora Lai, Stefano Cascinu, Gavino Faa, Mario Scartozzi
Publikováno v:
Cancers
Volume 15
Issue 4
Pages: 1212
Volume 15
Issue 4
Pages: 1212
Background: The transmembrane glycoprotein CD44, the major hyaluronan (HA) receptor, has been proven to regulate cell growth, survival, differentiation, and migration. It is therefore widely considered to be involved in carcinogenesis. Its role as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91e44ba10f3ca006c23b5a30a21fda19
Autor:
Maria Giovanna Marrosu1 gmarrosu@unica.it, Raffaele Murru1 rmurru@unica.it, Gianna Costa1 csm@unica.it, Maria Cristina Melis1 csm@unica.it, Marcella Rolesu1 csm@unica.it, Lucia Schirru1 csm@unica.it, Elisabetta Solla1 csm@unica.it, Stefania Cuccu1 csm@unica.it, Maria Antonietta Secci1 csm@unica.it, Whalen, Michael B2 whalenmb@hotmail.com, Cocco, Eleonora1 ecocco@unica.it, Pugliatti, Maura3 maurap@uniss.it, Sotgiu, Stefano3 stefanos@uniss.it, Rosati, Giulio3 webmed@uniss.it, Cucca, Francesco2 fcucca@uniss.it
Publikováno v:
BMC Genetics. 2007, Vol. 8, p25-10. 10p. 2 Charts, 3 Graphs.
Autor:
M. Conti, Cristina Mancosu, Maria Valeria Cherchi, Raffaele Murru, Nicola Carboni, Gabriella Spinicci
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 22:539-544
Journal of Stroke and C Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a disease caused by alterations in the NOTCH3 gene.Methods:Wedescribe the clinical, instrumental, and genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e74b87fd70a9d876136c01bbfb962e8
https://doi.org/10.1016/j.jstrokecerebrovasdis.2013.02.002
https://doi.org/10.1016/j.jstrokecerebrovasdis.2013.02.002
Autor:
Simone Poddighe, Eleonora Cocco, Maria Rita Murru, Lorena Lorefice, Federica Murgia, Jessica Frau, Luigi Atzori, Giancarlo Coghe, Giuseppe Fenu, Raffaele Murru, Luigi Barberini, Francesco Del Carratore, Maria Giovanna Marrosu
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation
Cocco, E, Murgia, F, Lorefice, L, Barberini, L, Poddighe, S, Frau, J, Fenu, G, Coghe, G, Murru, M R, Murru, R, Del Carratore, F, Atzori, L & Marrosu, M G 2015, ' 1 H-NMR analysis provides a metabolomic profile of patients with multiple sclerosis ', Neurology: Neuroimmunology and NeuroInflammation . https://doi.org/10.1212/NXI.0000000000000185
Cocco, E, Murgia, F, Lorefice, L, Barberini, L, Poddighe, S, Frau, J, Fenu, G, Coghe, G, Murru, M R, Murru, R, Del Carratore, F, Atzori, L & Marrosu, M G 2015, ' 1 H-NMR analysis provides a metabolomic profile of patients with multiple sclerosis ', Neurology: Neuroimmunology and NeuroInflammation . https://doi.org/10.1212/NXI.0000000000000185
Objective: To investigate the metabolomic profiles of patients with multiple sclerosis (MS) and to define the metabolic pathways potentially related to MS pathogenesis. Methods: Plasma samples from 73 patients with MS (therapy-free for at least 90 da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::760e3f052555a6b0e146f3d3000ab653
http://europepmc.org/articles/PMC4694073
http://europepmc.org/articles/PMC4694073
Publikováno v:
Neurological Sciences. 31:631-634
Neurofibromatosis 1 (NF1), also called von Recklinghausen disease or peripheral NF, is a common autosomal-dominant neurocutaneous disorder associated with mutations of the NF 1 gene. The pathogenesis is poorly understood and the disease is characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4d5ce31001d0ba69b0620a8463b5160
https://doi.org/10.1007/s10072-010-0252-2
https://doi.org/10.1007/s10072-010-0252-2
Autor:
Raffaele Murru, Jessica Frau, Eleonora Cocco, E Mamusa, Claudia Sardu, Lorena Lorefice, Paolo Contu, Maria Giovanna Marrosu
Publikováno v:
Multiple Sclerosis Journal. 15:1030-1036
Background The island of Sardinia features a high incidence of multiple sclerosis (MS) characterized by early age at onset and a progressively increasing trend. The current study was aimed at examining variations in human leukocyte antigen–risk gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a52553a2edcc078c08f75245517e9971
https://doi.org/10.1177/1352458509106745
https://doi.org/10.1177/1352458509106745
Autor:
Maristella Pitzalis, Laura Cornelia Clotilde Morelli, Stefano Sotgiu, Francesco Cucca, Michael B. Whalen, Maura Pugliatti, Magdalena Zoledziewska, P Pusceddu, M Bajorek, Am Satta, Rosanna Lampis, A Chessa, Patrizia Frongia, Patrizia Zavattari, A Marras, Eleonora Cocco, Loredana Moi, Gianna Costa, Cristina Melis, Maria Giovanna Marrosu, Giulio Rosati, Fausto Pier'Angelo Poddie, Raffaele Murru
Publikováno v:
Genes & Immunity. 10:15-17
Variation within intron 19 of the CLEC16A (KIAA0350) gene region was recently found to be unequivocally associated with type 1 diabetes (T1D) in genome-wide association (GWA) studies in Northern European populations. A variant in intron 22 that is ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::225de19ca8922eefb207296aeefe3532
https://doi.org/10.1038/gene.2008.84
https://doi.org/10.1038/gene.2008.84