Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Dalila Bevilacqua"'
Autor:
Sara Costa, Dalila Bevilacqua, Elena Caveggion, Sara Gasperini, Elena Zenaro, Francesca Pettinella, Marta Donini, Stefano Dusi, Gabriela Constantin, Silvia Lonardi, William Vermi, Francesco De Sanctis, Stefano Ugel, Tiziana Cestari, Clare L. Abram, Clifford A. Lowell, Pamela Rodegher, Franco Tagliaro, Giampiero Girolomoni, Marco A. Cassatella, Patrizia Scapini
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
BackgroundPsoriasis is a chronic skin disease associated with deregulated interplays between immune cells and keratinocytes. Neutrophil accumulation in the skin is a histological feature that characterizes psoriasis. However, the role of neutrophils
Externí odkaz:
https://doaj.org/article/b8b37b1a6ace4838bb7bd76f755ac86f
Autor:
Robin R. Ali, Dalila Bevilacqua, Dimitra Athanasiou, Mònica Aguilà, Takao Iwawaki, Alexander J. Smith, James Bellingham, David A. Parfitt, Ryea Maswood, Michael E. Cheetham, Yanai Duran, Giannis Spyrou
Publikováno v:
Human Molecular Genetics
Rhodopsin misfolding caused by the P23H mutation is a major cause of autosomal dominant retinitis pigmentosa (adRP). To date, there are no effective treatments for adRP. The BiP co-chaperone and reductase ERdj5 (DNAJC10) is part of the endoplasmic re
Autor:
Naheed Kanuga, Takao Iwawaki, J. Paul Chapple, Dimitra Athanasiou, Michael E. Cheetham, Caroline McCulley, Dalila Bevilacqua, Mònica Aguilà
Publikováno v:
Human Molecular Genetics
Hum Mol Genet
Hum Mol Genet
Mutations in rhodopsin, the light-sensitive protein of rod cells, are the most common cause of autosomal dominant retinitis pigmentosa (ADRP). Many rod opsin mutations, such as P23H, lead to misfolding of rod opsin with detrimental effects on photore
Autor:
Cecilia Spina, Olivia Marini, Dalila Bevilacqua, Donata de Sabata, Giorgio Gandini, Cristina Tecchio, William Vermi, Chiara Cavallini, Francesco Missale, Marco A. Cassatella, Sara Costa, Patrizia Scapini, Maurizio Cantini, Ilaria Tinazzi, Elisa Zoratti, Antonio Marchetta, Claudio Lunardi, Alfredo Guglielmi, Federica Calzetti, Elisa Tinazzi, Nicola Tamassia, A. Vassanelli, Andrea Ruzzenente, Maria Teresa Scupoli
Publikováno v:
Blood. 129:1343-1356
The identification of discrete neutrophil populations, as well as the characterization of their immunoregulatory properties, is an emerging topic under extensive investigation. In such regard, the presence of circulating CD66b+ neutrophil populations
Publikováno v:
Immunology. 156(1)
An increasing body of literature supports a role for neutrophils as players in the orchestration of adaptive immunity. During acute and chronic inflammatory conditions, neutrophils rapidly migrate not only to sites of inflammation, but also to draini
Autor:
Franco Tagliaro, Anna Panato, Sara Costa, Olivia Marini, Pamela Rodegher, Clifford A. Lowell, Marco A. Cassatella, Giampiero Girolomoni, William Vermi, Silvia Lonardi, Anthony L. DeFranco, Dalila Bevilacqua, Baidong Hou, Patrizia Scapini
Psoriasis is a chronic skin disease associated with deregulated activation of immune cells and keratinocytes. In this study, we used the imiquimod (IMQ)-induced mouse model of psoriasis to dissect better the contribution of hematopoietic and skin-res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::803efef7ffc29ca16860ce5bf142042f
http://hdl.handle.net/11379/493846
http://hdl.handle.net/11379/493846
Autor:
Michael E. Cheetham, David A. Parfitt, Dimitra Athanasiou, Dalila Bevilacqua, Mònica Aguilà, Sergey S. Novoselov
Publikováno v:
FEBS Letters. 587:2008-2017
Retinal degenerations are a group of clinically and genetically heterogeneous disorders characterised by progressive loss of vision due to neurodegeneration. The retina is a highly specialised tissue with a unique architecture and maintaining homeost
Autor:
Dimitra, Athanasiou, Monica, Aguila, Chikwado A, Opefi, Kieron, South, James, Bellingham, Dalila, Bevilacqua, Peter M, Munro, Naheed, Kanuga, Francesca E, Mackenzie, Adam M, Dubis, Anastasios, Georgiadis, Anna B, Graca, Rachael A, Pearson, Robin R, Ali, Sanae, Sakami, Krzysztof, Palczewski, Michael Y, Sherman, Philip J, Reeves, Michael E, Cheetham
Publikováno v:
Human Molecular Genetics
Protein misfolding caused by inherited mutations leads to loss of protein function and potentially toxic ‘gain of function’, such as the dominant P23H rhodopsin mutation that causes retinitis pigmentosa (RP). Here, we tested whether the AMPK acti
Autor:
Olivia, Marini, Sara, Costa, Dalila, Bevilacqua, Federica, Calzetti, Nicola, Tamassia, Cecilia, Spina, Donata, De Sabata, Elisa, Tinazzi, Claudio, Lunardi, Maria T, Scupoli, Chiara, Cavallini, Elisa, Zoratti, Ilaria, Tinazzi, Antonio, Marchetta, Aurora, Vassanelli, Maurizio, Cantini, Giorgio, Gandini, Andrea, Ruzzenente, Alfredo, Guglielmi, Francesco, Missale, William, Vermi, Cristina, Tecchio, Marco A, Cassatella, Patrizia, Scapini
Publikováno v:
Blood. 129(10)
The identification of discrete neutrophil populations, as well as the characterization of their immunoregulatory properties, is an emerging topic under extensive investigation. In such regard, the presence of circulating CD66b
Autor:
Michel Michaelides, Michael B. Gorin, Dawn L. Thiselton, David A. Parfitt, Naheed Kanuga, Jacob H.C. Ressa, Jessica C. Gardner, I Zito, Nele Schwarz, Ariadna Martinez, Alison J. Hardcastle, Tom R. Webb, Michael E. Cheetham, Alice E. Davidson, Dalila Bevilacqua, Marina Apergi
X-linked retinitis pigmentosa (XLRP) is genetically heterogeneous with two causative genes identified, RPGR and RP2. We previously mapped a locus for a severe form of XLRP, RP23, to a 10.71 Mb interval on Xp22.31-22.13 containing 62 genes. Candidate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c368e6acc54419a3e1505a673fd9005
https://europepmc.org/articles/PMC3406759/
https://europepmc.org/articles/PMC3406759/