Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Alberto, Gandini"'
Autor:
Luca Dalle Carbonare, Arianna Minoia, Anna Vareschi, Francesca Cristiana Piritore, Sharazed Zouari, Alberto Gandini, Mirko Meneghel, Rossella Elia, Pamela Lorenzi, Franco Antoniazzi, João Pessoa, Donato Zipeto, Maria Grazia Romanelli, Daniele Guardavaccaro, Maria Teresa Valenti
Publikováno v:
Cells, Vol 13, Iss 5, p 408 (2024)
Overexpression of the Runt-related transcription factor 2 (RUNX2) has been reported in several cancer types, and the C-X-C motif chemokine receptor 4 (CXCR4) has an important role in tumour progression. However, the interplay between CXCR4 and RUNX2
Externí odkaz:
https://doaj.org/article/3117fad34242428d8ec9dd54f6c35a9d
Autor:
Luca Dalle Carbonare, Jessica Bertacco, Salvatore Calogero Gaglio, Arianna Minoia, Mattia Cominacini, Samuele Cheri, Michela Deiana, Giulia Marchetto, Anna Bisognin, Alberto Gandini, Franco Antoniazzi, Massimiliano Perduca, Monica Mottes, Maria Teresa Valenti
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Flavonoids may modulate the bone formation process. Among flavonoids, fisetin is known to counteract tumor growth, osteoarthritis, and rheumatoid arthritis. In addition, fisetin prevents inflammation-induced bone loss. In order to evaluate its favora
Externí odkaz:
https://doaj.org/article/298fa8d4efa74553addf1819288fb077
Autor:
Federica Cavalcoli, Alberto Gandini, Irene Aglaia Matelloni, Francesca Catalano, Saverio Alicante, Guido Manfredi, Gianfranco Brambilla, Fernanda Menozzi, Federica Perolini, Egon Costi, Roberto Bertè, Elisabetta Buscarini
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-6 (2020)
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) is a multisystemic inherited vascular disease characterized by a heterogeneous clinical presentation and prognosis. Dietary evaluation is relevant in HHT patients to provide adequate iro
Externí odkaz:
https://doaj.org/article/e827bb12bdd141a0b3e7a43aa998f3c3
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 11, Iss 1 (2019)
West Nile virus is a zoonotic agent causing life-threatening encephalitis in a proportion of infected patients. Older age, immunosuppression and mutations in specific host genes (e.g. CCR5 delta-32 mutation) predispose to neuroinvasive infection. We
Externí odkaz:
https://doaj.org/article/cfb5e639c8f14d348ef931eb02595b27
Autor:
Luca Dalle Carbonare, Macarena Gomez Lira, Arianna Minoia, Jessica Bertacco, Silvia Orsi, Angela Lauriola, Veronica Li Vigni, Alberto Gandini, Franco Antoniazzi, Donato Zipeto, Monica Mottes, Lekhana Bhandary, Daniele Guardavaccaro, Maria Teresa Valenti
Publikováno v:
Journal of Cellular and Molecular Medicine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1800815f67f6ebab9a2b47575c37bea
https://doi.org/10.1111/jcmm.17767
https://doi.org/10.1111/jcmm.17767
Autor:
Michela Deiana, Luca Dalle Carbonare, Michela Serena, Samuele Cheri, Simona Mutascio, Alberto Gandini, Giulio Innamorati, Pamela Lorenzi, Michela Cumerlato, Jessica Bertacco, Franco Antoniazzi, Maria Grazia Romanelli, Monica Mottes, Donato Zipeto, Maria Teresa Valenti
Publikováno v:
Cells, Vol 9, Iss 3, p 751 (2020)
Ectopic expression of RUNX2 has been reported in several tumors. In melanoma cells, the RUNT domain of RUNX2 increases cell proliferation and migration. Due to the strong link between RUNX2 and skeletal development, we hypothesized that the RUNT doma
Externí odkaz:
https://doaj.org/article/94861e385b224bbaa55d8086abaa378c
Autor:
Michela Deiana, Luca Dalle Carbonare, Michela Serena, Samuele Cheri, Francesca Parolini, Alberto Gandini, Giulia Marchetto, Giulio Innamorati, Marcello Manfredi, Emilio Marengo, Jessica Brandi, Daniela Cecconi, Antonio Mori, Maria Mihaela Mina, Franco Antoniazzi, Monica Mottes, Natascia Tiso, Giovanni Malerba, Donato Zipeto, Maria Teresa Valenti
Publikováno v:
Cells, Vol 7, Iss 11, p 220 (2018)
The mortality rate for malignant melanoma (MM) is very high, since it is highly invasive and resistant to chemotherapeutic treatments. The modulation of some transcription factors affects cellular processes in MM. In particular, a higher expression o
Externí odkaz:
https://doaj.org/article/6f997a9227dd4a0f8e560eb4e31775c4
Publikováno v:
Biomicrofluidics
We describe RapidQ, a fast, disposable, easy-to-use microfluidic assay for the quantitation of the anti-SARS-CoV-2 spike (S) protein IgG in plasma samples. The assay utilizes antigen-coated paramagnetic microbeads, which are induced to aggregate insi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0161ebaf1f20d05e71f2202d7841da7e
https://pubmed.ncbi.nlm.nih.gov/35356130
https://pubmed.ncbi.nlm.nih.gov/35356130
Autor:
Massimiliano Perduca, Veronica Li Vigni, Luca Dalle Carbonare, Alberto Gandini, Silvia Orsi, Franco Antoniazzi, Jessica Bertacco, Monica Mottes, Arianna Minoia, Francesca Griggio, Maria Teresa Valenti
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 19
International Journal of Molecular Sciences, Vol 22, Iss 10336, p 10336 (2021)
Volume 22
Issue 19
International Journal of Molecular Sciences, Vol 22, Iss 10336, p 10336 (2021)
Cleidocranial dysplasia (CCD), a dominantly inherited skeletal disease, is characterized by a variable phenotype ranging from dental alterations to severe skeletal defects. Either de novo or inherited mutations in the RUNX2 gene have been identified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39e0c890f30e5a0ae3248f25790af984
http://europepmc.org/articles/PMC8508986
http://europepmc.org/articles/PMC8508986
Autor:
Alberto Gandini, Federica Perolini, Egon Costi, Gianfranco Brambilla, Francesca Catalano, Guido Manfredi, Fernanda Menozzi, Saverio Alicante, Federica Cavalcoli, Irene Aglaia Matelloni, Elisabetta Buscarini, Roberto Bertè
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-6 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Hereditary hemorrhagic telangiectasia (HHT) is a multisystemic inherited vascular disease characterized by a heterogeneous clinical presentation and prognosis. Dietary evaluation is relevant in HHT patients to provide adequate iron and nut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ab3431c44cffea91f0663fc6cacd71
https://doi.org/10.1186/s13023-020-01554-x
https://doi.org/10.1186/s13023-020-01554-x