Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Serena Somma"'
Autor:
Anna Maria Pinto, Valentina Imperatore, Aurora Currò, Francesca Ariani, Sonia De Francesco, Serena Somma, Mirella Bruttini, Theodora Hadjistilianou, Alessandra Renieri, Elisa Gelli, Francesca Mari, Marta Giulia Cannone, Daniela Galimberti
Publikováno v:
Human mutation. 40(2)
Retinoblastoma (RB), which represents the most common childhood eye cancer, is caused by biallelic inactivation of RB1 gene. Promoter hypermethylation is quite frequent in RB tissues but conclusive evidence of soma-wide predisposing epimutations is c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::185f94e63b765c0f9420d82a040604ea
https://pubmed.ncbi.nlm.nih.gov/30427563
https://pubmed.ncbi.nlm.nih.gov/30427563
Autor:
Giulia Carignani, Maria Antonietta Mencarelli, Paolo Toti, Francesca Mari, Chiara Di Marco, Francesca Ariani, Daniela Galimberti, Annabella Marozza, Serena Somma, Theodora Hadjistilianou, Ilaria Meloni, Pietro Piu, Caterina Lo Rizzo, Sonia De Francesco, Valentina Imperatore, Sara Amitrano, Laura Dosa, Francesco Cetta, Alessandra Renieri
Publikováno v:
European Journal of Human Genetics. 23:1523-1530
In about 50% of sporadic cases of retinoblastoma, no constitutive RB1 mutations are detected by conventional methods. However, recent research suggests that, at least in some of these cases, there is somatic mosaicism with respect to RB1 normal and m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e0092d3365856b220ad8bb2e976100a
https://doi.org/10.1038/ejhg.2015.6
https://doi.org/10.1038/ejhg.2015.6
Autor:
Joëlle Wiels, Martine Raphael, Serena Somma, Cristiana Bellan, Alessandro Gozzetti, Massimo Granai, Evelyne May, Awa Oumar Touré, Lorenzo Leoncini, Yonis Ahmed, Michele Iacono, Tandakha Ndiaye Dieye, Charles Henry Gattiollat, Pier Paolo Piccaluga, Abibatou Sall, Teresa Amato, Saliou Diop, Maria Raffaella Ambrosio
Publikováno v:
American journal of clinical pathology. 148(6)
Objectives: Chronic lymphocytic leukemia (CLL) is the most common type of leukemia in Western populations, being rarer in Asian and African people. It has been suggested that patients with CLL from Africa might have a more aggressive disease compared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a8387a6e9c9879e83b94194fb4f02be
https://pubmed.ncbi.nlm.nih.gov/29165569
https://pubmed.ncbi.nlm.nih.gov/29165569
Autor:
Gelli, Elisa, Pinto, Anna Maria, Somma, Serena, Imperatore, Valentina, Cannone, Marta G., Hadjistilianou, Theodora, Francesco, Sonia, Galimberti, Daniela, Currò, Aurora, Bruttini, Mirella, Mari, Francesca, Renieri, Alessandra, Ariani, Francesca
Publikováno v:
Human Mutation; Feb2019, Vol. 40 Issue 2, p201-206, 6p
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