Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Annalisa Ranieri"'
Autor:
Carmine De Angelis, Carmela Nardelli, Paola Concolino, Martina Pagliuca, Mario Setaro, Elisa De Paolis, Pietro De Placido, Valeria Forestieri, Giovanni Luca Scaglione, Annalisa Ranieri, Barbara Lombardo, Lucio Pastore, Sabino De Placido, Ettore Capoluongo
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
The partner and localizer of BRCA2 (PALB2) is a major BRCA2 binding partner that participates in homologous recombination repair in response to DNA double-strand breaks. Germline alterations of the PALB2 gene have recently been associated with a high
Externí odkaz:
https://doaj.org/article/6c2560cc8a3d452da31845c3dd0cda98
Autor:
Maura Bozzali, Daniela Leonardi, Angelo Coco, Lidia Sava, Annalisa Ranieri, Massimo Buscema, Francesca Calaciura, Carmela Cisternino, Vittorio Tassi, Vincenzo Trischitta, Concetto Regalbuto, Giueppe Miscio, Anna Carta, Raffaella Maiorana
Publikováno v:
Scopus-Elsevier
Congenital hypothyroidism (CH) may cause severe and irreversible neurologic and developmental abnormalities when not recognized early. Many millions of newborns have now been screened and many thousands of patients with CH have been identified. Appro
Autor:
Alessandro Cama, M C Verì, Francesco Nardi, G Colletta, Raffaele Palmirotta, Renato Mariani-Costantini, Annalisa Ranieri, Davide Lazzereschi, Laura Ottini, Francesco Cetta
Publikováno v:
British Journal of Cancer
Fifty-one thyroid tumours and tumour-like lesions were analysed for instability at ten dinucleotide microsatellite loci and at two coding mononucleotide repeats within the transforming growth factor β (TGF-β) type II receptor (TβRII) and insulin-l
Autor:
Francesco Nardi, Giulia Colletta, Caterina Carnovale Scalzo, Laura Sambuco, Annalisa Ranieri, Davide Lazzereschi, Gabriella Mincione
Publikováno v:
International Journal of Cancer. 76:806-811
Evidence of the involvement of cyclin gene alterations in human cancer is growing. In this study, we sought to determine the pattern of expression of cyclin D1 and cyclin E in normal and malignant thyroid cells. Quiescent rat thyroid cells in culture
Autor:
Susanna Scarpa, Giulia Colletta, Annalisa Ranieri, Davide Lazzereschi, Maria Ragano-Caracciolo, Barbara Lucignano, Gabriella Mincione, Alessandra Turco, Anna Coppa
Publikováno v:
Journal of Cellular Physiology. 172:200-208
Transforming growth factor beta 1 (TGF beta 1) inhibits the growth of normal rat epithelial thyroid cells (FRTL-5 strain) by counteracting thyrotropin (TSH)-stimulated DNA synthesis and by slowing the cells in the G1 phase of the cell cycle. Here, we
Autor:
R. Mariani Costantini, Annalisa Ranieri, P Battista, Alfredo Pontecorvi, Alessandro Cama, G Colletta, Salvatore Sciacchitano, E Zanella, Raffaele Palmirotta
Publikováno v:
British Journal of Cancer
Familial adenomatous polyposis (FAP) is known to be associated with neoplasia of various tissues, including thyroid carcinoma. Germline mutations of the tumour-suppressor gene APC, responsible for the predisposition to FAP, may therefore be involved
Autor:
Fulvio Della Loggia, Pasquale Battista, Fabio Capani, Alessandro Cama, Annalisa Ranieri, Agostino Consoli, Diana L. Esposito, Sandra Mammarella, Felice Giacomo Caramia, Renato Mariani-Costantini
Publikováno v:
Human Mutation. 7:364-366
Publikováno v:
The Journal of biological chemistry. 277(29)
Serpins are responsible for regulating a variety of proteolytic processes through a unique irreversible suicide substrate mechanism. To discover novel genes regulated by transforming growth factor-beta1 (TGF-beta 1), we performed differential display
Autor:
Renato Mariani-Costantini, Diana L. Esposito, Francesco Tonelli, Maria Cristina Curia, Rosa Valanzano, Raffaele Palmirotta, Andrea Modesti, Annalisa Ranieri, Alessandro Cama, Pasquale Battista, Ferdinando Ficari
Publikováno v:
Human mutation. 5(2)
Germline mutations of the adenomatous polyposis coli (APC) gene tend to cluster in discrete regions, Some of these mutations occur frequently in familial adenomatous polyposis coli (FAP) patients, and strategies for genetic diagnosis of the disease s
Autor:
Maria Cristina Curia, Rosa Valanzano, Diana L. Esposito, Ferdinando Ficari, Raffaele Palmirotta, Renato Mariani-Costantini, Annalisa Ranieri, Andrea Modesti, Alessandro Cama, Pasquale Battista, Francesco Tonelli
Publikováno v:
Human mutation. 3(3)