Zobrazeno 1 - 10
of 1 539
pro vyhledávání: '"A. Barili"'
Autor:
Giulia Vitetta, Laura Desiderio, Ilaria Baccolini, Vera Uliana, Giulia Lanzoni, Tullio Ghi, Gianluigi Pilu, Enrico Ambrosini, Patrizia Caggiati, Valeria Barili, Anna Carmela Trotta, Maria Rosaria Liuti, Elisabetta Malpezzi, Maria Carla Pittalis, Antonio Percesepe
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-12 (2024)
Abstract Mosaic chromosomal anomalies arising in the product of conception and the final fetal chromosomal arrangement are expression of complex biological mechanisms. The rescue of unbalanced chromosome with selection of the most viable cell line/s
Externí odkaz:
https://doaj.org/article/18d73d17a527428b9867a1ae6e70c7b1
Autor:
Maahs, Ricardo, Kuchle, Juliano, Rodrigues, Amanda Goulart, Trombetta, Mariane Cristina, Alvarenga, Renata dos Santos, Barili, Rosalia, Freitas, William
Publikováno v:
In Marine and Petroleum Geology September 2024 167
Autor:
Antonio Giovanni Cammardella, Marco Russo, Michele Di Mauro, Claudia Romagnoni, Fabrizio Ceresa, Francesco Patanè, Guido Gelpi, Francesco Pollari, Fabio Barili, Alessandro Parolari, Federico Ranocchi
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 15, p 4471 (2024)
Background: The transfemoral (TF) approach is the most common route in TAVI, but it is still associated with a risk of bleeding and vascular complications. The aim of this study was to compare the clinical outcomes between surgical cut-down (SC) and
Externí odkaz:
https://doaj.org/article/734e5669f0324b07a52709974326847a
Autor:
Vera Uliana, Enrico Ambrosini, Antonietta Taiani, Sofia Cesarini, Ilenia Rita Cannizzaro, Anna Negrotti, Walter Serra, Gabriele Quintavalle, Lucia Micale, Carmela Fusco, Marco Castori, Davide Martorana, Beatrice Bortesi, Laura Belli, Antonio Percesepe, Francesco Pisani, Valeria Barili
Publikováno v:
Genes, Vol 15, Iss 7, p 916 (2024)
Leucine zipper-like transcription regulator 1 (LZTR1) acts as a negative factor that suppresses RAS function and MAPK signaling; mutations in this protein may dysregulate RAS ubiquitination and lead to impaired degradation of RAS superfamily proteins
Externí odkaz:
https://doaj.org/article/4c573e6da5cd499180db11cd6e37b2e5
Autor:
Alberto Achcar, Jorge1 achcar@fmrp.usp.br, Barili, Emerson1 ebarili2@gmail.com
Publikováno v:
Pakistan Journal of Statistics & Operation Research. 2024, Vol. 20 Issue 2, p157-170. 14p.
Autor:
Santos, Victor Hugo Jacks Mendes dos, Pontin, Darlan, Engelmann, Pâmela de Medeiros, Cescani, Victor Kovaski, Zielinski, João Pedro Tauscheck, Barili, Rosalia, Melo, Clarissa Lovato, Dalla Vecchia, Felipe
Publikováno v:
In Applied Geochemistry April 2024 165
Publikováno v:
In European Economic Review February 2024 162
Autor:
Çağla Aytaş, Raffaele Gilardini, Annalisa Beghelli, Paolo Andrea Barili, Melissa Ori, Carlo Cantile
Publikováno v:
Veterinary Sciences, Vol 11, Iss 4, p 177 (2024)
A 13-month-old, neutered, male, domestic shorthair cat was referred with a history of progressive paraparesis, proprioceptive ataxia, and lumbar spinal pain. Neurological examination revealed non-ambulatory paraparesis consistent with L4-S1 myelopath
Externí odkaz:
https://doaj.org/article/53e405d310a34cca812e520ed4f66f25
High CD49a+ NK cell infiltrate is associated with poor clinical outcomes in Hepatocellular Carcinoma
Autor:
Alessandra Zecca, Valeria Barili, Carolina Boni, Paola Fisicaro, Andrea Vecchi, Marzia Rossi, Valentina Reverberi, Anna Montali, Giuseppe Pedrazzi, Carlo Ferrari, Elisabetta Cariani, Gabriele Missale
Publikováno v:
Heliyon, Vol 9, Iss 12, Pp e22680- (2023)
NK cells infiltrating Hepatocellular Carcinoma (HCC) may express residency markers such as Integrin Subunit Alpha 1 (CD49a) that have been associated with nurturing functions in the decidua, and characterized by the production of angiogenic factors a
Externí odkaz:
https://doaj.org/article/9cb91cef7d1848ba8120be1bd442b707
Autor:
Béatrice Bocquet, Caroline Borday, Nejla Erkilic, Daria Mamaeva, Alicia Donval, Christel Masson, Karine Parain, Karolina Kaminska, Mathieu Quinodoz, Irene Perea-Romero, Gema Garcia-Garcia, Carla Jimenez-Medina, Hassan Boukhaddaoui, Arthur Coget, Nicolas Leboucq, Giacomo Calzetti, Stefano Gandolfi, Antonio Percesepe, Valeria Barili, Vera Uliana, Marco Delsante, Francesca Bozzetti, Hendrik P.N. Scholl, Marta Corton, Carmen Ayuso, Jose M. Millan, Carlo Rivolta, Isabelle Meunier, Muriel Perron, Vasiliki Kalatzis
Publikováno v:
JCI Insight, Vol 8, Iss 21 (2023)
Retinitis pigmentosa (RP) is the most common inherited retinal disease (IRD) and is characterized by photoreceptor degeneration and progressive vision loss. We report 4 patients presenting with RP from 3 unrelated families with variants in TBC1D32, w
Externí odkaz:
https://doaj.org/article/95febfe0764a45129e5a016236db8fd5