Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Santamaria G"'
Autor:
Sanna Cherchi, S, Sampogna, Rv, Papeta, N, Burgess, Ke, Nees, Sn, Perry, Bj, Choi, M, Bodria, M, Liu, Y, Weng, Pl, Lozanovski, Vj, Verbitsky, M, Lugani, F, Sterken, R, Paragas, N, Caridi, G, Carrea, A, Dagnino, M, Materna Kiryluk, A, Santamaria, G, Murtas, C, Ristoska Bojkovska, N, Izzi, C, Kacak, N, Bianco, B, Giberti, S, Gigante, M, Piaggio, G, Gesualdo, L, Kosuljandic Vukic, D, Vukojevic, K, Saraga Babic, M, Saraga, M, Gucev, Z, Allegri, L, Latos Bielenska, A, Casu, D, State, M, Scolari, F, Ravazzolo, Roberto, Kiryluk, K, Al Awqati, Q, D'Agati, Vd, Drummond, Ia, Tasic, V, Lifton, Rp, Ghiggeri, Gm, Gharavi, Ag
Publikováno v:
The New England journal of medicine, vol 369, iss 7
BackgroundCongenital abnormalities of the kidney and the urinary tract are the most common cause of pediatric kidney failure. These disorders are highly heterogeneous, and the etiologic factors are poorly understood.MethodsWe performed genomewide lin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cbd40e690159fac589ca0d19f1b485a
https://escholarship.org/uc/item/2hg4p0g8
https://escholarship.org/uc/item/2hg4p0g8
Autor:
Stefanie Sudhop, Harald Lahm, Thomas Brade, Sharon L. Paige, Alexander Goedel, Svenja Laue, Thomas Meitinger, Markus Krane, Stefanie A. Doppler, Alessandra Moretti, Connie R. Bezzina, Pedro Schneider, Zhong Zhang, Makoto Sahara, Neil E. Bowles, Hilansi Rawat, Riccardo Berutti, Nazan Puluca, Ilaria My, Peter J. Gruber, Andreas Dendorfer, Ralf Gilsbach, Nora Lang, M. Dreßen, Christine M. Schneider, S. Schwarz, Daniel Sinnecker, I. Neb, Gianluca Santamaria, Karl-Ludwig Laugwitz, Rüdiger Lange, Sean M. Wu, Bruce D. Gelb, C. Abou-Ajram, Tatjana Dorn, Fleur V.Y. Tjong, Lia Crotti, Maria Rijlaarsdam, Matthias Mann, Christian Kupatt, Lutz Hein, Julie Cleuziou, Elisa Mastantuono, Lesca M. Holdt, Sophia Doll, Bernd H. Northoff
Publikováno v:
Circulation 144, 1409-1428 (2021)
Circulation
bioRxiv
Circulation, 144(17), 1409-1428. Lippincott Williams and Wilkins
Circulation
bioRxiv
Circulation, 144(17), 1409-1428. Lippincott Williams and Wilkins
Supplemental Digital Content is available in the text.
Background: Complex molecular programs in specific cell lineages govern human heart development. Hypoplastic left heart syndrome (HLHS) is the most common and severe manifestation within the
Background: Complex molecular programs in specific cell lineages govern human heart development. Hypoplastic left heart syndrome (HLHS) is the most common and severe manifestation within the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f0de69ffa304c5f2a963a861f6f795c
https://doi.org/10.1101/2021.04.24.441110
https://doi.org/10.1101/2021.04.24.441110
Autor:
Elisa R. Zanier, Francesca Pischiutta, Claudia Balducci, Gloria Vegliante, Pietro La Vitola, Giovanni Battista Ferrara, Edoardo Brandi, Giulia Santamaria, Federica Grandi, Francesca Re, Gianluigi Forloni, Antonio Uccelli, Nicole Kerlero de Rosbo
Publikováno v:
Cell Death and Differentiation
The multiplicity of systems affected in Alzheimer’s disease (AD) brains calls for multi-target therapies. Although mesenchymal stem cells (MSC) are promising candidates, their clinical application is limited because of risks related to their direct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63da9b8d06a390580200d923a37dacf6
http://hdl.handle.net/11567/1087200
http://hdl.handle.net/11567/1087200
Autor:
Isabella Ceccherini, Giuseppe Santamaria, Francesca Antonini, Anna Rubartelli, Rita Consolini, Ryuta Nishikomori, Federica Penco, Denise Lasigliè, Francesca Santarelli, Marco Di Duca, Antonella Insalaco, Genny Del Zotto, Marco Cattalini, Juan I. Aróstegui, Denise Ferrera, Mariasavina Severino, Alberto Martini, Giulia Amico, Anna Mensa-Vilaro, Marco Gattorno, Roberto Ravazzolo, Laura Obici, Kenji Nakagawa, Silvia Borghini, Roberta Caorsi, Alberto Tommasini, Romina Gallizzi
Objective.To evaluate the rate of somatic NLRP3 mosaicism in an Italian cohort of mutation-negative patients with cryopyrin-associated periodic syndrome (CAPS).Methods.The study enrolled 14 patients with a clinical phenotype consistent with CAPS in w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c7893d277729fe5191b8c11b6e589a5
http://hdl.handle.net/11570/3121587
http://hdl.handle.net/11570/3121587