Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Boschetti, Elisa"'
Autor:
Pierluigi Martelli, Tom J. de Koning, Takema Kato, Irene Liparulo, Mariko Taniguchi-Ikeda, Tatsushi Toda, Hisayoshi Nakamura, Wilfred F. A. den Dunnen, Giovanna Cenacchi, Sanjiban Chakrabarty, Yu Sheng Yeh, Sushil Kumar Mishra, Rita Casadio, Akira Ohtake, Ichizo Nishino, Roberto De Giorgio, Paolo Picco, Pasquale Striano, Chiara Fiorillo, Isabella Ceccherini, Tsuyoshi Goto, Elisa Boschetti, Makiko Tsutsumi, Eleonora Aronica, Georgios Kellaris, Mariel Alders, Gabor E. Linthorst, Jantima Tanboon, Angela Rita Sementa, Floor A. M. Duijkers, Yu Ichi Goto, Hiroki Kurahashi, Masakazu Mimaki, Gerard Dijkstra, Dik C. van Gent, Mariasavina Severino, Yoshinobu Oyazato, Christian Bergamini, Ikuya Nonaka, Yoshiki Yamaguchi, Ivana Matera, Giuseppe Raiola, Karin Van Spaendonck, Nicholas Katsanis, Luca Masin, Shumpei Uchino, Kenjiro Kosaki, Sara Signa, Anja Raams, Federica Isidori, Elena Bonora, Serena Arrigo, Kandai Nozu, Marc Engelen, Farid Ullah, Ichiro Morioka, Chiara Diquigiovanni, Marco Seri, Valerio Carelli, Francesca Bianco, Mariapia Giuditta Cratere, Nicola Rizzardi, Romana Fato, Alessandra Maresca, Alyson W. MacInnes, Valentina Papa, Kazumoto Iijima
Publikováno v:
Brain : a Journal of Neurology, 144(5), 1451-1466. Oxford University Press
Brain, 144(5), 1451-1466. Oxford University Press
Brain, 144(5), 1451-1466. Oxford University Press
Abnormal gut motility is a feature of several mitochondrial encephalomyopathies, and mutations in genes such as TYMP and POLG, have been linked to these rare diseases. The human genome encodes three DNA ligases, of which only one, ligase III (LIG3),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e470f830e056717e954489f79a11efb4
http://hdl.handle.net/11567/1065221
http://hdl.handle.net/11567/1065221
Autor:
Leonardo Caporali, Valerio Carelli, Maria Teresa Dotti, Rita Rinaldi, Antonio Daniele Pinna, Elisa Boschetti, Roberto D'Angelo, Susan Mohamed, Manuela Contin, Loris Pironi, Roberto De Giorgio, Mariantonietta Capristo
Publikováno v:
Mitochondrion. 34
Autor:
Roberto D'Alessandro, Leonardo Caporali, Maria Cristina Morelli, Roberto De Giorgio, Carlo Casali, Antonietta D'Errico, Laura Ludovica Gramegna, Vitaliano Tugnoli, Raffaele Lodi, Elisa Boschetti, Manuela Contin, Mariantonietta Capristo, Roberto D'Angelo, Giovanna Cenacchi, Caterina Tonon, Rita Rinaldi, Valerio Carelli, Susan Mohamed, Valentina Papa, Antonio Daniele Pinna, Alessandra Maresca, Loris Pironi
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is a fatal, recessive disease caused by mutations in the gene encoding thymidine phosphorylase, leading to reduced enzymatic activity, toxic nucleoside accumulation, and secondary mitochon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39d4b2c446c443136b6abba613e951e9
http://hdl.handle.net/11392/2374935
http://hdl.handle.net/11392/2374935
Autor:
Cesare Castellini, Alessandra Bordoni, Federico Sirri, A. Dal Bosco, Adele Meluzzi, Elisa Boschetti
Publikováno v:
Animal, Vol 10, Iss 4, Pp 700-708 (2016)
In Western countries the dietary guidance emphasizes the need to decrease the intake of saturated fatty acids and to replace them with polyunsaturated fatty acids (PUFA), particularly long chain n-3 PUFA (LC-PUFA). The production of poultry meat havi