Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jessica Lenzi"'
Autor:
Luca Caputo, Alice Granados, Jessica Lenzi, Alessandro Rosa, Slimane Ait-Si-Ali, Pier Lorenzo Puri, Sonia Albini
Publikováno v:
Skeletal Muscle, Vol 10, Iss 1, Pp 1-11 (2020)
Abstract Background In Duchenne muscular dystrophy (DMD), DYSTROPHIN deficiency exposes myofibers to repeated cycles of contraction/degeneration, ultimately leading to muscle loss and replacement by fibrotic tissue. DMD pathology is typically exacerb
Externí odkaz:
https://doaj.org/article/ffd85596464f467c8fd9803fd2d2c5f7
Autor:
Jessica Lenzi, Francesca Pagani, Riccardo De Santis, Cristina Limatola, Irene Bozzoni, Silvia Di Angelantonio, Alessandro Rosa
Publikováno v:
Stem Cell Research, Vol 17, Iss 1, Pp 140-147 (2016)
Amyotrophic Lateral Sclerosis (ALS) is a severe and fatal neurodegenerative disease characterized by progressive loss of motoneurons, muscle atrophy and paralysis. Recent evidence suggests that ALS should be considered as a multi-systemic disease, in
Externí odkaz:
https://doaj.org/article/b70a634417a64de4a344041f44d4b821
Autor:
Jessica Lenzi, Riccardo De Santis, Valeria de Turris, Mariangela Morlando, Pietro Laneve, Andrea Calvo, Virginia Caliendo, Adriano Chiò, Alessandro Rosa, Irene Bozzoni
Publikováno v:
Disease Models & Mechanisms, Vol 8, Iss 7, Pp 755-766 (2015)
Patient-derived induced pluripotent stem cells (iPSCs) provide an opportunity to study human diseases mainly in those cases for which no suitable model systems are available. Here, we have taken advantage of in vitro iPSCs derived from patients affec
Externí odkaz:
https://doaj.org/article/77c86d0d8f104629ba0303f1ec93a855
Autor:
Sonia Albini, Alice Granados, Pier Lorenzo Puri, Jessica Lenzi, Slimane Ait-Si-Ali, Luca Caputo, Alessandro Rosa
Publikováno v:
Skeletal Muscle
Skeletal Muscle, BioMed Central, 2020, 10 (1), ⟨10.1186/s13395-020-00224-7⟩
Skeletal Muscle, Vol 10, Iss 1, Pp 1-11 (2020)
Skeletal Muscle, BioMed Central, 2020, 10 (1), ⟨10.1186/s13395-020-00224-7⟩
Skeletal Muscle, Vol 10, Iss 1, Pp 1-11 (2020)
Background In Duchenne muscular dystrophy (DMD), DYSTROPHIN deficiency exposes myofibers to repeated cycles of contraction/degeneration, ultimately leading to muscle loss and replacement by fibrotic tissue. DMD pathology is typically exacerbated by e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc15fd51200be7361bf6af8b66d82eb8
https://hal.archives-ouvertes.fr/hal-03051525
https://hal.archives-ouvertes.fr/hal-03051525
Autor:
Cristina Limatola, Silvia Di Angelantonio, Francesca Pagani, Irene Bozzoni, Jessica Lenzi, Riccardo De Santis, Alessandro Rosa
Publikováno v:
Stem Cell Research, Vol 17, Iss 1, Pp 140-147 (2016)
Stem Cell Research
Stem Cell Research
Amyotrophic Lateral Sclerosis (ALS) is a severe and fatal neurodegenerative disease characterized by progressive loss of motoneurons, muscle atrophy and paralysis. Recent evidence suggests that ALS should be considered as a multi-systemic disease, in
Autor:
Augusto Orlandi, M Fiore, Jessica Lenzi, Marianna Desideri, Pierangela Totta, Daniela Passeri, Helder Maiato, Marin Barisic, F. Degrassi, Dd Bufalo, M Orticello, Alessandro Rosa
Publikováno v:
Oncogene (Basingstoke) 34 (2015): 3325–3335. doi:10.1038/onc.2014.265doi
info:cnr-pdr/source/autori:Orticello, Michela; Fiore, Mario; Totta, Pierangela; Desideri, Marianna; Barisic, Marin; Passeri, Daniela; Lenzi, Jessica; Rosa, Alessandro; Orlandi, Augusto; Maiato, Hélder; Del Bufalo, Donatella; Degrassi, Francesca/titolo:N-terminus-modified Hec1 suppresses tumour growth by interfering with kinetochore-microtubule dynamics/doi:10.1038%2Fonc.2014.265doi:/rivista:Oncogene (Basingstoke)/anno:2015/pagina_da:3325/pagina_a:3335/intervallo_pagine:3325–3335/volume:34
info:cnr-pdr/source/autori:Orticello, Michela; Fiore, Mario; Totta, Pierangela; Desideri, Marianna; Barisic, Marin; Passeri, Daniela; Lenzi, Jessica; Rosa, Alessandro; Orlandi, Augusto; Maiato, Hélder; Del Bufalo, Donatella; Degrassi, Francesca/titolo:N-terminus-modified Hec1 suppresses tumour growth by interfering with kinetochore-microtubule dynamics/doi:10.1038%2Fonc.2014.265doi:/rivista:Oncogene (Basingstoke)/anno:2015/pagina_da:3325/pagina_a:3335/intervallo_pagine:3325–3335/volume:34
Mitotic proteins are attractive targets to develop molecular cancer therapeutics due to the intimate interdependence between cell proliferation and mitosis. In this work, we have explored the therapeutic potential of the kinetochore (KT) protein Hec1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a99d5e5d5e98e5b8f1613e86f07c6e66
http://hdl.handle.net/11573/602782
http://hdl.handle.net/11573/602782
Autor:
Mariangela Morlando, Riccardo De Santis, Irene Bozzoni, Jessica Lenzi, Virginia Caliendo, Valeria de Turris, Andrea Calvo, Pietro Laneve, Alessandro Rosa, Adriano Chiò
Publikováno v:
Disease models & mechanisms
8 (2015): 755–766.
info:cnr-pdr/source/autori:Lenzi, Jessica; De Santis, Riccardo; de Turris, Valeria; Morlando, Mariangela; Laneve, Pietro; Calvo, Andrea; Caliendo, Virginia; Chio, Adriano; Rosa, Alessandro; Bozzoni, Irene/titolo:ALS mutant FUS proteins are recruited into stress granules in induced pluripotent stem cell-derived motoneurons/doi:/rivista:Disease models & mechanisms (Print)/anno:2015/pagina_da:755/pagina_a:766/intervallo_pagine:755–766/volume:8
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 8, Iss 7, Pp 755-766 (2015)
8 (2015): 755–766.
info:cnr-pdr/source/autori:Lenzi, Jessica; De Santis, Riccardo; de Turris, Valeria; Morlando, Mariangela; Laneve, Pietro; Calvo, Andrea; Caliendo, Virginia; Chio, Adriano; Rosa, Alessandro; Bozzoni, Irene/titolo:ALS mutant FUS proteins are recruited into stress granules in induced pluripotent stem cell-derived motoneurons/doi:/rivista:Disease models & mechanisms (Print)/anno:2015/pagina_da:755/pagina_a:766/intervallo_pagine:755–766/volume:8
Disease Models & Mechanisms
Disease Models & Mechanisms, Vol 8, Iss 7, Pp 755-766 (2015)
Patient-derived induced pluripotent stem cells (iPSCs) provide an opportunity to study human diseases mainly in those cases for which no suitable model systems are available. Here, we have taken advantage of in vitro iPSCs derived from patients affec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74ab767c98373ddbfc4ae500e796d0e5
https://publications.cnr.it/doc/384360
https://publications.cnr.it/doc/384360