Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Michela Ortolani"'
Autor:
Giovanna, Lattanzi, Michela, Ortolani, Marta, Columbaro, Sabino, Prencipe, Elisabetta, Mattioli, Catia, Lanzarini, Nadir M, Maraldi, Vittoria, Cenni, Paolo, Garagnani, Stefano, Salvioli, Gianluca, Storci, Massimiliano, Bonafè, Cristina, Capanni, Claudio, Franceschi
Publikováno v:
Journal of Cell Science; Vol 127
The dynamic organisation of the cell nucleus is profoundly modified during growth, development and senescence as a result of changes in chromatin arrangement and gene transcription. A plethora of data suggests that the nuclear lamina is a key player
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::25420e77c82f46e8e59fb42b8e183e45
http://hdl.handle.net/11585/250536
http://hdl.handle.net/11585/250536
Autor:
Paolo Garagnani, Gianluca Storci, Stefano Salvioli, Giovanna Lattanzi, Marta Columbaro, Michela Ortolani, Nadir M. Maraldi, Elisabetta Mattioli, Vittoria Cenni, Massimiliano Bonafè, Cristina Capanni, Claudio Franceschi, Catia Lanzarini, Sabino Prencipe
Publikováno v:
Journal of Cell Science.
The dynamic organisation of the cell nucleus is profoundly modified during growth, development and senescence as a result of changes in chromatin arrangement and gene transcription. A plethora of data suggests that the nuclear lamina is a key player
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::561e78c28f8624e4d3a2961f7dd52514
https://doi.org/10.1242/jcs.133983
https://doi.org/10.1242/jcs.133983
Autor:
Michela Ortolani, Giovanna Lattanzi, Elisabetta Mattioli, Maria Rosaria D'Apice, Marta Columbaro, Sofia Avnet, Diana Postorivo, Pietro Cortelli, Nadir M. Maraldi, Laura Gasparini, Anna Maria Nardone, Rocco Liguori
Adult-onset autosomal dominant leukodystrophy (ADLD) is a slowly progressive neurological disorder characterised by pyramidal, cerebellar, and autonomic disturbances. Duplication of the LMNB1 gene is the genetic cause of ADLD, yet the pathogenetic me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::509a10c27cbb3b48ff77fde4d1fc3f59
http://hdl.handle.net/11585/145898
http://hdl.handle.net/11585/145898
Autor:
Giuseppe Novelli, Elisa Schena, Cristina Capanni, Marta Columbaro, Michela Ortolani, Maria Rosaria D'Apice, Nadir M. Maraldi, Vittoria Cenni, Giovanna Lattanzi, Stefano Squarzoni, Daria Camozzi
Publikováno v:
Histochemistry and Cell Biology
Mandibuloacral dysplasia type A (MADA) is a rare laminopathy characterized by growth retardation, craniofacial anomalies, bone resorption at specific sites including clavicles, phalanges and mandibula, mottled cutaneous pigmentation, skin rigidity, p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::128f85c8d73c713ca728e74206789cae
http://hdl.handle.net/11585/132790
http://hdl.handle.net/11585/132790
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria
Autor:
Stefano Squarzoni, Michela Ortolani, Giovanna Lattanzi, N.M. Maraldi, Cristina Capanni, Sandra Marmiroli, Maria Rosaria D'Apice, Giuseppe Novelli, Vittoria Cenni, Sabino Prencipe, Emanuela Scarano, Milena Fini, Marta Columbaro
Publikováno v:
European Journal of Histochemistry, Vol 55, Iss 4, Pp e36-e36 (2011)
European Journal of Histochemistry : EJH
European Journal of Histochemistry : EJH
Farnesylated prelamin A is a processing intermediate produced in the lamin A maturation pathway. Accumulation of a truncated farnesylated prelamin A form, called progerin, is a hallmark of the severe premature ageing syndrome, Hutchinson-Gilford prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d1dbeb23f8d811cadda39b320cfe7ad
http://www.ejh.it/index.php/ejh/article/view/1895
http://www.ejh.it/index.php/ejh/article/view/1895
Autor:
Michela Zago, Lorenzo Breschi, Alessandra Ruggeri, Mirella Falconi, Susi Pelotti, Gabriella Teti, Giovanni Mazzotti, Michela Ortolani
2-Hydroxyethyl methacrylate (HEMA) can be released from restorative materials and diffused into the tooth Pulp over long periods of time. Although cytotoxicity due to high concentrations of monomers has been well e is known about the risk of chronic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::517e50190d166a1c8b7498837e7c270e
https://hdl.handle.net/11368/2282191
https://hdl.handle.net/11368/2282191
Autor:
Susi Pelotti, Gabriella Teti, Giovanni Mazzotti, Michela Zago, Lorenzo Breschi, Alessandra Ruggeri, Michela Ortolani, Mirella Falconi
In the dental pulp extracellular matrix, the main macromolecules are collagenous proteins, non-collagenous proteins and proteoglycans. Regulated synthesis of the interstitial collagens, in particular, type I collagen, is important during development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43352bfe74d9f2cfb6e3368d10c33e34
http://hdl.handle.net/11368/1857768
http://hdl.handle.net/11368/1857768
Autor:
Maria Cappuccilli, Francesca Bianchi, S Nascetti, Giorgio Feliciangeli, Giorgia Comai, Michela Ortolani, G. La Manna, Alessandro Faenza, Elisa Persici, Maria Scolari, G D. Mina, Sergio Stefoni, Gabriele Donati
Publikováno v:
Transplantation. 78:618
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c30f615f0e51e465872d174ea2419eea
https://doi.org/10.1097/00007890-200407271-01662
https://doi.org/10.1097/00007890-200407271-01662
Autor:
Manfred Wehnert, Cristina Capanni, Nadir M. Maraldi, Jessika Bertacchini, Elisabetta Mattioli, Vittoria Cenni, Michela Ortolani, Giuseppe Novelli, Giovanna Lattanzi, Stefano Squarzoni, Sandra Marmiroli, Maria Rosaria D'Apice, Marta Columbaro, Milena Fini, Sabino Prencipe
Publikováno v:
ResearcherID
Aging (Albany NY)
Scopus-Elsevier
Europe PubMed Central
Aging (Albany NY)
Scopus-Elsevier
Europe PubMed Central
Lamin A is a key component of the nuclear lamina produced through post-translational processing of its precursor known as prelamin A. LMNA mutations leading to farnesylated prelamin A accumulation are known to cause lipodystrophy, progeroid and devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f8d7fbdaf340d7fd13bb6a5fcae97f5
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000345431200006&KeyUID=WOS:000345431200006
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000345431200006&KeyUID=WOS:000345431200006
Autor:
Giovanna Lattanzi, Sofia Avnet, Laura Gasparini, Pietro Cortelli, Marta Columbaro, Nadir M. Maraldi, Rocco Liguori, Diana Postorivo, Elisabetta Mattioli, Maria Rosaria D'Apice, Michela Ortolani, Anna Maria Nardone
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. (12):2244
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5df667266b48546ccfad279d33884a2c