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231 results

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Page 1
Genomic loci mispositioning in Tmem120a knockout mice yields latent lipodystrophy.
Czapiewski R, Batrakou DG, de Las Heras JI, Carter RN, Sivakumar A, Sliwinska M, Dixon CR, Webb S, Lattanzi G, Morton NM, Schirmer EC. Czapiewski R, et al. Among authors: lattanzi g. Nat Commun. 2022 Jan 13;13(1):321. doi: 10.1038/s41467-021-27869-2. Nat Commun. 2022. PMID: 35027552 Free PMC article.
Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning.
Pellegrini C, Columbaro M, Schena E, Prencipe S, Andrenacci D, Iozzo P, Angela Guzzardi M, Capanni C, Mattioli E, Loi M, Araujo-Vilar D, Squarzoni S, Cinti S, Morselli P, Giorgetti A, Zanotti L, Gambineri A, Lattanzi G. Pellegrini C, et al. Among authors: lattanzi g. Exp Mol Med. 2019 Aug 2;51(8):1-17. doi: 10.1038/s12276-019-0289-0. Exp Mol Med. 2019. PMID: 31375660 Free PMC article.
Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcription.
Capanni C, Cenni V, Mattioli E, Sabatelli P, Ognibene A, Columbaro M, Parnaik VK, Wehnert M, Maraldi NM, Squarzoni S, Lattanzi G. Capanni C, et al. Among authors: lattanzi g. Exp Cell Res. 2003 Nov 15;291(1):122-34. doi: 10.1016/s0014-4827(03)00395-1. Exp Cell Res. 2003. PMID: 14597414
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy.
Capanni C, Mattioli E, Columbaro M, Lucarelli E, Parnaik VK, Novelli G, Wehnert M, Cenni V, Maraldi NM, Squarzoni S, Lattanzi G. Capanni C, et al. Among authors: lattanzi g. Hum Mol Genet. 2005 Jun 1;14(11):1489-502. doi: 10.1093/hmg/ddi158. Epub 2005 Apr 20. Hum Mol Genet. 2005. PMID: 15843404
Laminopathies and lamin-associated signaling pathways.
Maraldi NM, Capanni C, Cenni V, Fini M, Lattanzi G. Maraldi NM, et al. Among authors: lattanzi g. J Cell Biochem. 2011 Apr;112(4):979-92. doi: 10.1002/jcb.22992. J Cell Biochem. 2011. PMID: 21400569 Review.
Inhibition of DNA damage response at telomeres improves the detrimental phenotypes of Hutchinson-Gilford Progeria Syndrome.
Aguado J, Sola-Carvajal A, Cancila V, Revêchon G, Ong PF, Jones-Weinert CW, Wallén Arzt E, Lattanzi G, Dreesen O, Tripodo C, Rossiello F, Eriksson M, d'Adda di Fagagna F. Aguado J, et al. Among authors: lattanzi g. Nat Commun. 2019 Nov 18;10(1):4990. doi: 10.1038/s41467-019-13018-3. Nat Commun. 2019. PMID: 31740672 Free PMC article.
European lipodystrophy registry: background and structure.
von Schnurbein J, Adams C, Akinci B, Ceccarini G, D'Apice MR, Gambineri A, Hennekam RCM, Jeru I, Lattanzi G, Miehle K, Nagel G, Novelli G, Santini F, Santos Silva E, Savage DB, Sbraccia P, Schaaf J, Sorkina E, Tanteles G, Vantyghem MC, Vatier C, Vigouroux C, Vorona E, Araújo-Vilar D, Wabitsch M. von Schnurbein J, et al. Among authors: lattanzi g. Orphanet J Rare Dis. 2020 Jan 15;15(1):17. doi: 10.1186/s13023-020-1295-y. Orphanet J Rare Dis. 2020. PMID: 31941540 Free PMC article.
Lamin A involvement in ageing processes.
Cenni V, Capanni C, Mattioli E, Schena E, Squarzoni S, Bacalini MG, Garagnani P, Salvioli S, Franceschi C, Lattanzi G. Cenni V, et al. Among authors: lattanzi g. Ageing Res Rev. 2020 Sep;62:101073. doi: 10.1016/j.arr.2020.101073. Epub 2020 May 21. Ageing Res Rev. 2020. PMID: 32446955 Review.
231 results