Rocchi A - Search Results

1

Prelamin A is involved in early steps of muscle differentiation.

Capanni C, Del Coco R, Squarzoni S, Columbaro M, Mattioli E, Camozzi D, Rocchi A, Scotlandi K, Maraldi N, Foisner R, Lattanzi G. Capanni C, et al. Among authors: rocchi a. Exp Cell Res. 2008 Dec 10;314(20):3628-37. doi: 10.1016/j.yexcr.2008.09.026. Epub 2008 Oct 11. Exp Cell Res. 2008. PMID: 18951892

2

Apoptotic genes as potential markers of metastatic phenotype in human osteosarcoma cell lines.

Zucchini C, Rocchi A, Manara MC, De Sanctis P, Capanni C, Bianchini M, Carinci P, Scotlandi K, Valvassori L. Zucchini C, et al. Among authors: rocchi a. Int J Oncol. 2008 Jan;32(1):17-31. Int J Oncol. 2008. PMID: 18097539

3

A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case Report.

Montano V, Mancuso M, Simoncini C, Torri F, Chico L, Ali G, Rocchi A, Baldinotti F, Caligo MA, Lattanzi G, Mattioli E, Cenacchi G, Barison A, Siciliano G, Ricci G. Montano V, et al. Among authors: rocchi a. J Neuromuscul Dis. 2022;9(3):457-462. doi: 10.3233/JND-220802. J Neuromuscul Dis. 2022. PMID: 35466949

4

CD99 inhibits neural differentiation of human Ewing sarcoma cells and thereby contributes to oncogenesis.

Rocchi A, Manara MC, Sciandra M, Zambelli D, Nardi F, Nicoletti G, Garofalo C, Meschini S, Astolfi A, Colombo MP, Lessnick SL, Picci P, Scotlandi K. Rocchi A, et al. J Clin Invest. 2010 Mar;120(3):668-80. doi: 10.1172/JCI36667. Epub 2010 Feb 8. J Clin Invest. 2010. PMID: 20197622 Free PMC article.

5

CD99 isoforms dictate opposite functions in tumour malignancy and metastases by activating or repressing c-Src kinase activity.

Scotlandi K, Zuntini M, Manara MC, Sciandra M, Rocchi A, Benini S, Nicoletti G, Bernard G, Nanni P, Lollini PL, Bernard A, Picci P. Scotlandi K, et al. Among authors: rocchi a. Oncogene. 2007 Oct 11;26(46):6604-18. doi: 10.1038/sj.onc.1210481. Epub 2007 Apr 30. Oncogene. 2007. PMID: 17471235

6

An "inflammatory" mitochondrial myopathy. A case report.

Mancuso M, Orsucci D, Ienco EC, Ricci G, Ali G, Servadio A, Fontanini G, Filosto M, Vielmi V, Rocchi A, Petrozzi L, Logerfo A, Siciliano G. Mancuso M, et al. Among authors: rocchi a. Neuromuscul Disord. 2013 Nov;23(11):907-10. doi: 10.1016/j.nmd.2013.07.011. Epub 2013 Aug 8. Neuromuscul Disord. 2013. PMID: 24011700

7

A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation.

Mancuso M, Filosto M, Forli F, Rocchi A, Berrettini S, Siciliano G, Murri L. Mancuso M, et al. Among authors: rocchi a. Acta Neurol Scand. 2004 Jul;110(1):72-4. doi: 10.1111/j.1600-0404.2004.00254.x. Acta Neurol Scand. 2004. PMID: 15180810

8

Myopathic involvement and mitochondrial pathology in Kennedy disease and in other motor neuron diseases.

Orsucci D, Rocchi A, Caldarazzo Ienco E, Alì G, LoGerfo A, Petrozzi L, Scarpelli M, Filosto M, Carlesi C, Siciliano G, Bonuccelli U, Mancuso M. Orsucci D, et al. Among authors: rocchi a. Curr Mol Med. 2014;14(5):598-602. doi: 10.2174/1566524014666140603100131. Curr Mol Med. 2014. PMID: 24894177 Review.

9

MERRF syndrome without ragged-red fibers: the need for molecular diagnosis.

Mancuso M, Petrozzi L, Filosto M, Nesti C, Rocchi A, Choub A, Pistolesi S, Massetani R, Fontanini G, Siciliano G. Mancuso M, et al. Among authors: rocchi a. Biochem Biophys Res Commun. 2007 Mar 23;354(4):1058-60. doi: 10.1016/j.bbrc.2007.01.099. Epub 2007 Jan 26. Biochem Biophys Res Commun. 2007. PMID: 17275787

10

Mitochondrial DNA haplogroups do not influence the Huntington's disease phenotype.

Mancuso M, Kiferle L, Petrozzi L, Nesti C, Rocchi A, Ceravolo R, Orsucci D, Maluccio MR, Bonuccelli U, Filosto M, Siciliano G, Murri L. Mancuso M, et al. Among authors: rocchi a. Neurosci Lett. 2008 Oct 17;444(1):83-6. doi: 10.1016/j.neulet.2008.08.013. Epub 2008 Aug 8. Neurosci Lett. 2008. PMID: 18706972

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