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Items: 17

1.

Lysosome signaling controls the migration of dendritic cells.

Bretou M, Sáez PJ, Sanséau D, Maurin M, Lankar D, Chabaud M, Spampanato C, Malbec O, Barbier L, Muallem S, Maiuri P, Ballabio A, Helft J, Piel M, Vargas P, Lennon-Duménil AM.

Sci Immunol. 2017 Oct 27;2(16). pii: eaak9573. doi: 10.1126/sciimmunol.aak9573.

PMID:
29079589
2.

Duplication of Yq- and proximal Yp-arms with deletion of almost all PAR1 (including SHOX) in a young man with non-obstructive azoospermia, short stature and skeletal defects.

Cancemi D, Iannuzzi A, Perucatti A, Montano L, Capozzi O, Spampanato C, Ventruto ML, Urciuoli M, Iannuzzi L, Ventruto V.

J Appl Genet. 2017 Nov;58(4):481-486. doi: 10.1007/s13353-017-0412-7. Epub 2017 Oct 6.

PMID:
29019057
3.

A case of polimalformed fetus with a microdeletion of CTNNA3 gene.

Cancemi D, Urciuoli M, Morelli F, Lonardo MC, Lonardo V, Spampanato C, Ventruto M, Ventruto V, Sica C.

J Prenat Med. 2016 Jul-Dec;10(3-4):20-22. doi: 10.11138/jpm/2016.10.3.020.

4.

Early outcome of high energy Laser (Excimer) facilitated coronary angioplasty ON hARD and complex calcified and balloOn-resistant coronary lesions: LEONARDO Study.

Ambrosini V, Sorropago G, Laurenzano E, Golino L, Casafina A, Schiano V, Gabrielli G, Ettori F, Chizzola G, Bernardi G, Spedicato L, Armigliato P, Spampanato C, Furegato M.

Cardiovasc Revasc Med. 2015 Apr-May;16(3):141-6. doi: 10.1016/j.carrev.2015.02.002. Epub 2015 Feb 11.

PMID:
25708003
5.

Congenital megaurethra in a fetus with Meckel syndrome and in a fetus with female pseudoermanphroditism. The first report of these occurrences.

Di Meglio L, Mazzarelli LL, Boscaino A, Cancemi D, Morelli F, Lonardo MC, Lonardo V, Friso P, Spampanato C, Urciuoli M, Ventruto M, Ventruto V.

J Prenat Med. 2014 Apr-Jun;8(3-4):42-6.

6.

Simvastatin reduces melanoma progression in a murine model.

Zanfardino M, Spampanato C, De Cicco R, Buommino E, De Filippis A, Baiano S, Barra A, Morelli F.

Int J Oncol. 2013 Dec;43(6):1763-70. doi: 10.3892/ijo.2013.2126. Epub 2013 Oct 4.

7.

What else is in store for autophagy? Exocytosis of autolysosomes as a mechanism of TFEB-mediated cellular clearance in Pompe disease.

Feeney EJ, Spampanato C, Puertollano R, Ballabio A, Parenti G, Raben N.

Autophagy. 2013 Jul;9(7):1117-8. doi: 10.4161/auto.24920. Epub 2013 May 6.

8.

Transcription factor EB (TFEB) is a new therapeutic target for Pompe disease.

Spampanato C, Feeney E, Li L, Cardone M, Lim JA, Annunziata F, Zare H, Polishchuk R, Puertollano R, Parenti G, Ballabio A, Raben N.

EMBO Mol Med. 2013 May;5(5):691-706. doi: 10.1002/emmm.201202176. Epub 2013 Apr 18.

9.

A highly secreted sulphamidase engineered to cross the blood-brain barrier corrects brain lesions of mice with mucopolysaccharidoses type IIIA.

Sorrentino NC, D'Orsi L, Sambri I, Nusco E, Monaco C, Spampanato C, Polishchuk E, Saccone P, De Leonibus E, Ballabio A, Fraldi A.

EMBO Mol Med. 2013 May;5(5):675-90. doi: 10.1002/emmm.201202083. Epub 2013 Apr 9.

10.

Simvastatin inhibits cancer cell growth by inducing apoptosis correlated to activation of Bax and down-regulation of BCL-2 gene expression.

Spampanato C, De Maria S, Sarnataro M, Giordano E, Zanfardino M, Baiano S, Cartenì M, Morelli F.

Int J Oncol. 2012 Apr;40(4):935-41. doi: 10.3892/ijo.2011.1273. Epub 2011 Nov 29.

11.

Transcriptional activation of lysosomal exocytosis promotes cellular clearance.

Medina DL, Fraldi A, Bouche V, Annunziata F, Mansueto G, Spampanato C, Puri C, Pignata A, Martina JA, Sardiello M, Palmieri M, Polishchuk R, Puertollano R, Ballabio A.

Dev Cell. 2011 Sep 13;21(3):421-30. doi: 10.1016/j.devcel.2011.07.016. Epub 2011 Sep 1.

12.

Efficacy of a combined intracerebral and systemic gene delivery approach for the treatment of a severe lysosomal storage disorder.

Spampanato C, De Leonibus E, Dama P, Gargiulo A, Fraldi A, Sorrentino NC, Russo F, Nusco E, Auricchio A, Surace EM, Ballabio A.

Mol Ther. 2011 May;19(5):860-9. doi: 10.1038/mt.2010.299. Epub 2011 Feb 15.

13.

Lysosomal fusion and SNARE function are impaired by cholesterol accumulation in lysosomal storage disorders.

Fraldi A, Annunziata F, Lombardi A, Kaiser HJ, Medina DL, Spampanato C, Fedele AO, Polishchuk R, Sorrentino NC, Simons K, Ballabio A.

EMBO J. 2010 Nov 3;29(21):3607-20. doi: 10.1038/emboj.2010.237. Epub 2010 Sep 24.

14.

Multistep, sequential control of the trafficking and function of the multiple sulfatase deficiency gene product, SUMF1 by PDI, ERGIC-53 and ERp44.

Fraldi A, Zito E, Annunziata F, Lombardi A, Cozzolino M, Monti M, Spampanato C, Ballabio A, Pucci P, Sitia R, Cosma MP.

Hum Mol Genet. 2008 Sep 1;17(17):2610-21. doi: 10.1093/hmg/ddn161. Epub 2008 May 28.

PMID:
18508857
15.

A block of autophagy in lysosomal storage disorders.

Settembre C, Fraldi A, Jahreiss L, Spampanato C, Venturi C, Medina D, de Pablo R, Tacchetti C, Rubinsztein DC, Ballabio A.

Hum Mol Genet. 2008 Jan 1;17(1):119-29. Epub 2007 Oct 3.

PMID:
17913701
16.

Mutations in splicing factor PRPF3, causing retinal degeneration, form detrimental aggregates in photoreceptor cells.

Comitato A, Spampanato C, Chakarova C, Sanges D, Bhattacharya SS, Marigo V.

Hum Mol Genet. 2007 Jul 15;16(14):1699-707. Epub 2007 May 20.

PMID:
17517693
17.

Systemic inflammation and neurodegeneration in a mouse model of multiple sulfatase deficiency.

Settembre C, Annunziata I, Spampanato C, Zarcone D, Cobellis G, Nusco E, Zito E, Tacchetti C, Cosma MP, Ballabio A.

Proc Natl Acad Sci U S A. 2007 Mar 13;104(11):4506-11. Epub 2007 Mar 6.

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