Valente EM - Search Results

1

A subcellular analysis of genetic modulation of PINK1 on mitochondrial alterations, autophagy and cell death.

Lenzi P, Marongiu R, Falleni A, Gelmetti V, Busceti CL, Michiorri S, Valente EM, Fornai F. Lenzi P, et al. Among authors: valente em. Arch Ital Biol. 2012 Jun-Sep;150(2-3):194-217. doi: 10.4449/aib.v150i2/3.1417. Arch Ital Biol. 2012. PMID: 23165879

2

PINK1 mutations are associated with sporadic early-onset parkinsonism.

Valente EM, Salvi S, Ialongo T, Marongiu R, Elia AE, Caputo V, Romito L, Albanese A, Dallapiccola B, Bentivoglio AR. Valente EM, et al. Ann Neurol. 2004 Sep;56(3):336-41. doi: 10.1002/ana.20256. Ann Neurol. 2004. PMID: 15349860

3

PINK1 homozygous W437X mutation in a patient with apparent dominant transmission of parkinsonism.

Criscuolo C, Volpe G, De Rosa A, Varrone A, Marongiu R, Mancini P, Salvatore E, Dallapiccola B, Filla A, Valente EM, De Michele G. Criscuolo C, et al. Among authors: valente em. Mov Disord. 2006 Aug;21(8):1265-7. doi: 10.1002/mds.20933. Mov Disord. 2006. PMID: 16700027

4

Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum.

Marongiu R, Brancati F, Antonini A, Ialongo T, Ceccarini C, Scarciolla O, Capalbo A, Benti R, Pezzoli G, Dallapiccola B, Goldwurm S, Valente EM. Marongiu R, et al. Among authors: valente em. Hum Mutat. 2007 Jan;28(1):98. doi: 10.1002/humu.9472. Hum Mutat. 2007. PMID: 17154281

5

Late onset sporadic Parkinson's disease caused by PINK1 mutations: clinical and functional study.

Gelmetti V, Ferraris A, Brusa L, Romano F, Lombardi F, Barzaghi C, Stanzione P, Garavaglia B, Dallapiccola B, Valente EM. Gelmetti V, et al. Among authors: valente em. Mov Disord. 2008 Apr 30;23(6):881-5. doi: 10.1002/mds.21960. Mov Disord. 2008. PMID: 18307263

6

PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum.

Marongiu R, Ferraris A, Ialongo T, Michiorri S, Soleti F, Ferrari F, Elia AE, Ghezzi D, Albanese A, Altavista MC, Antonini A, Barone P, Brusa L, Cortelli P, Martinelli P, Pellecchia MT, Pezzoli G, Scaglione C, Stanzione P, Tinazzi M, Zecchinelli A, Zeviani M, Cassetta E, Garavaglia B, Dallapiccola B, Bentivoglio AR, Valente EM; Italian PD Study Group. Marongiu R, et al. Among authors: valente em. Hum Mutat. 2008 Apr;29(4):565. doi: 10.1002/humu.20719. Hum Mutat. 2008. PMID: 18330912 Free article.

7

Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson's disease by disturbing calcium flux.

Marongiu R, Spencer B, Crews L, Adame A, Patrick C, Trejo M, Dallapiccola B, Valente EM, Masliah E. Marongiu R, et al. Among authors: valente em. J Neurochem. 2009 Mar;108(6):1561-74. doi: 10.1111/j.1471-4159.2009.05932.x. Epub 2009 Jan 24. J Neurochem. 2009. PMID: 19166511 Free PMC article.

8

The Parkinson-associated protein PINK1 interacts with Beclin1 and promotes autophagy.

Michiorri S, Gelmetti V, Giarda E, Lombardi F, Romano F, Marongiu R, Nerini-Molteni S, Sale P, Vago R, Arena G, Torosantucci L, Cassina L, Russo MA, Dallapiccola B, Valente EM, Casari G. Michiorri S, et al. Among authors: valente em. Cell Death Differ. 2010 Jun;17(6):962-74. doi: 10.1038/cdd.2009.200. Epub 2010 Jan 8. Cell Death Differ. 2010. PMID: 20057503

9

Molecular pathways in sporadic PD.

Valente EM, Arena G, Torosantucci L, Gelmetti V. Valente EM, et al. Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S71-3. doi: 10.1016/S1353-8020(11)70023-2. Parkinsonism Relat Disord. 2012. PMID: 22166460 Review.

10

PINK1 protects against cell death induced by mitochondrial depolarization, by phosphorylating Bcl-xL and impairing its pro-apoptotic cleavage.

Arena G, Gelmetti V, Torosantucci L, Vignone D, Lamorte G, De Rosa P, Cilia E, Jonas EA, Valente EM. Arena G, et al. Among authors: valente em. Cell Death Differ. 2013 Jul;20(7):920-30. doi: 10.1038/cdd.2013.19. Epub 2013 Mar 22. Cell Death Differ. 2013. PMID: 23519076 Free PMC article.

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