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Publications prior to 2004
1. Musicco C, Cormio
A, Calvaruso MA, Iommarini L, Gasparre G, Porcelli AM,
Timperio AM, Zolla L, Gadaleta MN. Analysis of mitochondrial
proteome of cybrid cells harbouring a truncative mitochondrial DNA
mutation in respiratory complex I. Mol. BioSyst. 2014. Accepted
Manuscript. doi: 10.1039/C3MB70542K.
2. Giordano C,
Iommarini L, Giordano L, Maresca A, Pisano A, Valentino ML,
Caporali L, Liguori R, Deceglie S, Roberti M, Fanelli F, Fracasso
F, Ross-Cisneros FN, D'Adamo P, Hudson G, Pyle A, Yu-Wai-Man P,
Chinnery PF, Zeviani M, Salomao SR, Berezovsky A, Belfort R Jr,
Ventura DF, Moraes M, Moraes Filho M, Barboni P, Sadun F, De Negri
A, Sadun AA, Tancredi A, Mancini M, d'Amati G, Loguercio Polosa P,
Cantatore P, Carelli V. Efficient mitochondrial biogenesis drives
incomplete penetrance in Leber's hereditary optic neuropathy.
Brain. 2014 Feb;137(Pt 2):335-53. doi: 10.1093/brain/awt343.
3. Calabrese C,
Iommarini L, Kurelac I, Calvaruso MA, Capristo M, Lollini
PL, Nanni P, Bergamini C, Nicoletti G, Giovanni CD, Ghelli A,
Giorgio V, Caratozzolo MF, Marzano F, Manzari C, Betts CM, Carelli
V, Ceccarelli C, Attimonelli M, Romeo G, Fato R, Rugolo M, Tullo A,
Gasparre G, Porcelli AM. Respiratory complex I is essential to
induce a Warburg profile in mitochondria-defective tumor cells.
Cancer Metab. 2013 Mar 18;1(1):11. doi: 10.1186/2049-3002-1-11.
5. Srivastava S, Diaz F, Iommarini L, Aure K, Lombes A,
Moraes CT. PGC-1alpha/beta induced expression partially compensates
for respiratory chain defects in cells from patients with
mitochondrial disorders. Hum Mol Genet. 2009 May 15;18(10):1805-12.
doi: 10.1093/hmg/ddp093.
6. Ramos Cdo V, Bellusci C, Savini G, Carbonelli M, Berezovsky
A, Tamaki C, Cinoto R, Sacai PY, Moraes-Filho MN, Miura HM,
Valentino ML, Iommarini L, De Negri AM, Sadun F, Cortelli P,
Montagna P, Salomao SR, Sadun AA, Carelli V, Barboni P. Association
of optic disc size with development and prognosis of Leber's
hereditary optic neuropathy. Invest Ophthalmol Vis Sci. 2009
Apr;50(4):1666-74. doi: 10.1167/iovs.08-2695.
7. Amati-Bonneau P, Valentino ML, Reynier P, Gallardo ME,
Bornstein B, Boissière A, Campos Y, Rivera H, de la Aleja JG,
Carroccia R, Iommarini L, Labauge P, Figarella-Branger D,
Marcorelles P, Furby A, Beauvais K, Letournel F, Liguori R, La
Morgia C, Montagna P, Liguori M, Zanna C, Rugolo M, Cossarizza A,
Wissinger B, Verny C, Schwarzenbacher R, Martín MA, Arenas J, Ayuso
C, Garesse R, Lenaers G, Bonneau D, Carelli V. OPA1 mutations
induce mitochondrial DNA instability and optic atrophy 'plus'
phenotypes. Brain. 2008 Feb;131(Pt 2):338-51.
