M. Capristo

发表

DNMT1 mutations leading to neurodegeneration paradoxically reflect on mitochondrial metabolism

E. Mignot, G. Plazzi, C. La Morgia, 2020, Human molecular genetics.

Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells

M. Attimonelli, P. Lollini, V. Giorgio, 2013, Cancer & Metabolism.

The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilization.

M. Attimonelli, A. Melcarne, A. Martinuzzi, 2010, Human molecular genetics.

Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome

G. Savini, P. Barboni, M. Carbonelli, 2020, Scientific Reports.

Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNALys

C. La Morgia, M. Montopoli, V. Carelli, 2022, Molecular medicine.

ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy

M. Zeviani, R. Schüle, L. Schöls, 2020, Annals of neurology.

Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic Variants

C. La Morgia, E. Lamantea, V. Carelli, 2021, Frontiers in Neurology.

Expanding and validating the biomarkers for mitochondrial diseases

C. La Morgia, V. Carelli, L. Di Vito, 2020, Journal of Molecular Medicine.

Preclinical Effectiveness of Selective Inhibitor of IRS-1/2 NT157 in Osteosarcoma Cell Lines

P. Picci, C. Garofalo, K. Scotlandi, 2015, Front. Endocrinol..

Incomplete penetrance in mitochondrial optic neuropathies.

C. La Morgia, V. Carelli, M. Valentino, 2017, Mitochondrion.

Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy

R. Lodi, M. Contin, C. Casali, 2016, Annals of neurology.

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy

A. Torroni, P. Barboni, M. Carbonelli, 2018, PLoS genetics.

Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment.

P. Lollini, V. Giorgio, A. Porcelli, 2014, Human molecular genetics.

Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells

M. Attimonelli, P. Lollini, V. Giorgio, 2013, Cancer & metabolism.

A mutation threshold distinguishes the antitumorigenic effects of the mitochondrial gene MTND1, an oncojanus function.

Giovanni Romeo, Giuseppe Gasparre, Anna Ghelli, 2011, Cancer research.

Liver transplantation in mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical long-term follow-up and pathogenic implications

L. Fasano, L. Pisani, R. Lodi, 2020, Journal of Neurology.

Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy

T. Strom, H. Prokisch, P. Charbel Issa, 2021, The Journal of clinical investigation.

Metformin as an Adjuvant Drug against Pediatric Sarcomas: Hypoxia Limits Therapeutic Effects of the Drug

P. Lollini, P. Picci, A. Belfiore, 2013, PloS one.

Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome

G. Savini, P. Barboni, M. Carbonelli, 2020, Scientific Reports.

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy

G. Plazzi, D. Manners, R. Lodi, 2018, American Journal of Neuroradiology.

ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy

R. Lodi, C. Casali, C. Tonon, 2016, Neurological Sciences.

A novel ALG14 missense variant in an alive child with myopathy, epilepsy, and progressive cerebral atrophy

V. Carelli, F. Pisani, M. Capristo, 2021, American Journal of Medical Genetics. Part A.

Liver transplant reverses biochemical imbalance in mitochondrial neurogastrointestinal encephalomyopathy.

M. Contin, M. Dotti, R. De Giorgio, 2017, Mitochondrion.