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Items: 14

1.

Extracts from Cell Suspension Cultures of Strawberry (Fragaria x ananassa Duch): Cytotoxic Effects on Human Cancer Cells.

Lucioli S, Pastorino F, Nota P, Ballan G, Frattarelli A, Fabbri A, Forni C, Caboni E.

Molecules. 2019 May 4;24(9). pii: E1738. doi: 10.3390/molecules24091738.

2.

Anthocyanic pigments from elicited in vitro grown shoot cultures of Vaccinium corymbosum L., cv. Brigitta Blue, as photosensitizer in natural dye-sensitized solar cells (NDSSC).

Lucioli S, Di Bari C, Forni C, Di Carlo A, Barrajón-Catalán E, Micol V, Nota P, Teoli F, Matteocci F, Frattarelli A, Caboni E.

J Photochem Photobiol B. 2018 Nov;188:69-76. doi: 10.1016/j.jphotobiol.2018.09.002. Epub 2018 Sep 6.

PMID:
30219632
3.

Characterization of the response of in vitro cultured Myrtus communis L. plants to high concentrations of NaCl.

Di Cori P, Lucioli S, Frattarelli A, Nota P, Tel-Or E, Benyamini E, Gottlieb H, Caboni E, Forni C.

Plant Physiol Biochem. 2013 Dec;73:420-6. doi: 10.1016/j.plaphy.2013.10.026. Epub 2013 Oct 30.

PMID:
24239614
4.

Peroxisomal acyl-CoA-oxidase deficiency: two new cases.

Carrozzo R, Bellini C, Lucioli S, Deodato F, Cassandrini D, Cassanello M, Caruso U, Rizzo C, Rizza T, Napolitano ML, Wanders RJ, Jakobs C, Bruno C, Santorelli FM, Dionisi-Vici C, Bonioli E.

Am J Med Genet A. 2008 Jul 1;146A(13):1676-81. doi: 10.1002/ajmg.a.32298.

PMID:
18536048
5.

Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.

Dimmock DP, Zhang Q, Dionisi-Vici C, Carrozzo R, Shieh J, Tang LY, Truong C, Schmitt E, Sifry-Platt M, Lucioli S, Santorelli FM, Ficicioglu CH, Rodriguez M, Wierenga K, Enns GM, Longo N, Lipson MH, Vallance H, Craigen WJ, Scaglia F, Wong LJ.

Hum Mutat. 2008 Feb;29(2):330-1. doi: 10.1002/humu.9519.

PMID:
18205204
6.

Infantile mitochondrial disorders.

Carrozzo R, Piemonte F, Tessa A, Lucioli S, Rizza T, Meschini MC, Fattori F, Santorelli FM.

Biosci Rep. 2007 Jun;27(1-3):105-12. Review.

PMID:
17486440
7.

SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.

Carrozzo R, Dionisi-Vici C, Steuerwald U, Lucioli S, Deodato F, Di Giandomenico S, Bertini E, Franke B, Kluijtmans LA, Meschini MC, Rizzo C, Piemonte F, Rodenburg R, Santer R, Santorelli FM, van Rooij A, Vermunt-de Koning D, Morava E, Wevers RA.

Brain. 2007 Mar;130(Pt 3):862-74. Epub 2007 Feb 14.

PMID:
17301081
8.

Human mitochondrial pyrophosphatase: cDNA cloning and analysis of the gene in patients with mtDNA depletion syndromes.

Curbo S, Lagier-Tourenne C, Carrozzo R, Palenzuela L, Lucioli S, Hirano M, Santorelli F, Arenas J, Karlsson A, Johansson M.

Genomics. 2006 Mar;87(3):410-6. Epub 2005 Nov 21.

9.

Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patient.

Lucioli S, Hoffmeier K, Carrozzo R, Tessa A, Ludwig B, Santorelli FM.

Neurogenetics. 2006 Mar;7(1):51-7. Epub 2005 Nov 12.

PMID:
16284789
10.

Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy.

Giusti B, Lucarini L, Pietroni V, Lucioli S, Bandinelli B, Sabatelli P, Squarzoni S, Petrini S, Gartioux C, Talim B, Roelens F, Merlini L, Topaloglu H, Bertini E, Guicheney P, Pepe G.

Ann Neurol. 2005 Sep;58(3):400-10.

PMID:
16130093
11.

Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathy.

Lucioli S, Giusti B, Mercuri E, Vanegas OC, Lucarini L, Pietroni V, Urtizberea A, Ben Yaou R, de Visser M, van der Kooi AJ, Bönnemann C, Iannaccone ST, Merlini L, Bushby K, Muntoni F, Bertini E, Chu ML, Pepe G.

Neurology. 2005 Jun 14;64(11):1931-7.

PMID:
15955946
12.

A mitochondrial ATPase 6 mutation is associated with Leigh syndrome in a family and affects proton flow and adenosine triphosphate output when modeled in Escherichia coli.

Carrozzo R, Rizza T, Lucioli S, Pierini R, Bertini E, Santorelli FM.

Acta Paediatr Suppl. 2004 May;93(445):65-7.

PMID:
15176724
13.

Mutation analysis in 16 patients with mtDNA depletion.

Carrozzo R, Bornstein B, Lucioli S, Campos Y, de la Pena P, Petit N, Dionisi-Vici C, Vilarinho L, Rizza T, Bertini E, Garesse R, Santorelli FM, Arenas J.

Hum Mutat. 2003 Apr;21(4):453-4.

PMID:
12655576
14.

Poliovirus Sabin type 1 neutralization epitopes recognized by immunoglobulin A monoclonal antibodies.

Fiore L, Ridolfi B, Genovese D, Buttinelli G, Lucioli S, Lahm A, Ruggeri FM.

J Virol. 1997 Sep;71(9):6905-12.

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