Tiranti V - Search Results

1

Identification of novel mutations in five patients with mitochondrial encephalomyopathy.

Valente L, Piga D, Lamantea E, Carrara F, Uziel G, Cudia P, Zani A, Farina L, Morandi L, Mora M, Spinazzola A, Zeviani M, Tiranti V. Valente L, et al. Among authors: tiranti v. Biochim Biophys Acta. 2009 May;1787(5):491-501. doi: 10.1016/j.bbabio.2008.10.001. Epub 2008 Oct 15. Biochim Biophys Acta. 2009. PMID: 18977334 Free article.

2

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Zeviani M, Gellera C, Antozzi C, Rimoldi M, Morandi L, Villani F, Tiranti V, DiDonato S. Zeviani M, et al. Among authors: tiranti v. Lancet. 1991 Jul 20;338(8760):143-7. doi: 10.1016/0140-6736(91)90136-d. Lancet. 1991. PMID: 1677065

3

A full-length cDNA encoding a mitochondrial DNA-specific single-stranded DNA binding protein from Xenopus laevis.

Tiranti V, Barat-Gueride B, Bijl J, DiDonato S, Zeviani M. Tiranti V, et al. Nucleic Acids Res. 1991 Aug 11;19(15):4291. doi: 10.1093/nar/19.15.4291. Nucleic Acids Res. 1991. PMID: 1870981 Free PMC article. No abstract available.

4

The gene (NFE2L1) for human NRF-1, an activator involved in nuclear-mitochondrial interactions, maps to 7q32.

Tiranti V, Rossi E, Rocchi M, DiDonato S, Zuffardi O, Zeviani M. Tiranti V, et al. Genomics. 1995 Jun 10;27(3):555-7. doi: 10.1006/geno.1995.1094. Genomics. 1995. PMID: 7558044 No abstract available.

5

Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNASer(UCN) gene.

Tiranti V, Chariot P, Carella F, Toscano A, Soliveri P, Girlanda P, Carrara F, Fratta GM, Reid FM, Mariotti C, Zeviani M. Tiranti V, et al. Hum Mol Genet. 1995 Aug;4(8):1421-7. doi: 10.1093/hmg/4.8.1421. Hum Mol Genet. 1995. PMID: 7581383

6

Searching for genes affecting the structural integrity of the mitochondrial genome.

Zeviani M, Amati P, Comi G, Fratta G, Mariotti C, Tiranti V. Zeviani M, et al. Among authors: tiranti v. Biochim Biophys Acta. 1995 May 24;1271(1):153-8. doi: 10.1016/0925-4439(95)00022-v. Biochim Biophys Acta. 1995. PMID: 7599202 Free article. Review.

7

Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis.

Tiranti V, Rossi E, Ruiz-Carrillo A, Rossi G, Rocchi M, DiDonato S, Zuffardi O, Zeviani M. Tiranti V, et al. Genomics. 1995 Jan 20;25(2):559-64. doi: 10.1016/0888-7543(95)80058-t. Genomics. 1995. PMID: 7789991

8

A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.

Zeviani M, Muntoni F, Savarese N, Serra G, Tiranti V, Carrara F, Mariotti C, DiDonato S. Zeviani M, et al. Among authors: tiranti v. Eur J Hum Genet. 1993;1(1):80-7. doi: 10.1159/000472390. Eur J Hum Genet. 1993. PMID: 8069654

9

Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy.

Mariotti C, Tiranti V, Carrara F, Dallapiccola B, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: tiranti v. J Clin Invest. 1994 Mar;93(3):1102-7. doi: 10.1172/JCI117061. J Clin Invest. 1994. PMID: 8132749 Free PMC article.

10

Cloning of human and rat cDNAs encoding the mitochondrial single-stranded DNA-binding protein (SSB).

Tiranti V, Rocchi M, DiDonato S, Zeviani M. Tiranti V, et al. Gene. 1993 Apr 30;126(2):219-25. doi: 10.1016/0378-1119(93)90370-i. Gene. 1993. PMID: 8482537

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