Esposito T - Search Results

1

Transcriptome analysis provides new molecular signatures in sporadic Cerebral Cavernous Malformation endothelial cells.

Scimone C, Donato L, Alibrandi S, Esposito T, Alafaci C, D'Angelo R, Sidoti A. Scimone C, et al. Among authors: esposito t. Biochim Biophys Acta Mol Basis Dis. 2020 Dec 1;1866(12):165956. doi: 10.1016/j.bbadis.2020.165956. Epub 2020 Aug 30. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 32877751 Free article.

2

Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations.

Gianfrancesco F, Cannella M, Martino T, Maglione V, Esposito T, Innocenzi G, Vitale E, Liquori CL, Marchuk DA, Squitieri F. Gianfrancesco F, et al. Among authors: esposito t. Am J Med Genet B Neuropsychiatr Genet. 2007 Jul 5;144B(5):691-5. doi: 10.1002/ajmg.b.30381. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17440989

3

FMO3 allelic variants in Sicilian and Sardinian populations: trimethylaminuria and absence of fish-like body odor.

D'Angelo R, Esposito T, Calabrò M, Rinaldi C, Robledo R, Varriale B, Sidoti A. D'Angelo R, et al. Among authors: esposito t. Gene. 2013 Feb 25;515(2):410-5. doi: 10.1016/j.gene.2012.12.047. Epub 2012 Dec 21. Gene. 2013. PMID: 23266626

4

Fish odor syndrome (trimethylaminuria) supporting the possible FMO3 down expression in childhood: a case report.

D'Angelo R, Scimone C, Esposito T, Bruschetta D, Rinaldi C, Ruggeri A, Sidoti A. D'Angelo R, et al. Among authors: esposito t. J Med Case Rep. 2014 Oct 6;8:328. doi: 10.1186/1752-1947-8-328. J Med Case Rep. 2014. PMID: 25288227 Free PMC article.

5

Regulation of flavin-containing mono-oxygenase (Fmo3) gene expression by steroids in mice and humans.

Esposito T, Varriale B, D'Angelo R, Amato A, Sidoti A. Esposito T, et al. Horm Mol Biol Clin Investig. 2014 Dec;20(3):99-109. doi: 10.1515/hmbci-2014-0012. Horm Mol Biol Clin Investig. 2014. PMID: 25460299

6

A novel RLBP1 gene geographical area-related mutation present in a young patient with retinitis punctata albescens.

Scimone C, Donato L, Esposito T, Rinaldi C, D'Angelo R, Sidoti A. Scimone C, et al. Among authors: esposito t. Hum Genomics. 2017 Aug 1;11(1):18. doi: 10.1186/s40246-017-0114-6. Hum Genomics. 2017. PMID: 28764803 Free PMC article.

7

ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations.

Gianfrancesco F, Esposito T, Penco S, Maglione V, Liquori CL, Patrosso MC, Zuffardi O, Ciccodicola A, Marchuk DA, Squitieri F. Gianfrancesco F, et al. Among authors: esposito t. Neuroscience. 2008 Aug 13;155(2):345-9. doi: 10.1016/j.neuroscience.2008.05.030. Epub 2008 Jul 16. Neuroscience. 2008. PMID: 18632209

8

Paget disease of bone-associated UBA domain mutations of SQSTM1 exert distinct effects on protein structure and function.

Goode A, Long JE, Shaw B, Ralston SH, Visconti MR, Gianfrancesco F, Esposito T, Gennari L, Merlotti D, Rendina D, Rea SL, Sultana M, Searle MS, Layfield R. Goode A, et al. Among authors: esposito t. Biochim Biophys Acta. 2014 Jul;1842(7):992-1000. doi: 10.1016/j.bbadis.2014.03.006. Epub 2014 Mar 16. Biochim Biophys Acta. 2014. PMID: 24642144 Free PMC article.

9

The identification of H3F3A mutation in giant cell tumour of the clivus and the histological diagnostic algorithm of other clival lesions permit the differential diagnosis in this location.

Scotto di Carlo F, Divisato G, Iacoangeli M, Esposito T, Gianfrancesco F. Scotto di Carlo F, et al. Among authors: esposito t. BMC Cancer. 2018 Apr 2;18(1):358. doi: 10.1186/s12885-018-4291-z. BMC Cancer. 2018. PMID: 29609578 Free PMC article. Review.

10

Characterization of the murine orthologue of a novel human subtelomeric multigene family.

Gianfrancesco F, Falco G, Esposito T, Rocchi M, D'Urso M. Gianfrancesco F, et al. Among authors: esposito t. Cytogenet Cell Genet. 2001;94(1-2):98-100. doi: 10.1159/000048796. Cytogenet Cell Genet. 2001. PMID: 11701968 No abstract available.

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