Esposito T - Search Results

1

Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix.

Sampaolo S, Napolitano F, Tirozzi A, Reccia MG, Lombardi L, Farina O, Barra A, Cirillo F, Melone MAB, Gianfrancesco F, Iorio GD, Esposito T. Sampaolo S, et al. Among authors: esposito t. J Med Genet. 2017 Oct;54(10):710-720. doi: 10.1136/jmedgenet-2017-104555. Epub 2017 Jul 22. J Med Genet. 2017. PMID: 28735299

2

A synaptobrevin-like gene in the Xq28 pseudoautosomal region undergoes X inactivation.

D'Esposito M, Ciccodicola A, Gianfrancesco F, Esposito T, Flagiello L, Mazzarella R, Schlessinger D, D'Urso M. D'Esposito M, et al. Among authors: esposito t. Nat Genet. 1996 Jun;13(2):227-9. doi: 10.1038/ng0696-227. Nat Genet. 1996. PMID: 8640232

3

Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome.

Gianfrancesco F, Esposito T, Ruini L, Houlgatte R, Nagaraja R, D'Esposito M, Rocchi M, Auffray C, Schlessinger D, D'Urso M, Forabosco A. Gianfrancesco F, et al. Among authors: esposito t. Gene. 1997 Mar 18;187(2):179-84. doi: 10.1016/s0378-1119(96)00743-3. Gene. 1997. PMID: 9099878

4

A novel pseudoautosomal gene encoding a putative GTP-binding protein resides in the vicinity of the Xp/Yp telomere.

Gianfrancesco F, Esposito T, Montanini L, Ciccodicola A, Mumm S, Mazzarella R, Rao E, Giglio S, Rappold G, Forabosco A. Gianfrancesco F, et al. Among authors: esposito t. Hum Mol Genet. 1998 Mar;7(3):407-14. doi: 10.1093/hmg/7.3.407. Hum Mol Genet. 1998. PMID: 9466997

5

Molecular cloning and fine mapping of API5L1, a novel human gene strongly related to an antiapoptotic gene.

Gianfrancesco F, Esposito T, Ciccodicola A, D'Esposito M, Mazzarella R, D'Urso M, Forabosco A. Gianfrancesco F, et al. Among authors: esposito t. Cytogenet Cell Genet. 1999;84(3-4):164-6. doi: 10.1159/000015247. Cytogenet Cell Genet. 1999. PMID: 10393420 No abstract available.

6

Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region.

Ciccodicola A, D'Esposito M, Esposito T, Gianfrancesco F, Migliaccio C, Miano MG, Matarazzo MR, Vacca M, Franzè A, Cuccurese M, Cocchia M, Curci A, Terracciano A, Torino A, Cocchia S, Mercadante G, Pannone E, Archidiacono N, Rocchi M, Schlessinger D, D'Urso M. Ciccodicola A, et al. Among authors: esposito t. Hum Mol Genet. 2000 Feb 12;9(3):395-401. doi: 10.1093/hmg/9.3.395. Hum Mol Genet. 2000. PMID: 10655549

7

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.

8

Emergence of Talanin protein associated with human uric acid nephrolithiasis in the Hominidae lineage.

Gianfrancesco F, Esposito T, Casu G, Maninchedda G, Roberto R, Pirastu M. Gianfrancesco F, et al. Among authors: esposito t. Gene. 2004 Sep 15;339:131-8. doi: 10.1016/j.gene.2004.06.030. Gene. 2004. PMID: 15363853

9

[Multifactorial disorder: molecular and evolutionary insights of uric acid nephrolithiasis].

Gianfrancesco F, Esposito T. Gianfrancesco F, et al. Among authors: esposito t. Minerva Med. 2005 Dec;96(6):409-16. Minerva Med. 2005. PMID: 16518303 Review. Italian.

10

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

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