Esposito T - Search Results

1

ZNF687 Mutations in an Extended Cohort of Neoplastic Transformations in Paget's Disease of Bone: Implications for Clinical Pathology.

Scotto di Carlo F, Pazzaglia L, Mumm S, Benassi MS, De Chiara A, Franchi A, Parafioriti A, Righi A, Esposito T, Whyte MP, Gianfrancesco F. Scotto di Carlo F, et al. Among authors: esposito t. J Bone Miner Res. 2020 Oct;35(10):1974-1980. doi: 10.1002/jbmr.3993. Epub 2020 Mar 11. J Bone Miner Res. 2020. PMID: 32106343 Free article.

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

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

4

X/autosomal translocations in the Xq critical region associated with premature ovarian failure fall within and outside genes.

Mumm S, Herrera L, Waeltz PW, Scardovi A, Nagaraja R, Esposito T, Schlessinger D, Rocchi M, Forabosco A. Mumm S, et al. Among authors: esposito t. Genomics. 2001 Aug;76(1-3):30-6. doi: 10.1006/geno.2001.6611. Genomics. 2001. PMID: 11560122

5

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.

6

Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution.

Gianfrancesco F, Sanges R, Esposito T, Tempesta S, Rao E, Rappold G, Archidiacono N, Graves JA, Forabosco A, D'Urso M. Gianfrancesco F, et al. Among authors: esposito t. Genome Res. 2001 Dec;11(12):2095-100. doi: 10.1101/gr.197001. Genome Res. 2001. PMID: 11731500 Free PMC article.

7

Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate.

Gianfrancesco F, Esposito T, Ombra MN, Forabosco P, Maninchedda G, Fattorini M, Casula S, Vaccargiu S, Casu G, Cardia F, Deiana I, Melis P, Falchi M, Pirastu M. Gianfrancesco F, et al. Among authors: esposito t. Am J Hum Genet. 2003 Jun;72(6):1479-91. doi: 10.1086/375628. Epub 2003 May 9. Am J Hum Genet. 2003. PMID: 12740763 Free PMC article.

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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