Miano MG - Search Results

1

Ovarian dysfunction and FMR1 alleles in a large Italian family with POF and FRAXA disorders: case report.

Miano MG, Laperuta C, Chiurazzi P, D'Urso M, Ursini MV. Miano MG, et al. BMC Med Genet. 2007 Apr 11;8:18. doi: 10.1186/1471-2350-8-18. BMC Med Genet. 2007. PMID: 17428316 Free PMC article.

2

Construction of a pilot human YAC library in a recombination-defective yeast strain.

Palmieri G, Miano MG, Casamassimi A, Lania A, Kohno K, Schlessinger D, D'Urso M, Featherstone T. Palmieri G, et al. Among authors: miano mg. Gene. 1997 Apr 1;188(2):169-74. doi: 10.1016/s0378-1119(96)00751-2. Gene. 1997. PMID: 9133588

3

Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity.

de Crecchio G, Simonelli F, Nunziata G, Mazzeo S, Greco GM, Rinaldi E, Ventruto V, Ciccodicola A, Miano MG, Testa F, Curci A, D'Urso M, Rinaldi MM, Cavaliere ML, Castelluccio P. de Crecchio G, et al. Among authors: miano mg. Clin Genet. 1998 Oct;54(4):315-20. doi: 10.1034/j.1399-0004.1998.5440409.x. Clin Genet. 1998. PMID: 9831343

4

Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa.

Miano MG, Testa F, Strazzullo M, Trujillo M, De Bernardo C, Grammatico B, Simonelli F, Mangino M, Torrente I, Ruberto G, Beneyto M, Antinolo G, Rinaldi E, Danesino C, Ventruto V, D'Urso M, Ayuso C, Baiget M, Ciccodicola A. Miano MG, et al. Eur J Hum Genet. 1999 Sep;7(6):687-94. doi: 10.1038/sj.ejhg.5200352. Eur J Hum Genet. 1999. PMID: 10482958

5

Human and mouse SYBL1 gene structure and expression.

Matarazzo MR, Cuccurese M, Strazzullo M, Vacca M, Curci A, Miano MG, Cocchia M, Mercadante G, Torino A, D'Urso M, Ciccodicola A, D'Esposito M. Matarazzo MR, et al. Among authors: miano mg. Gene. 1999 Nov 15;240(1):233-8. doi: 10.1016/s0378-1119(99)00375-3. Gene. 1999. PMID: 10564831

6

Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. Online.

Miano MG, Valverde D, Solans T, Grammatico B, Migliaccio C, Cirigliano V, DeBernardo C, Ventruto V, Meitinger T, Wright A, Del Porto G, Baiget M, D'Urso M, Ciccodicola A. Miano MG, et al. Hum Mutat. 1998;12(3):212-3. Hum Mutat. 1998. PMID: 10651485

7

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: miano mg. Hum Mol Genet. 2000 Feb 12;9(3):395-401. doi: 10.1093/hmg/9.3.395. Hum Mol Genet. 2000. PMID: 10655549

8

Identification of novel RP2 mutations in a subset of X-linked retinitis pigmentosa families and prediction of new domains.

Miano MG, Testa F, Filippini F, Trujillo M, Conte I, Lanzara C, Millán JM, De Bernardo C, Grammatico B, Mangino M, Torrente I, Carrozzo R, Simonelli F, Rinaldi E, Ventruto V, D'Urso M, Ayuso C, Ciccodicola A. Miano MG, et al. Hum Mutat. 2001 Aug;18(2):109-19. doi: 10.1002/humu.1160. Hum Mutat. 2001. PMID: 11462235

9

Mapping of MRX81 in Xp11.2-Xq12 suggests the presence of a new gene involved in nonspecific X-linked mental retardation.

Annunziata I, Lanzara C, Conte I, Zullo A, Ventruto V, Rinaldi MM, D'Urso M, Casari G, Ciccodicola A, Miano MG. Annunziata I, et al. Among authors: miano mg. Am J Med Genet A. 2003 Apr 30;118A(3):217-22. doi: 10.1002/ajmg.a.10144. Am J Med Genet A. 2003. PMID: 12673650

10

Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-kappaB activation.

Fusco F, Bardaro T, Fimiani G, Mercadante V, Miano MG, Falco G, Israël A, Courtois G, D'Urso M, Ursini MV. Fusco F, et al. Among authors: miano mg. Hum Mol Genet. 2004 Aug 15;13(16):1763-73. doi: 10.1093/hmg/ddh192. Epub 2004 Jun 30. Hum Mol Genet. 2004. PMID: 15229184

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