Miano MG - Search Results

1

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

2

Sequence-tagged sites (STSs) from YAC insert-ends and X-specific flow-sorted chromosomes.

Ciccodicola A, Cinti C, Esposito T, Campanile C, Casamassimi A, Miano MG, Maraldi NM, Vitale M, Johnson D, Molini B, et al. Ciccodicola A, et al. Among authors: miano mg. Mamm Genome. 1994 Aug;5(8):511-4. doi: 10.1007/BF00369322. Mamm Genome. 1994. PMID: 7949737 No abstract available.

3

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

4

Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosa.

Simonelli F, Rinaldi M, Nesti A, Testa F, Rinaldi E, Ciccodicola A, Flagiello L, Miano MG, Ventruto V, D'Urso M. Simonelli F, et al. Among authors: miano mg. Br J Ophthalmol. 1998 Jun;82(6):709. doi: 10.1136/bjo.82.6.709. Br J Ophthalmol. 1998. PMID: 9797678 Free PMC article. No abstract available.

5

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

6

Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family.

Rozzo C, Fossarello M, Galleri G, Miano MG, Ciccodicola A, Sole G, Pirastu M. Rozzo C, et al. Among authors: miano mg. Eur J Hum Genet. 1999 Jul;7(5):574-8. doi: 10.1038/sj.ejhg.5200332. Eur J Hum Genet. 1999. PMID: 10439964

7

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

8

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

9

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

10

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

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