Mirisola M - Search Results

1

Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families.

Romano V, Calì F, Seidita G, Mirisola M, D'Anna RP, Gambino G, Schinocca P, Romano S, Ayala GF, Canziani F, De Leo G, Elia M. Romano V, et al. Among authors: mirisola m. Psychiatr Genet. 2005 Jun;15(2):149-50. doi: 10.1097/00041444-200506000-00013. Psychiatr Genet. 2005. PMID: 15900231

2

Mutagenic alteration of the distal switch II region of RAS blocks CDC25-dependent signaling functions.

Mirisola MG, Seidita G, Verrotti AC, Di Blasi F, Fasano O. Mirisola MG, et al. J Biol Chem. 1994 Jun 3;269(22):15740-8. J Biol Chem. 1994. PMID: 8195227 Free article.

3

PAH gene mutations in the Sicilian population: association with minihaplotypes and expression analysis.

Mirisola MG, Cali F, Gloria A, Schinocca P, D'Amato M, Cassara G, Leo GD, Palillo L, Meli C, Romano V. Mirisola MG, et al. Mol Genet Metab. 2001 Nov;74(3):353-61. doi: 10.1006/mgme.2001.3211. Mol Genet Metab. 2001. PMID: 11708866

4

Continental and subcontinental distributions of mtDNA control region types.

Forster P, Calì F, Röhl A, Metspalu E, D'Anna R, Mirisola M, De Leo G, Flugy A, Salerno A, Ayala G, Kouvatsi A, Villems R, Romano V. Forster P, et al. Among authors: mirisola m. Int J Legal Med. 2002 Apr;116(2):99-108. doi: 10.1007/s00414-001-0261-z. Int J Legal Med. 2002. PMID: 12056528

5

DXYS156: a multi-purpose short tandem repeat locus for determination of sex, paternal and maternal geographic origins and DNA fingerprinting.

Calì F, Forster P, Kersting C, Mirisola MG, D'Anna R, De Leo G, Romano V. Calì F, et al. Int J Legal Med. 2002 Jun;116(3):133-8. doi: 10.1007/s00414-001-0272-9. Int J Legal Med. 2002. PMID: 12111315

6

The phenylketonuria mouse model: a meeting review.

McDonald JD, Andriolo M, Calì F, Mirisola M, Puglisi-Allegra S, Romano V, Sarkissian CN, Smith CB. McDonald JD, et al. Among authors: mirisola m. Mol Genet Metab. 2002 Aug;76(4):256-61. doi: 10.1016/s1096-7192(02)00115-4. Mol Genet Metab. 2002. PMID: 12208130 No abstract available.

7

Lack of association of HOXA1 and HOXB1 mutations and autism in Sicilian (Italian) patients.

Romano V, Calì F, Mirisola M, Gambino G, D' Anna R, Di Rosa P, Seidita G, Chiavetta V, Aiello F, Canziani F, De Leo G, Ayala GF, Elia M. Romano V, et al. Among authors: mirisola m. Mol Psychiatry. 2003 Aug;8(8):716-7. doi: 10.1038/sj.mp.4001285. Mol Psychiatry. 2003. PMID: 12888798 No abstract available.

8

Screening of subtelomeric rearrangements in autistic disorder: identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation.

Di Bella MA, Calì F, Seidita G, Mirisola M, Ragusa A, Ragalmuto A, Galesi O, Elia M, Greco D, Zingale M, Gambino G, D'Anna RP, Regan R, Carbone MC, Gallo A, Romano V. Di Bella MA, et al. Among authors: mirisola m. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):584-90. doi: 10.1002/ajmg.b.30328. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16823807

9

Ras-pathway has a dual role in yeast galactose metabolism.

Mirisola MG, Gallo A, De Leo G. Mirisola MG, et al. FEBS Lett. 2007 May 15;581(10):2009-16. doi: 10.1016/j.febslet.2007.04.018. Epub 2007 Apr 23. FEBS Lett. 2007. PMID: 17475260 Free article.

10

Yeast vectors for the integration/expression of any sequence at the TYR1 locus.

Mirisola MG, Colomba L, Gallo A, Amodeo R, De Leo G. Mirisola MG, et al. Yeast. 2007 Sep;24(9):761-6. doi: 10.1002/yea.1511. Yeast. 2007. PMID: 17597490

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