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Characteristics and quality of illness behavior in celiac disease.
de Rosa A, Troncone A, Vacca M, Ciacci C. de Rosa A, et al. Among authors: vacca m. Psychosomatics. 2004 Jul-Aug;45(4):336-42. doi: 10.1176/appi.psy.45.4.336. Psychosomatics. 2004. PMID: 15232048
Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region.
Vacca M, Matarazzo MR, Jones J, Spalluto C, Archidiacono N, Ma P, Rocchi M, D'Urso M, Chen EY, D'Esposito M, Mumm S. Vacca M, et al. Genomics. 1999 Dec 1;62(2):293-6. doi: 10.1006/geno.1999.5996. Genomics. 1999. PMID: 10610725
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: vacca m. Hum Mol Genet. 2000 Feb 12;9(3):395-401. doi: 10.1093/hmg/9.3.395. Hum Mol Genet. 2000. PMID: 10655549
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.
Vacca M, Filippini F, Budillon A, Rossi V, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, MacDonald F, Kerr A, Dhanjal S, Hultén M. Vacca M, et al. J Mol Med (Berl). 2001;78(11):648-55. doi: 10.1007/s001090000155. J Mol Med (Berl). 2001. PMID: 11269512
DHPLC analysis of the MECP2 gene in Italian Rett patients.
Nicolao P, Carella M, Giometto B, Tavolato B, Cattin R, Giovannucci-Uzielli ML, Vacca M, Della Regione F, Piva S, Bortoluzzi S, Gasparini P. Nicolao P, et al. Among authors: vacca m. Hum Mutat. 2001 Aug;18(2):132-40. doi: 10.1002/humu.1162. Hum Mutat. 2001. PMID: 11462237
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: vacca m. Gene. 1999 Nov 15;240(1):233-8. doi: 10.1016/s0378-1119(99)00375-3. Gene. 1999. PMID: 10564831
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region.
Vacca M, Filippini F, Budillon A, Rossi V, Della Ragione F, De Bonis ML, Mercadante G, Manzati E, Gualandi F, Bigoni S, Trabanelli C, Pini G, Calzolari E, Ferlini A, Meloni I, Hayek G, Zappella M, Renieri A, D'Urso M, D'Esposito M, Macdonald F, Kerr A, Dhanjal S, Hulten M. Vacca M, et al. Brain Dev. 2001 Dec;23 Suppl 1:S246-50. doi: 10.1016/s0387-7604(01)00343-6. Brain Dev. 2001. PMID: 11738884
Lessons from two human chromatin diseases, ICF syndrome and Rett syndrome.
Matarazzo MR, De Bonis ML, Vacca M, Della Ragione F, D'Esposito M. Matarazzo MR, et al. Among authors: vacca m. Int J Biochem Cell Biol. 2009 Jan;41(1):117-26. doi: 10.1016/j.biocel.2008.07.026. Epub 2008 Aug 22. Int J Biochem Cell Biol. 2009. PMID: 18786650 Review.
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