D'Esposito M - Search Results

1

Molecular cloning and characterization of the clock gene period2 in the testis of lizard Podarcis sicula and its expression during seasonal reproductive cycle.

Della Ragione F, Comitato R, Angelini F, D'Esposito M, Cardone A. Della Ragione F, et al. Gene. 2005 Dec 19;363:105-12. doi: 10.1016/j.gene.2005.08.018. Epub 2005 Nov 14. Gene. 2005. PMID: 16289937

2

Mapping of 59 EST gene markers in 31 intervals spanning the human X chromosome.

Gianfrancesco F, Esposito T, Ruini L, Houlgatte R, Nagaraja R, D'Esposito M, Rocchi M, Auffray C, Schlessinger D, D'Urso M, Forabosco A. Gianfrancesco F, et al. Gene. 1997 Mar 18;187(2):179-84. doi: 10.1016/s0378-1119(96)00743-3. Gene. 1997. PMID: 9099878

3

Expressed STSs and transcription of human Xq28.

Esposito T, Ciccodicola A, Flagiello L, Matarazzo MR, Migliaccio C, Cifarelli RA, Visone R, Campanile C, Mazzarella R, Schlessinger D, D'Urso M, D'Esposito M. Esposito T, et al. Gene. 1997 Mar 18;187(2):185-91. doi: 10.1016/s0378-1119(96)00772-x. Gene. 1997. PMID: 9099879

4

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. Gene. 1999 Nov 15;240(1):233-8. doi: 10.1016/s0378-1119(99)00375-3. Gene. 1999. PMID: 10564831

5

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

6

The X-linked methyl binding protein gene Kaiso is highly expressed in brain but is not mutated in Rett syndrome patients.

Della Ragione F, Tiunova A, Vacca M, Strazzullo M, González E, Armstrong J, Valero R, Campanile C, Pineda M, Hulten M, Monros E, D'Esposito M, Prokhortchouk E. Della Ragione F, et al. Gene. 2006 May 24;373:83-9. doi: 10.1016/j.gene.2006.01.015. Epub 2006 Mar 13. Gene. 2006. PMID: 16530985

7

Wide gene expression profiling of ischemia-reperfusion injury in human liver transplantation.

Conti A, Scala S, D'Agostino P, Alimenti E, Morelli D, Andria B, Tammaro A, Attanasio C, Della Ragione F, Scuderi V, Fabbrini F, D'Esposito M, Di Florio E, Nitsch L, Calise F, Faiella A. Conti A, et al. Liver Transpl. 2007 Jan;13(1):99-113. doi: 10.1002/lt.20960. Liver Transpl. 2007. PMID: 17192907 Free article.

8

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. 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.

9

Epigenetic alteration of microRNAs in DNMT3B-mutated patients of ICF syndrome.

Gatto S, Della Ragione F, Cimmino A, Strazzullo M, Fabbri M, Mutarelli M, Ferraro L, Weisz A, D'Esposito M, Matarazzo MR. Gatto S, et al. Epigenetics. 2010 Jul 1;5(5):427-43. doi: 10.4161/epi.5.5.11999. Epub 2010 Jul 1. Epigenetics. 2010. PMID: 20448464 Free article.

10

Differential DNA methylation as a tool for noninvasive prenatal diagnosis (NIPD) of X chromosome aneuploidies.

Della Ragione F, Mastrovito P, Campanile C, Conti A, Papageorgiou EA, Hultén MA, Patsalis PC, Carter NP, D'Esposito M. Della Ragione F, et al. J Mol Diagn. 2010 Nov;12(6):797-807. doi: 10.2353/jmoldx.2010.090199. Epub 2010 Sep 16. J Mol Diagn. 2010. PMID: 20847278 Free PMC article.

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