Tabolacci E - Search Results

1

Defining the role of the CGGBP1 protein in FMR1 gene expression.

Goracci M, Lanni S, Mancano G, Palumbo F, Chiurazzi P, Neri G, Tabolacci E. Goracci M, et al. Among authors: tabolacci e. Eur J Hum Genet. 2016 May;24(5):697-703. doi: 10.1038/ejhg.2015.182. Epub 2015 Aug 26. Eur J Hum Genet. 2016. PMID: 26306647 Free PMC article.

2

Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine.

Pietrobono R, Pomponi MG, Tabolacci E, Oostra B, Chiurazzi P, Neri G. Pietrobono R, et al. Among authors: tabolacci e. Nucleic Acids Res. 2002 Jul 15;30(14):3278-85. doi: 10.1093/nar/gkf434. Nucleic Acids Res. 2002. PMID: 12136110 Free PMC article.

3

[L-acetylcarnitine treatment on fragile X patients hyperactive behaviour].

Calvani M, D'Iddio S, de Gaetano A, Mariotti P, Mosconi L, Pomponi MG, Tabolacci E, Torrioli MG, Vernacotola S, Neri G. Calvani M, et al. Among authors: tabolacci e. Rev Neurol. 2001 Oct;33 Suppl 1:S65-70. Rev Neurol. 2001. PMID: 12447823 Free article. Clinical Trial. Spanish.

4

X-linked mental retardation (XLMR): from clinical conditions to cloned genes.

Chiurazzi P, Tabolacci E, Neri G. Chiurazzi P, et al. Among authors: tabolacci e. Crit Rev Clin Lab Sci. 2004;41(2):117-58. doi: 10.1080/10408360490443013. Crit Rev Clin Lab Sci. 2004. PMID: 15270552 Review.

5

Assisted reproductive technology and congenital overgrowth: some speculations on a case of Pallister-Killian syndrome.

Chiurazzi P, Bajer J, Tabolacci E, Pomponi MG, Lecce R, Zollino M, Neri G. Chiurazzi P, et al. Among authors: tabolacci e. Am J Med Genet A. 2004 Oct 15;130A(3):315-6. doi: 10.1002/ajmg.a.30300. Am J Med Genet A. 2004. PMID: 15378537

6

Molecular dissection of the events leading to inactivation of the FMR1 gene.

Pietrobono R, Tabolacci E, Zalfa F, Zito I, Terracciano A, Moscato U, Bagni C, Oostra B, Chiurazzi P, Neri G. Pietrobono R, et al. Among authors: tabolacci e. Hum Mol Genet. 2005 Jan 15;14(2):267-77. doi: 10.1093/hmg/ddi024. Epub 2004 Nov 24. Hum Mol Genet. 2005. PMID: 15563507

7

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments.

Tabolacci E, Pietrobono R, Moscato U, Oostra BA, Chiurazzi P, Neri G. Tabolacci E, et al. Eur J Hum Genet. 2005 May;13(5):641-8. doi: 10.1038/sj.ejhg.5201393. Eur J Hum Genet. 2005. PMID: 15741991

8

Two brothers with 22q13 deletion syndrome and features suggestive of the Clark-Baraitser syndrome.

Tabolacci E, Zollino M, Lecce R, Sangiorgi E, Gurrieri F, Leuzzi V, Opitz JM, Neri G. Tabolacci E, et al. Clin Dysmorphol. 2005 Jul;14(3):127-132. Clin Dysmorphol. 2005. PMID: 15930901

9

A truncating mutation in the IL1RAPL1 gene is responsible for X-linked mental retardation in the MRX21 family.

Tabolacci E, Pomponi MG, Pietrobono R, Terracciano A, Chiurazzi P, Neri G. Tabolacci E, et al. Am J Med Genet A. 2006 Mar 1;140(5):482-7. doi: 10.1002/ajmg.a.31107. Am J Med Genet A. 2006. PMID: 16470793

10

Prevalence of spinocerebellar ataxia type 2 mutation among Italian Parkinsonian patients.

Modoni A, Contarino MF, Bentivoglio AR, Tabolacci E, Santoro M, Calcagni ML, Tonali PA, Neri G, Silvestri G. Modoni A, et al. Among authors: tabolacci e. Mov Disord. 2007 Feb 15;22(3):324-7. doi: 10.1002/mds.21228. Mov Disord. 2007. PMID: 17149720

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