Antonucci I - Search Results

1

Genetics of syndromic and nonsyndromic cleft lip and palate.

Stuppia L, Capogreco M, Marzo G, La Rovere D, Antonucci I, Gatta V, Palka G, Mortellaro C, Tetè S. Stuppia L, et al. Among authors: antonucci i. J Craniofac Surg. 2011 Sep;22(5):1722-6. doi: 10.1097/SCS.0b013e31822e5e4d. J Craniofac Surg. 2011. PMID: 21959420 Review.

2

C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy.

Stuppia L, Gatta V, Gaspari AR, Antonucci I, Morizio E, Calabrese G, Palka G. Stuppia L, et al. Among authors: antonucci i. Eur J Hum Genet. 2002 Jun;10(6):388-90. doi: 10.1038/sj.ejhg.5200819. Eur J Hum Genet. 2002. PMID: 12080391

3

Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene.

Stuppia L, Gatta V, Scarciolla O, Antonucci I, Morizio E, Calabrese G, Palka G. Stuppia L, et al. Among authors: antonucci i. Genomics. 2005 Feb;85(2):280-3. doi: 10.1016/j.ygeno.2004.10.015. Genomics. 2005. PMID: 15676287

4

Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs.

Stuppia L, Antonucci I, Binni F, Brandi A, Grifone N, Colosimo A, De Santo M, Gatta V, Gelli G, Guida V, Majore S, Calabrese G, Palka C, Ravani A, Rinaldi R, Tiboni GM, Ballone E, Venturoli A, Ferlini A, Torrente I, Grammatico P, Calzolari E, Dallapiccola B. Stuppia L, et al. Among authors: antonucci i. Eur J Hum Genet. 2005 Aug;13(8):959-64. doi: 10.1038/sj.ejhg.5201437. Eur J Hum Genet. 2005. PMID: 15870824

5

Reduced thromboxane biosynthesis in carriers of toll-like receptor 4 polymorphisms in vivo.

Patrignani P, Di Febbo C, Tacconelli S, Moretta V, Baccante G, Sciulli MG, Ricciotti E, Capone ML, Antonucci I, Guglielmi MD, Stuppia L, Porreca E. Patrignani P, et al. Among authors: antonucci i. Blood. 2006 May 1;107(9):3572-4. doi: 10.1182/blood-2005-12-4811. Epub 2006 Jan 5. Blood. 2006. PMID: 16397127 Free article.

6

Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay.

Gatta V, Antonucci I, Morizio E, Palka C, Fischetto R, Mokini V, Tumini S, Calabrese G, Stuppia L. Gatta V, et al. Among authors: antonucci i. J Hum Genet. 2007;52(1):21-27. doi: 10.1007/s10038-006-0074-5. Epub 2006 Nov 8. J Hum Genet. 2007. PMID: 17091221

7

Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring.

Coppedè F, Migheli F, Bargagna S, Siciliano G, Antonucci I, Stuppia L, Palka G, Migliore L. Coppedè F, et al. Among authors: antonucci i. Neurosci Lett. 2009 Jan 2;449(1):15-9. doi: 10.1016/j.neulet.2008.10.074. Epub 2008 Oct 25. Neurosci Lett. 2009. PMID: 18983896

8

Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol.

Antonucci I, Iezzi I, Morizio E, Mastrangelo F, Pantalone A, Mattioli-Belmonte M, Gigante A, Salini V, Calabrese G, Tetè S, Palka G, Stuppia L. Antonucci I, et al. BMC Biotechnol. 2009 Feb 16;9:9. doi: 10.1186/1472-6750-9-9. BMC Biotechnol. 2009. PMID: 19220883 Free PMC article.

9

Testis transcriptome analysis in male infertility: new insight on the pathogenesis of oligo-azoospermia in cases with and without AZFc microdeletion.

Gatta V, Raicu F, Ferlin A, Antonucci I, Scioletti AP, Garolla A, Palka G, Foresta C, Stuppia L. Gatta V, et al. Among authors: antonucci i. BMC Genomics. 2010 Jun 24;11:401. doi: 10.1186/1471-2164-11-401. BMC Genomics. 2010. PMID: 20576090 Free PMC article.

10

Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols.

Giuliani R, Antonucci I, Torrente I, Grammatico P, Palka G, Stuppia L. Giuliani R, et al. Among authors: antonucci i. Asian J Androl. 2010 Nov;12(6):819-26. doi: 10.1038/aja.2010.58. Epub 2010 Jul 26. Asian J Androl. 2010. PMID: 20657600 Free PMC article.

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