Arrigo G - Search Results

1

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome.

Bonaglia MC, Giorda R, Beri S, De Agostini C, Novara F, Fichera M, Grillo L, Galesi O, Vetro A, Ciccone R, Bonati MT, Giglio S, Guerrini R, Osimani S, Marelli S, Zucca C, Grasso R, Borgatti R, Mani E, Motta C, Molteni M, Romano C, Greco D, Reitano S, Baroncini A, Lapi E, Cecconi A, Arrigo G, Patricelli MG, Pantaleoni C, D'Arrigo S, Riva D, Sciacca F, Dalla Bernardina B, Zoccante L, Darra F, Termine C, Maserati E, Bigoni S, Priolo E, Bottani A, Gimelli S, Bena F, Brusco A, di Gregorio E, Bagnasco I, Giussani U, Nitsch L, Politi P, Martinez-Frias ML, Martínez-Fernández ML, Martínez Guardia N, Bremer A, Anderlid BM, Zuffardi O. Bonaglia MC, et al. Among authors: arrigo g. PLoS Genet. 2011 Jul;7(7):e1002173. doi: 10.1371/journal.pgen.1002173. Epub 2011 Jul 14. PLoS Genet. 2011. PMID: 21779178 Free PMC article.

2

Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.

De Gregori M, Ciccone R, Magini P, Pramparo T, Gimelli S, Messa J, Novara F, Vetro A, Rossi E, Maraschio P, Bonaglia MC, Anichini C, Ferrero GB, Silengo M, Fazzi E, Zatterale A, Fischetto R, Previderé C, Belli S, Turci A, Calabrese G, Bernardi F, Meneghelli E, Riegel M, Rocchi M, Guerneri S, Lalatta F, Zelante L, Romano C, Fichera M, Mattina T, Arrigo G, Zollino M, Giglio S, Lonardo F, Bonfante A, Ferlini A, Cifuentes F, Van Esch H, Backx L, Schinzel A, Vermeesch JR, Zuffardi O. De Gregori M, et al. Among authors: arrigo g. J Med Genet. 2007 Dec;44(12):750-62. doi: 10.1136/jmg.2007.052787. Epub 2007 Aug 31. J Med Genet. 2007. PMID: 17766364 Free PMC article.

3

13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.

Ballarati L, Rossi E, Bonati MT, Gimelli S, Maraschio P, Finelli P, Giglio S, Lapi E, Bedeschi MF, Guerneri S, Arrigo G, Patricelli MG, Mattina T, Guzzardi O, Pecile V, Police A, Scarano G, Larizza L, Zuffardi O, Giardino D. Ballarati L, et al. Among authors: arrigo g. J Med Genet. 2007 Jan;44(1):e60. doi: 10.1136/jmg.2006.043059. J Med Genet. 2007. PMID: 17209130 Free PMC article.

4

Unexpected results in the constitution of small supernumerary marker chromosomes.

Vetro A, Manolakos E, Petersen MB, Thomaidis L, Liehr T, Croci G, Franchi F, Marinelli M, Meneghelli E, Dal Bello B, Cesari S, Iasci A, Arrigo G, Zuffardi O. Vetro A, et al. Among authors: arrigo g. Eur J Med Genet. 2012 Mar;55(3):185-90. doi: 10.1016/j.ejmg.2012.01.010. Epub 2012 Jan 28. Eur J Med Genet. 2012. PMID: 22342433 Free article.

5

Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements.

Giglio S, Pirola B, Arrigo G, Dagrada P, Bardoni B, Bernardi F, Russo G, Argentiero L, Forabosco A, Carrozzo R, Zuffardi O. Giglio S, et al. Among authors: arrigo g. Eur J Hum Genet. 2000 Jan;8(1):63-70. doi: 10.1038/sj.ejhg.5200394. Eur J Hum Genet. 2000. PMID: 10713889

6

Assignment of the tenascin-R gene (Tnr) to mouse chromosome 4 band E2 by fluorescence in situ hybridization; refinement of the human TNR location to chromosome 1q24.

Arrigo G, Gherzi R, Bonaglia MC, Leprini A, Zuffardi O, Zardi L. Arrigo G, et al. Cytogenet Cell Genet. 1997;78(2):145-6. doi: 10.1159/000134650. Cytogenet Cell Genet. 1997. PMID: 9371410 No abstract available.

7

Cell-cycle phases and genetic profile of bone marrow-derived mesenchymal stromal cells expanded in vitro from healthy donors.

Achille V, Mantelli M, Arrigo G, Novara F, Avanzini MA, Bernardo ME, Zuffardi O, Barosi G, Zecca M, Maccario R. Achille V, et al. Among authors: arrigo g. J Cell Biochem. 2011 Jul;112(7):1817-21. doi: 10.1002/jcb.23100. J Cell Biochem. 2011. PMID: 21400572

8

Identification of two paralogous regions mapping to the short and long arms of human chromosome 2 comprising LIS1 pseudogenes.

Fogli A, Giglio S, Arrigo G, Lo Nigro C, Zollo M, Viggiano L, Rocchi M, Archidiacono N, Zuffardi O, Carrozzo R. Fogli A, et al. Among authors: arrigo g. Cytogenet Cell Genet. 1999;86(3-4):225-32. doi: 10.1159/000015344. Cytogenet Cell Genet. 1999. PMID: 10575211

9

Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivation.

Carrozzo R, Arrigo G, Rossi E, Bardoni B, Cammarata M, Gandullia P, Gatti R, Zuffardi O. Carrozzo R, et al. Among authors: arrigo g. Am J Med Genet. 1997 Oct 31;72(3):329-34. Am J Med Genet. 1997. PMID: 9332664

10

In vitro biosafety profile evaluation of multipotent mesenchymal stem cells derived from the bone marrow of sarcoma patients.

Lucarelli E, Bellotti C, Mantelli M, Avanzini MA, Maccario R, Novara F, Arrigo G, Zuffardi O, Zuntini M, Pandolfi M, Sangiorgi L, Lisini D, Donati D, Duchi S. Lucarelli E, et al. Among authors: arrigo g. J Transl Med. 2014 Apr 9;12:95. doi: 10.1186/1479-5876-12-95. J Transl Med. 2014. PMID: 24716831 Free PMC article.

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