Isolation from the horse genome of a new DNA transposon belonging to the Tigger family.
Paulis M
Mamm Genome. 15(5):399-403.
Prion-like Doppel gene (PRND) in the goat: genomic structure, cDNA, and polymorphisms.
Uboldi C
Mamm Genome. 2005 Dec 8;16(12):963-71.
A set of duplicons on human chromosome 9 is involved in the origin of a supernumerary marker chromosome.
Paulis M
Genomics. 2006 Apr 4;87(6):747-57.
Cloning of the bovine prion-like Shadoo (SPRN) gene by comparative analysis of the predicted genomic locus.
Uboldi C
Mamm Genome. 2006 Nov 7;17(11):1130-9.
Transfer of a human chromosomal vector from a hamster cell line to a mouse embryonic stem cell line.
Paulis M
Stem Cells. 2007 Jul 5;25(10):2543-50.
Claspin inhibition leads to fragile site expression.
Focarelli ML
Genes Chromosomes Cancer. 48(12):1083-90. doi: 10.1002/gcc.20710
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA.
Revenkova E
Hum Mol Genet. 2008 Nov 7;18(3):418-27. doi: 10.1093/hmg/ddn369
Chromosome transfer via cell fusion.
Paulis M
Methods Mol Biol. 738:57-67. doi: 10.1007/978-1-61779-099-7_4
Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implications.
Marrella V
Blood. 2012 Jun 21;120(5):1005-14. doi: 10.1182/blood-2012-01-406827
Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO.
Lo Iacono N
J Bone Miner Res. 27(12):2501-10. doi: 10.1002/jbmr.1712