G. Giorgio

Functional characterization of the OFD1 protein reveals a nuclear localization and physical interaction with subunits of a chromatin remodeling complex.

S. Cairo, Clelia Prattichizzo, B. Franco, 2007, Molecular biology of the cell.

Identification of the gene for oral-facial-digital type I syndrome.

A. Ballabio, R. Winter, A. Woolf, 2001, American journal of human genetics.

Novel Functional Features of the LIS-H Domain: Role in Protein Dimerization, Half-Life and Cellular Localization

G. Gerlitz, O. Reiner, B. Franco, 2005, Cell cycle.

Mutational spectrum of the oral‐facial‐digital type I syndrome: a study on a large collection of patients

V. Novelli, Clelia Prattichizzo, B. Franco, 2008, Human mutation.

OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cells.

A. Woolf, M. Porteous, P. Winyard, 2003, Journal of the American Society of Nephrology : JASN.

Inhibition of HERG1 K+ channels by the novel second‐generation antihistamine mizolastine

L. Annunziato, M. Taglialatela, M Taglialatela, 2000, British journal of pharmacology.