Gene silencing at the nuclear peripherySigal Shaklai; Ninette Amariglio; Gideon Rechavi; Amos J. Simon · 2007

Genetic Linkage of Autosomal-Dominant Alport Syndrome with Leukocyte Inclusions and Macrothrombocytopenia (Fechtner Syndrome) to Chromosome 22q11-13Amos Toren; Ninette Amariglio; Galit Rozenfeld-Granot; Amos J. Simon; Frida Brok-Simoni; Elon Pras; Gideon Rechavi · 1999

A facile route to paclitaxel C-10 carbamatesCarlo Ballatore; Simon E. Aspland; Rosario Castillo; Joel Desharnais; Trisha Eustaquio; Chengzao Sun; Angelo J. Castellino; Amos B. Smith III · 2005

The strainscope: an optical device for field measurement of homogeneous finite strainJ. Simon; M.S. Japas; A.J. Amos · 1989

Increased RNA editing in children with cyanotic congenital heart diseaseSharon Borik; Amos J. Simon; Yael Nevo-Caspi; David Mishali; Ninette Amariglio; Gideon Rechavi; Gideon Paret · 2011

The human granulocyte nucleus: Unusual nuclear envelope and heterochromatin compositionAda L. Olins; Monika Zwerger; Harald Herrmann; Hanswalter Zentgraf; Amos J. Simon; Marc Monestier; Donald E. Olins · 2008

Fetuin-A deficiency is associated with infantile cortical hyperostosis (Caffey disease)Merdler-Rabinowicz, Rona; Grinberg, Anna; Jacobson, Jeffrey M.; Somekh, Ido; Klein, Christoph; Lev, Atar; Ihsan, Salama; Habib, Adib; Somech, Raz; Simon, Amos J. · Pediatric Research · 2019