- Small molecule inhibitor screening identified HSP90 inhibitor 17-AAG as potential therapeutic agent for gallbladder cancer. Weber H, Valbuena JR, Barbhuiya MA, Stein S, Kunkel H, García P, Bizama C, Riquelme I, Espinoza JA, Kurtz SE, Tyner JW, Calderon JF, Corvalán AH, Grez M, Pandey A, Leal-Rojas P, Roa JC. Oncotarget. 2017 epub. doi: 10.18632/oncotarget.15410
- Regulation of Connexins Expression Levels by MicroRNAs, an Update. Calderón JF1, Retamal MA2. Front Physiol. 2016 Nov 25;7:558. eCollection 2016.
- Elevated expression levels of lysyl oxidases protect against aortic aneurysm progression in Marfan syndrome. Busnadiego O, del Blanco D, Gonzalez-Santamaría J, Habashi J, Calderón JF, Sandoval P, Bedja D, Guinea-Viniegra J, Lopez-Cabrera M, Rosell-Garcia T, Snabel JM, Hanemaaijer R, Forteza A, Dietz HC, Egea G, Rodríguez-Pascual F. Journal of Molecular and Cellular Cardiology. 2015. In press.
- Current Controversies in Diagnosis and Management of Cleft Palate and Velopharyngeal Insufficiency. Ysunza PA, Repetto GM, Pamplona MC, Calderón JF, Shaheen K, Chaiyasate K, Rontal M. BioMed Research International. 2015; Article ID 196240.
- Angiotensin II-dependent TGF-β signaling contributes to Loeys-Dietz syndrome vascular pathogenesis. Gallo EM, Loch DC, Habashi JP, Calderon JF, Chen Y, Bedja D, van Erp C, Gerber EE, Parker SJ, Sauls K, Judge DP, Cooke SK, Lindsay ME, Rouf R, Myers L, Ap Rhys CM, Kent KC, Norris RA, Huso DL, Dietz HC. J Clin Invest. 2014 Jan 2;124(1):448-60.
- GluA3-deficiency in Mice is Associated with Increased Social and Aggressive Behavior and Elevated Dopamine in Striatum. Adamczyk A, Mejias R, Takamiya K, Yocum J, Krasnova I, Calderón JF, Cadet JL, Huganir R, Pletnikov M, Wang T. Behavioural Brain Research 2012 Apr 1;229(1):265-72.
- VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study. Calderón JF, Puga AR, Guzmán ML, Astete CP, Arriaza M, Aracena M, Aravena T, Sanz P, Repetto GM. Biol Res. 2009;42(4):461-8.
- Clinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients. Repetto GM, Guzmán ML, Puga A, Calderón JF, Astete CP, Aracena M, Arriaza M, Aravena T, Sanz P. Clin Genet. 2009 Nov;76(5):465-70. Epub 2009 Sep 8.
