Prevention of Ventricular Arrhythmia and Calcium Dysregulation in a Catecholaminergic Polymorphic Ventricular Tachycardia Mouse Model Carrying Calsequestrin-2 Mutation

Por Alcalai, Ronny, Wakimoto, Hiroko, Arad, Michael, Planer, David, Konno, Tetsuo, Wang, Libin, Seidman, Jon G., Seidman, Christine E., Berul, Charles I
Publicado em 2010

Allele-specific expression in the human heart and its application to postoperative atrial fibrillation and myocardial ischemia

Por Sigurdsson, Martin I., Saddic, Louis, Heydarpour, Mahyar, Chang, Tzuu-Wang, Shekar, Prem, Aranki, Sary, Couper, Gregory S., Shernan, Stanton K., Seidman, Jon G., Body, Simon C., Muehlschlegel, Jochen D.
Publicado no Genome Med (2016)

The Long Noncoding RNA Landscape of the Ischemic Human Left Ventricle

Por Saddic, Louis A., Sigurdsson, Martin I., Chang, Tzuu-Wang, Mazaika, Erica, Heydarpour, Mahyar, Shernan, Stanton K., Seidman, Christine E., Seidman, Jon G., Aranki, Sary F., Body, Simon C., Muehlschlegel, Jochen D.
Publicado no Circ Cardiovasc Genet (2017)

Genome-wide identification of mouse congenital heart disease loci

Por Kamp, Anna, Peterson, Michael A., Svenson, Karen L., Bjork, Bryan C., Hentges, Kathryn E., Rajapaksha, Tharinda W., Moran, Jennifer, Justice, Monica J., Seidman, Jon G., Seidman, Christine E., Moskowitz, Ivan P., Beier, David R.
Publicado em 2010

Joint analysis of left ventricular expression and circulating plasma levels of Omentin after myocardial ischemia

Por Saddic, Louis A., Nicoloro, Sarah M., Gupta, Olga T., Czech, Michael P., Gorham, Joshua, Shernan, Stanton K., Seidman, Christine E., Seidman, Jon G., Aranki, Sary F., Body, Simon C., Fitzgibbons, Timothy P., Muehlschlegel, Jochen D.
Publicado no Cardiovasc Diabetol (2017)

Using Next-generation RNA Sequencing to Examine Ischemic Changes Induced by Cold Blood Cardioplegia on the Human Left Ventricular Myocardium Transcriptome

Por Muehlschlegel, Jochen D., Christodoulou, Danos C., McKean, David, Gorham, Joshua, Mazaika, Erica, Heydarpour, Mahyar, Lee, Grace, DePalma, Steven R., Perry, Tjorvi E., Fox, Amanda F., Shernan, Stanton, Seidman, Christine E., Aranki, Sary F., Seidman, Jon G., Body, Simon C.
Publicado no Anesthesiology (2015)

Pitx2 modulates a Tbx5-dependent gene regulatory network to maintain atrial rhythm

Por Nadadur, Rangarajan D., Broman, Michael T., Boukens, Bastiaan, Mazurek, Stefan R., Yang, Xinan, van den Boogaard, Malou, Bekeny, Jenna, Gadek, Margaret, Ward, Tarsha, Zhang, Min, Qiao, Yun, Martin, James F., Seidman, Christine E., Seidman, Jon, Christoffels, Vincent, Efimov, Igor R., McNally, Elizabeth M., Weber, Christopher R., Moskowitz, Ivan P.
Publicado no Sci Transl Med (2016)

Loss-of-Function Mutations in PTPN11 Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome

Por Bowen, Margot E., Boyden, Eric D., Holm, Ingrid A., Campos-Xavier, Belinda, Bonafé, Luisa, Superti-Furga, Andrea, Ikegawa, Shiro, Cormier-Daire, Valerie, Bovée, Judith V., Pansuriya, Twinkal C., de Sousa, Sérgio B., Savarirayan, Ravi, Andreucci, Elena, Vikkula, Miikka, Garavelli, Livia, Pottinger, Caroline, Ogino, Toshihiko, Sakai, Akinori, Regazzoni, Bianca M., Wuyts, Wim, Sangiorgi, Luca, Pedrini, Elena, Zhu, Mei, Kozakewich, Harry P., Kasser, James R., Seidman, Jon G., Kurek, Kyle C., Warman, Matthew L.
Publicado em 2011