Transcription factor haploinsufficiency: when half a loaf is not enough

Por Seidman, J.G., Seidman, Christine
Publicado em 2002

Identifying Sarcomere Gene Mutations in HCM: A Personal History

Por Seidman, Christine E., Seidman, J.G.
Publicado em 2011

The impact of genetic testing on hypertrophic cardiomyopathy and heart failure (As of 12072009 by HIRO)

Por Morita, Hiroyuki, Nagai, Ryozo, Seidman, JG, Seidman, Christine E
Publicado em 2010

Hypertrophic cardiomyopathy: Translating cellular cross talk into therapeutics

Por Teekakirikul, Polakit, Padera, Robert F., Seidman, J.G., Seidman, Christine E.
Publicado em 2012

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

Por Kasahara, Hideko, Lee, Bora, Schott, Jean-Jacques, Benson, D. Woodrow, Seidman, J.G., Seidman, Christine E., Izumo, Seigo
Publicado em 2000

Eya4-deficient mice are a model for heritable otitis media

Por Depreux, Frederic F.S., Darrow, Keith, Conner, David A., Eavey, Roland D., Liberman, M. Charles, Seidman, Christine E., Seidman, J.G.
Publicado em 2008

Sequencing of TGF-β pathway genes in familial cases of intracranial aneurysm

Por Santiago-Sim, Teresa, Mathew-Joseph, Sumy, Pannu, Hariyadarshi, Milewicz, Dianna M., Seidman, Christine E., Seidman, J.G., Kim, Dong H.
Publicado em 2009

Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis

Por Delgado-Olguín, Paul, Huang, Yu, Li, Xue, Christodoulou, Danos, Seidman, Christine E., Seidman, J.G., Tarakhovsky, Alexander, Bruneau, Benoit G.
Publicado em 2012

β–Myosin Heavy Chain Variant Met606Val Causes Very Mild Hypertrophic Cardiomyopathy in Mice, but Exacerbates HCM Phenotypes in Mice Carrying Other HCM Mutations

Por Blankenburg, Robert, Hackert, Katarzyna, Wurster, Sebastian, Deenen, René, Seidman, J.G., Seidman, Christine E., Lohse, Martin J., Schmitt, Joachim P.
Publicado em 2014

Cardiac Myosin Binding Protein-C Is Essential for Thick-Filament Stability and Flexural Rigidity

Por Nyland, Lori R., Palmer, Bradley M., Chen, Zengyi, Maughan, David W., Seidman, Christine E., Seidman, J.G., Kreplak, Laurent, Vigoreaux, Jim O.
Publicado em 2009

Pheochromocytoma-Induced Cardiomyopathy is Modulated by the Synergistic Effects of Cell-Secreted Factors: Mobine. Cell-Secreted Factors in Pheo-Induced CM

Por Mobine, Hector R., Baker, Aaron B., Wang, Libin, Wakimoto, Hiroko, Jacobsen, Kurt C., Seidman, Christine E., Seidman, J.G., Edelman, Elazer R.
Publicado em 2009

Dynamic Cellular Integration Drives Functional Assembly of the Heart’s Pacemaker Complex

Por Bressan, Michael, Henley, Trevor, Louie, Jonathan D., Liu, Gary, Christodoulou, Danos, Bai, Xue, Taylor, Joan, Seidman, Christine E., Seidman, J.G., Mikawa, Takashi
Publicado no Cell Rep (2018)

Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

Por Morita, Hiroyuki, Rehm, Heidi L., Menesses, Andres, McDonough, Barbara, Roberts, Amy E., Kucherlapati, Raju, Towbin, Jeffrey A., Seidman, J.G., Seidman, Christine E.
Publicado em 2008

Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene

Por Fatkin, Diane, Christe, Michael E., Aristizabal, Orlando, McConnell, Bradley K., Srinivasan, Shardha, Schoen, Frederick J., Seidman, Christine E., Turnbull, Daniel H., Seidman, J.G.
Publicado em 1999

Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia

Por Song, Lei, Alcalai, Ronny, Arad, Michael, Wolf, Cordula M., Toka, Okan, Conner, David A., Berul, Charles I., Eldar, Michael, Seidman, Christine E., Seidman, J.G.
Publicado em 2007

An abnormal Ca(2+) response in mutant sarcomere protein–mediated familial hypertrophic cardiomyopathy

Por Fatkin, Diane, McConnell, Bradley K., Mudd, James O., Semsarian, Christopher, Moskowitz, Ivan G.P., Schoen, Frederick J., Giewat, Michael, Seidman, Christine E., Seidman, J.G.
Publicado em 2000

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

Por Arad, Michael, Benson, D. Woodrow, Perez-Atayde, Antonio R., McKenna, William J., Sparks, Elizabeth A., Kanter, Ronald J., McGarry, Kate, Seidman, J.G., Seidman, Christine E.
Publicado em 2002

UBQLN2 Mutation Causing Heterogeneous X-linked Dominant Neurodegeneration

Por Fahed, Akl C., McDonough, Barbara, Gouvion, Cynthia M., Newell, Kathy L., Dure, Leon S., Bebin, Martina, Bick, Alexander G., Seidman, J.G., Harter, Donald H., Seidman, Christine E.
Publicado em 2014

Reversibility of PRKAG2 Glycogen-Storage Cardiomyopathy and Electrophysiological Manifestations

Por Wolf, Cordula M., Arad, Michael, Ahmad, Ferhaan, Sanbe, Atsushi, Bernstein, Scott A., Toka, Okan, Konno, Tetsuo, Morley, Gregory, Robbins, Jeffrey, Seidman, J.G., Seidman, Christine E., Berul, Charles I.
Publicado em 2007

A Classic Twin Study of External Ear Malformations, Including Microtia

Por Artunduaga, Maria A., Quintanilla-Dieck, Maria D.L., Greenway, Steven, Betensky, Rebecca, Nicolau, Yamileth, Hamdan, Usama, Jarrin, Patricia, Osorno, Gabriel, Brent, Burt, Eavey, Roland, Seidman, Christine, Seidman, J.G.
Publicado em 2009