Transcription factor haploinsufficiency: when half a loaf is not enough

Tekijä Seidman, J.G., Seidman, Christine
Julkaistu 2002

Identifying Sarcomere Gene Mutations in HCM: A Personal History

Tekijä Seidman, Christine E., Seidman, J.G.
Julkaistu 2011

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

Tekijä Morita, Hiroyuki, Nagai, Ryozo, Seidman, JG, Seidman, Christine E
Julkaistu 2010

Hypertrophic cardiomyopathy: Translating cellular cross talk into therapeutics

Tekijä Teekakirikul, Polakit, Padera, Robert F., Seidman, J.G., Seidman, Christine E.
Julkaistu 2012

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

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

Eya4-deficient mice are a model for heritable otitis media

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

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

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

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

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

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

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

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

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

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

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

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

Tekijä Bressan, Michael, Henley, Trevor, Louie, Jonathan D., Liu, Gary, Christodoulou, Danos, Bai, Xue, Taylor, Joan, Seidman, Christine E., Seidman, J.G., Mikawa, Takashi
Julkaisussa Cell Rep (2018)

Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults

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

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

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

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

Tekijä 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.
Julkaistu 2007

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

Tekijä 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.
Julkaistu 2000

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

Tekijä 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.
Julkaistu 2002

UBQLN2 Mutation Causing Heterogeneous X-linked Dominant Neurodegeneration

Tekijä 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.
Julkaistu 2014

Reversibility of PRKAG2 Glycogen-Storage Cardiomyopathy and Electrophysiological Manifestations

Tekijä 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.
Julkaistu 2007

A Classic Twin Study of External Ear Malformations, Including Microtia

Tekijä 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.
Julkaistu 2009