Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease von Bosse, Kevin, Hans, Chetan P, Zhao, Ning, Koenig, Sara N, Huang, Nianyuan, Guggilam, Anuradha, LaHaye, Stephanie, Tao, Ge, Lucchesi, Pamela A, Lincoln, Joy, Lilly, Brenda, Garg, Vidu

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Isolation and characterization of a SARS-CoV-2 variant with a Q677H mutation in the spike protein von Niu, Xiaoyu, Xu, Jiayu, Liu, Mingde, Tu, Huolin, Koenig, Sara N., Saif, Linda J., Jones, Daniel M., Wang, Qiuhong

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Inhibitory role of Notch1 in calcific aortic valve disease von Acharya, Asha, Hans, Chetan P, Koenig, Sara N, Nichols, Haley A, Galindo, Cristi L, Garner, Harold R, Merrill, Walter H, Hinton, Robert B, Garg, Vidu

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Novel Identification of Ankyrin-R in Cardiac Fibroblasts and a Potential Role in Heart Failure von Argall, Aaron D, Sucharski-Argall, Holly C, Comisford, Luke G, Jurs, Sallie J, Seminetta, Jack T, Wallace, Michael J, Crawford, Casey A, Takenaka, Sarah S, Han, Mei, El Refaey, Mona, Hund, Thomas J, Mohler, Peter J, Koenig, Sara N

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Endothelial Notch1 Is Required for Proper Development of the Semilunar Valves and Cardiac Outflow Tract von Koenig, Sara N., Bosse, Kevin, Majumdar, Uddalak, Bonachea, Elizabeth M., Radtke, Freddy, Garg, Vidu

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Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo von Misra, Chaitali, Sachan, Nita, McNally, Caryn Rothrock, Koenig, Sara N, Nichols, Haley A, Guggilam, Anuradha, Lucchesi, Pamela A, Pu, William T, Srivastava, Deepak, Garg, Vidu

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Developmental origins for semilunar valve stenosis identified in mice harboring congenital heart disease-associated GATA4 mutation von LaHaye, Stephanie, Majumdar, Uddalak, Yasuhara, Jun, Koenig, Sara N, Matos-Nieves, Adrianna, Kumar, Rahul, Garg, Vidu

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Humanized Dsp ACM Mouse Model Displays Stress-Induced Cardiac Electrical and Structural Phenotypes von Stevens, Tyler L, Manring, Heather R, Wallace, Michael J, Argall, Aaron, Dew, Trevor, Papaioannou, Peter, Antwi-Boasiako, Steve, Xu, Xianyao, Campbell, Stuart G, Akar, Fadi G, Borzok, Maegen A, Hund, Thomas J, Mohler, Peter J, Koenig, Sara N, El Refaey, Mona

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Mechanisms and Alterations of Cardiac Ion Channels Leading to Disease: Role of Ankyrin-B in Cardiac Function von Sucharski, Holly C., Dudley, Emma K., Keith, Caullin B. R., El Refaey, Mona, Koenig, Sara N., Mohler, Peter J.

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Arrhythmogenic Cardiomyopathy: Molecular Insights for Improved Therapeutic Design von Stevens, Tyler L., Wallace, Michael J., El Refaey, Mona, Roberts, Jason D., Koenig, Sara N., Mohler, Peter J.

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Notch1 haploinsufficiency causes ascending aortic aneurysms in mice von Koenig, Sara N, LaHaye, Stephanie, Feller, James D, Rowland, Patrick, Hor, Kan N, Trask, Aaron J, Janssen, Paul Ml, Radtke, Freddy, Lilly, Brenda, Garg, Vidu

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Altered Expression of Zonula occludens-1 Affects Cardiac Na + Channels and Increases Susceptibility to Ventricular Arrhythmias von El Refaey, Mona, Coles, Sara, Musa, Hassan, Stevens, Tyler L, Wallace, Michael J, Murphy, Nathaniel P, Antwi-Boasiako, Steve, Young, Lindsay J, Manring, Heather R, Curran, Jerry, Makara, Michael A, Sas, Kelli, Han, Mei, Koenig, Sara N, Skaf, Michel, Kline, Crystal F, Janssen, Paul M L, Accornero, Federica, Borzok, Maegen A, Mohler, Peter J

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The evolving role of ankyrin-B in cardiovascular disease von Koenig, Sara N., Mohler, Peter J.

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Genetic basis of aortic valvular disease von Koenig, Sara N, Lincoln, Joy, Garg, Vidu

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Evidence of Aortopathy in Mice with Haploinsufficiency of Notch1 in Nos3 -Null Background von Koenig, Sara N, Bosse, Kevin M, Nadorlik, Holly A, Lilly, Brenda, Garg, Vidu

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Identification of GATA6 Sequence Variants in Patients With Congenital Heart Defects von Maitra, Meenakshi, Koenig, Sara N, Srivastava, Deepak, Garg, Vidu

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Dynamic Heterogeneity of the Heart Valve Interstitial Cell Population in Mitral Valve Health and Disease von Horne, Tori E, VandeKopple, Matthew, Sauls, Kimberly, Koenig, Sara N, Anstine, Lindsey J, Garg, Vidu, Norris, Russell A, Lincoln, Joy

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MicroRNA miR145 Regulates TGFBR2 Expression and Matrix Synthesis in Vascular Smooth Muscle Cells von Zhao, Ning, Koenig, Sara N, Trask, Aaron J, Lin, Cho-Hao, Hans, Chetan P, Garg, Vidu, Lilly, Brenda

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Aberrant Expression of a Non-muscle RBFOX2 Isoform Triggers Cardiac Conduction Defects in Myotonic Dystrophy von Misra, Chaitali, Bangru, Sushant, Lin, Feikai, Lam, Kin, Koenig, Sara N., Lubbers, Ellen R., Hedhli, Jamila, Murphy, Nathaniel P., Parker, Darren J., Dobrucki, Lawrence W., Cooper, Thomas A., Tajkhorshid, Emad, Mohler, Peter J., Kalsotra, Auinash

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Potential use of ivabradine for treatment of atrial fibrillation von Koenig, Sara N., Mohler, Peter J.

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