Impaired lymphatic contraction associated with immunosuppression von Liao, Shan, Cheng, Gang, Conner, David A., Huang, Yuhui, Kucherlapati, Raju S., Munn, Lance L., Ruddle, Nancy H., Jain, Rakesh K., Fukumura, Dai, Padera, Timothy P.

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Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome-associated PTPN11 mutation von Marin, Talita M, Keith, Kimberly, Davies, Benjamin, Conner, David A, Guha, Prajna, Kalaitzidis, Demetrios, Wu, Xue, Lauriol, Jessica, Wang, Bo, Bauer, Michael, Bronson, Roderick, Franchini, Kleber G, Neel, Benjamin G, Kontaridis, Maria I

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Regulation of tendon differentiation by scleraxis distinguishes force-transmitting tendons from muscle-anchoring tendons von Murchison, Nicholas D, Price, Brian A, Conner, David A, Keene, Douglas R, Olson, Eric N, Tabin, Clifford J, Schweitzer, Ronen

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Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model von Raja, Anna Axelsson, Wakimoto, Hiroko, DeLaughter, Daniel M., Reichart, Daniel, Gorham, Joshua, Conner, David A., Lun, Mingyue, Probst, Clemens K., Sakai, Norihiko, Knipe, Rachel S., Montesi, Sydney B., Shea, Barry, Adam, Leonard P., Leinwand, Leslie A., Wan, William, Choi, Esther Sue, Lindberg, Eric L., Patone, Giannino, Noseda, Michela, Hübner, Norbert, Seidman, Christine E., Tager, Andrew M., Seidman, J. G., Ho, Carolyn Y.

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Wnt9a signaling is required for joint integrity and regulation of Ihh during chondrogenesis von Später, Daniela, Hill, Theo P., O'Sullivan, Roderick J., Gruber, Michaela, Conner, David A., Hartmann, Christine

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

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Surfactant protein-C chromatin-bound green fluorescence protein reporter mice reveal heterogeneity of surfactant protein C-expressing lung cells von Lee, Joo-Hyeon, Kim, Jonghwan, Gludish, David, Roach, Rebecca R, Saunders, Arven H, Barrios, Juliana, Woo, Andrew Jonghan, Chen, Huaiyong, Conner, David A, Fujiwara, Yuko, Stripp, Barry R, Kim, Carla F

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Lamin A/C haploinsufficiency causes dilated cardiomyopathy and apoptosis-triggered cardiac conduction system disease von Wolf, Cordula M, Wang, Libin, Alcalai, Ronny, Pizard, Anne, Burgon, Patrick G, Ahmad, Ferhaan, Sherwood, Megan, Branco, Dorothy M, Wakimoto, Hiroko, Fishman, Glenn I, See, Vincent, Stewart, Colin L, Conner, David A, Berul, Charles I, Seidman, Christine E, Seidman, J.G

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β-Arrestin 1 and 2 Differentially Regulate Heptahelical Receptor Signaling and Trafficking von Kohout, Trudy A., Lin, Fang-Tsyr, Perry, Stephen J., Conner, David A., Lefkowitz, Robert J.

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Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice von Reichart, Daniel, Newby, Gregory A., Wakimoto, Hiroko, Lun, Mingyue, Gorham, Joshua M., Curran, Justin J., Raguram, Aditya, DeLaughter, Daniel M., Conner, David A., Marsiglia, Júlia D. C., Kohli, Sajeev, Chmatal, Lukas, Page, David C., Zabaleta, Nerea, Vandenberghe, Luk, Liu, David R., Seidman, Jonathan G., Seidman, Christine

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Cardiac Myosin Missense Mutations Cause Dilated Cardiomyopathy in Mouse Models and Depress Molecular Motor Function von Schmitt, Joachim P., Debold, Edward P., Ahmad, Ferhaan, Armstrong, Amy, Frederico, Andrea, Conner, David A., Mende, Ulrike, Lohse, Martin J., Warshaw, David, Seidman, Christine E., Seidman, J. G.

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The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy von Ahmad, Ferhaan, Banerjee, Sanjay K, Lage, Michele L, Huang, Xueyin N, Smith, Stephen H, Saba, Samir, Rager, Jennifer, Conner, David A, Janczewski, Andrzej M, Tobita, Kimimasa, Tinney, Joseph P, Moskowitz, Ivan P, Perez-Atayde, Antonio R, Keller, Bradley B, Mathier, Michael A, Shroff, Sanjeev G, Seidman, Christine E, Seidman, J G

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A Mouse Model of Familial Hypertrophic Cardiomyopathy von Anja A. T. Geisterfer-Lowrance, Christe, Michael, Conner, David A., Ingwall, Joanne S., Schoen, Frederick J., Seidman, Christine E., Seidman, J. G.

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LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart von Alcalai, Ronny, Arad, Michael, Wakimoto, Hiroko, Yadin, Dor, Gorham, Joshua, Wang, Libin, Burns, Elia, Maron, Barry J, Roberts, William C, Konno, Tetsuo, Conner, David A, Perez-Atayde, Antonio R, Seidman, Jon G, Seidman, Christine E

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beta-Arrestin1 Knockout Mice Appear Normal but Demonstrate Altered Cardiac Responses to beta-Adrenergic Stimulation von Conner, David. A, Mathier, Michael A, Mortensen, Richard M, Christe, Michael, Vatner, Stephen F, Seidman, Christine E, Seidman, J.G

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CRISPR/Cas9‐Mediated Fluorescent Tagging of Endogenous Proteins in Human Pluripotent Stem Cells von Sharma, Arun, Toepfer, Christopher N., Ward, Tarsha, Wasson, Lauren, Agarwal, Radhika, Conner, David A., Hu, Johnny H., Seidman, Christine E.

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5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy von Christodoulou, Danos C, Wakimoto, Hiroko, Onoue, Kenji, Eminaga, Seda, Gorham, Joshua M, DePalma, Steve R, Herman, Daniel S, Teekakirikul, Polakit, Conner, David A, McKean, David M, Domenighetti, Andrea A, Aboukhalil, Anton, Chang, Stephen, Srivastava, Gyan, McDonough, Barbara, De Jager, Philip L, Chen, Ju, Bulyk, Martha L, Muehlschlegel, Jochen D, Seidman, Christine E, Seidman, J G

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Molecular profiling of dilated cardiomyopathy that progresses to heart failure von Burke, Michael A, Chang, Stephen, Wakimoto, Hiroko, Gorham, Joshua M, Conner, David A, Christodoulou, Danos C, Parfenov, Michael G, DePalma, Steve R, Eminaga, Seda, Konno, Tetsuo, Seidman, Jonathan G, Seidman, Christine E

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BET bromodomain proteins regulate transcriptional reprogramming in genetic dilated cardiomyopathy von Antolic, Andrew, Wakimoto, Hiroko, Jiao, Zhe, Gorham, Joshua M, DePalma, Steven R, Lemieux, Madeleine E, Conner, David A, Lee, Da Young, Qi, Jun, Seidman, Jonathan G, Bradner, James E, Brown, Jonathan D, Haldar, Saptarsi M, Seidman, Christine E, Burke, Michael A

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Eya4-deficient mice are a model for heritable otitis media von Depreux, Frederic F S, Darrow, Keith, Conner, David A, Eavey, Roland D, Liberman, M Charles, Seidman, Christine E, Seidman, J G

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