Ngā hua rapu - Conner, David A

β-Arrestin 1 and 2 differentially regulate heptahelical receptor signaling and trafficking mā Kohout, Trudy A., Lin, Fang-Tsyr, Perry, Stephen J., Conner, David A., Lefkowitz, Robert J.

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Eya4-deficient mice are a model for heritable otitis media mā 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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CRISPR/Cas9 Mediated Fluorescent Tagging of Endogenous Proteins in Human Pluripotent Stem Cells mā Sharma, Arun, Toepfer, Christopher N., Ward, Tarsha, Wasson, Lauren, Agarwal, Radhika, Conner, David A., Hu, Johnny H., Seidman, Christine E.

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Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia mā 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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Impaired lymphatic contraction associated with immunosuppression mā 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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Cardiac myosin missense mutations cause dilated cardiomyopathy in mouse models and depress molecular motor function mā 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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Surfactant Protein–C Chromatin-Bound Green Fluorescence Protein Reporter Mice Reveal Heterogeneity of Surfactant Protein C–Expressing Lung Cells mā 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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Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome–associated PTPN11 mutation mā 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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Molecular profiling of dilated cardiomyopathy that progresses to heart failure mā 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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LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart mā 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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Lamin A/C Haploinsufficiency Causes Dilated Cardiomyopathy and Apoptosis-Triggered Cardiac Conduction System Disease mā 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, JG

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BET bromodomain proteins regulate transcriptional reprogramming in genetic dilated cardiomyopathy mā 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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Cardiomyopathy in Irx4-Deficient Mice Is Preceded by Abnormal Ventricular Gene Expression mā Bruneau, Benoit G., Bao, Zheng-Zheng, Fatkin, Diane, Xavier-Neto, Jose, Georgakopoulos, Dimitrios, Maguire, Colin T., Berul, Charles I., Kass, David A., Kuroski-de Bold, Mercedes L., de Bold, Adolfo J., Conner, David A., Rosenthal, Nadia, Cepko, Constance L., 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 mā 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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5′RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy mā 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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Ablation of lysophosphatidic acid receptor 1 attenuates hypertrophic cardiomyopathy in a mouse model mā Axelsson Raja, Anna, 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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