Connective tissue growth factor dependent collagen gene expression induced by MAS agonist AR234960 in human cardiac fibroblasts

por Chatterjee, Arunachal, Barnard, John, Moravec, Christine, Desnoyer, Russell, Tirupula, Kalyan, Karnik, Sadashiva S.
Publicado 2017

KChIP2 is a core transcriptional regulator of cardiac excitability

por Nassal, Drew M, Wan, Xiaoping, Liu, Haiyan, Maleski, Danielle, Ramirez-Navarro, Angelina, Moravec, Christine S, Ficker, Eckhard, Laurita, Kenneth R, Deschênes, Isabelle
Publicado 2017

Bayesian integration of genetics and epigenetics detects causal regulatory SNPs underlying expression variability

por Das, Avinash, Morley, Michael, Moravec, Christine S., Tang, W. H. W., Hakonarson, Hakon, Margulies, Kenneth B., Cappola, Thomas P., Jensen, Shane, Hannenhalli, Sridhar
Publicado 2015

Cardiomyocyte contractile impairment in heart failure results from reduced BAG3-mediated sarcomeric protein turnover

por Martin, Thomas G., Myers, Valerie D., Dubey, Praveen, Dubey, Shubham, Perez, Edith, Moravec, Christine S., Willis, Monte S., Feldman, Arthur M., Kirk, Jonathan A.
Publicado 2021

MetaDiff: differential isoform expression analysis using random-effects meta-regression

por Jia, Cheng, Guan, Weihua, Yang, Amy, Xiao, Rui, Tang, W. H. Wilson, Moravec, Christine S., Margulies, Kenneth B., Cappola, Thomas P., Li, Chun, Li, Mingyao
Publicado 2015

Genomic selection of reference genes for real-time PCR in human myocardium

por Pilbrow, Anna P, Ellmers, Leigh J, Black, Michael A, Moravec, Christine S, Sweet, Wendy E, Troughton, Richard W, Richards, A Mark, Frampton, Chris M, Cameron, Vicky A
Publicado 2008

Association of Noninvasively Measured Left Ventricular Mechanics With In Vitro Muscle Contractile Performance: A Prospective Study in Hypertrophic Cardiomyopathy Patients

por Dhillon, Ashwat, Sweet, Wendy, Popovic, Zoran B., Smedira, Nicholas G., Thamilarasan, Maran, Lytle, Bruce W., Tan, Carmela, Starling, Randall C., Lever, Harry M., Moravec, Christine S., Desai, Milind Y.
Publicado 2014

Atrial Fibrillation Associated Chromosome 4q25 Variants Are Not Associated with PITX2c Expression in Human Adult Left Atrial Appendages

por Gore-Panter, Shamone R., Hsu, Jeffery, Hanna, Peter, Gillinov, A. Marc, Pettersson, Gosta, Newton, David W., Moravec, Christine S., Van Wagoner, David R., Chung, Mina K., Barnard, John, Smith, Jonathan D.
Publicado 2014

The rs11515 Polymorphism Is More Frequent and Associated With Aggressive Breast Tumors with Increased ANRIL and Decreased p16(INK4a) Expression

por Royds, Janice A., Pilbrow, Anna P., Ahn, Antonio, Morrin, Helen R., Frampton, Chris, Russell, I. Alasdair, Moravec, Christine S., Sweet, Wendy E., Tang, W. H. Wilson, Currie, Margaret J., Hung, Noelyn A., Slatter, Tania L.
Publicado 2016

A unique microRNA profile in end-stage heart failure indicates alterations in specific cardiovascular signaling networks

por Naga Prasad, Sathyamangla V., Gupta, Manveen K., Duan, Zhong-Hui, Surampudi, Venkata Suresh K., Liu, Chang-Gong, Kotwal, Ashwin, Moravec, Christine S., Starling, Randall C., Perez, Dianne M., Sen, Subha, Wu, Qingyu, Plow, Edward F., Karnik, Sadashiva
Publicado 2017

Yes-Associated Protein (Yap) Is Up-Regulated in Heart Failure and Promotes Cardiac Fibroblast Proliferation

por Sharifi-Sanjani, Maryam, Berman, Mariah, Goncharov, Dmitry, Alhamaydeh, Mohammad, Avolio, Theodore Guy, Baust, Jeffrey, Chang, Baojun, Kobir, Ahasanul, Ross, Mark, St. Croix, Claudette, Nouraie, Seyed Mehdi, McTiernan, Charles F., Moravec, Christine S., Goncharova, Elena, Al Ghouleh, Imad
Publicado 2021

Novel and Annotated Long Noncoding RNAs Associated with Ischemia in the Human Heart

por Ward, Zoe, Schmeier, Sebastian, Saddic, Louis, Sigurdsson, Martin I., Cameron, Vicky A., Pearson, John, Miller, Allison, Morley-Bunker, Arthur, Gorham, Josh, Seidman, Jonathan G., Moravec, Christine S., Sweet, Wendy E., Aranki, Sary F., Body, Simon, Muehlschlegel, Jochen D., Pilbrow, Anna P.
Publicado 2021

The Chromosome 9p21.3 Coronary Heart Disease Risk Allele Is Associated with Altered Gene Expression in Normal Heart and Vascular Tissues

por Pilbrow, Anna P., Folkersen, Lasse, Pearson, John F., Brown, Chris M., McNoe, Les, Wang, Nancy M., Sweet, Wendy E., Tang, W. H. Wilson, Black, Michael A., Troughton, Richard W., Richards, A. Mark, Franco-Cereceda, Anders, Gabrielsen, Anders, Eriksson, Per, Moravec, Christine S., Cameron, Vicky A.
Publicado 2012

Epistasis regulates genetic control of cardiac hypertrophy

por Wang, Qianru, Tang, Tiffany, Youlton, Nathan, Weldy, Chad, Kenney, Ana, Ronen, Omer, Hughes, John, Chin, Elizabeth, Sutton, Shirley, Agarwal, Abhineet, Li, Xiao, Behr, Merle, Kumbier, Karl, Moravec, Christine, Tang, W. H. Wilson, Margulies, Kenneth, Cappola, Thomas, Butte, Atul, Arnaout, Rima, Brown, James, Priest, James, Parikh, Victoria, Yu, Bin, Ashley, Euan
Publicado 2023

Epistasis regulates genetic control of cardiac hypertrophy

por Wang, Qianru, Tang, Tiffany M., Youlton, Nathan, Weldy, Chad S., Kenney, Ana M., Ronen, Omer, Hughes, J. Weston, Chin, Elizabeth T., Sutton, Shirley C., Agarwal, Abhineet, Li, Xiao, Behr, Merle, Kumbier, Karl, Moravec, Christine S., Tang, W. H. Wilson, Margulies, Kenneth B., Cappola, Thomas P., Butte, Atul J., Arnaout, Rima, Brown, James B., Priest, James R., Parikh, Victoria N., Yu, Bin, Ashley, Euan A.
Publicado 2023

Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failure

por Cordero, Pablo, Parikh, Victoria N., Chin, Elizabeth T., Erbilgin, Ayca, Gloudemans, Michael J., Shang, Ching, Huang, Yong, Chang, Alex C., Smith, Kevin S., Dewey, Frederick, Zaleta, Kathia, Morley, Michael, Brandimarto, Jeff, Glazer, Nicole, Waggott, Daryl, Pavlovic, Aleksandra, Zhao, Mingming, Moravec, Christine S., Tang, W. H. Wilson, Skreen, Jamie, Malloy, Christine, Hannenhalli, Sridhar, Li, Hongzhe, Ritter, Scott, Li, Mingyao, Bernstein, Daniel, Connolly, Andrew, Hakonarson, Hakon, Lusis, Aldons J., Margulies, Kenneth B., Depaoli-Roach, Anna A., Montgomery, Stephen B., Wheeler, Matthew T., Cappola, Thomas, Ashley, Euan A.
Publicado 2019

Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure

por Smith, J. Gustav, Felix, Janine F., Morrison, Alanna C., Kalogeropoulos, Andreas, Trompet, Stella, Wilk, Jemma B., Gidlöf, Olof, Wang, Xinchen, Morley, Michael, Mendelson, Michael, Joehanes, Roby, Ligthart, Symen, Shan, Xiaoyin, Bis, Joshua C., Wang, Ying A., Sjögren, Marketa, Ngwa, Julius, Brandimarto, Jeffrey, Stott, David J., Aguilar, David, Rice, Kenneth M., Sesso, Howard D., Demissie, Serkalem, Buckley, Brendan M., Taylor, Kent D., Ford, Ian, Yao, Chen, Liu, Chunyu, Sotoodehnia, Nona, van der Harst, Pim, Stricker, Bruno H. Ch., Kritchevsky, Stephen B., Liu, Yongmei, Gaziano, J. Michael, Hofman, Albert, Moravec, Christine S., Uitterlinden, André G., Kellis, Manolis, van Meurs, Joyce B., Margulies, Kenneth B., Dehghan, Abbas, Levy, Daniel, Olde, Björn, Psaty, Bruce M., Cupples, L. Adrienne, Jukema, J. Wouter, Djousse, Luc, Franco, Oscar H., Boerwinkle, Eric, Boyer, Laurie A., Newton-Cheh, Christopher, Butler, Javed, Vasan, Ramachandran S., Cappola, Thomas P., Smith, Nicholas L.
Publicado 2016

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

por Arking, Dan E., Pulit, Sara L., Crotti, Lia, van der Harst, Pim, Munroe, Patricia B., Koopmann, Tamara T., Sotoodehnia, Nona, Rossin, Elizabeth J., Morley, Michael, Wang, Xinchen, Johnson, Andrew D., Lundby, Alicia, Gudbjartsson, Daníel F., Noseworthy, Peter A., Eijgelsheim, Mark, Bradford, Yuki, Tarasov, Kirill V., Dörr, Marcus, Müller-Nurasyid, Martina, Lahtinen, Annukka M., Nolte, Ilja M., Smith, Albert Vernon, Bis, Joshua C., Isaacs, Aaron, Newhouse, Stephen J., Evans, Daniel S., Post, Wendy S., Waggott, Daryl, Lyytikäinen, Leo-Pekka, Hicks, Andrew A., Eisele, Lewin, Ellinghaus, David, Hayward, Caroline, Navarro, Pau, Ulivi, Sheila, Tanaka, Toshiko, Tester, David J., Chatel, Stéphanie, Gustafsson, Stefan, Kumari, Meena, Morris, Richard W., Naluai, Åsa T., Padmanabhan, Sandosh, Kluttig, Alexander, Strohmer, Bernhard, Panayiotou, Andrie G., Torres, Maria, Knoflach, Michael, Hubacek, Jaroslav A., Slowikowski, Kamil, Raychaudhuri, Soumya, Kumar, Runjun D., Harris, Tamara B., Launer, Lenore J., Shuldiner, Alan R., Alonso, Alvaro, Bader, Joel S., Ehret, Georg, Huang, Hailiang, Kao, W.H. Linda, Strait, James B., Macfarlane, Peter W., Brown, Morris, Caulfield, Mark J., Samani, Nilesh J., Kronenberg, Florian, Willeit, Johann, Smith, J. Gustav, Greiser, Karin H., zu Schwabedissen, Henriette Meyer, Werdan, Karl, Carella, Massimo, Zelante, Leopoldo, Heckbert, Susan R., Psaty, Bruce M., Rotter, Jerome I., Kolcic, Ivana, Polašek, Ozren, Wright, Alan F., Griffin, Maura, Daly, Mark J., Arnar, David O., Hólm, Hilma, Thorsteinsdottir, Unnur, Denny, Joshua C., Roden, Dan M., Zuvich, Rebecca L., Emilsson, Valur, Plump, Andrew S., Larson, Martin G., O'Donnell, Christopher J., Yin, Xiaoyan, Bobbo, Marco, D'Adamo, Adamo P., Iorio, Annamaria, Sinagra, Gianfranco, Carracedo, Angel, Cummings, Steven R., Nalls, Michael A., Jula, Antti, Kontula, Kimmo K., Marjamaa, Annukka, Oikarinen, Lasse, Perola, Markus, Porthan, Kimmo, Erbel, Raimund, Hoffmann, Per, Jöckel, Karl-Heinz, Kälsch, Hagen, Nöthen, Markus M., consortium, HRGEN, den Hoed, Marcel, Loos, Ruth J.F., Thelle, Dag S., Gieger, Christian, Meitinger, Thomas, Perz, Siegfried, Peters, Annette, Prucha, Hanna, Sinner, Moritz F., Waldenberger, Melanie, de Boer, Rudolf A., Franke, Lude, van der Vleuten, Pieter A., Beckmann, Britt Maria, Martens, Eimo, Bardai, Abdennasser, Hofman, Nynke, Wilde, Arthur A.M., Behr, Elijah R., Dalageorgou, Chrysoula, Giudicessi, John R., Medeiros-Domingo, Argelia, Barc, Julien, Kyndt, Florence, Probst, Vincent, Ghidoni, Alice, Insolia, Roberto, Hamilton, Robert M., Scherer, Stephen W., Brandimarto, Jeffrey, Margulies, Kenneth, Moravec, Christine E., Fabiola Del, Greco M., Fuchsberger, Christian, O'Connell, Jeffrey R., Lee, Wai K., Watt, Graham C.M., Campbell, Harry, Wild, Sarah H., El Mokhtari, Nour E., Frey, Norbert, Asselbergs, Folkert W., Leach, Irene Mateo, Navis, Gerjan, van den Berg, Maarten P., van Veldhuisen, Dirk J., Kellis, Manolis, Krijthe, Bouwe P., Franco, Oscar H., Hofman, Albert, Kors, Jan A., Uitterlinden, André G., Witteman, Jacqueline C.M., Kedenko, Lyudmyla, Lamina, Claudia, Oostra, Ben A., Abecasis, Gonçalo R., Lakatta, Edward G., Mulas, Antonella, Orrú, Marco, Schlessinger, David, Uda, Manuela, Markus, Marcello R.P., Völker, Uwe, Snieder, Harold, Spector, Timothy D., Ärnlöv, Johan, Lind, Lars, Sundström, Johan, Syvänen, Ann-Christine, Kivimaki, Mika, Kähönen, Mika, Mononen, Nina, Raitakari, Olli T., Viikari, Jorma S., Adamkova, Vera, Kiechl, Stefan, Brion, Maria, Nicolaides, Andrew N., Paulweber, Bernhard, Haerting, Johannes, Dominiczak, Anna F., Nyberg, Fredrik, Whincup, Peter H., Hingorani, Aroon, Schott, Jean-Jacques, Bezzina, Connie R., Ingelsson, Erik, Ferrucci, Luigi, Gasparini, Paolo, Wilson, James F., Rudan, Igor, Franke, Andre, Mühleisen, Thomas W., Pramstaller, Peter P., Lehtimäki, Terho J., Paterson, Andrew D., Parsa, Afshin, Liu, Yongmei, van Duijn, Cornelia, Siscovick, David S., Gudnason, Vilmundur, Jamshidi, Yalda, Salomaa, Veikko, Felix, Stephan B., Sanna, Serena, Ritchie, Marylyn D., Stricker, Bruno H., Stefansson, Kari, Boyer, Laurie A., Cappola, Thomas P., Olsen, Jesper V., Lage, Kasper, Schwartz, Peter J., Kääb, Stefan, Chakravarti, Aravinda, Ackerman, Michael J., Pfeufer, Arne, de Bakker, Paul I.W., Newton-Cheh, Christopher
Publicado 2014