Topical Collection on Regenerative Medicine and Stem Cell Therapy: Pluripotent Stem Cells as a Platform for Cardiac Arrhythmia Drug Screening

Por Leyton-Mange, Jordan S., Milan, David J.
Publicado no Curr Treat Options Cardiovasc Med (2014)

Dexamethasone suppresses long QT phenotype in patient with acute promyelocytic leukemia treated with arsenic

Por Winterfield, Jeffrey R., Milan, David J.
Publicado no HeartRhythm Case Rep (2015)

Zebrafish Genetic Models for Arrhythmia

Por Milan, David J., MacRae, Calum A.
Publicado em 2009

Patterning and Development of the Atrioventricular Canal in Zebrafish

Por Peal, David S., Lynch, Stacey N., Milan, David J.
Publicado em 2011

Genome Wide Association Studies in Cardiac Electrophysiology: Recent Discoveries and Implications for Clinical Practice

Por Milan, David J., Lubitz, Steven A., Kääb, Stefan, Ellinor, Patrick T.
Publicado em 2010

Monogenic atrial fibrillation as pathophysiological paradigms

Por Mahida, Saagar, Lubitz, Steven A., Rienstra, Michiel, Milan, David J., Ellinor, Patrick T.
Publicado em 2011

Rapid Cellular Phenotyping of Human Pluripotent Stem Cell-Derived Cardiomyocytes using a Genetically Encoded Fluorescent Voltage Sensor

Por Leyton-Mange, Jordan S., Mills, Robert W., Macri, Vincenzo S., Jang, Min Young, Butte, Faraz N., Ellinor, Patrick T., Milan, David J.
Publicado em 2014

Novel Chemical Suppressors of Long QT Syndrome Identified by an in vivo Functional Screen

Por Peal, David S., Mills, Robert W., Lynch, Stacey N., Mosley, Janet M., Lim, Evi, Elllinor, Patrick T., January, Craig T., Peterson, Randall T., Milan, David J.
Publicado em 2010

Overexpression of KCNN3 results in sudden cardiac death

Por Mahida, Saagar, Mills, Robert W., Tucker, Nathan R., Simonson, Bridget, Macri, Vincenzo, Lemoine, Marc D., Das, Saumya, Milan, David J., Ellinor, Patrick T.
Publicado em 2014

miR-21 represses Pdcd4 during cardiac valvulogenesis

Por Kolpa, Heather J., Peal, David S., Lynch, Stacey N., Giokas, Andrea C., Ghatak, Shibnath, Misra, Suniti, Norris, Russell A., MacRae, Calum A., Markwald, Roger R., Ellinor, Patrick, Bischoff, Joyce, Milan, David J.
Publicado em 2013

Bioengineering Human Myocardium on Native Extracellular Matrix

Por Guyette, Jacques P., Charest, Jonathan M, Mills, Robert W, Jank, Bernhard J., Moser, Philipp T., Gilpin, Sarah E., Gershlak, Joshua R., Okamoto, Tatsuya, Gonzalez, Gabriel, Milan, David J., Gaudette, Glenn R., Ott, Harald C.
Publicado no Circ Res (2015)

A Novel Trafficking-defective HCN4 Mutation is Associated with Early-Onset Atrial Fibrillation

Por Macri, Vincenzo, Mahida, Saagar N., Zhang, Michael L., Sinner, Moritz F., Dolmatova, Elena V., Tucker, Nathan R., McLellan, Micheal, Shea, Marisa A., Milan, David J., Lunetta, Kathryn L., Benjamin, Emelia J., Ellinor, Patrick T.
Publicado em 2014

A Drug-Sensitized Zebrafish Screen Identifies Multiple Genes, Including GINS3, as Regulators of Myocardial Repolarization

Por Milan, David J., Kim, Albert M., Winterfield, Jeffrey R., Jones, Ian L., Pfeufer, Arne, Sanna, Serena, Arking, Dan E., Amsterdam, Adam H., Sabeh, Khaled M., Mably, John D., Rosenbaum, David S., Peterson, Randall T., Chakravarti, Aravinda, Kääb, Stefan, Roden, Dan M., MacRae, Calum A.
Publicado em 2009

Photochemical activation of TRPA1 channels in neurons and animals

Por Kokel, David, Cheung, Chung Yan J., Mills, Robert, Coutinho-Budd, Jaeda, Huang, Liyi, Setola, Vincent, Sprague, Jared, Jin, Shan, Jin, Youngnam N., Huang, Xi-Ping, Bruni, Giancarlo, Woolf, Clifford, Roth, Bryan L., Hamblin, Michael R, Zylka, Mark J., Milan, David J., Peterson, Randall T.
Publicado em 2013

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

Por Sroubek, Jakub, Probst, Vincent, Mazzanti, Andrea, Delise, Pietro, Hevia, Jesus Castro, Ohkubo, Kimie, Zorzi, Alessandro, Champagne, Jean, Kostopoulou, Anna, Yin, Xiaoyan, Napolitano, Carlo, Milan, David J., Wilde, Arthur, Sacher, Frederic, Borggrefe, Martin, Ellinor, Patrick T., Theodorakis, George, Nault, Isabelle, Corrado, Domenico, Watanabe, Ichiro, Antzelevitch, Charles, Allocca, Giuseppe, Priori, Silvia, Lubitz, Steven A.
Publicado no Circulation (2016)

Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

Por Wang, Xinchen, Tucker, Nathan R, Rizki, Gizem, Mills, Robert, Krijger, Peter HL, de Wit, Elzo, Subramanian, Vidya, Bartell, Eric, Nguyen, Xinh-Xinh, Ye, Jiangchuan, Leyton-Mange, Jordan, Dolmatova, Elena V, van der Harst, Pim, de Laat, Wouter, Ellinor, Patrick T, Newton-Cheh, Christopher, Milan, David J, Kellis, Manolis, Boyer, Laurie A
Publicado no eLife (2016)

Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics

Por Lundby, Alicia, Rossin, Elizabeth J., Steffensen, Annette B., Rav Acha, Moshe, Newton-Cheh, Christopher, Pfeufer, Arne, Lynch, Stacey N., Olesen, Søren-Peter, Brunak, Søren, Ellinor, Patrick T., Jukema, J.Wouter, Trompet, Stella, Ford, Ian, Macfarlane, Peter W., Krijthe, Bouwe P., Hofman, Albert, Uitterlinden, Andre G., Stricker, Bruno H., Nathoe, Hendrik M., Spiering, Wilko, Daly, Mark J., Asselbergs, Folkert W., van der Harst, Pim, Milan, David J., de Bakker, Paul I.W., Lage, Kasper, Olsen, Jesper V.
Publicado em 2014

PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance

Por Kiando, Soto Romuald, Tucker, Nathan R., Castro-Vega, Luis-Jaime, Katz, Alexander, D’Escamard, Valentina, Tréard, Cyrielle, Fraher, Daniel, Albuisson, Juliette, Kadian-Dodov, Daniella, Ye, Zi, Austin, Erin, Yang, Min-Lee, Hunker, Kristina, Barlassina, Cristina, Cusi, Daniele, Galan, Pilar, Empana, Jean-Philippe, Jouven, Xavier, Gimenez-Roqueplo, Anne-Paule, Bruneval, Patrick, Hyun Kim, Esther Soo, Olin, Jeffrey W., Gornik, Heather L., Azizi, Michel, Plouin, Pierre-François, Ellinor, Patrick T., Kullo, Iftikhar J., Milan, David J., Ganesh, Santhi K., Boutouyrie, Pierre, Kovacic, Jason C., Jeunemaitre, Xavier, Bouatia-Naji, Nabila
Publicado no PLoS Genet (2016)

Macrophages Facilitate Electrical Conduction in the Heart

Por Hulsmans, Maarten, Clauss, Sebastian, Xiao, Ling, Aguirre, Aaron D., King, Kevin R., Hanley, Alan, Hucker, William J., Wülfers, Eike M., Seemann, Gunnar, Courties, Gabriel, Iwamoto, Yoshiko, Sun, Yuan, Savol, Andrej J., Sager, Hendrik B., Lavine, Kory J., Fishbein, Gregory A., Capen, Diane E., Da Silva, Nicolas, Miquerol, Lucile, Wakimoto, Hiroko, Seidman, Christine E., Seidman, Jonathan G., Sadreyev, Ruslan I., Naxerova, Kamila, Mitchell, Richard N., Brown, Dennis, Libby, Peter, Weissleder, Ralph, Swirski, Filip K., Kohl, Peter, Vinegoni, Claudio, Milan, David J., Ellinor, Patrick T., Nahrendorf, Matthias
Publicado no Cell (2017)

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

Por Dina, Christian, Bouatia-Naji, Nabila, Tucker, Nathan, Delling, Francesca N., Toomer, Katelynn, Durst, Ronen, Perrocheau, Maelle, Fernandez-Friera, Leticia, Solis, Jorge, Le Tourneau, Thierry, Chen, Ming-Huei, Probst, Vincent, Bosse, Yohan, Pibarot, Philippe, Zelenika, Diana, Lathrop, Mark, Hercberg, Serge, Roussel, Ronan, Benjamin, Emelia J., Bonnet, Fabrice, Su Hao, LO, Dolmatova, Elena, Simonet, Floriane, Lecointe, Simon, Kyndt, Florence, Redon, Richard, Le Marec, Hervé, Froguel, Philippe, Ellinor, Patrick T., Vasan, Ramachandran S., Bruneval, Patrick, Norris, Russell A., Milan, David J., Slaugenhaupt, Susan A., Levine, Robert A., Schott, Jean-Jacques, Hagege, Albert A., Jeunemaitre, Xavier
Publicado no Nat Genet (2015)