Resultados da busca - Enkhsaikhan Purevjav

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  1. 1
    Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling

    Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling por Michelle Chintanaphol, Buyan‐Ochir Orgil, Neely R. Alberson, Jeffrey A. Towbin, Enkhsaikhan Purevjav

    Publicado em 2022
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  2. 2
    GSK3- and PRMT-1–dependent modifications of desmoplakin control desmoplakin–cytoskeleton dynamics

    GSK3- and PRMT-1–dependent modifications of desmoplakin control desmoplakin–cytoskeleton dynamics por Lauren V. Albrecht, Lichao Zhang, Jeffrey Shabanowitz, Enkhsaikhan Purevjav, Jeffrey A. Towbin, Donald F. Hunt, Kathleen J. Green

    Publicado em 2015
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  3. 3
    Accelerated cardiac remodeling in desmoplakin transgenic mice in response to endurance exercise is associated with perturbed Wnt/β-catenin signaling

    Accelerated cardiac remodeling in desmoplakin transgenic mice in response to endurance exercise is associated with perturbed Wnt/β-catenin signaling por Ruben Martherus, Rahul Jain, Ken Takagi, Uzmee Mendsaikhan, Subat Turdi, Hanna Osińska, Jeanne James, Kristen Kramer, Enkhsaikhan Purevjav, Jeffrey A. Towbin

    Publicado em 2015
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  4. 4
    Pediatric and adult dilated cardiomyopathy represent distinct pathological entities

    Pediatric and adult dilated cardiomyopathy represent distinct pathological entities por Meghna D. Patel, Mohan Jayaram, C. Schneider, Geetika Bajpai, Enkhsaikhan Purevjav, Charles E. Canter, Jeffrey A. Towbin, Andrea Bredemeyer, Kory J. Lavine

    Publicado em 2017
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  5. 5
    Unraveling the genetic blueprint of doxorubicin-induced cardiotoxicity through systems genetics approaches

    Unraveling the genetic blueprint of doxorubicin-induced cardiotoxicity through systems genetics approaches por Buyan‐Ochir Orgil, Akhilesh Kumar Bajpai, Neely R. Alberson, Morgan Lander, Batsaikhan Enkhzul, Hugo R. Martinez, Jeffrey A. Towbin, Lu Lu, Enkhsaikhan Purevjav

    Publicado em 2025
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  6. 6
    Cardiac Metabolic Pathways Affected in the Mouse Model of Barth Syndrome

    Cardiac Metabolic Pathways Affected in the Mouse Model of Barth Syndrome por Yan Huang, Corey Powers, Satish K. Madala, Kenneth D. Greis, Wendy D. Haffey, Jeffrey A. Towbin, Enkhsaikhan Purevjav, Sabzali Javadov, Arnold W. Strauss, Zaza Khuchua

    Publicado em 2015
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  7. 7
    Myopathic Cardiac Genotypes Increase Risk for Myocarditis

    Myopathic Cardiac Genotypes Increase Risk for Myocarditis por Amy Kontorovich, Nihir Patel, Arden Moscati, Felix Richter, Inga Peter, Enkhsaikhan Purevjav, Simina Selejan, Ingrid Kindermann, Jeffrey A. Towbin, Michael Böhm, Karin Klingel, Bruce D. Gelb

    Publicado em 2021
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  8. 8
    Genomics of pediatric cardiomyopathy

    Genomics of pediatric cardiomyopathy por Teresa M. Lee, Stephanie M. Ware, Alicia M. Kamsheh, Surbhi Bhatnagar, Mohammed Absi, Erin Miller, Enkhsaikhan Purevjav, Kaitlin A. Ryan, Jeffrey A. Towbin, Steven E. Lipshultz

    Publicado em 2025
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  9. 9
    Disturbance in Z-Disk Mechanosensitive Proteins Induced by a Persistent Mutant Myopalladin Causes Familial Restrictive Cardiomyopathy

    Disturbance in Z-Disk Mechanosensitive Proteins Induced by a Persistent Mutant Myopalladin Causes Familial Restrictive Cardiomyopathy por Anne-Cécile Huby, Uzmee Mendsaikhan, Ken Takagi, Ruben Martherus, Janaka Wansapura, Nan Gong, Hanna Osińska, Jeanne James, Kristen Kramer, Kazuyoshi Saito, Jeffrey Robbins, Zaza Khuchua, Jeffrey A. Towbin, Enkhsaikhan Purevjav

    Publicado em 2014
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  10. 10
    α-1-Syntrophin Mutation and the Long-QT Syndrome

    α-1-Syntrophin Mutation and the Long-QT Syndrome por Geru Wu, Tomohiko Ai, Jeffrey J. Kim, Bhagyalaxmi Mohapatra, Yutao Xi, Zhaohui Li, Shahrzad Abbasi, Enkhsaikhan Purevjav, Kaveh Samani, Michael J. Ackerman, Ming Qi, Arthur J. Moss, Wataru Shimizu, Jeffrey A. Towbin, Jie Cheng, Matteo Vatta

    Publicado em 2008
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  11. 11
    Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

    Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis por Enkhsaikhan Purevjav, Jaquelin Varela, Micaela Morgado, Debra L. Kearney, Hua Li, Michael D. Taylor, Takuro Arimura, Carole L. Moncman, William J. McKenna, Ross T. Murphy, Siegfried Labeit, Matteo Vatta, Neil E. Bowles, Akinori Kimura, Aladin M. Boriek, Jeffrey A. Towbin

    Publicado em 2010
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  12. 12
    Sickle cell anemia mice develop a unique cardiomyopathy with restrictive physiology

    Sickle cell anemia mice develop a unique cardiomyopathy with restrictive physiology por Nihal Bakeer, Jeanne James, Swarnava Roy, Janaka Wansapura, Shiva Kumar Shanmukhappa, John N. Lorenz, Hanna Osińska, Kristin Backer, Anne-Cécile Huby, Archana Shrestha, Omar Niss, Robert J. Fleck, Charles T. Quinn, Michael D. Taylor, Enkhsaikhan Purevjav, Bruce J. Aronow, Jeffrey A. Towbin, Punam Malik

    Publicado em 2016
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  13. 13
    Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy

    Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy por Satoko Miyatake, Satomi Mitsuhashi, Yukiko Hayashi, Enkhsaikhan Purevjav, Atsuko Nishikawa, Eriko Koshimizu, Mikiya Suzuki, K Yatabe, Yuzo Tanaka, Katsuhisa Ogata, Satoshi Kuru, Masaaki Shiina, Yoshinori Tsurusaki, Mitsuko Nakashima, Takeshi Mizuguchi, Noriko Miyake, Hirotomo Saitsu, Kazuhiro Ogata, Mitsuru Kawai, Jeffrey A. Towbin, Ikuya Nonaka, Ichizo Nishino, Naomichi Matsumoto

    Publicado em 2016
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  14. 14
    Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations

    Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations por Enkhsaikhan Purevjav, Takuro Arimura, Sibylle Augustin, Anne-Cécile Huby, Ken Takagi, Shinichi Nunoda, Debra L. Kearney, Michael D. Taylor, Fumio Terasaki, J. Martijn Bos, Steve R. Ommen, Hiroki Shibata, Megumi Takahashi, Manatsu Itoh-Satoh, William J. McKenna, Ross T. Murphy, Siegfried Labeit, Yoichi Yamanaka, Noboru Machida, Jeong-Euy Park, Peta Alexander, Robert G. Weintraub, Yasushi Kitaura, Michael J. Ackerman, Akinori Kimura, Jeffrey A. Towbin

    Publicado em 2012
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