Результати пошуку - Enkhsaikhan Purevjav

  • Показ 1 - 14 результатів із 14
Уточнити результати
  1. 1
    Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling

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

    Опубліковано 2022
    Отримати повний текст Отримати повний текст
    Revisão
    Додати у Вибране
    Збережено в:
  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 за авторством Lauren V. Albrecht, Lichao Zhang, Jeffrey Shabanowitz, Enkhsaikhan Purevjav, Jeffrey A. Towbin, Donald F. Hunt, Kathleen J. Green

    Опубліковано 2015
    Отримати повний текст Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  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 за авторством Ruben Martherus, Rahul Jain, Ken Takagi, Uzmee Mendsaikhan, Subat Turdi, Hanna Osińska, Jeanne James, Kristen Kramer, Enkhsaikhan Purevjav, Jeffrey A. Towbin

    Опубліковано 2015
    Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  4. 4
    Pediatric and adult dilated cardiomyopathy represent distinct pathological entities

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

    Опубліковано 2017
    Отримати повний текст Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  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 за авторством Buyan‐Ochir Orgil, Akhilesh Kumar Bajpai, Neely R. Alberson, Morgan Lander, Batsaikhan Enkhzul, Hugo R. Martinez, Jeffrey A. Towbin, Lu Lu, Enkhsaikhan Purevjav

    Опубліковано 2025
    Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  6. 6
    Cardiac Metabolic Pathways Affected in the Mouse Model of Barth Syndrome

    Cardiac Metabolic Pathways Affected in the Mouse Model of Barth Syndrome за авторством 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

    Опубліковано 2015
    Отримати повний текст Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  7. 7
    Myopathic Cardiac Genotypes Increase Risk for Myocarditis

    Myopathic Cardiac Genotypes Increase Risk for Myocarditis за авторством 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

    Опубліковано 2021
    Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  8. 8
    Genomics of pediatric cardiomyopathy

    Genomics of pediatric cardiomyopathy за авторством 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

    Опубліковано 2025
    Отримати повний текст
    Revisão
    Додати у Вибране
    Збережено в:
  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 за авторством 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

    Опубліковано 2014
    Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  10. 10
    α-1-Syntrophin Mutation and the Long-QT Syndrome

    α-1-Syntrophin Mutation and the Long-QT Syndrome за авторством 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

    Опубліковано 2008
    Отримати повний текст Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  11. 11
    Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

    Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis за авторством 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

    Опубліковано 2010
    Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  12. 12
    Sickle cell anemia mice develop a unique cardiomyopathy with restrictive physiology

    Sickle cell anemia mice develop a unique cardiomyopathy with restrictive physiology за авторством 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

    Опубліковано 2016
    Отримати повний текст Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  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 за авторством 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

    Опубліковано 2016
    Отримати повний текст Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:
  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 за авторством 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

    Опубліковано 2012
    Отримати повний текст
    Artigo
    Додати у Вибране
    Збережено в:

Інструменти для пошуку: