Ohcanbohtosat - Enkhsaikhan Purevjav
- Čájehuvvo 1 - 14 / 14
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GSK3- and PRMT-1–dependent modifications of desmoplakin control desmoplakin–cytoskeleton dynamics Dahkki Lauren V. Albrecht, Lichao Zhang, Jeffrey Shabanowitz, Enkhsaikhan Purevjav, Jeffrey A. Towbin, Donald F. Hunt, Kathleen J. Green
Almmustuhtton 2015Artigo -
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Accelerated cardiac remodeling in desmoplakin transgenic mice in response to endurance exercise is associated with perturbed Wnt/β-catenin signaling Dahkki Ruben Martherus, Rahul Jain, Ken Takagi, Uzmee Mendsaikhan, Subat Turdi, Hanna Osińska, Jeanne James, Kristen Kramer, Enkhsaikhan Purevjav, Jeffrey A. Towbin
Almmustuhtton 2015Artigo -
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Pediatric and adult dilated cardiomyopathy represent distinct pathological entities Dahkki Meghna D. Patel, Mohan Jayaram, C. Schneider, Geetika Bajpai, Enkhsaikhan Purevjav, Charles E. Canter, Jeffrey A. Towbin, Andrea Bredemeyer, Kory J. Lavine
Almmustuhtton 2017Artigo -
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Unraveling the genetic blueprint of doxorubicin-induced cardiotoxicity through systems genetics approaches Dahkki Buyan‐Ochir Orgil, Akhilesh Kumar Bajpai, Neely R. Alberson, Morgan Lander, Batsaikhan Enkhzul, Hugo R. Martinez, Jeffrey A. Towbin, Lu Lu, Enkhsaikhan Purevjav
Almmustuhtton 2025Artigo -
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Cardiac Metabolic Pathways Affected in the Mouse Model of Barth Syndrome Dahkki 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
Almmustuhtton 2015Artigo -
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Myopathic Cardiac Genotypes Increase Risk for Myocarditis Dahkki 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
Almmustuhtton 2021Artigo -
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Genomics of pediatric cardiomyopathy Dahkki 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
Almmustuhtton 2025Revisão -
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Disturbance in Z-Disk Mechanosensitive Proteins Induced by a Persistent Mutant Myopalladin Causes Familial Restrictive Cardiomyopathy Dahkki 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
Almmustuhtton 2014Artigo -
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α-1-Syntrophin Mutation and the Long-QT Syndrome Dahkki 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
Almmustuhtton 2008Artigo -
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Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis Dahkki 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
Almmustuhtton 2010Artigo -
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Sickle cell anemia mice develop a unique cardiomyopathy with restrictive physiology Dahkki 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
Almmustuhtton 2016Artigo -
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Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy Dahkki 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
Almmustuhtton 2016Artigo -
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Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations Dahkki 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
Almmustuhtton 2012Artigo
Ohcanreaiddut:
Laktáseaddji fáttát
Biology
Gene
Medicine
Genetics
Internal medicine
Cardiomyopathy
Heart failure
Cardiology
Cell biology
Phenotype
Desmoplakin
Endocrinology
Pathology
Biochemistry
Desmin
Dilated cardiomyopathy
Disease
Fibrosis
Genetically modified mouse
Immunohistochemistry
Missense mutation
Molecular biology
Mutation
Myocarditis
Myocyte
Pathological
Restrictive cardiomyopathy
Sudden cardiac death
Sudden death
Transgene