Torthaí cuardaigh - Enkhsaikhan Purevjav
- 1 - 14 toradh as 14 á dtaispeáint
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1
Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling de réir Michelle Chintanaphol, Buyan‐Ochir Orgil, Neely R. Alberson, Jeffrey A. Towbin, Enkhsaikhan Purevjav
Foilsithe / Cruthaithe 2022Revisão -
2
GSK3- and PRMT-1–dependent modifications of desmoplakin control desmoplakin–cytoskeleton dynamics de réir Lauren V. Albrecht, Lichao Zhang, Jeffrey Shabanowitz, Enkhsaikhan Purevjav, Jeffrey A. Towbin, Donald F. Hunt, Kathleen J. Green
Foilsithe / Cruthaithe 2015Artigo -
3
Accelerated cardiac remodeling in desmoplakin transgenic mice in response to endurance exercise is associated with perturbed Wnt/β-catenin signaling de réir Ruben Martherus, Rahul Jain, Ken Takagi, Uzmee Mendsaikhan, Subat Turdi, Hanna Osińska, Jeanne James, Kristen Kramer, Enkhsaikhan Purevjav, Jeffrey A. Towbin
Foilsithe / Cruthaithe 2015Artigo -
4
Pediatric and adult dilated cardiomyopathy represent distinct pathological entities de réir Meghna D. Patel, Mohan Jayaram, C. Schneider, Geetika Bajpai, Enkhsaikhan Purevjav, Charles E. Canter, Jeffrey A. Towbin, Andrea Bredemeyer, Kory J. Lavine
Foilsithe / Cruthaithe 2017Artigo -
5
Unraveling the genetic blueprint of doxorubicin-induced cardiotoxicity through systems genetics approaches de réir Buyan‐Ochir Orgil, Akhilesh Kumar Bajpai, Neely R. Alberson, Morgan Lander, Batsaikhan Enkhzul, Hugo R. Martinez, Jeffrey A. Towbin, Lu Lu, Enkhsaikhan Purevjav
Foilsithe / Cruthaithe 2025Artigo -
6
Cardiac Metabolic Pathways Affected in the Mouse Model of Barth Syndrome de réir 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
Foilsithe / Cruthaithe 2015Artigo -
7
Myopathic Cardiac Genotypes Increase Risk for Myocarditis de réir 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
Foilsithe / Cruthaithe 2021Artigo -
8
Genomics of pediatric cardiomyopathy de réir 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
Foilsithe / Cruthaithe 2025Revisão -
9
Disturbance in Z-Disk Mechanosensitive Proteins Induced by a Persistent Mutant Myopalladin Causes Familial Restrictive Cardiomyopathy de réir 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
Foilsithe / Cruthaithe 2014Artigo -
10
α-1-Syntrophin Mutation and the Long-QT Syndrome de réir 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
Foilsithe / Cruthaithe 2008Artigo -
11
Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis de réir 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
Foilsithe / Cruthaithe 2010Artigo -
12
Sickle cell anemia mice develop a unique cardiomyopathy with restrictive physiology de réir 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
Foilsithe / Cruthaithe 2016Artigo -
13
Biallelic Mutations in MYPN , Encoding Myopalladin, Are Associated with Childhood-Onset, Slowly Progressive Nemaline Myopathy de réir 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
Foilsithe / Cruthaithe 2016Artigo -
14
Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations de réir 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
Foilsithe / Cruthaithe 2012Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
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