Canlyniadau Chwilio - Jin‐Hong Shin
- Dangos 1 - 16 canlyniadau o 16
-
1
The evolution of heart gene delivery vectors gan Nalinda B. Wasala, Jin‐Hong Shin, Dongsheng Duan
Cyhoeddwyd 2011Revisão -
2
-
3
-
4
-
5
-
6
AAV micro-dystrophin gene therapy alleviates stress-induced cardiac death but not myocardial fibrosis in > 21-m-old mdx mice, an end-stage model of Duchenne muscular dystrophy c... gan Benjamín C. Bostick, Jin‐Hong Shin, Yongping Yue, Nalinda B. Wasala, Yi Lai, Dongsheng Duan
Cyhoeddwyd 2012Artigo -
7
-
8
An intronic LINE-1 element insertion in the dystrophin gene aborts dystrophin expression and results in Duchenne-like muscular dystrophy in the corgi breed gan B. F. Smith, Yongping Yue, Philip R. Woods, Joe N. Kornegay, Jin‐Hong Shin, Regina R Williams, Dongsheng Duan
Cyhoeddwyd 2010Artigo -
9
-
10
Safe and bodywide muscle transduction in young adult Duchenne muscular dystrophy dogs with adeno-associated virus gan Yongping Yue, Xiufang Pan, Chady H. Hakim, Kasun Kodippili, Keqing Zhang, Jin‐Hong Shin, H. T. Yang, Thomas McDonald, Dongsheng Duan
Cyhoeddwyd 2015Artigo -
11
-
12
Adeno-Associated Virus Serotype 6 Capsid Tyrosine-to-Phenylalanine Mutations Improve Gene Transfer to Skeletal Muscle gan Chunping Qiao, Wei Zhang, Zhenhua Yuan, Jin‐Hong Shin, Jianbin Li, Giridhara R. Jayandharan, Zhong Li, Arun Srivastava, Xiao Xiao, Dongsheng Duan
Cyhoeddwyd 2010Artigo -
13
Genetic Variants Associated with Episodic Ataxia in Korea gan Kwang‐Dong Choi, Ji‐Soo Kim, Hyo‐Jung Kim, Ileok Jung, Seong‐Hae Jeong, Seung‐Han Lee, Dong Uk Kim, Sang-Ho Kim, Seo‐Young Choi, Jin‐Hong Shin, Dae‐Seong Kim, Kyung‐Pil Park, Hyang-Sook Kim, Jae‐Hwan Choi
Cyhoeddwyd 2017Artigo -
14
Myo‐Guide: A Machine Learning‐Based Web Application for Neuromuscular Disease Diagnosis With MRI gan José Verdú-Díaz, C. Bolano-Díaz, A. Gonzalez-Chamorro, S Fitzsimmons, Jodi Warman‐Chardon, Goknur Selen Kocak, Debora Mucida‐Alvim, Ian C. P. Smith, John Vissing, Nanna Scharff Poulsen, Sushan Luo, Cristina Domínguez‐González, Laura Bermejo‐Guerrero, David Gómez‐Andrés, J. Sotoca, Anna Pichiecchio, Silvia Nicolosi, Mauro Monforte, Claudia Brogna, Eugenio Mercuri, Jorge A. Bevilacqua, Jorge Díaz‐Jara, Benjamín Pizarro‐Galleguillos, Peter Krkoška, Jorge Alonso‐Pérez, Montse Olivé, Erik H. Niks, Hermien E. Kan, James B Lilleker, Mark Roberts, Bianca Buchignani, Jin‐Hong Shin, Florence Esselin, Emmanuelle Le Bars, Anne Marie Childs, Edoardo Malfatti, Anna Sárközy, Luke Perry, Sniya Sudhakar, Edmar Zanoteli, Filipe Tupinamba Di Pace, Emma Matthews, Shahram Attarian, David Bendahan, Matteo Garibaldi, Laura Fionda, Alicia Alonso‐Jiménez, Robert Carlier, Ali Asghar Okhovat, Shahriar Nafissi, Atchayaram Nalini, Seena Vengalil, Kieren G. Hollingsworth, Chiara Marini‐Bettolo, Volker Straub, Giorgio Tasca, Jaume Bacardit, Jordi Díaz‐Manera
Cyhoeddwyd 2025Artigo -
15
Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study gan Marianela Schiava, Chiseko Ikenaga, Rocío N. Villar‐Quiles, Marta Caballero‐Ávila, Ana Töpf, Ichizo Nishino, Virginia Kimonis, Bjarne Udd, Benedikt Schoser, Edmar Zanoteli, Paulo Victor Sgobbi de Souza, Giorgio Tasca, Thomas Lloyd, Adolfo Lopez-de Munain, Carmen Paradas, Elena Pegoraro, Aleksandra Nadaj-Pakleza, Jan De Bleecker, Umesh A. Badrising, Alicia Alonso‐Jiménez, Anna Kostera‐Pruszczyk, Francesc X. Miralles, Jin‐Hong Shin, Jorge A. Bevilacqua, Montse Olivé, Matthias Vorgerd, Rudi Kley, Stefen Brady, Timothy L. Williams, Cristina Domínguez‐González, George K. Papadimas, Jodi Warman‐Chardon, Kristl G. Claeys, Marianne de Visser, Nuria Muelas, Pascal Laforêt, Edoardo Malfatti, Lindsay N. Alfano, Sruthi Nair, Georgios Manousakis, Hani Kushlaf, Matthew Harms, Christopher Nance, Alba Ramos‐Fransí, Carmelo Rodolico, Channa Hewamadduma, Hakan Çetin, Jorge García‐García, Endre Pál, Maria Elena Farrugia, Phillipa J. Lamont, Colin Quinn, Velina Nedkova-Hristova, Stojan Peric, Sushan Luo, Anders Oldfors, Kate Taylor, Stuart H. Ralston, Tanya Stojkovic, Conrad C. Weihl, Jordi Díaz‐Manera
Cyhoeddwyd 2022Artigo -
16
104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07) gan Benedikt Schoser, Priya S. Kishnani, Drago Bratkovic, Barry J. Byrne, Kristl G. Claeys, Jordi Díaz‐Manera, Pascal Laforêt, Mark Roberts, António Toscano, Ans T. van der Ploeg, Jeff Castelli, Mitchell Goldman, Fred Holdbrook, Sheela Sitaraman Das, Y. Wasfi, Tahseen Mozaffar, Ágnes Sebök, Alan Pestronk, Aleksandra Dominović-Kovačević, Anzalee Khan, Blaž Koritnik, Céline Tard, Christopher Lindberg, Colin Quinn, Crystal Eldridge, Cynthia Bodkin, David Reyes‐Leiva, Derralynn Hughes, Ela Stefanescu, Emmanuelle Salort‐Campana, Ernest Butler, Françoise Bouhour, Gee Kim, George K. Papadimas, Giancarlo Parenti, Halina Bartosik-Psujek, Hani Kushlaf, Akihiro Hashiguchi, Heather Lau, Hélio Pedro, Henning Andersen, Hernán Amartino, Hideaki Shiraishi, Hiroshi Kobayashi, Ivaylo Tarnev, Jaime Vengoechea, Jennifer Avelar, Jin‐Hong Shin, John Nevin, Jonathan Cauci, Jorge Alonso‐Pérez, József Janszky, Julie Berthy, Cornelia Kornblum, Kristina Gutschmidt, Mária Judit Molnár, Marie Wencel, Mark A. Tarnopolsky, Matthias Boentert, Michel Tchan, Miriam Freimer, Nicola Longo, Nicolas J. Abreu, Nuria Vidal-Fernandez, Olimpia Musumeci, Özlem Göker-Alpan, Patrick Deegan, Paula R. Clemens, Richard Roxburgh, Robert Henderson, Robert J. Hopkin, Sabrina Sacconi, Simona Fecarotta, Shahram Attarian, Stephan Wenninger, Stephanie DeArmey, Tarekegn Hiwot, Thomas Andrew Burrow, Tobias Ruck, Tomo Sawada, Vescei Laszlo, Wolfgang N. Löscher, Yin‐Hsiu Chien
Cyhoeddwyd 2024Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Gene
Genetics
Medicine
Duchenne muscular dystrophy
Dystrophin
Internal medicine
Genetic enhancement
Muscular dystrophy
Gene delivery
Recombinant DNA
Vector (molecular biology)
Adeno-associated virus
Biochemistry
Cardiology
Cardiomyopathy
Disease
Endocrinology
Heart failure
Transduction (biophysics)
Bioinformatics
Computational biology
Dilated cardiomyopathy
Gene transfer
Genotype
Molecular biology
Muscle disorder
Muscle weakness
Mutation
Pathology