Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tatianna Wai Ying Wong"'
Autor:
Matthew Rok, Tatianna Wai Ying Wong, Eleonora Maino, Abdalla Ahmed, Grace Yang, Elzbieta Hyatt, Kyle Lindsay, Sina Fatehi, Ryan Marks, Paul Delgado-Olguín, Evgueni A. Ivakine, Ronald D. Cohn
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 30, Iss , Pp 246-258 (2023)
Duchenne muscular dystrophy (DMD) is a disease with a life-threatening trajectory resulting from mutations in the dystrophin gene, leading to degeneration of skeletal muscle and fibrosis of cardiac muscle. The overwhelming majority of mutations are m
Externí odkaz:
https://doaj.org/article/f6f44eb7d6ec40c3ab0d3efbe103235b
Autor:
Tatianna Wai Ying Wong, Abdalla Ahmed, Grace Yang, Eleonora Maino, Sydney Steiman, Elzbieta Hyatt, Parry Chan, Kyle Lindsay, Nicole Wong, Diane Golebiowski, Joel Schneider, Paul Delgado-Olguín, Evgueni A. Ivakine, Ronald D. Cohn
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 9 (2020)
Duchenne muscular dystrophy (DMD) is a life-threatening neuromuscular disease caused by the lack of dystrophin, resulting in progressive muscle wasting and locomotor dysfunctions. By adulthood, almost all patients also develop cardiomyopathy, which i
Externí odkaz:
https://doaj.org/article/331a1839953f44fc84ba83fead6d8655
Targeted genome editing in vivo corrects a Dmd duplication restoring wild‐type dystrophin expression
Autor:
Eleonora Maino, Matthew J. Rok, Tatianna Wai Ying Wong, Michelle Schneeweiss, Ori Scott, Sonia L Evagelou, Amanda Chiodo, Daria Wojtal, Lindsay K, Ronald D. Cohn, Evgueni A. Ivakine, Aiman Farheen, Samar Z Rizvi, Shagana Visuvanathan, Elzbieta Hyatt
Publikováno v:
EMBO Molecular Medicine, Vol 13, Iss 5, Pp n/a-n/a (2021)
EMBO Molecular Medicine
EMBO Molecular Medicine
Tandem duplication mutations are increasingly found to be the direct cause of many rare heritable diseases, accounting for up to 10% of cases. Unfortunately, animal models recapitulating such mutations are scarce, limiting our ability to study them a
Autor:
Nicole Wong, Diane Golebiowski, Parry Chan, Sydney Steiman, Elzbieta Hyatt, Abdalla Ahmed, Evgueni A. Ivakine, Grace J. Yang, Eleonora Maino, Tatianna Wai Ying Wong, Lindsay K, Ronald D. Cohn, Joel S. Schneider, Paul Delgado-Olguin
Publikováno v:
Disease Models & Mechanisms, Vol 13, Iss 9 (2020)
Disease Models & Mechanisms
article-version (VoR) Version of Record
Disease Models & Mechanisms
article-version (VoR) Version of Record
Duchenne muscular dystrophy (DMD) is a life-threatening neuromuscular disease caused by the lack of dystrophin, resulting in progressive muscle wasting and locomotor dysfunctions. By adulthood, almost all patients also develop cardiomyopathy, which i
Autor:
Tatianna Wai Ying Wong, Ronald D. Cohn
Publikováno v:
Current Gene Therapy. 17
Background Duchenne muscular dystrophy (DMD) is an X-linked neuromuscular disease caused by the lack of dystrophin due to mutations in the DMD gene. Since dystrophin is essential in maintaining the integrity of the sarcolemmal membrane, the absence o
Autor:
Dorothee Heincke, Louisa Wilcke, Susann Herrmann, Tim W. Gilberger, Tobias Spielmann, Caroline Bruns, Maya Kono, Tatianna Wai Ying Wong
Publikováno v:
Journal of Cell Science
The intraerythrocytic developmental cycle of Plasmodium falciparum is completed with the release of up to 32 invasive daughter cells, the merozoites, into the blood stream. Before release, the final step of merozoite development is the assembly of th
Autor:
Sergio L. Pereira, Zeenat Malam, Michael D. Wilson, Vincent Mouly, Dwi U. Kemaladewi, Hernan Gonorazky, Sarah Abdullah, Elzbieta Hyatt, James Stavropoulos, Francesco Muntoni, Ronald D. Cohn, Roberto Mendoza-Londono, Kamel Mamchaoui, Evgueni A. Ivakine, Zahra Baghestani, James J. Dowling, Daria Wojtal, Tatianna Wai Ying Wong, Thomas Voit
Clustered regularly interspaced short palindromic repeat (CRISPR) has arisen as a frontrunner for efficient genome engineering. However, the potentially broad therapeutic implications are largely unexplored. Here, to investigate the therapeutic poten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eb67a2f6f91352aee2c50d1871f99b4
https://europepmc.org/articles/PMC4716669/
https://europepmc.org/articles/PMC4716669/
Autor:
Susann Herrmann, Maya Kono, Lakshmipuram S. Swapna, Tim W. Gilberger, Sidharth Saini, Louisa Wilcke, Srinivas Nellimarla, Christian Ungermann, Laura Biller, Arun T. John Peter, Johanna Wetzel, Tatianna Wai Ying Wong, Karen L. Mossman, Tobias Spielmann, Olivia Ramsay, Dhaneswar Prusty, Ana Cabrera, Dorothee Heincke, John Parkinson
Publikováno v:
The Journal of biological chemistry. 290(3)
To survive and persist within its human host, the malaria parasite Plasmodium falciparum utilizes a battery of lineage-specific innovations to invade and multiply in human erythrocytes. With central roles in invasion and cytokinesis, the inner membra