Zobrazeno 1 - 10
of 1 656
pro vyhledávání: '"Wernig, A."'
Autor:
Gernot Neumayer, Jessica L. Torkelson, Shengdi Li, Kelly McCarthy, Hanson H. Zhen, Madhuri Vangipuram, Marius M. Mader, Gulilat Gebeyehu, Taysir M. Jaouni, Joanna Jacków-Malinowska, Avina Rami, Corey Hansen, Zongyou Guo, Sadhana Gaddam, Keri M. Tate, Alberto Pappalardo, Lingjie Li, Grace M. Chow, Kevin R. Roy, Thuylinh Michelle Nguyen, Koji Tanabe, Patrick S. McGrath, Amber Cramer, Anna Bruckner, Ganna Bilousova, Dennis Roop, Jean Y. Tang, Angela Christiano, Lars M. Steinmetz, Marius Wernig, Anthony E. Oro
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract We present Dystrophic Epidermolysis Bullosa Cell Therapy (DEBCT), a scalable platform producing autologous organotypic iPS cell-derived induced skin composite (iSC) grafts for definitive treatment. Clinical-grade manufacturing integrates CRI
Externí odkaz:
https://doaj.org/article/beaa5273b9ae4861a2bf161a05a28b1a
Autor:
Wernig, Jakob1 (AUTHOR) jakob.wernig@stud.medunigraz.at, Pilz, Stefan1 (AUTHOR), Trummer, Christian1 (AUTHOR), Theiler-Schwetz, Verena1 (AUTHOR), Schmitt, Lisa Maria1 (AUTHOR), Tsybrovskyy, Oleksiy2 (AUTHOR)
Publikováno v:
JCEM Case Reports. Oct2024, Vol. 2 Issue 10, p1-6. 6p.
Autor:
Ingrid M. Saldana-Guerrero, Luis F. Montano-Gutierrez, Katy Boswell, Christoph Hafemeister, Evon Poon, Lisa E. Shaw, Dylan Stavish, Rebecca A. Lea, Sara Wernig-Zorc, Eva Bozsaky, Irfete S. Fetahu, Peter Zoescher, Ulrike Pötschger, Marie Bernkopf, Andrea Wenninger-Weinzierl, Caterina Sturtzel, Celine Souilhol, Sophia Tarelli, Mohamed R. Shoeb, Polyxeni Bozatzi, Magdalena Rados, Maria Guarini, Michelle C. Buri, Wolfgang Weninger, Eva M. Putz, Miller Huang, Ruth Ladenstein, Peter W. Andrews, Ivana Barbaric, George D. Cresswell, Helen E. Bryant, Martin Distel, Louis Chesler, Sabine Taschner-Mandl, Matthias Farlik, Anestis Tsakiridis, Florian Halbritter
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-25 (2024)
Abstract Early childhood tumours arise from transformed embryonic cells, which often carry large copy number alterations (CNA). However, it remains unclear how CNAs contribute to embryonic tumourigenesis due to a lack of suitable models. Here we empl
Externí odkaz:
https://doaj.org/article/869f81138e26465185ec2a1246dd0cf6
Autor:
Hao, Yukun A., Lee, Sungmoo, Roth, Richard H., Natale, Silvia, Gomez, Laura, Taxidis, Jiannis, O’Neill, Philipp S., Villette, Vincent, Bradley, Jonathan, Wang, Zeguan, Jiang, Dongyun, Zhang, Guofeng, Sheng, Mengjun, Lu, Di, Boyden, Edward, Delvendahl, Igor, Golshani, Peyman, Wernig, Marius, Feldman, Daniel E., Ji, Na, Ding, Jun, Südhof, Thomas C., Clandinin, Thomas R., Lin, Michael Z.
Publikováno v:
In Neuron 20 November 2024 112(22):3680-3696
Autor:
Susanto, Teodorus Theo, Hung, Victoria, Levine, Andrew G., Chen, Yuxiang, Kerr, Craig H., Yoo, Yongjin, Oses-Prieto, Juan A., Fromm, Lisa, Zhang, Zijian, Lantz, Travis C., Fujii, Kotaro, Wernig, Marius, Burlingame, Alma L., Ruggero, Davide, Barna, Maria
Publikováno v:
In Molecular Cell 19 September 2024 84(18):3545-3563
Autor:
Gintautas Vainorius, Maria Novatchkova, Georg Michlits, Juliane Christina Baar, Cecilia Raupach, Joonsun Lee, Ramesh Yelagandula, Marius Wernig, Ulrich Elling
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Ascl1 and Ngn2, closely related proneural transcription factors, are able to convert mouse embryonic stem cells into induced neurons. Despite their similarities, these factors elicit only partially overlapping transcriptional programs, and i
Externí odkaz:
https://doaj.org/article/be3b505e9315435b88d215c8c6ad0e64
Autor:
Wernig-Zorc, Sara1,2 (AUTHOR) sara.wernig-zorc@ccri.at, Schwartz, Uwe3 (AUTHOR), Martínez-Rodríguez, Paulina4 (AUTHOR) paulinaconstanza.martinez@ufrontera.cl, Inalef, Josefa5 (AUTHOR) ingridehrenfeld@uach.cl, Pavicic, Francisca5 (AUTHOR), Ehrenfeld, Pamela5,6 (AUTHOR), Längst, Gernot1 (AUTHOR), Maldonado, Rodrigo7 (AUTHOR) rodrigo.maldonado@uss.cl
Publikováno v:
International Journal of Molecular Sciences. May2024, Vol. 25 Issue 10, p5515. 16p.
Publikováno v:
In Current Opinion in Genetics & Development December 2023 83
A cell therapy approach to restore microglial Trem2 function in a mouse model of Alzheimer’s disease
Publikováno v:
In Cell Stem Cell 3 August 2023 30(8):1043-1053
Autor:
Bahareh Haddad Derafshi, Tamas Danko, Soham Chanda, Pedro J. Batista, Ulrike Litzenburger, Qian Yi Lee, Yi Han Ng, Anu Sebin, Howard Y. Chang, Thomas C. Südhof, Marius Wernig
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-28 (2022)
Abstract The chromodomain helicase DNA-binding protein CHD8 is the most frequently mutated gene in autism spectrum disorder. Despite its prominent disease involvement, little is known about its molecular function in the human brain. CHD8 is a chromat
Externí odkaz:
https://doaj.org/article/f6144c8eb12747dd9d2726213f094bb0