Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yassin Harim"'
Autor:
Changwen Wang, Meng Sun, Chunxuan Shao, Lisa Schlicker, Yue Zhuo, Yassin Harim, Tianping Peng, Weili Tian, Nadja Stöffler, Martin Schneider, Dominic Helm, Youjun Chu, Beibei Fu, Xiaoliang Jin, Jan-Philipp Mallm, Moritz Mall, Yonghe Wu, Almut Schulze, Hai-Kun Liu
Publikováno v:
npj Precision Oncology, Vol 8, Iss 1, Pp 1-21 (2024)
Abstract Recent advances in the genomics of glioblastoma (GBM) led to the introduction of molecular neuropathology but failed to translate into treatment improvement. This is largely attributed to the genetic and phenotypic heterogeneity of GBM, whic
Externí odkaz:
https://doaj.org/article/d63afc60087d40eba8fc806d9ff1af6b
Autor:
Weijun Feng, Daisuke Kawauchi, Huiqin Körkel-Qu, Huan Deng, Elisabeth Serger, Laura Sieber, Jenna Ariel Lieberman, Silvia Jimeno-González, Sander Lambo, Bola S. Hanna, Yassin Harim, Malin Jansen, Anna Neuerburg, Olga Friesen, Marc Zuckermann, Vijayanad Rajendran, Jan Gronych, Olivier Ayrault, Andrey Korshunov, David T. W. Jones, Marcel Kool, Paul A. Northcott, Peter Lichter, Felipe Cortés-Ledesma, Stefan M. Pfister, Hai-Kun Liu
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
Mutations in the chromatin modifier Chd7 have been associated with CHARGE syndrome and other developmental disorders. Here the authors show that Chd7 is required for the activation of genes essential for cerebellar granule cell differentiation, and t
Externí odkaz:
https://doaj.org/article/a402443280f6419d867e3b5b78b484b1
Autor:
Changwen Wang, Meng Sun, Chunxuan Shao, Lisa Schlicker, Yue Zhuo, Yassin Harim, Tianping Peng, Weili Tian, Nadja Stöffler, Martin Schneider, Dominic Helm, Jan-Philipp Mallm, Yonghe Wu, Almut Schulze, Hai-Kun Liu
Recent advances in the genomics of glioblastoma (GBM) led to the introduction of molecular neuropathology but failed to translate into treatment improvement. This is largely attributed to the genetic and phenotypic heterogeneity of GBM, which are con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b3ee9c69783e22c4450a50222b77f27
https://doi.org/10.1101/2023.01.24.525374
https://doi.org/10.1101/2023.01.24.525374
Autor:
Peter Lichter, Hai-Kun Liu, Huiqin Körkel-Qu, Elisabeth Serger, Sander Lambo, Laura Sieber, Felipe Cortés-Ledesma, Anna Neuerburg, Jan Gronych, Weijun Feng, Daisuke Kawauchi, Jenna Ariel Lieberman, David T.W. Jones, Bola S. Hanna, Marc Zuckermann, Malin Jansen, Huan Deng, Vijayanad Rajendran, Paul A. Northcott, Yassin Harim, Marcel Kool, Olivier Ayrault, Andrey Korshunov, Olga Friesen, Silvia Jimeno-González, Stefan M. Pfister
Publikováno v:
Nature Communications
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
idUS. Depósito de Investigación de la Universidad de Sevilla
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
idUS. Depósito de Investigación de la Universidad de Sevilla
Feng, Weijun et al.
Mutations in chromatin modifier genes are frequently associated with neurodevelopmental diseases. We herein demonstrate that the chromodomain helicase DNA-binding protein 7 (Chd7), frequently associated with CHARGE syndrome,
Mutations in chromatin modifier genes are frequently associated with neurodevelopmental diseases. We herein demonstrate that the chromodomain helicase DNA-binding protein 7 (Chd7), frequently associated with CHARGE syndrome,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3cca4dc85383e0fca03e272844684fc2
http://hdl.handle.net/10261/165442
http://hdl.handle.net/10261/165442