Editing the Neuronal Genome: a CRISPR View of Chromatin Regulation in Neuronal Development, Function, and Plasticity

por Yang, Marty G., West, Anne E.
Publicado 2016

Characterization of sequence determinants of enhancer function using natural genetic variation

por Yang, Marty G, Ling, Emi, Cowley, Christopher J, Greenberg, Michael E, Vierbuchen, Thomas
Publicado 2022

Regulation of chromatin accessibility and Zic binding at enhancers in the developing cerebellum

por Frank, Christopher L., Liu, Fang, Wijayatunge, Ranjula, Song, Lingyun, Biegler, Matthew T., Yang, Marty G., Vockley, Christopher M., Safi, Alexias, Gersbach, Charles A., Crawford, Gregory E., West, Anne E.
Publicado 2015

Enhancer Histone Acetylation Modulates Transcriptional Bursting Dynamics of Neuronal Activity-Inducible Genes

por Chen, Liang-Fu, Lin, Yen Ting, Gallegos, David A., Hazlett, Mariah F., Gómez-Schiavon, Mariana, Yang, Marty G., Kalmeta, Breanna, Zhou, Allen S., Holtzman, Liad, Gersbach, Charles A., Grandl, Jörg, Buchler, Nicolas E., West, Anne E.
Publicado 2019

Activity-dependent regulome of human GABAergic neurons reveals new patterns of gene regulation and neurological disease heritability

por Boulting, Gabriella L., Durresi, Ershela, Ataman, Bulent, Sherman, Maxwell A., Mei, Kevin, Harmin, David A., Carter, Ava C., Hochbaum, Daniel R., Granger, Adam J., Engreitz, Jesse M, Hrvatin, Sinisa, Blanchard, Michael R., Yang, Marty G., Griffith, Eric C., Greenberg, Michael E.
Publicado 2021

Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations

por Van Schil, Kristof, Naessens, Sarah, Van de Sompele, Stijn, Carron, Marjolein, Aslanidis, Alexander, Van Cauwenbergh, Caroline, Kathrin Mayer, Anja, Van Heetvelde, Mattias, Bauwens, Miriam, Verdin, Hannah, Coppieters, Frauke, Greenberg, Michael E, Yang, Marty G, Karlstetter, Marcus, Langmann, Thomas, De Preter, Katleen, Kohl, Susanne, Cherry, Timothy J, Leroy, Bart P, De Baere, Elfride
Publicado 2018

Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations

por Van Schil, Kristof, Naessens, Sarah, Van de Sompele, Stijn, Carron, Marjolein, Aslanidis, Alexander, Van Cauwenbergh, Caroline, Mayer, Anja K., Van Heetvelde, Mattias, Bauwens, Miriam, Verdin, Hannah, Coppieters, Frauke, Greenberg, Michael E., Yang, Marty G., Karlstetter, Marcus, Langmann, Thomas, De Preter, Katleen, Kohl, Susanne, Cherry, Timothy J., Leroy, Bart P., De Baere, Elfride
Publicado 2018