Distinct features of brain perivascular fibroblasts and mural cells revealed by in vivo two-photon imaging

por Bonney, Stephanie K, Sullivan, Liam T, Cherry, Timothy J, Daneman, Richard, Shih, Andy Y
Publicado 2021

Monocarboxylate Transporter 1 (MCT1) Mediates Succinate Export in the Retina

por Bisbach, Celia M., Hass, Daniel T., Thomas, Eric D., Cherry, Timothy J., Hurley, James B.
Publicado 2022

Machine Learning Prediction of Non-Coding Variant Impact in Human Retinal cis-Regulatory Elements

por VandenBosch, Leah S., Luu, Kelsey, Timms, Andrew E., Challam, Shriya, Wu, Yue, Lee, Aaron Y., Cherry, Timothy J.
Publicado 2022

Lipid nanoparticle-mediated delivery of mRNA into the mouse and human retina and other ocular tissues

por Chambers, Cheri Z., Soo, Gillian L., Engel, Abbi L., Glass, Ian A., Frassetto, Andrea, Martini, Paolo G. V., Cherry, Timothy J.
Publicado 2023

Chromatin Environment and Cellular Context Specify Compensatory Activity of Paralogous MEF2 Transcription Factors

por Majidi, Shahriyar P., Reddy, Naveen C., Moore, Michael J., Chen, Hao, Yamada, Tomoko, Andzelm, Milena M., Cherry, Timothy J., Hu, Linda S., Greenberg, Michael E., Bonni, Azad
Publicado 2019

Contribution of non-coding mutations to RPGRIP1-mediated inherited retinal degeneration

por Jamshidi, Farzad, Place, Emily M., Mehrotra, Sudeep, Navarro-Gomez, Daniel, Maher, Mathew, Branham, Kari E., Valkanas, Elise, Cherry, Timothy J., Lek, Monkol, MacArthur, Daniel, Pierce, Eric A., Bujakowska, Kinga M.
Publicado 2018

Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina

por Lyu, Pin, Hoang, Thanh, Santiago, Clayton P., Thomas, Eric D., Timms, Andrew E., Appel, Haley, Gimmen, Megan, Le, Nguyet, Jiang, Lizhi, Kim, Dong Won, Chen, Siqi, Espinoza, David F., Telger, Ariel E., Weir, Kurt, Clark, Brian S., Cherry, Timothy J., Qian, Jiang, Blackshaw, Seth
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