Generation of isogenic models of Angelman syndrome and Prader-Willi syndrome in CRISPR/Cas9-engineered human embryonic stem cells

por Gilmore, Rachel B., Gorka, Dea, Stoddard, Christopher E., Cotney, Justin L., Chamberlain, Stormy J
Publicado 2023

Identifying key underlying regulatory networks and predicting targets of orphan C/D box SNORD116 snoRNAs in Prader-Willi syndrome

por Gilmore, Rachel B., Liu, Yaling, Stoddard, Christopher E., Chung, Michael S., Carmichael, Gordon G., Cotney, Justin
Publicado 2023

The role of UBE3A in the autism and epilepsy-related Dup15q syndrome using patient-derived, CRISPR-corrected neurons

por Elamin, Marwa, Dumarchey, Aurelie, Stoddard, Christopher, Robinson, Tiwanna M., Cowie, Christopher, Gorka, Dea, Chamberlain, Stormy J., Levine, Eric S.
Publicado 2023

Examining the role of the surfactant family member SFTA3 in interneuron specification

por Chen, Christopher Y., Anderson, Nickesha C., Becker, Sandy, Schicht, Martin, Stoddard, Christopher, Bräuer, Lars, Paulsen, Friedrich, Grabel, Laura
Publicado 2018

Human retinal organoids harboring IMPG2 mutations exhibit a photoreceptor outer segment phenotype that models advanced retinitis pigmentosa

por Mayerl, Steven J., Bajgai, Simona, Ludwig, Allison L., Jager, Lindsey D., Williams, Brittany N., Bacig, Cole, Stoddard, Christopher, Sinha, Divya, Philpot, Benjamin D., Gamm, David M.
Publicado 2022

TET3 epigenetically controls feeding and stress response behaviors via AGRP neurons

por Xie, Di, Stutz, Bernardo, Li, Feng, Chen, Fan, Lv, Haining, Sestan-Pesa, Matija, Catarino, Jonatas, Gu, Jianlei, Zhao, Hongyu, Stoddard, Christopher E., Carmichael, Gordon G., Shanabrough, Marya, Taylor, Hugh S., Liu, Zhong-Wu, Gao, Xiao-Bing, Horvath, Tamas L., Huang, Yingqun
Publicado 2022