Papillorenal Syndrome-Causing Missense Mutations in PAX2/Pax2 Result in Hypomorphic Alleles in Mouse and Human

por Alur, Ramakrishna P., Vijayasarathy, Camasamudram, Brown, Jacob D., Mehtani, Mohit, Onojafe, Ighovie F., Sergeev, Yuri V., Boobalan, Elangovan, Jones, MaryPat, Tang, Ke, Liu, Haiquan, Xia, Chun-hong, Gong, Xiaohua, Brooks, Brian P.
Publicado 2010

Nolz1 expression is required in dopaminergic axon guidance and striatal innervation

por Soleilhavoup, Clement, Travaglio, Marco, Patrick, Kieran, Garção, Pedro, Boobalan, Elangovan, Adolfs, Youri, Spriggs, Ruth V., Moles-Garcia, Emma, Dhiraj, Dalbir, Oosterveen, Tony, Ferri, Sarah L., Abel, Ted, Brodkin, Edward S., Pasterkamp, R. Jeroen, Brooks, Brian P., Panman, Lia
Publicado 2020

Zfp503/Nlz2 Is Required for RPE Differentiation and Optic Fissure Closure

por Boobalan, Elangovan, Thompson, Amy H., Alur, Ramakrishna P., McGaughey, David M., Dong, Lijin, Shih, Grace, Vieta-Ferrer, Emile R., Onojafe, Ighovie F., Kalaskar, Vijay K., Arno, Gavin, Lotery, Andrew J., Guan, Bin, Bender, Chelsea, Memon, Omar, Brinster, Lauren, Soleilhavoup, Clement, Panman, Lia, Badea, Tudor C., Minella, Andrea, Lopez, Antonio Jacobo, Thomasy, Sara M., Moshiri, Ala, Blain, Delphine, Hufnagel, Robert B., Cogliati, Tiziana, Bharti, Kapil, Brooks, Brian P.
Publicado 2022