Defective proteostasis in induced pluripotent stem cell models of frontotemporal lobar degeneration

por Mahali, Sidhartha, Martinez, Rita, King, Melvin, Verbeck, Anthony, Harari, Oscar, Benitez, Bruno A., Horie, Kanta, Sato, Chihiro, Temple, Sally, Karch, Celeste M.
Publicado 2022

Conserved gene signatures shared among MAPT mutations reveal defects in calcium signaling

por Minaya, Miguel A., Mahali, Sidhartha, Iyer, Abhirami K., Eteleeb, Abdallah M., Martinez, Rita, Huang, Guangming, Budde, John, Temple, Sally, Nana, Alissa L., Seeley, William W., Spina, Salvatore, Grinberg, Lea T., Harari, Oscar, Karch, Celeste M.
Publicado 2023

Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation

por Filipello, Fabia, You, Shih-Feng, Mirfakhar, Farzaneh S., Mahali, Sidhartha, Bollman, Bryan, Acquarone, Mariana, Korvatska, Olena, Marsh, Jacob A., Sivaraman, Anirudh, Martinez, Rita, Cantoni, Claudia, De Feo, Luca, Ghezzi, Laura, Minaya, Miguel A., Renganathan, Arun, Cashikar, Anil G., Satoh, Jun-Ichi, Beatty, Wandy, Iyer, Abhirami K., Cella, Marina, Raskind, Wendy H., Piccio, Laura, Karch, Celeste M.
Publicado 2023