Bringing Light to Transcription: The Optogenetics Repertoire

by Lorena de Mena, Patrick Rizk, Diego E. Rincon-Limas, Diego E. Rincon-Limas
Published 2018-11-01

PhotoGal4: A Versatile Light-Dependent Switch for Spatiotemporal Control of Gene Expression in Drosophila Explants

by Lorena de Mena, Diego E. Rincon-Limas
Published 2020-07-01

Molecular, functional, and pathological aspects of TDP-43 fragmentation

by Deepak Chhangani, Alfonso Martín-Peña, Diego E. Rincon-Limas
Published 2021-05-01

Combined pharmacological induction of Hsp70 suppresses prion protein neurotoxicity in Drosophila.

by Yan Zhang, Sergio Casas-Tinto, Diego E Rincon-Limas, Pedro Fernandez-Funez
Published 2014-01-01

In vivo generation of neurotoxic prion protein: role for hsp70 in accumulation of misfolded isoforms.

by Pedro Fernandez-Funez, Sergio Casas-Tinto, Yan Zhang, Melisa Gómez-Velazquez, Marco A Morales-Garza, Ana C Cepeda-Nieto, Joaquín Castilla, Claudio Soto, Diego E Rincon-Limas
Published 2009-06-01

Data set of interactomes and metabolic pathways of proteins differentially expressed in brains with Alzheimer׳s disease

by Benito Minjarez, Karla Grisel Calderón-González, Ma Luz Valero Rustarazo, María Esther Herrera-Aguirre, María Luisa Labra-Barrios, Diego E. Rincon-Limas, Manuel M. Sánchez del Pino, Raul Mena, Juan Pedro Luna-Arias
Published 2016-06-01

NCBP2 modulates neurodevelopmental defects of the 3q29 deletion in Drosophila and Xenopus laevis models.

by Mayanglambam Dhruba Singh, Matthew Jensen, Micaela Lasser, Emily Huber, Tanzeen Yusuff, Lucilla Pizzo, Brian Lifschutz, Inshya Desai, Alexis Kubina, Sneha Yennawar, Sydney Kim, Janani Iyer, Diego E Rincon-Limas, Laura Anne Lowery, Santhosh Girirajan
Published 2020-02-01

Aß40 displays amyloidogenic properties in the non-transgenic mouse brain but does not exacerbate Aß42 toxicity in Drosophila

by Lorena De Mena, Michael A. Smith, Jason Martin, Katie L. Dunton, Carolina Ceballos-Diaz, Karen R. Jansen-West, Pedro E. Cruz, Kristy D. Dillon, Diego E. Rincon-Limas, Todd E. Golde, Brenda D. Moore, Yona Levites
Published 2020-10-01

KCNC3R420H, a K+ channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular trafficking

by Carolina Gallego-Iradi, Justin S. Bickford, Swati Khare, Alexis Hall, Jerelyn A. Nick, Donya Salmasinia, Kolja Wawrowsky, Serguei Bannykh, Duong P. Huynh, Diego E. Rincon-Limas, Stefan M. Pulst, Harry S. Nick, Pedro Fernandez-Funez, Michael F. Waters
Published 2014-11-01

A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking.

by Swati Khare, Jerelyn A Nick, Yalan Zhang, Kira Galeano, Brittany Butler, Habibeh Khoshbouei, Sruti Rayaprolu, Tyisha Hathorn, Laura P W Ranum, Lisa Smithson, Todd E Golde, Martin Paucar, Richard Morse, Michael Raff, Julie Simon, Magnus Nordenskjöld, Karin Wirdefeldt, Diego E Rincon-Limas, Jada Lewis, Leonard K Kaczmarek, Pedro Fernandez-Funez, Harry S Nick, Michael F Waters
Published 2017-01-01