Diflunisal inhibits prestin by chloride-dependent mechanism

por Duret, Guillaume, Pereira, Fred A., Raphael, Robert M.
Publicado 2017

DNA Sequence Analysis of SLC26A5, Encoding Prestin, in a Patient-Control Cohort: Identification of Fourteen Novel DNA Sequence Variations

por Minor, Jacob S., Tang, Hsiao-Yuan, Pereira, Fred A., Alford, Raye Lynn
Publicado 2009

High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss

por Tang, Hsiao-Yuan, Xia, Anping, Oghalai, John S, Pereira, Fred A, Alford, Raye L
Publicado 2005

A Coregulatory Network of NR2F1 and microRNA-140

por Chiang, David Y., Cuthbertson, David W., Ruiz, Fernanda R., Li, Na, Pereira, Fred A.
Publicado 2013

Genome-Wide Analysis of Binding Sites and Direct Target Genes of the Orphan Nuclear Receptor NR2F1/COUP-TFI

por Montemayor, Celina, Montemayor, Oscar A., Ridgeway, Alex, Lin, Feng, Wheeler, David A., Pletcher, Scott D., Pereira, Fred A.
Publicado 2010

Prestin Regulation and Function in Residual Outer Hair Cells after Noise-Induced Hearing Loss

por Xia, Anping, Song, Yohan, Wang, Rosalie, Gao, Simon S., Clifton, Will, Raphael, Patrick, Chao, Sung-il, Pereira, Fred A., Groves, Andrew K., Oghalai, John S.
Publicado 2013

Trehalose reduces retinal degeneration, neuroinflammation and storage burden caused by a lysosomal hydrolase deficiency

por Lotfi, Parisa, Tse, Dennis Y., Di Ronza, Alberto, Seymour, Michelle L., Martano, Giuseppe, Cooper, Jonathan D., Pereira, Fred A., Passafaro, Maria, Wu, Samuel M., Sardiello, Marco
Publicado 2018

An Allelic Series of Mice Reveals a Role for RERE in the Development of Multiple Organs Affected in Chromosome 1p36 Deletions

por Kim, Bum Jun, Zaveri, Hitisha P., Shchelochkov, Oleg A., Yu, Zhiyin, Hernández-García, Andrés, Seymour, Michelle L., Oghalai, John S., Pereira, Fred A., Stockton, David W., Justice, Monica J., Lee, Brendan, Scott, Daryl A.
Publicado 2013

Manipulations of MeCP2 in glutamatergic neurons highlight their contributions to Rett and other neurological disorders

por Meng, Xiangling, Wang, Wei, Lu, Hui, He, Ling-jie, Chen, Wu, Chao, Eugene S, Fiorotto, Marta L, Tang, Bin, Herrera, Jose A, Seymour, Michelle L, Neul, Jeffrey L, Pereira, Fred A, Tang, Jianrong, Xue, Mingshan, Zoghbi, Huda Y
Publicado 2016

mTORC1-independent TFEB activation via Akt inhibition promotes cellular clearance in neurodegenerative storage diseases

por Palmieri, Michela, Pal, Rituraj, Nelvagal, Hemanth R., Lotfi, Parisa, Stinnett, Gary R., Seymour, Michelle L., Chaudhury, Arindam, Bajaj, Lakshya, Bondar, Vitaliy V., Bremner, Laura, Saleem, Usama, Tse, Dennis Y., Sanagasetti, Deepthi, Wu, Samuel M., Neilson, Joel R., Pereira, Fred A., Pautler, Robia G., Rodney, George G., Cooper, Jonathan D., Sardiello, Marco
Publicado 2017

Corrigendum: mTORC1-independent TFEB activation via Akt inhibition promotes cellular clearance in neurodegenerative storage diseases

por Palmieri, Michela, Pal, Rituraj, Nelvagal, Hemanth R., Lotfi, Parisa, Stinnett, Gary R., Seymour, Michelle L., Chaudhury, Arindam, Bajaj, Lakshya, Bondar, Vitaliy V., Bremner, Laura, Saleem, Usama, Tse, Dennis Y., Sanagasetti, Deepthi, Wu, Samuel M., Neilson, Joel R., Pereira, Fred A., Pautler, Robia G., Rodney, George G., Cooper, Jonathan D., Sardiello, Marco
Publicado 2017