Despite WT1 binding sites in the promoter region of human and mouse nucleoporin glycoprotein 210, WT1 does not influence expression of GP210

por Olsson, Magnus, English, Milton A, Mason, Jacqueline, Licht, Jonathan D, Ekblom, Peter
Publicado 2004

A Novel ARL3 Gene Mutation Associated With Autosomal Dominant Retinal Degeneration

por Ratnapriya, Rinki, Jacobson, Samuel G., Cideciyan, Artur V., English, Milton A., Roman, Alejandro J., Sumaroka, Alexander, Sheplock, Rebecca, Swaroop, Anand
Publicado 2021

In vitro modeling and rescue of ciliopathy associated with IQCB1/NPHP5 mutations using patient-derived cells

por Kruczek, Kamil, Qu, Zepeng, Welby, Emily, Shimada, Hiroko, Hiriyanna, Suja, English, Milton A., Zein, Wadih M., Brooks, Brian P., Swaroop, Anand
Publicado 2022

Knockdown of Bardet-Biedl Syndrome Gene BBS9/PTHB1 Leads to Cilia Defects

por Veleri, Shobi, Bishop, Kevin, Dalle Nogare, Damian E., English, Milton A., Foskett, Trevor J., Chitnis, Ajay, Sood, Raman, Liu, Paul, Swaroop, Anand
Publicado 2012

Long wavelength-sensing cones of zebrafish retina exhibit multiple layers of transcriptional heterogeneity

por Farre, Ashley A., Sun, Chi, Starostik, Margaret R., Hunter, Samuel S., English, Milton A., Duncan, Audrey, Santhanam, Abirami, Shihabeddin, Eyad, O’Brien, John, Swaroop, Anand, Stenkamp, Deborah L.
Publicado 2023

Ultra-rare complement factor 8 coding variants in families with age-related macular degeneration

por Zelinger, Lina, Martin, Tammy M., Advani, Jayshree, Campello, Laura, English, Milton A., Kwong, Alan, Weber, Claire, Maykoski, Jennifer, Sergeev, Yuri V., Fariss, Robert, Chew, Emily Y., Klein, Michael L., Swaroop, Anand
Publicado 2023