Mechanistic Insights into Axenfeld–Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants

por French, Curtis R.
Publicado 2021

Meis1 specifies positional information in the retina and tectum to organize the zebrafish visual system

por Erickson, Timothy, French, Curtis R, Waskiewicz, Andrew J
Publicado 2010

Phytocannabinoids Reduce Seizures in Larval Zebrafish and Affect Endocannabinoid Gene Expression

por Kollipara, Roshni, Langille, Evan, Tobin, Cameron, French, Curtis R.
Publicado 2023

Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis

por Hawkey-Noble, Alexia, Pater, Justin A., Kollipara, Roshni, Fitzgerald, Meriel, Maekawa, Alexandre S., Kovacs, Christopher S., Young, Terry-Lynn, French, Curtis R.
Publicado 2022

Pbx homeodomain proteins pattern both the zebrafish retina and tectum

por French, Curtis R, Erickson, Timothy, Callander, Davon, Berry, Karyn M, Koss, Ron, Hagey, Daniel W, Stout, Jennifer, Wuennenberg-Stapleton, Katrin, Ngai, John, Moens, Cecilia B, Waskiewicz, Andrew J
Publicado 2007

The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left–Right Patterning

por Chrystal, Paul W., French, Curtis R., Jean, Francesca, Havrylov, Serhiy, van Baarle, Suey, Peturson, Ann-Marie, Xu, Pengfei, Crump, J. Gage, Pilgrim, David B., Lehmann, Ordan J., Waskiewicz, Andrew J.
Publicado 2021

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene

por Pater, Justin A., Penney, Cindy, O’Rielly, Darren D., Griffin, Anne, Kamal, Lara, Brownstein, Zippora, Vona, Barbara, Vinkler, Chana, Shohat, Mordechai, Barel, Ortal, French, Curtis R., Singh, Sushma, Werdyani, Salem, Burt, Taylor, Abdelfatah, Nelly, Houston, Jim, Doucette, Lance P., Squires, Jessica, Glaser, Fabian, Roslin, Nicole M., Vincent, Daniel, Marquis, Pascale, Woodland, Geoffrey, Benoukraf, Touati, Hawkey-Noble, Alexia, Avraham, Karen B., Stanton, Susan G., Young, Terry-Lynn
Publicado 2022

A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene

por Abdelfatah, Nelly, Mostafa, Ahmed A., French, Curtis R., Doucette, Lance P., Penney, Cindy, Lucas, Matthew B., Griffin, Anne, Booth, Valerie, Rowley, Christopher, Besaw, Jessica E., Tranebjærg, Lisbeth, Rendtorff, Nanna Dahl, Hodgkinson, Kathy A., Little, Leichelle A., Agrawal, Sumit, Parnes, Lorne, Batten, Tony, Moore, Susan, Hu, Pingzhao, Pater, Justin A., Houston, Jim, Galutira, Dante, Benteau, Tammy, MacDonald, Courtney, French, Danielle, O’Rielly, Darren D., Stanton, Susan G., Young, Terry-Lynn
Publicado 2021