Gait Analysis in a Mecp2 Knockout Mouse Model of Rett Syndrome Reveals Early-Onset and Progressive Motor Deficits

por Gadalla, Kamal K. E., Ross, Paul D., Riddell, John S., Bailey, Mark E. S., Cobb, Stuart R.
Publicado 2014

Development of a Novel AAV Gene Therapy Cassette with Improved Safety Features and Efficacy in a Mouse Model of Rett Syndrome

por Gadalla, Kamal K.E., Vudhironarit, Thishnapha, Hector, Ralph D., Sinnett, Sarah, Bahey, Noha G., Bailey, Mark E.S., Gray, Steven J., Cobb, Stuart R.
Publicado 2017

Radically truncated MeCP2 rescues Rett syndrome-like neurological defects

por Tillotson, Rebekah, Selfridge, Jim, Koerner, Martha V., Gadalla, Kamal K. E., Guy, Jacky, De Sousa, Dina, Hector, Ralph D., Cobb, Stuart R., Bird, Adrian
Publicado 2017

Improved MECP2 Gene Therapy Extends the Survival of MeCP2-Null Mice without Apparent Toxicity after Intracisternal Delivery

por Sinnett, Sarah E., Hector, Ralph D., Gadalla, Kamal K.E., Heindel, Clifford, Chen, Daphne, Zaric, Violeta, Bailey, Mark E.S., Cobb, Stuart R., Gray, Steven J.
Publicado 2017

Convergent cerebrospinal fluid proteomes and metabolic ontologies in humans and animal models of Rett syndrome

por Zlatic, Stephanie A., Duong, Duc, Gadalla, Kamal K.E., Murage, Brenda, Ping, Lingyan, Shah, Ruth, Fink, James J., Khwaja, Omar, Swanson, Lindsay C., Sahin, Mustafa, Rayaprolu, Sruti, Kumar, Prateek, Rangaraju, Srikant, Bird, Adrian, Tarquinio, Daniel, Carpenter, Randall, Cobb, Stuart, Faundez, Victor
Publicado 2022