Elevated Membrane Attack Complex in Human Choroid With High Risk Complement Factor H Genotypes

Por Mullins, Robert F., Dewald, Aaron D., Streb, Luan M., Wang, Kai, Kuehn, Markus H., Stone, Edwin M.
Publicado em 2011

Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa

Por Tucker, Budd A, Mullins, Robert F, Streb, Luan M, Anfinson, Kristin, Eyestone, Mari E, Kaalberg, Emily, Riker, Megan J, Drack, Arlene V, Braun, Terry A, Stone, Edwin M
Publicado em 2013

Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease

Por Stone, Edwin M., Andorf, Jeaneen L., Whitmore, S. Scott, DeLuca, Adam P., Giacalone, Joseph C., Streb, Luan M., Braun, Terry A., Mullins, Robert F., Scheetz, Todd E., Sheffield, Val C., Tucker, Budd A.
Publicado no Ophthalmology (2017)

North Carolina Macular Dystrophy is caused by dysregulation of the retinal transcription factor PRDM13

Por Small, Kent W., DeLuca, Adam P., Whitmore, S. Scott, Rosenberg, Thomas, Silva-Garcia, Rosemary, Udar, Nitin, Puech, Bernard, Garcia, Charles A., Rice, Thomas A., Fishman, Gerald A., Héon, Elise, Folk, James C., Streb, Luan M., Haas, Christine M., Wiley, Luke A., Scheetz, Todd E., Fingert, John H., Mullins, Robert F., Tucker, Budd A., Stone, Edwin. M.
Publicado no Ophthalmology (2015)