Prescreening whole exome sequencing results from patients with retinal degeneration for variants in genes associated with retinal degeneration

por Bryant, Laura, Lozynska, Olga, Maguire, Albert M, Aleman, Tomas S, Bennett, Jean
Publicado 2017

Translational Regulation of Utrophin by miRNAs

por Basu, Utpal, Lozynska, Olga, Moorwood, Catherine, Patel, Gopal, Wilton, Steve D., Khurana, Tejvir S.
Publicado 2011

Drug Discovery for Duchenne Muscular Dystrophy via Utrophin Promoter Activation Screening

por Moorwood, Catherine, Lozynska, Olga, Suri, Neha, Napper, Andrew D., Diamond, Scott L., Khurana, Tejvir S.
Publicado 2011

QSulf1 remodels the 6-O sulfation states of cell surface heparan sulfate proteoglycans to promote Wnt signaling

por Ai, Xingbin, Do, Anh-Tri, Lozynska, Olga, Kusche-Gullberg, Marion, Lindahl, Ulf, Emerson, Charles P.
Publicado 2003

Identification of a novel pathogenic missense mutation in PRPF31 using whole exome sequencing: a case report

por Bryant, Laura, Lozynska, Olga, Marsh, Anson, Papp, Tyler E, van Gorder, Lucas, Serrano, Leona W, Gai, Xiaowu, Maguire, Albert M, Aleman, Tomas S, Bennett, Jean
Publicado 2019