Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Austin J Reutzel"'
Autor:
Val C. Sheffield, Ian C. Han, Jeaneen L. Andorf, Erin R Burnight, Austin J Reutzel, Edwin M. Stone, Malia M. Collins, Budd A. Tucker, Robert F. Mullins, Qihong Zhang, Joseph C. Giacalone, Dalyz Ochoa
Publikováno v:
Human Gene Therapy. 30:967-974
In a screen of 1,000 consecutively ascertained families, we recently found that mutations in the gene RPGR are the third most common cause of all inherited retinal disease. As the two most frequent disease-causing genes, ABCA4 and USH2A, are far too
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44a0b032439e4494f12a95303a6f622d
https://doi.org/10.1089/hum.2018.244
https://doi.org/10.1089/hum.2018.244
Autor:
Robert F. Mullins, Austin J Reutzel, Matthew J. Miller, Joseph C. Giacalone, S. Scott Whitmore, Budd A. Tucker, Edwin M. Stone, Dalyz Ochoa, Grefachew Workalemahu
Publikováno v:
Microvasc Res
Age-related macular degeneration (AMD) is a common cause of blindness worldwide. While recent studies have revealed that the loss of choroidal endothelial cells (ChECs) is critical to the disease pathogenesis of dry AMD, in vitro studies are needed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a89f929ece0681d436c1c766508e7493
https://doi.org/10.1016/j.mvr.2018.12.002
https://doi.org/10.1016/j.mvr.2018.12.002
Autor:
Joseph C, Giacalone, Jeaneen L, Andorf, Qihong, Zhang, Erin R, Burnight, Dalyz, Ochoa, Austin J, Reutzel, Malia M, Collins, Val C, Sheffield, Robert F, Mullins, Ian C, Han, Edwin M, Stone, Budd A, Tucker
Publikováno v:
Hum Gene Ther
In a screen of 1,000 consecutively ascertained families, we recently found that mutations in the gene RPGR are the third most common cause of all inherited retinal disease. As the two most frequent disease-causing genes, ABCA4 and USH2A, are far too
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a262fab7c0aaeb3d177ab70bad61b4e1
https://pubmed.ncbi.nlm.nih.gov/31106594
https://pubmed.ncbi.nlm.nih.gov/31106594