Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Guoxing Yang"'
Autor:
Zhiqiang Liu, Lina Lv, Guoxing Yang, Shipeng Xie, Chengquan Li, Jialiang Zhao, Minglian Zhang
Publikováno v:
Scientific Reports
Fundus albipunctatus (FA) is a rare autosomal recessive form of stationary night blindness characterized by the presence of white or white-yellow dots in the perimacular area and the periphery of the retina, with or without macular involvement. In th
Publikováno v:
Scientific Reports
Congenital cataract disease is a clinically and genetically heterogeneous lens disorder. The purpose of this study was to identify the genetic defects and to investigate the relationships between disease-causing genes and lens morphology in congenita
Publikováno v:
Molecular Vision
Purpose Congenital cataracts are a clinically and genetically heterogeneous lens disorder. The purpose of this study was to identify the genetic mutation and the molecular phenotype responsible for the presence of an autosomal dominant congenital nuc
Autor:
Paul A. Sieving, Lucia Ziccardi, Camasamudram Vijayasarathy, Richard A. Lewis, Ruifang Sui, Guoxing Yang, Yong Zeng, Rafael C. Caruso, Fei Xu
Retinoschisin (RS1) is a cell-surface adhesion molecule expressed by photoreceptor and bipolar cells of the retina. The 24-kDa protein encodes two conserved sequence motifs: the initial signal sequence targets the protein for secretion while the larg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e799a254cc3b4d039cff9313a1de8298
https://europepmc.org/articles/PMC2991635/
https://europepmc.org/articles/PMC2991635/