Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sowjanya Kallakuri"'
Autor:
Yuanyuan Li, Norihito Kishimoto, Zhaoxia Sun, Lu Zhao, Ying Cao, Shiaulou Yuan, Linda M. DiBella, Sowjanya Kallakuri
Publikováno v:
Proceedings of the National Academy of Sciences. 110:12697-12702
Primary ciliary dyskinesia (PCD) is an autosomal recessive disease caused by defective cilia motility. The identified PCD genes account for about half of PCD incidences and the underlying mechanisms remain poorly understood. We demonstrate that Repti
Autor:
Bernard M. Mechler, István Kiss, Tolga Eichhorn, Istvan Török, Mátyás Gorjánácz, Erika Viragh, Tamás Szlanka, Sowjanya Kallakuri
Publikováno v:
G3: Genes|Genomes|Genetics
The multifunctional factors Imp-α and Imp-β are involved in nuclear protein import, mitotic spindle dynamics, and nuclear membrane formation. Furthermore, each of the three members of the Imp-α family exerts distinct tasks during development. In D
Autor:
Sowjanya Kallakuri, Philip W. Ingham
Publikováno v:
Mechanisms of Development. 145:S53
Autor:
Jianxin A. Yu, Stefania Nicoli, Sowjanya Kallakuri, Jade Li, Yuanyuan Li, Zhaoxia Sun, Brant M. Weinstein
Publikováno v:
Journal of the American Society of Nephrology : JASN. 26(4)
The cilium is a signaling platform of the vertebrate cell. It has a critical role in polycystic kidney disease and nephronophthisis. Cilia have been detected on endothelial cells, but the function of these organelles in the vasculature remains incomp