Search Results - "Gete, Yantenew G."

Mechanisms of angiogenic incompetence in Hutchinson–Gilford progeria via downregulation of endothelial NOS by Gete, Yantenew G., Koblan, Luke W., Mao, Xiaojing, Trappio, Mason, Mahadik, Bhushan, Fisher, John P., Liu, David R., Cao, Kan

“…Hutchinson–Gilford progeria syndrome (HGPS) is a rare genetic disorder with features of accelerated aging. The majority of HGPS cases are caused by a de novo…”
Get full text

Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome by Mao, Xiaojing, Xiong, Zheng-Mei, Xue, Huijing, Brown, Markus A, Gete, Yantenew G, Yu, Reynold, Sun, Linlin, Cao, Kan

“…Hutchinson-Gilford progeria syndrome (HGPS) is a detrimental premature aging disease caused by a point mutation in the human gene. This mutation results in the…”
Get full text

In vivo base editing rescues Hutchinson–Gilford progeria syndrome in mice by Koblan, Luke W., Erdos, Michael R., Wilson, Christopher, Cabral, Wayne A., Levy, Jonathan M., Xiong, Zheng-Mei, Tavarez, Urraca L., Davison, Lindsay M., Gete, Yantenew G., Mao, Xiaojing, Newby, Gregory A., Doherty, Sean P., Narisu, Narisu, Sheng, Quanhu, Krilow, Chad, Lin, Charles Y., Gordon, Leslie B., Cao, Kan, Collins, Francis S., Brown, Jonathan D., Liu, David R.

“…Hutchinson–Gilford progeria syndrome (HGPS or progeria) is typically caused by a dominant-negative C•G-to-T•A mutation (c.1824 C>T; p.G608G) in LMNA , the gene…”
Get full text