Evjenth Rune相关文献与解析，生知库 | 链接生命科学的每一步

Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency

利用VAAST基因检测鉴定出一种X连锁遗传疾病，该疾病由于N端乙酰转移酶缺乏而导致男性婴儿死亡。

doi:10.1016/j.ajhg.2011.05.017

Rope, Alan F; Wang, Kai; Evjenth, Rune; Xing, Jinchuan; Johnston, Jennifer J; Swensen, Jeffrey J; Johnson, W Evan; Moore, Barry; Huff, Chad D; Bird, Lynne M; Carey, John C; Opitz, John M; Stevens, Cathy A; Jiang, Tao; Schank, Christa; Fain, Heidi Deborah; Robison, Reid; Dalley, Brian; Chin, Steven; South, Sarah T; Pysher, Theodore J; Jorde, Lynn B; Hakonarson, Hakon; Lillehaug, Johan R; Biesecker, Leslie G; Yandell, Mark; Arnesen, Thomas; Lyon, Gholson J

发表日期：2011

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Proteomics analyses reveal the evolutionary conservation and divergence of N-terminal acetyltransferases from yeast and humans

蛋白质组学分析揭示了酵母和人类N端乙酰转移酶的进化保守性和分化。

期刊:Proceedings of the National Academy of Sciences of the United States of America

影响因子:9.1

doi:10.1073/pnas.0901931106

Arnesen, Thomas; Van Damme, Petra; Polevoda, Bogdan; Helsens, Kenny; Evjenth, Rune; Colaert, Niklaas; Varhaug, Jan Erik; Vandekerckhove, Joël; Lillehaug, Johan R; Sherman, Fred; Gevaert, Kris

发表日期：2009

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Knockdown of human N alpha-terminal acetyltransferase complex C leads to p53-dependent apoptosis and aberrant human Arl8b localization.

人类 N α 末端乙酰转移酶复合物 C 的敲除导致 p53 依赖性细胞凋亡和人类 Arl8b 异常定位

期刊:Molecular and Cellular Biology

影响因子:2.7

doi:10.1128/MCB.01909-08

Starheim Kristian K, Gromyko Darina, Evjenth Rune, Ryningen Anita, Varhaug Jan Erik, Lillehaug Johan R, Arnesen Thomas

Application of reverse-phase HPLC to quantify oligopeptide acetylation eliminates interference from unspecific acetyl CoA hydrolysis

应用反相高效液相色谱法定量寡肽乙酰化可消除非特异性乙酰辅酶A水解的干扰。

期刊:BMC Proceedings

影响因子:

doi:10.1186/1753-6561-3-S6-S5

Evjenth, Rune; Hole, Kristine; Ziegler, Mathias; Lillehaug, Johan R

Interaction between HIF-1 alpha (ODD) and hARD1 does not induce acetylation and destabilization of HIF-1 alpha

HIF-1α (ODD) 与 hARD1 之间的相互作用不会诱导 HIF-1α 的乙酰化和不稳定。

期刊:

影响因子:

doi:10.1016/j.febslet.2005.10.036

Arnesen, Thomas; Kong, Xianguo; Evjenth, Rune; Gromyko, Darina; Varhaug, Jan Erik; Lin, Zhao; Sang, Nianli; Caro, Jaime; Lillehaug, Johan R

Protein N-terminal acetyltransferases act as N-terminal propionyltransferases in vitro and in vivo

蛋白质N端乙酰转移酶在体外和体内均发挥N端丙酰转移酶的作用。

Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency

利用VAAST基因检测鉴定出一种X连锁遗传疾病，该疾病由于N端乙酰转移酶缺乏而导致男性婴儿死亡。

Proteomics analyses reveal the evolutionary conservation and divergence of N-terminal acetyltransferases from yeast and humans

蛋白质组学分析揭示了酵母和人类N端乙酰转移酶的进化保守性和分化。

Knockdown of human N alpha-terminal acetyltransferase complex C leads to p53-dependent apoptosis and aberrant human Arl8b localization.

人类 N α 末端乙酰转移酶复合物 C 的敲除导致 p53 依赖性细胞凋亡和人类 Arl8b 异常定位

Application of reverse-phase HPLC to quantify oligopeptide acetylation eliminates interference from unspecific acetyl CoA hydrolysis

应用反相高效液相色谱法定量寡肽乙酰化可消除非特异性乙酰辅酶A水解的干扰。

Interaction between HIF-1 alpha (ODD) and hARD1 does not induce acetylation and destabilization of HIF-1 alpha

HIF-1α (ODD) 与 hARD1 之间的相互作用不会诱导 HIF-1α 的乙酰化和不稳定。