日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

TRAF7 in signaling and disease: emerging mechanisms and clinical implications

TRAF7 在信号传导和疾病中的作用:新兴机制和临床意义

Orock, Albert; Zuccato, Jeffrey A; Phan, Khanh; Liu, Yufeng; Ihuoma, Jennifer; Tavakol, Sherwin; Tsytsykova, Alla V; Tsitsikov, Erdyni N; Tarantini, Stefano; Johnson, Anthony C; Dunn, Ian F

GSTM1 null genotype underpins recurrence of NF2 meningiomas

GSTM1 基因缺失型是 NF2 脑膜瘤复发的基础

Johnson, Anthony C; Tsitsikov, Erdyni N; Phan, Khanh P; Zuccato, Jeffrey A; Bauer, Andrew M; Graffeo, Christopher S; Hameed, Sanaa; Stephens, Tressie M; Liu, Yufeng; Dunn, Gavin P; Tsytsykova, Alla V; Jones, Pamela S; Dunn, Ian F

Spontaneous mutation in 2310061I04Rik results in reduced expression of mitochondrial genes and impaired brain myelination

2310061I04Rik 的自发突变导致线粒体基因表达减少和脑髓鞘形成受损

Erdyni N Tsitsikov, Khanh P Phan, Yufeng Liu, Alla V Tsytsykova, Rosalia Paterno, David M Sherry, Anthony C Johnson, Ian F Dunn

TRAF7 is an essential regulator of blood vessel integrity during mouse embryonic and neonatal development

TRAF7 是小鼠胚胎和新生儿发育过程中血管完整性的重要调节剂

Erdyni N Tsitsikov, Khanh P Phan, Yufeng Liu, Alla V Tsytsykova, Mike Kinter, Lauren Selland, Lori Garman, Courtney Griffin, Ian F Dunn

Specific gene expression signatures of low grade meningiomas

低级别脑膜瘤的特定基因表达特征

Tsitsikov, Erdyni N; Hameed, Sanaa; Tavakol, Sherwin A; Stephens, Tressie M; Tsytsykova, Alla V; Garman, Lori; Bi, Wenya Linda; Dunn, Ian F

COMMD10 Is Essential for Neural Plate Development during Embryogenesis

COMMD10 对胚胎发生过程中神经板的发育至关重要

Khanh P Phan, Panayiotis Pelargos, Alla V Tsytsykova, Erdyni N Tsitsikov, Graham Wiley, Chuang Li, Melissa Bebak, Ian F Dunn

Mutated KLF4(K409Q) in meningioma binds STRs and activates FGF3 gene expression

脑膜瘤中突变的 KLF4(K409Q) 与 STR 结合并激活 FGF3 基因表达

Alla V Tsytsykova, Graham Wiley, Chuang Li, Richard C Pelikan, Lori Garman, Francis A Acquah, Blaine H M Mooers, Erdyni N Tsitsikov, Ian F Dunn

A novel mutation in the POLE2 gene causing combined immunodeficiency

POLE2基因中的一种新突变导致联合免疫缺陷

Frugoni, Francesco; Dobbs, Kerry; Felgentreff, Kerstin; Aldhekri, Hasan; Al Saud, Bandar K; Arnaout, Rand; Ali, Afshan Ashraf; Abhyankar, Avinash; Alroqi, Fayhan; Giliani, Silvia; Ojeda, Mayra Martinez; Tsitsikov, Erdyni; Pai, Sung-Yun; Casanova, Jean Laurent; Notarangelo, Luigi D; Manis, John P

Ligase-4 Deficiency Causes Distinctive Immune Abnormalities in Asymptomatic Individuals

连接酶-4 缺乏导致无症状个体出现明显免疫异常

Kerstin Felgentreff, Sachin N Baxi, Yu Nee Lee, Kerry Dobbs, Lauren A Henderson, Krisztian Csomos, Erdyni N Tsitsikov, Mary Armanios, Jolan E Walter, Luigi D Notarangelo

Human HOIP and LUBAC deficiency underlies autoinflammation, immunodeficiency, amylopectinosis, and lymphangiectasia

人类HOIP和LUBAC缺陷是自身炎症、免疫缺陷、支链淀粉病和淋巴管扩张症的根本原因。

Bertrand Boisson ,Emmanuel Laplantine ,Kerry Dobbs ,Aurélie Cobat ,Nadine Tarantino ,Melissa Hazen ,Hart G W Lidov ,Gregory Hopkins ,Likun Du ,Aziz Belkadi ,Maya Chrabieh ,Yuval Itan ,Capucine Picard ,Jean-Christophe Fournet ,Hermann Eibel ,Erdyni Tsitsikov ,Sung-Yun Pai ,Laurent Abel ,Waleed Al-Herz ,Jean-Laurent Casanova ,Alain Israel ,Luigi D Notarangelo