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

Mitochondrial DNA lineages determine tumor progression through T cell reactive oxygen signaling

线粒体DNA谱系通过T细胞活性氧信号传导决定肿瘤进展

Yardeni, Tal; Olali, Arnold Z; Chen, Hsiao-Wen; Wang, Liqing; Haltom, Jeffrey A; Zenab, Angi; Morrow, Ryan; Butic, Arrienne; Murdock, Deborah G; Waymire, Katrina G; MacGregor, Grant R; Boursi, Ben; Beier, Ulf H; Hancock, Wayne W; Wallace, Douglas C

Bioenergetic Signatures of DLD Deficiency: Dissecting PDHc- and α-KGDHc-Linked Defects

DLD 缺乏症的生物能量学特征:剖析 PDHc 和 α-KGDHc 相关缺陷

Haham Zarbib, Yarden; Huri Ohev-Shalom, Shira; Lyskov, Shani Kassia; Mazor, Yuval; Anekstein-Spigel, Mika; Shalva, Nechama; Spiegel, Ronen; Staretz-Chacham, Orna; Manor, Joshua; Saada, Ann; Rock, Rachel; Anikster, Yair; Yardeni, Tal

Improved CAR-T cell activity associated with increased mitochondrial function primed by galactose.

半乳糖促进线粒体功能增强,从而提高 CAR-T 细胞活性

Gross Golda, Alkadieri Suha, Meir Amilia, Itzhaki Orit, Aharony-Tevet Yarden, Yosef Shahar Ben, Zenab Angi, Shbiro Liat, Toren Amos, Yardeni Tal, Jacoby Elad

An mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypes

线粒体DNA突变小鼠表明,线粒体缺陷可导致自闭症内表型。

Yardeni, Tal; Cristancho, Ana G; McCoy, Almedia J; Schaefer, Patrick M; McManus, Meagan J; Marsh, Eric D; Wallace, Douglas C

Rationale and Design for a Phase 1 Study of N-Acetylmannosamine for Primary Glomerular Diseases

N-乙酰甘露糖胺治疗原发性肾小球疾病的I期研究的理论依据和设计

Huizing, Marjan; Yardeni, Tal; Fuentes, Federico; Malicdan, May C V; Leoyklang, Petcharat; Volkov, Alexander; Dekel, Benjamin; Brede, Emily; Blake, Jodi; Powell, Alva; Chatrathi, Harish; Anikster, Yair; Carrillo, Nuria; Gahl, William A; Kopp, Jeffrey B

A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C-methyltransferase deficiency

辅酶Q10生物合成途径的一种新型先天性缺陷:由COQ5 C-甲基转移酶缺乏引起的共济失调和静止性脑肌病

Malicdan, May Christine V; Vilboux, Thierry; Ben-Zeev, Bruria; Guo, Jennifer; Eliyahu, Aviva; Pode-Shakked, Ben; Dori, Amir; Kakani, Sravan; Chandrasekharappa, Settara C; Ferreira, Carlos R; Shelestovich, Natalia; Marek-Yagel, Dina; Pri-Chen, Hadass; Blatt, Ilan; Niederhuber, John E; He, Langping; Toro, Camilo; Taylor, Robert W; Deeken, John; Yardeni, Tal; Wallace, Douglas C; Gahl, William A; Anikster, Yair

UDP-GlcNAc 2-Epimerase/ManNAc Kinase (GNE): A Master Regulator of Sialic Acid Synthesis

UDP-GlcNAc 2-差向异构酶/ManNAc激酶(GNE):唾液酸合成的主要调节因子

Hinderlich, Stephan; Weidemann, Wenke; Yardeni, Tal; Horstkorte, Rüdiger; Huizing, Marjan

Non-specific accumulation of glycosphingolipids in GNE myopathy

GNE肌病中糖鞘脂的非特异性积累

Patzel, Katherine A; Yardeni, Tal; Le Poëc-Celic, Erell; Leoyklang, Petcharat; Dorward, Heidi; Alonzi, Dominic S; Kukushkin, Nikolay V; Xu, Bixue; Zhang, Yongmin; Sollogoub, Matthieu; Blériot, Yves; Gahl, William A; Huizing, Marjan; Butters, Terry D

Murine isoforms of UDP-GlcNAc 2-epimerase/ManNAc kinase: Secondary structures, expression profiles, and response to ManNAc therapy

小鼠UDP-GlcNAc 2-差向异构酶/ManNAc激酶同工酶:二级结构、表达谱及对ManNAc疗法的反应

Yardeni, Tal; Jacobs, Katherine; Niethamer, Terren K; Ciccone, Carla; Anikster, Yair; Kurochkina, Natalya; Gahl, William A; Huizing, Marjan

Hereditary inclusion body myopathy: single patient response to intravenous dosing of GNE gene lipoplex

遗传性包涵体肌病:单例患者对静脉注射GNE基因脂质体的反应

Nemunaitis, Gregory; Jay, Chris M; Maples, Phillip B; Gahl, William A; Huizing, Marjan; Yardeni, Tal; Tong, Alex W; Phadke, Anagha P; Pappen, Beena O; Bedell, Cynthia; Allen, Henry; Hernandez, Cathy; Templeton, Nancy S; Kuhn, Joseph; Senzer, Neil; Nemunaitis, John