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

Preclinical dose response study shows NR2E3 can attenuate retinal degeneration in the retinitis pigmentosa mouse model Rho(P23H+/)()

临床前剂量反应研究表明，NR2E3 可以减轻视网膜色素变性小鼠模型 Rho(P23H+/)() 中的视网膜变性。

期刊:Gene Therapy
影响因子:4.5
doi:10.1038/s41434-024-00440-6
McNamee, Shannon M; Chan, Natalie P; Akula, Monica; Avola, Marielle O; Whalen, Maiya; Nystuen, Kaden; Singh, Pushpendra; Upadhyay, Arun K; DeAngelis, Margaret M; Haider, Neena B
发表日期：2024
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Evaluating therapeutic potential of NR2E3 doses in the rd7 mouse model of retinal degeneration

评估NR2E3剂量在rd7小鼠视网膜变性模型中的治疗潜力

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-024-67095-6
McNamee, Shannon M; Akula, Monica; Love, Zoe; Nasraty, Neelaab; Nystuen, Kaden; Singh, Pushpendra; Upadhyay, Arun K; DeAngelis, Margaret M; Haider, Neena B
发表日期：2024
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Alzheimer's Disease: Models and Molecular Mechanisms Informing Disease and Treatments

阿尔茨海默病：疾病及治疗的模型和分子机制

期刊:Bioengineering-Basel
影响因子:3.8
doi:10.3390/bioengineering11010045
Nystuen, Kaden L; McNamee, Shannon M; Akula, Monica; Holton, Kristina M; DeAngelis, Margaret M; Haider, Neena B
阿尔茨海默症
发表日期：2024
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Seeing the Future: A Review of Ocular Therapy

展望未来：眼科治疗综述

期刊:Bioengineering-Basel
影响因子:3.8
doi:10.3390/bioengineering11020179
Whalen, Maiya; Akula, Monica; McNamee, Shannon M; DeAngelis, Margaret M; Haider, Neena B
发表日期：2024
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Differential dimerization of variants linked to enhanced S-cone sensitivity syndrome (ESCS) located in the NR2E3 ligand-binding domain.

NR2E3 配体结合域中与增强型 S 锥体敏感性综合征 (ESCS) 相关的变异体的差异性二聚化

期刊:Human Mutation
影响因子:3.7
doi:10.1002/humu.22775
von Alpen Désirée, Tran Hoai Viet, Guex Nicolas, Venturini Giulia, Munier Francis L, Schorderet Daniel F, Haider Neena B, Escher Pascal
其它
发表日期：2015
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Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology.

ROBO1 和 RORA 对年龄相关性黄斑变性风险的影响揭示了疾病病理生理学中遗传上不同的表型

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0025775
Jun Gyungah, Nicolaou Michael, Morrison Margaux A, Buros Jacqueline, Morgan Denise J, Radeke Monte J, Yonekawa Yoshihiro, Tsironi Evangelia E, Kotoula Maria G, Zacharaki Fani, Mollema Nissa, Yuan Yang, Miller Joan W, Haider Neena B, Hageman Gregory S, Kim Ivana K, Schaumberg Debra A, Farrer Lindsay A, DeAngelis Margaret M
其它
发表日期：2011
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Patterned neuroprotection in the Inpp4a(wbl) mutant mouse cerebellum correlates with the expression of Eaat4

Inpp4a(wbl)突变小鼠小脑中的模式化神经保护与Eaat4的表达相关

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0008270
Sachs, Andrew J; David, Samuel A; Haider, Neena B; Nystuen, Arne M
神经科学
发表日期：2009
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A novel mutation in Prph2, a gene regulated by Nr2e3, causes retinal degeneration and outer-segment defects similar to Nr2e3 ( rd7/rd7 ) retinas

Prph2基因（一种受Nr2e3调控的基因）中的一种新突变会导致视网膜变性和外节缺陷，类似于Nr2e3（rd7/rd7）视网膜。

期刊:Mammalian Genome
影响因子:2.7
doi:10.1007/s00335-008-9138-5
Nystuen, Arne M; Sachs, Andrew J; Yuan, Yang; Heuermann, Laura; Haider, Neena B
信号转导
发表日期：2008
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