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

A Novel SCA3 Knock-in Mouse Model Mimics the Human SCA3 Disease Phenotype Including Neuropathological, Behavioral, and Transcriptional Abnormalities Especially in Oligodendrocytes

新型 SCA3 基因敲入小鼠模型可模拟人类 SCA3 疾病表型，包括神经病理学、行为和转录异常（尤其是少突胶质细胞中的异常）

期刊:Molecular Neurobiology
影响因子:4.6
doi:10.1007/s12035-021-02610-8
Eva Haas, Rana D Incebacak, Thomas Hentrich, Chrisovalantou Huridou, Thorsten Schmidt, Nicolas Casadei, Yacine Maringer, Carola Bahl, Frank Zimmermann, James D Mills, Eleonora Aronica, Olaf Riess, Julia M Schulze-Hentrich, Jeannette Hübener-Schmid
神经
胶质细胞
IF
IHC-P
IP
WB
Mouse
MBP
发表日期：2022
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Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice

脊髓小脑共济失调 3 型中的神经丝：人类和小鼠共济失调前和共济失调阶段的血液生物标志物

期刊:EMBO Molecular Medicine
影响因子:9
doi:10.15252/emmm.201911803
Carlo Wilke, Eva Haas, Kathrin Reetz, Jennifer Faber, Hector Garcia-Moreno, Magda M Santana, Bart van de Warrenburg, Holger Hengel, Manuela Lima, Alessandro Filla, Alexandra Durr, Bela Melegh, Marcella Masciullo, Jon Infante, Paola Giunti, Manuela Neumann, Jeroen de Vries, Luis Pereira de Almeida, M
神经
Human
发表日期：2020
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Calpain-1 ablation partially rescues disease-associated hallmarks in models of Machado-Joseph disease

钙蛋白酶-1消融可部分挽救马查多-约瑟夫病模型中的疾病相关特征

期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddaa010
Jonasz J Weber, Eva Haas, Yacine Maringer, Stefan Hauser, Nicolas L P Casadei, Athar H Chishti, Olaf Riess, Jeannette Hübener-Schmid
信号转导
IHC
Goat
IgG Fc
发表日期：2020
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Greater Response Interference to Pain Faces Under Low Perceptual Load Conditions in Adolescents With Impairing Pain: A Role for Poor Attention Control Mechanisms in Pain Disability?

在感知负荷较低的情况下，疼痛障碍青少年对疼痛面孔的反应干扰更大：注意力控制机制不良在疼痛致残中的作用？

期刊:Journal of Pain
影响因子:4
doi:10.1016/j.jpain.2018.10.005
Lau, Jennifer Y F; Sprecher, Eva; Haas, Sara; Lisk, Stephen; Pagliaccio, David; Sharpe, Louise; Bar-Haim, Yair; Pine, Daniel S
发表日期：2019
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Development of an AAV-Based MicroRNA Gene Therapy to Treat Machado-Joseph Disease

开发基于 AAV 的 microRNA 基因疗法治疗 Machado-Joseph 病

期刊:Molecular Therapy-Methods & Clinical Development
影响因子:
doi:10.1016/j.omtm.2019.10.008
Raygene Martier, Marina Sogorb-Gonzalez, Janice Stricker-Shaver, Jeannette Hübener-Schmid, Sonay Keskin, Jiri Klima, Lodewijk J Toonen, Stefan Juhas, Jana Juhasova, Zdenka Ellederova, Jan Motlik, Eva Haas, Sander van Deventer, Pavlina Konstantinova, Huu Phuc Nguyen, Melvin M Evers
信号转导
发表日期：2019
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A mutation in the c-fos gene associated with congenital generalized lipodystrophy

c-fos基因突变与先天性全身性脂肪营养不良症相关

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/1750-1172-8-119
Knebel, Birgit; Kotzka, Jorg; Lehr, Stefan; Hartwig, Sonja; Avci, Haluk; Jacob, Sylvia; Nitzgen, Ulrike; Schiller, Martina; März, Winfried; Hoffmann, Michael M; Seemanova, Eva; Haas, Jutta; Muller-Wieland, Dirk
发表日期：2013
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