勘误：在表达人源化APOEε4和Trem2R47H的新型小鼠模型中揭示疾病机制
Corrigendum: Uncovering Disease Mechanisms in a Novel Mouse Model Expressing Humanized APOEε4 and Trem2R47H.
作者信息
Kotredes Kevin P, Oblak Adrian, Pandey Ravi S, Lin Peter Bor-Chian, Garceau Dylan, Williams Harriet, Uyar Asli, O'Rourke Rita, O'Rourke Sarah, Ingraham Cynthia, Bednarczyk Daria, Belanger Melisa, Cope Zackary, Foley Kate E, Logsdon Benjamin A, Mangravite Lara M, Sukoff Rizzo Stacey J, Territo Paul R, Carter Gregory W, Sasner Michael, Lamb Bruce T, Howell Gareth R
机构信息
The Jackson Laboratory, Bar Harbor, ME, United States.
Stark Neurosciences Research Institute, School of Medicine, Indiana University Bloomington, Indianapolis, IN, United States.
出版信息
Front Aging Neurosci. 2022 Feb 7;14:857628. doi: 10.3389/fnagi.2022.857628. eCollection 2022.
Abstract
[This corrects the article DOI: 10.3389/fnagi.2021.735524.].
摘要
[本文更正了文章的数字对象标识符：10.3389/fnagi.2021.735524。]
相似文献
1
Corrigendum: Uncovering Disease Mechanisms in a Novel Mouse Model Expressing Humanized APOEε4 and Trem2R47H.勘误：在表达人源化APOEε4和Trem2R47H的新型小鼠模型中揭示疾病机制
Front Aging Neurosci. 2022 Feb 7;14:857628. doi: 10.3389/fnagi.2022.857628. eCollection 2022.
2
Uncovering Disease Mechanisms in a Novel Mouse Model Expressing Humanized APOEε4 and Trem2*R47H.在表达人源化APOEε4和Trem2*R47H的新型小鼠模型中揭示疾病机制
Front Aging Neurosci. 2021 Oct 11;13:735524. doi: 10.3389/fnagi.2021.735524. eCollection 2021.
3
R47H Variant of TREM2 Associated With Alzheimer Disease in a Large Late-Onset Family: Clinical, Genetic, and Neuropathological Study.TREM2的R47H变异体与一个大型晚发型家族中的阿尔茨海默病相关：临床、遗传和神经病理学研究
JAMA Neurol. 2015 Aug;72(8):920-7. doi: 10.1001/jamaneurol.2015.0979.
4
Humanized TREM2 mice reveal microglia-intrinsic and -extrinsic effects of R47H polymorphism.人源化 Trem2 小鼠揭示了 R47H 多态性的小胶质细胞内在和外在作用。
J Exp Med. 2018 Mar 5;215(3):745-760. doi: 10.1084/jem.20171529. Epub 2018 Jan 10.
5
The Trem2 R47H Alzheimer's risk variant impairs splicing and reduces Trem2 mRNA and protein in mice but not in humans.Trem2 R47H 阿尔茨海默病风险变异体可损害剪接，并降低小鼠而非人类的 Trem2 mRNA 和蛋白。
Mol Neurodegener. 2018 Sep 6;13(1):49. doi: 10.1186/s13024-018-0280-6.
6
The Trem2 R47H variant confers loss-of-function-like phenotypes in Alzheimer's disease.Trem2 R47H 变异体在阿尔茨海默病中表现出类似功能丧失的表型。
Mol Neurodegener. 2018 Jun 1;13(1):29. doi: 10.1186/s13024-018-0262-8.
7
Plaque-associated human microglia accumulate lipid droplets in a chimeric model of Alzheimer's disease.斑块相关的人类小胶质细胞在阿尔茨海默病的嵌合模型中积累脂滴。
Mol Neurodegener. 2021 Jul 23;16(1):50. doi: 10.1186/s13024-021-00473-0.
8
Frontobasal gray matter loss is associated with the TREM2 p.R47H variant.额基底灰质丢失与TREM2基因p.R47H变体相关。
Neurobiol Aging. 2014 Dec;35(12):2681-2690. doi: 10.1016/j.neurobiolaging.2014.06.007. Epub 2014 Jun 17.
9
Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer's disease brains.阿尔茨海默病大脑中野生型和p.R47H TREM2变体的表达及加工分析
Mol Neurodegener. 2016 Nov 25;11(1):72. doi: 10.1186/s13024-016-0137-9.
10
The Alzheimer's Disease-Associated R47H Variant of TREM2 Has an Altered Glycosylation Pattern and Protein Stability.与阿尔茨海默病相关的TREM2基因R47H变异体具有改变的糖基化模式和蛋白质稳定性。
Front Neurosci. 2017 Jan 18;10:618. doi: 10.3389/fnins.2016.00618. eCollection 2016.
Zotero 插件