Corrigendum to "Acid ceramidase improves mitochondrial function and oxidative stress in Niemann-Pick type C disease by repressing STARD1 expression and mitochondrial cholesterol accumulation" [Redox Biol. 2021 45 102052].
作者信息
Torres S, Solsona-Vilarrasa E, Nuñez S, Matías N, Insausti-Urkia N, Castro F, Casasempere M, Fabriás G, Casas J, Enrich C, Fernández-Checa J C, Garcia-Ruiz C
机构信息
Cell Death and Proliferation, Institute of Biomedical Research of Barcelona (IIBB), CSIC, Barcelona, Spain; Liver Unit, Hospital Clinic I Provincial de Barcelona, IDIBAPS and CIBERehd, Barcelona, Spain.
Cell Death and Proliferation, Institute of Biomedical Research of Barcelona (IIBB), CSIC, Barcelona, Spain.
出版信息
Redox Biol. 2022 Apr;50:102231. doi: 10.1016/j.redox.2022.102231. Epub 2022 Jan 10.
Abstract
摘要
相似文献
1
Corrigendum to "Acid ceramidase improves mitochondrial function and oxidative stress in Niemann-Pick type C disease by repressing STARD1 expression and mitochondrial cholesterol accumulation" [Redox Biol. 2021 45 102052].对“酸性神经酰胺酶通过抑制STARD1表达和线粒体胆固醇积累改善尼曼-匹克C型病中的线粒体功能和氧化应激”的勘误 [《氧化还原生物学》。2021年，第45卷，第102052页]
Redox Biol. 2022 Apr;50:102231. doi: 10.1016/j.redox.2022.102231. Epub 2022 Jan 10.
2
Acid ceramidase improves mitochondrial function and oxidative stress in Niemann-Pick type C disease by repressing STARD1 expression and mitochondrial cholesterol accumulation.酸性鞘磷脂酶可通过抑制 STARD1 表达和线粒体胆固醇积累改善尼曼-匹克 C 病的线粒体功能和氧化应激。
Redox Biol. 2021 Sep;45:102052. doi: 10.1016/j.redox.2021.102052. Epub 2021 Jun 19.
3
Mitochondrial Cholesterol in Alzheimer's Disease and Niemann-Pick Type C Disease.阿尔茨海默病和尼曼-匹克C型病中的线粒体胆固醇
Front Neurol. 2019 Nov 7;10:1168. doi: 10.3389/fneur.2019.01168. eCollection 2019.
4
Decreased membrane cholesterol in liver mitochondria of the point mutation mouse model of juvenile Niemann-Pick C1, Npc1.少年型尼曼-匹克 C1 型（NPC1）点突变鼠模型肝线粒体膜胆固醇降低
Mitochondrion. 2020 Mar;51:15-21. doi: 10.1016/j.mito.2019.12.003. Epub 2019 Dec 17.
5
Mitochondrial dysfunction in fibroblasts derived from patients with Niemann-Pick type C disease.尼曼-匹克C型病患者来源的成纤维细胞中的线粒体功能障碍。
Arch Biochem Biophys. 2016 Mar 1;593:50-9. doi: 10.1016/j.abb.2016.02.012. Epub 2016 Feb 8.
6
Pathophysiological In Vitro Profile of Neuronal Differentiated Cells Derived from Niemann-Pick Disease Type C2 Patient-Specific iPSCs Carrying the Mutations c.58G>T/c.140G>T.源自携带突变 c.58G>T/c.140G>T 的尼曼-匹克病 C2 型患者特异性 iPS 细胞的神经元分化细胞的病理生理体外特征。
Int J Mol Sci. 2021 Apr 13;22(8):4009. doi: 10.3390/ijms22084009.
7
Lysosomal and Mitochondrial Liaisons in Niemann-Pick Disease.尼曼-匹克病中的溶酶体与线粒体联系
Front Physiol. 2017 Nov 30;8:982. doi: 10.3389/fphys.2017.00982. eCollection 2017.
8
Adult-onset Niemann-Pick type C disease. Clinical, biochemical, and genetic study.成人型尼曼-匹克C型病。临床、生化及遗传学研究。
Arch Neurol. 1997 Dec;54(12):1536-41. doi: 10.1001/archneur.1997.00550240084016.
9
Mitochondrial cholesterol import.线粒体胆固醇摄取。
Biochim Biophys Acta Mol Cell Biol Lipids. 2017 Jan;1862(1):90-101. doi: 10.1016/j.bbalip.2016.08.012. Epub 2016 Aug 23.
10
The ceramide activated protein phosphatase Sit4 impairs sphingolipid dynamics, mitochondrial function and lifespan in a yeast model of Niemann-Pick type C1.神经鞘氨醇激活的蛋白磷酸酶 Sit4 损害神经鞘氨醇脂动态平衡、线粒体功能和尼曼-匹克 C1 型酵母模型中的寿命。
Biochim Biophys Acta Mol Basis Dis. 2018 Jan;1864(1):79-88. doi: 10.1016/j.bbadis.2017.10.010. Epub 2017 Oct 6.
引用本文的文献
1
Lysosomal positioning diseases: beyond substrate storage.溶酶体定位疾病：超越底物存储。
Open Biol. 2022 Oct;12(10):220155. doi: 10.1098/rsob.220155. Epub 2022 Oct 26.
Zotero 插件