Immp2l Mutation Induces Mitochondrial Membrane Depolarization and Complex III Activity Suppression after Middle Cerebral Artery Occlusion in Mice
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s11596-023-2726-5.pdf
Reference45 articles.
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2. Patel C, Cooper-Charles L, McMullan DJ, et al. Translocation breakpoint at 7q31 associated with tics: further evidence for IMMP2L as a candidate gene for Tourette syndrome. Eur J Hum Genet, 2011,19(6):634–639
3. Swaminathan S, Shen L, Kim S, et al. Analysis of copy number variation in Alzheimer’s disease: the NIALOAD/NCRAD Family Study. Curr Alzheimer Res, 2012,9(7):801–814
4. Gimelli S, Capra V, Di Rocco M, et al. Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders. Mol Cytogenet, 2014,7:54
5. Uehara DT, Freitas É L, Alves LU, et al. A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplication segregating with nonsyndromic hearing loss in a Brazilian family. Hum Genome Var, 2015,2:15038
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1. Inner Mitochondrial Membrane Peptidase 2-Like Deletion Aggravates Mitochondrial Apoptosis and Inhibits Autophagy After Hyperglycemia Stroke;Molecular Neurobiology;2024-09-14
2. Immp2l Enhances the Structure and Function of Mitochondrial Gpd2 Dehydrogenase;International Journal of Molecular Sciences;2024-01-12
3. Antioxidant Behavioural Phenotype in the Immp2l Gene Knock-Out Mouse;Genes;2023-08-28
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