These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
305 related articles for article (PubMed ID: 32586831)
1. Mitochondrial damage and senescence phenotype of cells derived from a novel frataxin G127V point mutation mouse model of Friedreich's ataxia. Fil D; Chacko BK; Conley R; Ouyang X; Zhang J; Darley-Usmar VM; Zuberi AR; Lutz CM; Napierala M; Napierala JS Dis Model Mech; 2020 Jul; 13(7):. PubMed ID: 32586831 [TBL] [Abstract][Full Text] [Related]
2. Neurobehavioral deficits of mice expressing a low level of G127V mutant frataxin. Fil D; Conley RL; Zuberi AR; Lutz CM; Gemelli T; Napierala M; Napierala JS Neurobiol Dis; 2023 Feb; 177():105996. PubMed ID: 36638893 [TBL] [Abstract][Full Text] [Related]
3. Missense mutations linked to friedreich ataxia have different but synergistic effects on mitochondrial frataxin isoforms. Li H; Gakh O; Smith DY; Ranatunga WK; Isaya G J Biol Chem; 2013 Feb; 288(6):4116-27. PubMed ID: 23269675 [TBL] [Abstract][Full Text] [Related]
4. A Comprehensive Transcriptome Analysis Identifies FXN and BDNF as Novel Targets of miRNAs in Friedreich's Ataxia Patients. Misiorek JO; Schreiber AM; Urbanek-Trzeciak MO; Jazurek-Ciesiołka M; Hauser LA; Lynch DR; Napierala JS; Napierala M Mol Neurobiol; 2020 Jun; 57(6):2639-2653. PubMed ID: 32291635 [TBL] [Abstract][Full Text] [Related]
5. A novel GAA-repeat-expansion-based mouse model of Friedreich's ataxia. Anjomani Virmouni S; Ezzatizadeh V; Sandi C; Sandi M; Al-Mahdawi S; Chutake Y; Pook MA Dis Model Mech; 2015 Mar; 8(3):225-35. PubMed ID: 25681319 [TBL] [Abstract][Full Text] [Related]
6. Inhibition of the SUV4-20 H1 histone methyltransferase increases frataxin expression in Friedreich's ataxia patient cells. Vilema-Enríquez G; Quinlan R; Kilfeather P; Mazzone R; Saqlain S; Del Molino Del Barrio I; Donato A; Corda G; Li F; Vedadi M; Németh AH; Brennan PE; Wade-Martins R J Biol Chem; 2020 Dec; 295(52):17973-17985. PubMed ID: 33028632 [TBL] [Abstract][Full Text] [Related]
7. Effect of Mitochondrial and Cytosolic FXN Isoform Expression on Mitochondrial Dynamics and Metabolism. Agrò M; Díaz-Nido J Int J Mol Sci; 2020 Nov; 21(21):. PubMed ID: 33158039 [TBL] [Abstract][Full Text] [Related]
8. Mice harboring the FXN I151F pathological point mutation present decreased frataxin levels, a Friedreich ataxia-like phenotype, and mitochondrial alterations. Medina-Carbonero M; Sanz-Alcázar A; Britti E; Delaspre F; Cabiscol E; Ros J; Tamarit J Cell Mol Life Sci; 2022 Jan; 79(2):74. PubMed ID: 35038030 [TBL] [Abstract][Full Text] [Related]
9. GAA repeat expansion mutation mouse models of Friedreich ataxia exhibit oxidative stress leading to progressive neuronal and cardiac pathology. Al-Mahdawi S; Pinto RM; Varshney D; Lawrence L; Lowrie MB; Hughes S; Webster Z; Blake J; Cooper JM; King R; Pook MA Genomics; 2006 Nov; 88(5):580-90. PubMed ID: 16919418 [TBL] [Abstract][Full Text] [Related]
10. Posttranslational regulation of mitochondrial frataxin and identification of compounds that increase frataxin levels in Friedreich's ataxia. Hackett PT; Jia X; Li L; Ward DM J Biol Chem; 2022 Jun; 298(6):101982. PubMed ID: 35472330 [TBL] [Abstract][Full Text] [Related]
11. Comprehensive analysis of gene expression patterns in Friedreich's ataxia fibroblasts by RNA sequencing reveals altered levels of protein synthesis factors and solute carriers. Napierala JS; Li Y; Lu Y; Lin K; Hauser LA; Lynch DR; Napierala M Dis Model Mech; 2017 Nov; 10(11):1353-1369. PubMed ID: 29125828 [TBL] [Abstract][Full Text] [Related]
12. 'Mitochondrial energy imbalance and lipid peroxidation cause cell death in Friedreich's ataxia'. Abeti R; Parkinson MH; Hargreaves IP; Angelova PR; Sandi C; Pook MA; Giunti P; Abramov AY Cell Death Dis; 2016 May; 7(5):e2237. PubMed ID: 27228352 [TBL] [Abstract][Full Text] [Related]
13. A GAA repeat expansion reporter model of Friedreich's ataxia recapitulates the genomic context and allows rapid screening of therapeutic compounds. Lufino MM; Silva AM; Németh AH; Alegre-Abarrategui J; Russell AJ; Wade-Martins R Hum Mol Genet; 2013 Dec; 22(25):5173-87. PubMed ID: 23943791 [TBL] [Abstract][Full Text] [Related]
14. Alleviating GAA Repeat Induced Transcriptional Silencing of the Friedreich's Ataxia Gene During Somatic Cell Reprogramming. Polak U; Li Y; Butler JS; Napierala M Stem Cells Dev; 2016 Dec; 25(23):1788-1800. PubMed ID: 27615158 [TBL] [Abstract][Full Text] [Related]
15. Neurodegeneration in Friedreich's ataxia: from defective frataxin to oxidative stress. Gomes CM; Santos R Oxid Med Cell Longev; 2013; 2013():487534. PubMed ID: 23936609 [TBL] [Abstract][Full Text] [Related]
16. The displacement of frataxin from the mitochondrial cristae correlates with abnormal respiratory supercomplexes formation and bioenergetic defects in cells of Friedreich ataxia patients. Doni D; Rigoni G; Palumbo E; Baschiera E; Peruzzo R; De Rosa E; Caicci F; Passerini L; Bettio D; Russo A; Szabò I; Soriano ME; Salviati L; Costantini P FASEB J; 2021 Mar; 35(3):e21362. PubMed ID: 33629768 [TBL] [Abstract][Full Text] [Related]
17. The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis. Wong A; Yang J; Cavadini P; Gellera C; Lonnerdal B; Taroni F; Cortopassi G Hum Mol Genet; 1999 Mar; 8(3):425-30. PubMed ID: 9949201 [TBL] [Abstract][Full Text] [Related]
18. Targeting lipid peroxidation and mitochondrial imbalance in Friedreich's ataxia. Abeti R; Uzun E; Renganathan I; Honda T; Pook MA; Giunti P Pharmacol Res; 2015 Sep; 99():344-50. PubMed ID: 26141703 [TBL] [Abstract][Full Text] [Related]
19. DNA Base Damage Repair Crosstalks with Chromatin Structures to Contract Expanded GAA Repeats in Friedreich's Ataxia. Lai Y; Diaz N; Armbrister R; Agoulnik I; Liu Y Biomolecules; 2024 Jul; 14(7):. PubMed ID: 39062522 [TBL] [Abstract][Full Text] [Related]
20. Human frataxin maintains mitochondrial iron homeostasis in Saccharomyces cerevisiae. Cavadini P; Gellera C; Patel PI; Isaya G Hum Mol Genet; 2000 Oct; 9(17):2523-30. PubMed ID: 11030757 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]