Similar articles for PMID: 21147271

Year	Number of Results
1997	1
1999	2
2000	2
2001	4
2002	4
2003	1
2004	3
2006	3
2007	3
2008	2
2009	5
2010	4
2011	9
2012	9
2013	11
2014	10
2015	4
2016	4
2017	5
2018	2
2019	6
2020	5
2021	3
2022	5
2023	4
2024	1

1

Blood cells from Friedreich ataxia patients harbor frataxin deficiency without a loss of mitochondrial function.

Selak MA, Lyver E, Micklow E, Deutsch EC, Onder O, Selamoglu N, Yager C, Knight S, Carroll M, Daldal F, Dancis A, Lynch DR, Sarry JE. Selak MA, et al. Mitochondrion. 2011 Mar;11(2):342-50. doi: 10.1016/j.mito.2010.12.003. Epub 2010 Dec 13. Mitochondrion. 2011. PMID: 21147271 Free PMC article.

2

GRP75 overexpression rescues frataxin deficiency and mitochondrial phenotypes in Friedreich ataxia cellular models.

Dong YN, McMillan E, Clark EM, Lin H, Lynch DR. Dong YN, et al. Hum Mol Genet. 2019 May 15;28(10):1594-1607. doi: 10.1093/hmg/ddy448. Hum Mol Genet. 2019. PMID: 30590615 Free PMC article.

3

PPAR gamma agonist leriglitazone improves frataxin-loss impairments in cellular and animal models of Friedreich Ataxia.

Rodríguez-Pascau L, Britti E, Calap-Quintana P, Dong YN, Vergara C, Delaspre F, Medina-Carbonero M, Tamarit J, Pallardó FV, Gonzalez-Cabo P, Ros J, Lynch DR, Martinell M, Pizcueta P. Rodríguez-Pascau L, et al. Neurobiol Dis. 2021 Jan;148:105162. doi: 10.1016/j.nbd.2020.105162. Epub 2020 Nov 7. Neurobiol Dis. 2021. PMID: 33171227 Free article.

4

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. Fil D, et al. Dis Model Mech. 2020 Jul 27;13(7):dmm045229. doi: 10.1242/dmm.045229. Dis Model Mech. 2020. PMID: 32586831 Free PMC article.

5

Human frataxin, the Friedreich ataxia deficient protein, interacts with mitochondrial respiratory chain.

Doni D, Cavion F, Bortolus M, Baschiera E, Muccioli S, Tombesi G, d'Ettorre F, Ottaviani D, Marchesan E, Leanza L, Greggio E, Ziviani E, Russo A, Bellin M, Sartori G, Carbonera D, Salviati L, Costantini P. Doni D, et al. Cell Death Dis. 2023 Dec 8;14(12):805. doi: 10.1038/s41419-023-06320-y. Cell Death Dis. 2023. PMID: 38062036 Free PMC article.

6

Exenatide induces frataxin expression and improves mitochondrial function in Friedreich ataxia.

Igoillo-Esteve M, Oliveira AF, Cosentino C, Fantuzzi F, Demarez C, Toivonen S, Hu A, Chintawar S, Lopes M, Pachera N, Cai Y, Abdulkarim B, Rai M, Marselli L, Marchetti P, Tariq M, Jonas JC, Boscolo M, Pandolfo M, Eizirik DL, Cnop M. Igoillo-Esteve M, et al. JCI Insight. 2020 Jan 30;5(2):e134221. doi: 10.1172/jci.insight.134221. JCI Insight. 2020. PMID: 31877117 Free PMC article.

7

Friedreich ataxia: an update on animal models, frataxin function and therapies.

González-Cabo P, Llorens JV, Palau F, Moltó MD. González-Cabo P, et al. Adv Exp Med Biol. 2009;652:247-61. doi: 10.1007/978-90-481-2813-6_17. Adv Exp Med Biol. 2009. PMID: 20225031 Review.

8

Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia.

Rötig A, de Lonlay P, Chretien D, Foury F, Koenig M, Sidi D, Munnich A, Rustin P. Rötig A, et al. Nat Genet. 1997 Oct;17(2):215-7. doi: 10.1038/ng1097-215. Nat Genet. 1997. PMID: 9326946

9

Missense mutations linked to friedreich ataxia have different but synergistic effects on mitochondrial frataxin isoforms.

Li H, Gakh O, Smith DY 4th, Ranatunga WK, Isaya G. Li H, et al. J Biol Chem. 2013 Feb 8;288(6):4116-27. doi: 10.1074/jbc.M112.435263. Epub 2012 Dec 26. J Biol Chem. 2013. PMID: 23269675 Free PMC article.

10

Mitochondrial dysfunction in friedreich's ataxia.

Lodi R, Taylor DJ, Schapira AH. Lodi R, et al. Biol Signals Recept. 2001 May-Aug;10(3-4):263-70. doi: 10.1159/000046891. Biol Signals Recept. 2001. PMID: 11351132 Review.

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