170 related articles for article (PubMed ID: 38710404)
1. Galactose-replacement unmasks the biochemical consequences of the G11778A mitochondrial DNA mutation of LHON in patient-derived fibroblasts.
Pasqualotto BA; Tegeman C; Frame AK; McPhedrain R; Halangoda K; Sheldon CA; Rintoul GL
Exp Cell Res; 2024 Jun; 439(1):114075. PubMed ID: 38710404
[TBL] [Abstract][Full Text] [Related]
2. Impaired mitochondrial morphological plasticity and failure of mitophagy associated with the G11778A mutation of LHON.
Pasqualotto BA; Nelson A; Deheshi S; Sheldon CA; Vogl AW; Rintoul GL
Biochem Biophys Res Commun; 2024 Aug; 721():150119. PubMed ID: 38768545
[TBL] [Abstract][Full Text] [Related]
3. Mitochondrial transport mediates survival of retinal ganglion cells in affected LHON patients.
Yang TC; Yarmishyn AA; Yang YP; Lu PC; Chou SJ; Wang ML; Lin TC; Hwang DK; Chou YB; Chen SJ; Yu WK; Wang AG; Hsu CC; Chiou SH
Hum Mol Genet; 2020 Jun; 29(9):1454-1464. PubMed ID: 32277753
[TBL] [Abstract][Full Text] [Related]
4. Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration.
Carelli V; Rugolo M; Sgarbi G; Ghelli A; Zanna C; Baracca A; Lenaz G; Napoli E; Martinuzzi A; Solaini G
Biochim Biophys Acta; 2004 Jul; 1658(1-2):172-9. PubMed ID: 15282189
[TBL] [Abstract][Full Text] [Related]
5. Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy.
Floreani M; Napoli E; Martinuzzi A; Pantano G; De Riva V; Trevisan R; Bisetto E; Valente L; Carelli V; Dabbeni-Sala F
FEBS J; 2005 Mar; 272(5):1124-35. PubMed ID: 15720387
[TBL] [Abstract][Full Text] [Related]
6. The metabolomic signature of Leber's hereditary optic neuropathy reveals endoplasmic reticulum stress.
Chao de la Barca JM; Simard G; Amati-Bonneau P; Safiedeen Z; Prunier-Mirebeau D; Chupin S; Gadras C; Tessier L; Gueguen N; Chevrollier A; Desquiret-Dumas V; Ferré M; Bris C; Kouassi Nzoughet J; Bocca C; Leruez S; Verny C; Miléa D; Bonneau D; Lenaers G; Martinez MC; Procaccio V; Reynier P
Brain; 2016 Nov; 139(11):2864-2876. PubMed ID: 27633772
[TBL] [Abstract][Full Text] [Related]
7. Increased Protein
Zhou L; Chan JCY; Chupin S; Gueguen N; Desquiret-Dumas V; Koh SK; Li J; Gao Y; Deng L; Verma C; Beuerman RW; Chan ECY; Milea D; Reynier P
Int J Mol Sci; 2020 Apr; 21(8):. PubMed ID: 32344771
[TBL] [Abstract][Full Text] [Related]
8. Yeast NDI1 improves oxidative phosphorylation capacity and increases protection against oxidative stress and cell death in cells carrying a Leber's hereditary optic neuropathy mutation.
Park JS; Li YF; Bai Y
Biochim Biophys Acta; 2007 May; 1772(5):533-42. PubMed ID: 17320357
[TBL] [Abstract][Full Text] [Related]
9. The G11778A LHON mutation does not enhance ethambutol cytotoxicity in a cybrid model.
Pommer R; Schoeler S; Mawrin C; Szibor R; Kirches E
Clin Neuropathol; 2008; 27(6):414-23. PubMed ID: 19130740
[TBL] [Abstract][Full Text] [Related]
10. Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium.
Ghelli A; Zanna C; Porcelli AM; Schapira AH; Martinuzzi A; Carelli V; Rugolo M
J Biol Chem; 2003 Feb; 278(6):4145-50. PubMed ID: 12446713
[TBL] [Abstract][Full Text] [Related]
11. Emerging model systems and treatment approaches for Leber's hereditary optic neuropathy: Challenges and opportunities.
Bahr T; Welburn K; Donnelly J; Bai Y
Biochim Biophys Acta Mol Basis Dis; 2020 Jun; 1866(6):165743. PubMed ID: 32105823
[TBL] [Abstract][Full Text] [Related]
12. Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.
Giordano C; Montopoli M; Perli E; Orlandi M; Fantin M; Ross-Cisneros FN; Caparrotta L; Martinuzzi A; Ragazzi E; Ghelli A; Sadun AA; d'Amati G; Carelli V
Brain; 2011 Jan; 134(Pt 1):220-34. PubMed ID: 20943885
[TBL] [Abstract][Full Text] [Related]
13. Oxidative Stress Profile in Genetically Confirmed Cases of Leber's Hereditary Optic Neuropathy.
Rovcanin B; Jancic J; Pajic J; Rovcanin M; Samardzic J; Djuric V; Nikolic B; Ivancevic N; Novakovic I; Kostic V
J Mol Neurosci; 2021 May; 71(5):1070-1081. PubMed ID: 33095398
[TBL] [Abstract][Full Text] [Related]
14. Leber's hereditary optic neuropathy: a multifactorial disease.
Yen MY; Wang AG; Wei YH
Prog Retin Eye Res; 2006 Jul; 25(4):381-96. PubMed ID: 16829155
[TBL] [Abstract][Full Text] [Related]
15. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
Mao YJ; Qu J; Guan MX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
[TBL] [Abstract][Full Text] [Related]
16. The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity.
Ghelli A; Porcelli AM; Zanna C; Vidoni S; Mattioli S; Barbieri A; Iommarini L; Pala M; Achilli A; Torroni A; Rugolo M; Carelli V
PLoS One; 2009 Nov; 4(11):e7922. PubMed ID: 19936068
[TBL] [Abstract][Full Text] [Related]
17. Use of mitochondrial antioxidant defenses for rescue of cells with a Leber hereditary optic neuropathy-causing mutation.
Qi X; Sun L; Hauswirth WW; Lewin AS; Guy J
Arch Ophthalmol; 2007 Feb; 125(2):268-72. PubMed ID: 17296905
[TBL] [Abstract][Full Text] [Related]
18. The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.
Qu J; Li R; Zhou X; Tong Y; Lu F; Qian Y; Hu Y; Mo JQ; West CE; Guan MX
Invest Ophthalmol Vis Sci; 2006 Feb; 47(2):475-83. PubMed ID: 16431939
[TBL] [Abstract][Full Text] [Related]
19. Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNA
Zhang J; Ji Y; Liu X; Chen J; Wang B; Zhang M; Guan MX
Mitochondrion; 2018 Sep; 42():84-91. PubMed ID: 29225014
[TBL] [Abstract][Full Text] [Related]
20. Cigarette toxicity triggers Leber's hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways.
Giordano L; Deceglie S; d'Adamo P; Valentino ML; La Morgia C; Fracasso F; Roberti M; Cappellari M; Petrosillo G; Ciaravolo S; Parente D; Giordano C; Maresca A; Iommarini L; Del Dotto V; Ghelli AM; Salomao SR; Berezovsky A; Belfort R; Sadun AA; Carelli V; Loguercio Polosa P; Cantatore P
Cell Death Dis; 2015 Dec; 6(12):e2021. PubMed ID: 26673666
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]