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.
375 related articles for article (PubMed ID: 29366807)
1. Bioactivity and gene expression profiles of hiPSC-generated retinal ganglion cells in MT-ND4 mutated Leber's hereditary optic neuropathy. Wu YR; Wang AG; Chen YT; Yarmishyn AA; Buddhakosai W; Yang TC; Hwang DK; Yang YP; Shen CN; Lee HC; Chiou SH; Peng CH; Chen SJ Exp Cell Res; 2018 Feb; 363(2):299-309. PubMed ID: 29366807 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Glutamate Stimulation Dysregulates AMPA Receptors-Induced Signal Transduction Pathway in Leber's Inherited Optic Neuropathy Patient-Specific hiPSC-Derived Retinal Ganglion Cells. Yang YP; Nguyen PNN; Lin TC; Yarmishyn AA; Chen WS; Hwang DK; Chiou GY; Lin TW; Chien CS; Tsai CY; Chiou SH; Chen SJ; Peng CH; Hsu CC Cells; 2019 Jun; 8(6):. PubMed ID: 31234430 [TBL] [Abstract][Full Text] [Related]
4. Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON). Peron C; Mauceri R; Cabassi T; Segnali A; Maresca A; Iannielli A; Rizzo A; Sciacca FL; Broccoli V; Carelli V; Tiranti V Stem Cell Res; 2020 Oct; 48():101939. PubMed ID: 32771908 [TBL] [Abstract][Full Text] [Related]
5. Inhibition of angiogenesis by the secretome from iPSC-derived retinal ganglion cells with Leber's hereditary optic neuropathy-like phenotypes. Peng SY; Chen CY; Chen H; Yang YP; Wang ML; Tsai FT; Chien CS; Weng PY; Tsai ET; Wang IC; Hsu CC; Lin TC; Hwang DK; Chen SJ; Chiou SH; Chiao CC; Chien Y Biomed Pharmacother; 2024 Sep; 178():117270. PubMed ID: 39126773 [TBL] [Abstract][Full Text] [Related]
6. Generation of an induced pluripotent stem cell line from a patient with leber's hereditary optic neuropathy carrying a homoplasmic m.3635G > A mutation in the mitochondrial ND1 gene. Ji D; Su X; Hu C; Zhang Z; Wang M; Zou W; Shen L; Liu Y; Liang C; Du Y; Liang D; Cao Y Stem Cell Res; 2022 Aug; 63():102858. PubMed ID: 35905669 [TBL] [Abstract][Full Text] [Related]
7. Leber's Hereditary Optic Neuropathy as a Promising Disease for Gene Therapy Development. Karaarslan C Adv Ther; 2019 Dec; 36(12):3299-3307. PubMed ID: 31605306 [TBL] [Abstract][Full Text] [Related]
8. Mitochondrial replacement in an iPSC model of Leber's hereditary optic neuropathy. Wong RCB; Lim SY; Hung SSC; Jackson S; Khan S; Van Bergen NJ; De Smit E; Liang HH; Kearns LS; Clarke L; Mackey DA; Hewitt AW; Trounce IA; Pébay A Aging (Albany NY); 2017 Apr; 9(4):1341-1350. PubMed ID: 28455970 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathy. Nie Z; Wang C; Chen J; Ji Y; Zhang H; Zhao F; Zhou X; Guan MX Hum Mol Genet; 2023 Jan; 32(2):231-243. PubMed ID: 35947995 [TBL] [Abstract][Full Text] [Related]