242 related articles for article (PubMed ID: 34177786)
1. Dominant Optic Atrophy (DOA): Modeling the Kaleidoscopic Roles of OPA1 in Mitochondrial Homeostasis.
Del Dotto V; Carelli V
Front Neurol; 2021; 12():681326. PubMed ID: 34177786
[TBL] [Abstract][Full Text] [Related]
2. Establishing induced pluripotent stem cell lines from two dominant optic atrophy patients with distinct
Pohl KA; Zhang X; Pham AH; Chan JW; Sadun AA; Yang XJ
Front Genet; 2023; 14():1251216. PubMed ID: 37745862
[TBL] [Abstract][Full Text] [Related]
3. CRISPR-Cas9 correction of
Sladen PE; Perdigão PRL; Salsbury G; Novoselova T; van der Spuy J; Chapple JP; Yu-Wai-Man P; Cheetham ME
Mol Ther Nucleic Acids; 2021 Dec; 26():432-443. PubMed ID: 34589289
[TBL] [Abstract][Full Text] [Related]
4. Optimized OPA1 Isoforms 1 and 7 Provide Therapeutic Benefit in Models of Mitochondrial Dysfunction.
Maloney DM; Chadderton N; Millington-Ward S; Palfi A; Shortall C; O'Byrne JJ; Cassidy L; Keegan D; Humphries P; Kenna P; Farrar GJ
Front Neurosci; 2020; 14():571479. PubMed ID: 33324145
[TBL] [Abstract][Full Text] [Related]
5. OPA1: How much do we know to approach therapy?
Del Dotto V; Fogazza M; Lenaers G; Rugolo M; Carelli V; Zanna C
Pharmacol Res; 2018 May; 131():199-210. PubMed ID: 29454676
[TBL] [Abstract][Full Text] [Related]
6. OPA1 gene therapy prevents retinal ganglion cell loss in a Dominant Optic Atrophy mouse model.
Sarzi E; Seveno M; Piro-Mégy C; Elzière L; Quilès M; Péquignot M; Müller A; Hamel CP; Lenaers G; Delettre C
Sci Rep; 2018 Feb; 8(1):2468. PubMed ID: 29410463
[TBL] [Abstract][Full Text] [Related]
7. OPA1 functions in mitochondria and dysfunctions in optic nerve.
Lenaers G; Reynier P; Elachouri G; Soukkarieh C; Olichon A; Belenguer P; Baricault L; Ducommun B; Hamel C; Delettre C
Int J Biochem Cell Biol; 2009 Oct; 41(10):1866-74. PubMed ID: 19389483
[TBL] [Abstract][Full Text] [Related]
8. Dominant optic atrophy: updates on the pathophysiology and clinical manifestations of the optic atrophy 1 mutation.
Chun BY; Rizzo JF
Curr Opin Ophthalmol; 2016 Nov; 27(6):475-480. PubMed ID: 27585216
[TBL] [Abstract][Full Text] [Related]
9. OPA1 expression in the normal rat retina and optic nerve.
Ju WK; Misaka T; Kushnareva Y; Nakagomi S; Agarwal N; Kubo Y; Lipton SA; Bossy-Wetzel E
J Comp Neurol; 2005 Jul; 488(1):1-10. PubMed ID: 15912498
[TBL] [Abstract][Full Text] [Related]
10. OPA1 (Kjer type) dominant optic atrophy: a novel mitochondrial disease.
Delettre C; Lenaers G; Pelloquin L; Belenguer P; Hamel CP
Mol Genet Metab; 2002 Feb; 75(2):97-107. PubMed ID: 11855928
[TBL] [Abstract][Full Text] [Related]
11. Mutations in DNM1L, as in OPA1, result in dominant optic atrophy despite opposite effects on mitochondrial fusion and fission.
Gerber S; Charif M; Chevrollier A; Chaumette T; Angebault C; Kane MS; Paris A; Alban J; Quiles M; Delettre C; Bonneau D; Procaccio V; Amati-Bonneau P; Reynier P; Leruez S; Calmon R; Boddaert N; Funalot B; Rio M; Bouccara D; Meunier I; Sesaki H; Kaplan J; Hamel CP; Rozet JM; Lenaers G
Brain; 2017 Oct; 140(10):2586-2596. PubMed ID: 28969390
[TBL] [Abstract][Full Text] [Related]
12. OPA1 haploinsufficiency induces a BNIP3-dependent decrease in mitophagy in neurons: relevance to Dominant Optic Atrophy.
Moulis MF; Millet AM; Daloyau M; Miquel MC; Ronsin B; Wissinger B; Arnauné-Pelloquin L; Belenguer P
J Neurochem; 2017 Feb; 140(3):485-494. PubMed ID: 27861891
[TBL] [Abstract][Full Text] [Related]
13. OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology.
Chao de la Barca JM; Prunier-Mirebeau D; Amati-Bonneau P; Ferré M; Sarzi E; Bris C; Leruez S; Chevrollier A; Desquiret-Dumas V; Gueguen N; Verny C; Hamel C; Miléa D; Procaccio V; Bonneau D; Lenaers G; Reynier P
Neurobiol Dis; 2016 Jun; 90():20-6. PubMed ID: 26311407
[TBL] [Abstract][Full Text] [Related]
14. Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models.
Del Dotto V; Fogazza M; Musiani F; Maresca A; Aleo SJ; Caporali L; La Morgia C; Nolli C; Lodi T; Goffrini P; Chan D; Carelli V; Rugolo M; Baruffini E; Zanna C
Biochim Biophys Acta Mol Basis Dis; 2018 Oct; 1864(10):3496-3514. PubMed ID: 30293569
[TBL] [Abstract][Full Text] [Related]
15. Early-onset severe neuromuscular phenotype associated with compound heterozygosity for OPA1 mutations.
Schaaf CP; Blazo M; Lewis RA; Tonini RE; Takei H; Wang J; Wong LJ; Scaglia F
Mol Genet Metab; 2011 Aug; 103(4):383-7. PubMed ID: 21636302
[TBL] [Abstract][Full Text] [Related]
16. OPA1-associated disorders: phenotypes and pathophysiology.
Amati-Bonneau P; Milea D; Bonneau D; Chevrollier A; Ferré M; Guillet V; Gueguen N; Loiseau D; de Crescenzo MA; Verny C; Procaccio V; Lenaers G; Reynier P
Int J Biochem Cell Biol; 2009 Oct; 41(10):1855-65. PubMed ID: 19389487
[TBL] [Abstract][Full Text] [Related]
17. Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.
Sarzi E; Seveno M; Angebault C; Milea D; Rönnbäck C; Quilès M; Adrian M; Grenier J; Caignard A; Lacroux A; Lavergne C; Reynier P; Larsen M; Hamel CP; Delettre C; Lenaers G; Müller A
Hum Mol Genet; 2016 Jun; 25(12):2539-2551. PubMed ID: 27260406
[TBL] [Abstract][Full Text] [Related]
18. Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy.
Nolli C; Goffrini P; Lazzaretti M; Zanna C; Vitale R; Lodi T; Baruffini E
Mitochondrion; 2015 Nov; 25():38-48. PubMed ID: 26455272
[TBL] [Abstract][Full Text] [Related]
19. Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene.
Formichi P; Radi E; Giorgi E; Gallus GN; Brunetti J; Battisti C; Rufa A; Dotti MT; Franceschini R; Bracci L; Federico A
J Neurol Sci; 2015 Apr; 351(1-2):99-108. PubMed ID: 25796301
[TBL] [Abstract][Full Text] [Related]
20. Modeling autosomal dominant optic atrophy using induced pluripotent stem cells and identifying potential therapeutic targets.
Chen J; Riazifar H; Guan MX; Huang T
Stem Cell Res Ther; 2016 Jan; 7():2. PubMed ID: 26738566
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]