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OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28.
- Published in:
- Nature Genetics, 2000, v. 26, n. 2, p. 211, doi. 10.1038/79944
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- Article
A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene.
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- Human Genetics, 2002, v. 110, n. 1, p. 52, doi. 10.1007/s00439-001-0645-7
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- Article
A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect.
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- Human Genetics, 2001, v. 109, n. 5, p. 498, doi. 10.1007/s004390100600
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- Article
Saturating density of STSs (1/6 kb) in a 1.1 Mb region on 3q28-q29: a valuable resource for cloning of disease genes.
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- European Journal of Human Genetics, 2001, v. 9, n. 4, p. 307, doi. 10.1038/sj.ejhg.5200630
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- Article
SLP-2 is required for stress-induced mitochondrial hyperfusion.
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- EMBO Journal, 2009, v. 28, n. 11, p. 1589, doi. 10.1038/emboj.2009.89
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- Article
Characterization of protein‐binding to the spinach chloroplast psbA mRNA 5′ untranslated region.
- Published in:
- Nucleic Acids Research, 1998, v. 26, n. 10, p. 2265, doi. 10.1093/nar/26.10.2265
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- Article
OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L.
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- Journal of Cell Biology, 2007, v. 178, n. 5, p. 749, doi. 10.1083/jcb.200704110
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- Article
Lactobacillus paracasei DSMZ16671 Reduces Mutans Streptococci: A Short-Term Pilot Study.
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- Probiotics & Antimicrobial Proteins, 2013, v. 5, n. 4, p. 259, doi. 10.1007/s12602-013-9148-9
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- Article
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophy.
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- Molecular Neurodegeneration, 2010, v. 5, p. 25, doi. 10.1186/1750-1326-5-25
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- Article
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.
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- Human Molecular Genetics, 2001, v. 10, n. 13, p. 1359, doi. 10.1093/hmg/10.13.1359
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- Article
OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 13, doi. 10.1093/hmg/10.13.1359
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- Publication type:
- Article
Characterization of OPA1 isoforms isolated from mouse tissues.
- Published in:
- Journal of Neurochemistry, 2008, v. 106, n. 1, p. 372, doi. 10.1111/j.1471-4159.2008.05401.x
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- Article