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Literature DB >> 16563384

Focus on molecules: the OPA1 protein.

Vanessa Davies¹, Marcela Votruba.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2006 PMID： 16563384 DOI： 10.1016/j.exer.2005.11.021

Source DB: PubMed Journal: Exp Eye Res ISSN： 0014-4835 Impact factor: 3.467

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Cited

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12 in total

1. Correlation between polymorphisms in the MFN1 gene and myopia in Chinese population.

Authors: Yun-Chun Zou; Jia-Hong Lei; Ying Wang; Shuang Xu
Journal: Int J Ophthalmol Date: 2015-12-18 Impact factor: 1.779

2. AUTOPHAGY, MITOCHONDRIAL DYNAMICS AND RETINAL DISEASES.

Authors: Talia R Kaden; Wei Li
Journal: Asia Pac J Ophthalmol (Phila) Date: 2013 Sep-Oct

Review 3. Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.

Authors: Patrick Yu-Wai-Man; Philip G Griffiths; Patrick F Chinnery
Journal: Prog Retin Eye Res Date: 2010-11-26 Impact factor: 21.198

Review 4. Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.

Authors: Eleni Bagli; Anastasia K Zikou; Niki Agnantis; Georgios Kitsos
Journal: In Vivo Date: 2017 Jul-Aug Impact factor: 2.155

5. Multi-system neurological disease is common in patients with OPA1 mutations.

Authors: P Yu-Wai-Man; P G Griffiths; G S Gorman; C M Lourenco; A F Wright; M Auer-Grumbach; A Toscano; O Musumeci; M L Valentino; L Caporali; C Lamperti; C M Tallaksen; P Duffey; J Miller; R G Whittaker; M R Baker; M J Jackson; M P Clarke; B Dhillon; B Czermin; J D Stewart; G Hudson; P Reynier; D Bonneau; W Marques; G Lenaers; R McFarland; R W Taylor; D M Turnbull; M Votruba; M Zeviani; V Carelli; L A Bindoff; R Horvath; P Amati-Bonneau; P F Chinnery
Journal: Brain Date: 2010-02-15 Impact factor: 13.501

10. Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping.

Authors: Toby Andrew; Nikolas Maniatis; Francis Carbonaro; S H Melissa Liew; Winston Lau; Tim D Spector; Christopher J Hammond
Journal: PLoS Genet Date: 2008-10-10 Impact factor: 5.917

Focus on molecules: the OPA1 protein.

1. Correlation between polymorphisms in the MFN1 gene and myopia in Chinese population.

2. AUTOPHAGY, MITOCHONDRIAL DYNAMICS AND RETINAL DISEASES.

Review 3. Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.

Review 4. Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.

5. Multi-system neurological disease is common in patients with OPA1 mutations.

6. OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules.

7. Down-regulation of OPA1 in patients with primary open angle glaucoma.

8. Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy.

Review 9. Inherited mitochondrial optic neuropathies.

10. Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping.