Found: 11
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Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families.
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 3, p. 134, doi. 10.1038/jhg.2013.134
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- Publication type:
- Article
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.
- Published in:
- Nature Genetics, 2014, v. 46, n. 9, p. 1007, doi. 10.1038/ng.3061
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- Publication type:
- Article
Clinical Features of Combined Central Retinal Artery and Vein Occlusion.
- Published in:
- Journal of Ophthalmology, 2019, p. 1, doi. 10.1155/2019/7202731
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- Publication type:
- Article
A Novel BBS9 Mutation Identified via Whole-Exome Sequencing in a Chinese Family with Bardet-Biedl Syndrome.
- Published in:
- BioMed Research International, 2021, p. 1, doi. 10.1155/2021/4514967
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- Publication type:
- Article
Genetic and phenotypic characteristics of four Chinese families with fundus albipunctatus.
- Published in:
- Scientific Reports, 2017, p. 46285, doi. 10.1038/srep46285
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- Publication type:
- Article
PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.
- Published in:
- 2020
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- Publication type:
- journal article
Efficacy and Safety of Houttuynia Eye Drops Atomization Treatment for Meibomian Gland Dysfunction-Related Dry Eye Disease: A Randomized, Double-Blinded, Placebo-Controlled Clinical Trial.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 12, p. 4022, doi. 10.3390/jcm9124022
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- Publication type:
- Article
Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 9, p. 1515, doi. 10.1093/hmg/ddy450
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- Publication type:
- Article
The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 3, p. 584, doi. 10.1093/hmg/ddv498
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- Publication type:
- Article
Fragment type and water nutrient interact and affect the survival and establishment of Myriophyllum aquaticum.
- Published in:
- Hydrobiologia, 2018, v. 817, n. 1, p. 205, doi. 10.1007/s10750-017-3388-8
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- Publication type:
- Article
High Mobility Group Box-1 Promotes Inflammation-Induced Lymphangiogenesis via Toll-Like Receptor 4-Dependent Signalling Pathway.
- Published in:
- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0154187
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- Publication type:
- Article