| scholarly article | Q13442814 |
| P2093 | author name string | Qin Wang | |
| Panfeng Wang | |||
| Qingjiong Zhang | |||
| Shiqiang Li | |||
| Xiangming Guo | |||
| Xiaoyun Jia | |||
| Xueshan Xiao | |||
| Yong-Gang Yao | |||
| Qing-Peng Kong | |||
| P2860 | cites work | Phylogeographic differentiation of mitochondrial DNA in Han Chinese | Q24632824 |
| Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background | Q24678122 | ||
| Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA | Q27860870 | ||
| Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases | Q28269333 | ||
| Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease | Q29398392 | ||
| Detecting errors in mtDNA data by phylogenetic analysis | Q30666169 | ||
| A call for mtDNA data quality control in forensic science | Q30919522 | ||
| Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility | Q33358078 | ||
| Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping | Q33375038 | ||
| Nuclear cataract and myopia during hyperbaric oxygen therapy | Q33643093 | ||
| Mitochondrial DNA haplogroups associated with age-related macular degeneration. | Q34924260 | ||
| Tracing the origins of Hakka and Chaoshanese by mitochondrial DNA analysis | Q34991696 | ||
| 1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging | Q35644545 | ||
| The mitochondrial impairment, oxidative stress and neurodegeneration connection: reality or just an attractive hypothesis? | Q37134820 | ||
| Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation | Q37156232 | ||
| Candidate gene and locus analysis of myopia | Q37419384 | ||
| OPA1 functions in mitochondria and dysfunctions in optic nerve. | Q37457225 | ||
| Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations | Q40323552 | ||
| Down-regulation of mammalian mitochondrial RNAs during oxidative stress. | Q41143520 | ||
| Basic mechanisms underlying the production of photochemical lesions in the mammalian retina | Q41592673 | ||
| Lipid peroxidation products and antioxidants in human disease | Q42014480 | ||
| Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1. | Q43168499 | ||
| A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612. | Q46624890 | ||
| Low levels of pigment epithelium-derived factor in highly myopic eyes with chorioretinal atrophy | Q46822507 | ||
| Ocular refractive changes in patients receiving hyperbaric oxygen administered by oronasal mask or hood. | Q51636341 | ||
| Mitochondrial haplogroups associated with Japanese centenarians, Alzheimer's patients, Parkinson's patients, type 2 diabetic patients and healthy non-obese young males. | Q53303487 | ||
| Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD. | Q53369985 | ||
| Epidemiology of myopia | Q55880061 | ||
| mtDNA haplogroup distribution in Chinese patients with Leber’s hereditary optic neuropathy and G11778A mutation | Q59295408 | ||
| Evolutionary history of the mtDNA 9-bp deletion in Chinese populations and its relevance to the peopling of east and southeast Asia | Q59295632 | ||
| Lipid peroxidation products in human subretinal fluid | Q71354874 | ||
| Myopia associated with hyperbaric oxygen therapy | Q71618614 | ||
| F(2) isoprostanes, potential specific markers of oxidative damage in human retina | Q73828615 | ||
| mtDNA haplogroup J: a contributing factor of optic neuritis | Q77421708 | ||
| Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1 | Q79919265 | ||
| Identification of apolipoprotein A-I as a "STOP" signal for myopia | Q80142919 | ||
| Mitochondrial DNA haplogroups and age-related maculopathy | Q81229189 | ||
| Does the mitochondrial genome play a role in the etiology of Alzheimer's disease? | Q82242627 | ||
| P921 | main subject | mitochondrial DNA | Q27075 |
| myopia | Q168403 | ||
| P304 | page(s) | 303-309 | |
| P577 | publication date | 2010-02-26 | |
| P1433 | published in | Molecular Vision | Q6895981 |
| P1476 | title | Mitochondrial DNA haplogroup distribution in Chaoshanese with and without myopia | |
| P478 | volume | 16 |
| Q35863038 | A novel truncation mutation in GJA1 associated with open angle glaucoma and microcornea in a large Chinese family |
| Q36408718 | Association of markers at chromosome 15q14 in Chinese patients with moderate to high myopia |
| Q35158256 | Cerulean cataract mapped to 12q13 and associated with a novel initiation codon mutation in MIP. |
| Q33812331 | Exome sequencing of 18 Chinese families with congenital cataracts: a new sight of the NHS gene |
| Q28533822 | Exome sequencing of 47 chinese families with cone-rod dystrophy: mutations in 25 known causative genes |
| Q28546422 | Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis |
| Q37539168 | Mitochondrial DNA haplogroup confers genetic susceptibility to nasopharyngeal carcinoma in Chaoshanese from Guangdong, China. |
| Q35047341 | Mutational screening of six genes in Chinese patients with congenital cataract and microcornea |
| Q88098249 | Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing |
| Q91627466 | RPE65 mutation frequency and phenotypic variation according to exome sequencing in a tertiary centre for genetic eye diseases in China |
| Q35629086 | Replication study of significant single nucleotide polymorphisms associated with myopia from two genome-wide association studies. |
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