| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/J.MITO.2011.06.006 |
| P698 | PubMed publication ID | 21742061 |
| P2093 | author name string | Min Liang | |
| Min-Xin Guan | |||
| Jia Qu | |||
| Yaping Qian | |||
| Xiangtian Zhou | |||
| P2860 | cites work | Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder | Q24538459 |
| Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background | Q24678122 | ||
| Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation | Q29614475 | ||
| Release of infectious Epstein-Barr virus by transformed marmoset leukocytes | Q35093948 | ||
| P433 | issue | 6 | |
| P921 | main subject | hereditary optic neuropathy | Q55789244 |
| P304 | page(s) | 871-877 | |
| P577 | publication date | 2011-07-01 | |
| P1433 | published in | Mitochondrion | Q2122381 |
| P1476 | title | The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation | |
| P478 | volume | 11 |
| Q35786077 | A method for mutagenesis of mouse mtDNA and a resource of mouse mtDNA mutations for modeling human pathological conditions |
| Q33916058 | A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis |
| Q40386722 | Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation |
| Q46515103 | Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. |
| Q37193896 | Coronary heart disease is associated with a mutation in mitochondrial tRNA. |
| Q36089268 | Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families |
| Q53072695 | Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families. |
| Q45738904 | Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees |
| Q34172317 | Profiling the mitochondrial proteome of Leber's Hereditary Optic Neuropathy (LHON) in Thailand: down-regulation of bioenergetics and mitochondrial protein quality control pathways in fibroblasts with the 11778G>A mutation |
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