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PLoS Genetics, ISSN 1553-7390, 05/2015, Volume 11, Issue 5
  According to Luo and colleagues [20], the skewed persistence of paternal mtDNA in only one of the 4-cell blastomers followed by subsequent uneven... 
Haplotypes | Mitochondria | Noise | Sperm | Spermatogenesis | Mitochondrial DNA | Mammals | Embryos | Deoxyribonucleic acid--DNA
Journal Article
PLoS Genetics, ISSN 1553-7390, 05/2015, Volume 11, Issue 5, pp. e1005179 - e1005179
Journal Article
Mitochondrion, ISSN 1567-7249, 09/2015, Volume 24, pp. S37 - S37
Journal Article
Journal Article
Journal Article
Journal Article
Movement Disorders, ISSN 0885-3185, 03/2017, Volume 32, Issue 3, pp. 346 - 363
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2012, Volume 90, Issue 5, pp. 915 - 924
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2012, Volume 109, Issue 49, pp. 20065 - 20070
An animal model of Leber hereditary optic neuropathy (LHON) was produced by introducing the human optic atrophy mtDNA ND6 P25L mutation into the mouse. Mice... 
Axons | Mitochondria | Optic atrophy | Optic nerve | Leber hereditary optic atrophy | Cell lines | Mitochondrial DNA | Biochemistry | Synaptosomes | Genetic mutation | Neurodegenerative disease | Ophthalmology | Oxidative phosphorylation | Maternal inheritance | LIFE-SPAN | neurodegenerative disease | MULTIDISCIPLINARY SCIENCES | MITOCHONDRIAL-DNA MUTATION | CELL LINES | maternal inheritance | oxidative phosphorylation | GLUTAMATE TRANSPORT | ENCEPHALOPATHY | RESPIRATORY COMPLEX I | ophthalmology | MICE | CYBRIDS | DYSFUNCTION | SUPEROXIDE-DISMUTASE | Electroretinography | Optic Nerve - pathology | Optic Atrophy, Hereditary, Leber - complications | Reactive Oxygen Species - metabolism | Age Factors | Humans | Oxidative Stress - physiology | Immunoblotting | NADH Dehydrogenase - genetics | Optic Atrophy, Hereditary, Leber - genetics | Synaptosomes - metabolism | Mutation, Missense - genetics | Animals | DNA, Mitochondrial - genetics | Adenosine Triphosphate - metabolism | Demyelinating Diseases - etiology | Mice | Demyelinating Diseases - pathology | Optic Atrophy, Hereditary, Leber - physiopathology | Retina - pathology | Disease Models, Animal | Development and progression | Genetic aspects | Gene mutations | Health aspects | Oxidative stress | Rodents | Retina | Mutation | Adenosine triphosphatase | Index Medicus | Biological Sciences
Journal Article