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Cell Death and the Mitochondrial Encephalomyopathies

Flanigan, K. M., & Ratan, R. R. (1999) · Humana Press eBooks · doi:10.1007/978-1-4612-1602-5_13 · Cited by 4

Increased Prevalence 12308 A > G mutation in Mitochondrial tRNALeu (CUN) Gene Associated with earlier Age of Onset in Friedreich Ataxia

Heidari, M. M., Khatami, M., Houshmand, M., Mahmoudi, E., & Nafissi, S. (2011) · Iranian journal of child neurology. · doi:10.22037/ijcn.v5i4.2674 · Cited by 3

Loss of mutant mitochondrial DNA harboring the MELAS A3243G mutation in human cybrid cells after cell-cell fusion with normal tissue-derived fibroblast cells

Nagase (2009) · International Journal of Molecular Medicine · doi:10.3892/ijmm_00000325 · Cited by 3

A Novel Amplification-Refractory Mutation System-PCR Strategy to Screen MT-TL1 Pathogenic Variants in Patient Repositories

Bulduk, B. K., Kılıç, H. B., Bekircan‐Kurt, C. E., Haliloğlu, G., Erdem‐Özdamar, S., Topaloğlu, H., & Kocaefe, Ç. (2020) · Genetic Testing and Molecular Biomarkers · doi:10.1089/gtmb.2019.0079 · Cited by 3

The Human Mitochondrial Genome: Mechanisms of Expression and Maintenance

Berdanier, C. D. (2005) · CRC Press eBooks · doi:10.1201/9781420028843-8 · Cited by 3

The Human Mitochondrial Genome

Taanman, J., & Williams, S. L. (2005) · Oxidative stress and disease · doi:10.1201/9781420028843.ch3 · Cited by 3

Clinical and biochemical phenotype of the MELAS mutation

Miyabayashi, S., Hanamizu, H., Nakamura, R., Hayashi, J., & Tada, K. (1993) · Journal of Inherited Metabolic Disease · doi:10.1007/bf00714284 · Cited by 3

Cybrids in the Study of Animal Mitochondrial Genetics and Pathology

Pinkert, C. A., & Trounce, I. A. (2005) · Oxidative stress and disease · doi:10.1201/9781420028843.ch11 · Cited by 3

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts.

Chomyn, A., Martinuzzi, A., Yoneda, M., Daga, A., Hurko, O., Johns, D. R., Lai, S. T., Nonaka, I., Angelini, C. I., & Attardi, G. M. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4221 · Cited by 491

Quantification of tRNA3243Leu point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription

Suomalainen, A., Majander, A. S., Pihko, H. S., Peltonen, L., & Syvänen, A. (1993) · Human Molecular Genetics · doi:10.1093/hmg/2.5.525 · Cited by 66

Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS

Koga, Y., Davidson, M. M., Schon, E. A., & King, M. P. (1993) · Nucleic Acids Research · doi:10.1093/nar/21.3.657 · Cited by 44

The mitochondrial tRNALeu(UUR) mutation in MELAS: a model for pathogenesis

Schon, E. A., Koga, Y., Davidson, M. M., Moraes, C. T., & King, M. P. (1992) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/0005-2728(92)90226-r · Cited by 74

The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.

Moraes, C. T., Ricci, E., Bonilla, E., DiMauro, S., & Schon, E. A. (1992) · PubMed · Cited by 244