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Genetic Selection in Human Mitochondria

Lehtinen, S. K. (2001) · Tampere University Institutional Repository (Tampere University)

The potential risks of abnormal transmission of mtDNA through assisted reproductive

John, J. C. S., Lloyd, R. E. I., & Shourbagy, S. H. E. (2003)

Complex Ocular Motility Disorders in Children

Brodsky, M. C. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3384-6_7

Author response to the letter regarding the publication titled “Major cerebral vessels involvement in patients with MELAS syndrome: worth a scan? A systematic review”

Gramegna, L. L., Cortesi, I., Tonon, C., & Lodi, R. (2021) · Journal of Neuroradiology · doi:10.1016/j.neurad.2021.03.005

Originalités structurales et fonctionnelles du système d’aspartylation mitochondrial humain

Messmer, M. C. (2008) · Serveur des thèses de l'Université de Strasbourg (University of Strasbourg)

Stroke-Like Episodes in Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS)

Lin, V. W., & Pavlakis, S. G. (2024) · Springer eBooks · doi:10.1007/978-3-031-41777-1_7

Clinical and genetic analysis of essential hypertension with mitochondrial tRNAMet 4435A>G and YARS2 mutation

Guo, M., He, Y., Ade, C. H. E. N., Zhuang, Z., Pan, X., & Guan, M. (2024) · Journal of Zhejiang University (Medical Sciences) · doi:10.3724/zdxbyxb-2023-0571

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes with coexisting nemaline myopathy: a case report

Gunawardena, K., Somasundaram, P., Dissanayake, V. H. W., & Ratnayake, P. D. (2024) · Journal of Medical Case Reports · doi:10.1186/s13256-024-04723-9

Molekulargenetische Charakterisierung von Mutationen der mitochondrialen 12S rRNA bei Patienten mit bilateraler Vestibulopathie

Schmidt, C. (2007) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.7738

Etude de la dysfonction cellulaire et moléculaire du syndrome mitochondrial MELAS.

Geffroy, G. (2017) · theses.fr (ABES) · doi:10.70675/a2ae3815zb7a8z4cbcz9a2dz22dbcd055adb

Contribution de la protéine O-fucosyltransférase 1( POFUT1) à la différenciation myogénique et à la tumorigenèse colorectale

Chabanais, J. (2019) · theses.fr (ABES) · doi:10.70675/e92b8968z3dd2z4735z8091z1f5f9a03059e

Cell-free mtDNA drives pyroptosis and inflammation in m.3243A>G mitochondrial disease modelsPreprint

Moresco, M., Rapone, A., Tropeano, C. V., Capristo, M., Capirossi, G., Ormanbekova, D., Fiorini, C., Pasti, A. P., Valle, F., Danese, A., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.03.729489

L-citrulline treatment of nitric oxide deficiency in MELAS a phase I dose-finding and safety study

Almannai, M., Duong, J., El‐Hattab, A. W., Ali, M., Bauri, D., Hawk, N., Soler-Alfonso, C., DeLay, L., Chu, Z. D., Liu, N., et al. (2026) · Molecular Genetics and Metabolism · doi:10.1016/j.ymgme.2026.110209

How does mitochondrial heteroplasmy affect cell proliferation?

Sutton, S. K. (2006) · UC Research Repository (University of Canterbury) · doi:10.26021/9173

Search for Difference in Aminoacylation of Mitochondrial DNA‐encoded Wild‐type and Mutant Human tRNALeu?(UUR)

Wang, Z.-C., Xue‐min, W., You‐Xin, J., Jiao, B., Xu, F., Mingyong, M., & Ke‐Jun, Z. (2003) · IUBMB Life · doi:10.1080/1521654031000110190 · Cited by 1

Reduction of mitochondrial tRNALeu(UUR) aminoacylation by some MELAS‐associated mutations

Hao, R., Yao, Y., Zheng, Y., Xu, M., & Wang, E. (2004) · FEBS Letters · doi:10.1016/j.febslet.2004.11.004 · Cited by 26

The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2

Sasarman, F., Antonická, H., & Shoubridge, E. A. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn265 · Cited by 153

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

King, M. P., Koga, Y., Davidson, M., & Schon, E. A. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.2.480 · Cited by 458

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