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Academic Journal

Mitochondrial DNA Missense Mutations ChrMT: 8981A > G and ChrMT: 6268C > T Identified in a Caucasian Female with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Triggered by the Epstein–Barr Virus.

Authors : Tang-Siegel, Gaoyan G.¹ (AUTHOR) ; Maughan, David W.¹ (AUTHOR); Frownfelter, Milah B.² (AUTHOR)

Source: Case Reports in Genetics. 5/9/2024, Vol. 2024, p1-10. 10p.

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Academic Journal

Exploring the Interplay between Mitochondrial DNA and Lifestyle Factors in the Pathogenesis of Psychiatric Disorders.

Authors : Wei, Wenming¹ (AUTHOR); Cheng, Bolun¹ (AUTHOR); Zhao, Yijing¹ (AUTHOR)

Source: Depression & Anxiety (1091-4269). 3/20/2024, Vol. 2024, p1-10. 10p.

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Academic Journal

Relationship of Mitochondrial DNA Oxidation and Content with Metabolic Syndrome and Cardiovascular Risk in Obesity Phenotypes.

Authors : Rojo, Mailén^1,2 (AUTHOR); Pérez, Hernán^2,3 (AUTHOR); Millán, Andrea Liliana^1,2 (AUTHOR)

Source: Journal of Obesity. 9/11/2024, Vol. 2024, p1-11. 11p.

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Fulminant Neonatal Liver Failure in MPV 17-Related Mitochondrial DNA Depletion Syndrome.

Authors : Abduljalil, Razan¹ (AUTHOR); Ben Turkia, Hadhami¹ (AUTHOR); Fakhroo, Aysha¹ (AUTHOR)

Source: Case Reports in Hepatology. 6/20/2023, p1-4. 4p.

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Effects of Treadmill Exercise on Mitochondrial DNA Damage and Cardiomyocyte Telomerase Activity in Aging Model Rats Based on Classical Apoptosis Signaling Pathway.

Authors : Liang, Chao¹ (AUTHOR); Zhou, Xiaoli² (AUTHOR); Li, Meiling³ (AUTHOR)

Source: BioMed Research International. 4/14/2022, p1-8. 8p.

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Academic Journal

Kearns–Sayre Syndrome Minus: Two Cases of Identical Large-Scale Mitochondrial DNA Deletions with Presentations outside the Classical Triad.

Authors : Gloria Pang, Shir Wey¹ (AUTHOR); Chih Lee, Hencher Han² (AUTHOR); Ng Wing kei, Carol^1,3 (AUTHOR)

Source: Case Reports in Genetics. 4/23/2022, p1-8. 8p.

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Whole-Exome Sequencing Identifies a Novel POLG Frameshift Variant in an Adult Patient Presenting with Progressive External Ophthalmoplegia and Mitochondrial DNA Depletion.

Authors : Kurtz, Justin¹ (AUTHOR); Fernandes Jr, Joseph Americo² (AUTHOR); Mansukhani, Mahesh¹ (AUTHOR)

Source: Case Reports in Genetics. 11/5/2021, p1-7. 7p.

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Discovery of a Novel Shared Variant Among RTEL1 Gene and RTEL1-TNFRSF6B lncRNA at Chromosome 20q13.33 in Familial Progressive Myoclonus Epilepsy.

Authors : Chaudhari, Sima¹ (AUTHOR); Acharya, Lavanya Prakash¹ (AUTHOR); Jasti, Dushyanth Babu² (AUTHOR)

Source: International Journal of Genomics. 8/10/2024, Vol. 2024, p1-15. 15p.

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Mitogenomic Characterization of South African Leopards and the Effect of Past Climatic Events.

Authors : Tensen, Laura^1,2,3 (AUTHOR); Emami-Khoyi, Arsalan^2,4 (AUTHOR); Khan, Anubhab³ (AUTHOR)

Source: Journal of Zoological Systematics & Evolutionary Research. 5/4/2024, Vol. 2024, p1-14. 14p.

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Conflicting relationships of Vipera walser inferred from nuclear genes sequences and mitochondrial DNA.

Authors : Doniol‐Valcroze, Paul¹ (AUTHOR) ; Ursenbacher, Sylvain^2,3 (AUTHOR); Mebert, Konrad⁴ (AUTHOR)

Source: Journal of Zoological Systematics & Evolutionary Research. Nov2021, Vol. 59 Issue 8, p2307-2320. 14p.

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فلترة النتائج

Mitochondrial DNA Missense Mutations ChrMT: 8981A > G and ChrMT: 6268C > T Identified in a Caucasian Female with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Triggered by the Epstein–Barr Virus.

Exploring the Interplay between Mitochondrial DNA and Lifestyle Factors in the Pathogenesis of Psychiatric Disorders.

Relationship of Mitochondrial DNA Oxidation and Content with Metabolic Syndrome and Cardiovascular Risk in Obesity Phenotypes.

Fulminant Neonatal Liver Failure in MPV 17-Related Mitochondrial DNA Depletion Syndrome.

Effects of Treadmill Exercise on Mitochondrial DNA Damage and Cardiomyocyte Telomerase Activity in Aging Model Rats Based on Classical Apoptosis Signaling Pathway.

Kearns–Sayre Syndrome Minus: Two Cases of Identical Large-Scale Mitochondrial DNA Deletions with Presentations outside the Classical Triad.

Whole-Exome Sequencing Identifies a Novel POLG Frameshift Variant in an Adult Patient Presenting with Progressive External Ophthalmoplegia and Mitochondrial DNA Depletion.

Discovery of a Novel Shared Variant Among RTEL1 Gene and RTEL1-TNFRSF6B lncRNA at Chromosome 20q13.33 in Familial Progressive Myoclonus Epilepsy.

Mitogenomic Characterization of South African Leopards and the Effect of Past Climatic Events.

Conflicting relationships of Vipera walser inferred from nuclear genes sequences and mitochondrial DNA.

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