نتائج البحث

Extensive mitogenomic heteroplasmy and its implications in the phylogeny of the fish genus Megalobrama.

• Authors : Liu, Kai¹ (AUTHOR) ; Xie, Nan¹ (AUTHOR); Wang, Yuxi¹ (AUTHOR)

• Source: 3 Biotech. 3/10/2023, Vol. 13 Issue 4, p1-10. 10p.

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Heteroplasmy and ancient translocation of mitochondrial DNA to the nucleus in the Chinese Horseshoe Bat (Rhinolophus sinicus) complex.

• Authors : Mao X; Institute of Molecular Ecology and Evolution, Institute for Advanced Studies in Multidisciplinary Science and Technology, East China Normal University, Shanghai, China; School of Biological and Chemical Sciences, Queen Mary University of London, London, United Kingdom.

Subjects: Genetic Variation* ; Phylogeny*; Active Transport, Cell Nucleus/Active Transport, Cell Nucleus/Active Transport, Cell Nucleus/*physiology

• Source: PloS one [PLoS One] 2014 May 19; Vol. 9 (5), pp. e98035. Date of Electronic Publication: 2014 May 19 (Print Publication: 2014).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation.

• Authors : Zhu Y; Huang S; Kang D

Subjects: DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics ; RNA, Ribosomal/RNA, Ribosomal/RNA, Ribosomal/*genetics

• Source: BMC genetics [BMC Genet] 2014 Feb 17; Vol. 15, pp. 26. Date of Electronic Publication: 2014 Feb 17.Publisher: BioMed Central Country of Publication: England NLM ID: 100966978 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2156

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Heteroplasmy in the mitochondrial genomes of human lice and ticks revealed by high throughput sequencing.

• Authors : Xiong H; Parasitology Section, School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia.; Barker SC

Subjects: Genome, Mitochondrial* ; Polymorphism, Genetic*; Electron Transport Complex IV/Electron Transport Complex IV/Electron Transport Complex IV/*genetics

• Source: PloS one [PLoS One] 2013 Sep 13; Vol. 8 (9), pp. e73329. Date of Electronic Publication: 2013 Sep 13 (Print Publication: 2013).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Two-stage association study of mitochondrial DNA variants in allergic rhinitis.

• Authors : Yuan, Huajie¹ (AUTHOR); Wang, Lingling¹ (AUTHOR); Wang, Song¹ (AUTHOR)

• Source: Allergy, Asthma & Clinical Immunology. 2/23/2024, Vol. 20 Issue 1, p1-10. 10p.

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A New Mitochondrial Genome of Sogatella furcifera (Horváth) (Hemiptera: Delphacidae) and Mitogenome-Wide Investigation on Polymorphisms.

• Authors : Park, Jongsun¹ (AUTHOR) ; Xi, Hong¹ (AUTHOR) ; Park, Jonghyun¹ (AUTHOR)

• Source: Insects (2075-4450). Dec2021, Vol. 12 Issue 12, p1066-1066. 1p.

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Control region mutations and the 'common deletion' are frequent in the mitochondrial DNA of patients with esophageal squamous cell carcinoma.

• Authors : Abnet, Christian C.¹ ; Huppi, Konrad¹ ; Carrera, Ana²

• Source: BMC Cancer. 2004, Vol. 4, p30-8. 8p. 2 Charts, 1 Graph.

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Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation.

• Authors : Gu P; College of Otolaryngology Head and Neck Surgery, Chinese PLA General Hospital, Chinese PLA Medical School, Do.28 Fuxing Road, Beijing, 100853, People's Republic of China.; National Clinical Research Center for Otolaryngologic Diseases, State Key Lab of Hearing Science, Ministry of Education, Beijing, People's Republic of China.

Subjects: DNA, Mitochondrial*/DNA, Mitochondrial*/DNA, Mitochondrial*/genetics ; Deafness*/Deafness*/Deafness*/genetics; China

• Source: BMC medical genomics [BMC Med Genomics] 2022 May 25; Vol. 15 (1), pp. 121. Date of Electronic Publication: 2022 May 25.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Rapid Detection of the mt3243A > G Mutation Using Urine Sediment in Elderly Chinese Type 2 Diabetic Patients.

• Authors : Zhang Y; The Metabolic Diseases Biobank, Center for Translational Medicine, Shanghai Key Laboratory of Diabetes, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai 200233, China.; Du X

Subjects: Mutation*; Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*genetics ; RNA, Transfer, Leu/RNA, Transfer, Leu/RNA, Transfer, Leu/*genetics

• Source: Journal of diabetes research [J Diabetes Res] 2017; Vol. 2017, pp. 4683857. Date of Electronic Publication: 2017 Jun 21.Publisher: Hindawi Limited Country of Publication: England NLM ID: 101605237 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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The unique characteristics of Thai Leber hereditary optic neuropathy: analysis of 30 G11778A pedigrees.

• Authors : Phasukkijwatana N; Department of Biochemistry, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.; Chuenkongkaew WL

Subjects: Pedigree*; Optic Atrophies, Hereditary/Optic Atrophies, Hereditary/Optic Atrophies, Hereditary/*genetics; Adolescent

• Source: Journal of human genetics [J Hum Genet] 2006; Vol. 51 (4), pp. 298-304. Date of Electronic Publication: 2006 Feb 14.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Print ISSN:

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