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370 related items for PubMed ID: 9684291

  • 1. Molecular instability in the COII-tRNA(Lys) intergenic region of the human mitochondrial genome: multiple origins of the 9-bp deletion and heteroplasmy for expanded repeats.
    Thomas MG, Cook CE, Miller KW, Waring MJ, Hagelberg E.
    Philos Trans R Soc Lond B Biol Sci; 1998 Jun 29; 353(1371):955-65. PubMed ID: 9684291
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  • 2. Mitochondrial intergenic COII/tRNA(Lys) 9-bp deletion, a biomarker for hepatocellular carcinoma?
    Ren W, Li Y, Li R, Feng H, Wu S, Mao Y, Huang L.
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jul 29; 27(4):2520-2. PubMed ID: 26017042
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  • 3. Evolutionary history of the COII/tRNALys intergenic 9 base pair deletion in human mitochondrial DNAs from the Pacific.
    Redd AJ, Takezaki N, Sherry ST, McGarvey ST, Sofro AS, Stoneking M.
    Mol Biol Evol; 1995 Jul 29; 12(4):604-15. PubMed ID: 7659016
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  • 4. COII/tRNA(Lys) intergenic 9-bp deletion and other mtDNA markers clearly reveal that the Tharus (southern Nepal) have Oriental affinities.
    Passarino G, Semino O, Modiano G, Santachiara-Benerecetti AS.
    Am J Hum Genet; 1993 Sep 29; 53(3):609-18. PubMed ID: 8102506
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  • 5. mtDNA control-region sequence variation suggests multiple independent origins of an "Asian-specific" 9-bp deletion in sub-Saharan Africans.
    Soodyall H, Vigilant L, Hill AV, Stoneking M, Jenkins T.
    Am J Hum Genet; 1996 Mar 29; 58(3):595-608. PubMed ID: 8644719
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  • 6. Different population histories of the Mundari- and Mon-Khmer-speaking Austro-Asiatic tribes inferred from the mtDNA 9-bp deletion/insertion polymorphism in Indian populations.
    Thangaraj K, Sridhar V, Kivisild T, Reddy AG, Chaubey G, Singh VK, Kaur S, Agarawal P, Rai A, Gupta J, Mallick CB, Kumar N, Velavan TP, Suganthan R, Udaykumar D, Kumar R, Mishra R, Khan A, Annapurna C, Singh L.
    Hum Genet; 2005 May 29; 116(6):507-17. PubMed ID: 15772853
    [Abstract] [Full Text] [Related]

  • 7. The 9 bp Deletion between the Mitochondrial COII and Lysine tRNA Genes in a Caucasian Population with Cognitive Disorders: An Observational Study.
    Giuliano M, Santa Paola S, Borgione E, Lo Giudice M, Di Blasi FD, Pettinato R, Romano C, Scuderi C.
    Int J Mol Sci; 2024 Oct 09; 25(19):. PubMed ID: 39409155
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  • 8. Multiple independent origins of the COII/tRNA(Lys) intergenic 9-bp mtDNA deletion in aboriginal Australians.
    Betty DJ, Chin-Atkins AN, Croft L, Sraml M, Easteal S.
    Am J Hum Genet; 1996 Feb 09; 58(2):428-33. PubMed ID: 8571972
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  • 9. Mitochondrial insertion-deletion polymorphism: role in disease pathology.
    Komandur S, Venkatasubramanian S, Alluri RV, Rao P, Rao P, Hasan Q.
    Genet Test Mol Biomarkers; 2011 May 09; 15(5):361-4. PubMed ID: 21476899
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  • 20. Putative origin and function of the intergenic region between COI and COII of Apis mellifera L. mitochondrial DNA.
    Cornuet JM, Garnery L, Solignac M.
    Genetics; 1991 Jun 09; 128(2):393-403. PubMed ID: 1649072
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