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Journal Abstract Search

188 related items for PubMed ID: 21850008

  • 1. Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.
    Zhao D, Hong D, Zhang W, Yao S, Qi X, Lv H, Zheng R, Feng L, Huang Y, Yuan Y, Wang Z.
    J Hum Genet; 2011 Nov; 56(11):759-64. PubMed ID: 21850008
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  • 3. The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.
    Leng Y, Liu Y, Fang X, Li Y, Yu L, Yuan Y, Wang Z.
    Mitochondrial DNA; 2015 Apr; 26(2):208-12. PubMed ID: 24708134
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  • 4. The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.
    Shanske S, Coku J, Lu J, Ganesh J, Krishna S, Tanji K, Bonilla E, Naini AB, Hirano M, DiMauro S.
    Arch Neurol; 2008 Mar; 65(3):368-72. PubMed ID: 18332249
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  • 8. Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations?
    Liolitsa D, Rahman S, Benton S, Carr LJ, Hanna MG.
    Ann Neurol; 2003 Jan; 53(1):128-32. PubMed ID: 12509858
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  • 9. Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I.
    Danhelovska T, Kolarova H, Zeman J, Hansikova H, Vaneckova M, Lambert L, Kucerova-Vidrova V, Berankova K, Honzik T, Tesarova M.
    BMC Pediatr; 2020 Jan 29; 20(1):41. PubMed ID: 31996177
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  • 13. A MELAS syndrome family harboring two mutations in mitochondrial genome.
    Choi BO, Hwang JH, Kim J, Cho EM, Cho SY, Hwang SJ, Lee HW, Kim SJ, Chung KW.
    Exp Mol Med; 2008 Jun 30; 40(3):354-60. PubMed ID: 18587274
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  • 14. Clinical and genetic uniqueness in an individual with MELAS.
    Vanniarajan A, Nayak D, Reddy AG, Singh L, Thangaraj K.
    Am J Med Genet B Neuropsychiatr Genet; 2006 Jul 05; 141B(5):440-4. PubMed ID: 16741938
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  • 16. LHON/MELAS overlap mutation in ND1 subunit of mitochondrial complex I affects ubiquinone binding as revealed by modeling in Escherichia coli NDH-1.
    Pätsi J, Maliniemi P, Pakanen S, Hinttala R, Uusimaa J, Majamaa K, Nyström T, Kervinen M, Hassinen IE.
    Biochim Biophys Acta; 2012 Feb 05; 1817(2):312-8. PubMed ID: 22079202
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