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250 related items for PubMed ID: 17942074

  • 1. mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation.
    Ji Y, Jia X, Zhang Q, Yao YG.
    Biochem Biophys Res Commun; 2007 Dec 14; 364(2):238-42. PubMed ID: 17942074
    [Abstract] [Full Text] [Related]

  • 2. Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.
    Qu J, Zhou X, Zhang J, Zhao F, Sun YH, Tong Y, Wei QP, Cai W, Yang L, West CE, Guan MX.
    Ophthalmology; 2009 Mar 14; 116(3):558-564.e3. PubMed ID: 19167085
    [Abstract] [Full Text] [Related]

  • 3. Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.
    Khan NA, Govindaraj P, Soumittra N, Sharma S, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Bindu PS, Gayathri N, Taly AB, Thangaraj K.
    Invest Ophthalmol Vis Sci; 2017 Aug 01; 58(10):3923-3930. PubMed ID: 28768321
    [Abstract] [Full Text] [Related]

  • 4. [The analysis of mitochondrial DNA haplogroups and variants for Leber's hereditary optic neuropathy in Chinese families carrying the m.14484T >C mutation].
    Meng X, Zhu J, Gao M, Zhang S, Zhao F, Zhang J, Liu X, Wei Q, Tong Y, Zhang M, Qu J, Guan M.
    Yi Chuan; 2014 Apr 01; 36(4):336-45. PubMed ID: 24846978
    [Abstract] [Full Text] [Related]

  • 5. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
    Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P.
    J Neuroophthalmol; 2006 Dec 01; 26(4):264-7. PubMed ID: 17204919
    [Abstract] [Full Text] [Related]

  • 6. Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A.
    Wang HW, Jia X, Ji Y, Kong QP, Zhang Q, Yao YG, Zhang YP.
    Mutat Res; 2008 Aug 25; 643(1-2):48-53. PubMed ID: 18619472
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.
    Yu D, Jia X, Zhang AM, Li S, Zou Y, Zhang Q, Yao YG.
    PLoS One; 2010 Oct 18; 5(10):e13426. PubMed ID: 20976138
    [Abstract] [Full Text] [Related]

  • 8. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
    Zhou X, Zhang H, Zhao F, Ji Y, Tong Y, Zhang J, Zhang Y, Yang L, Qian Y, Lu F, Qu J, Guan MX.
    Mol Genet Metab; 2010 Aug 18; 100(4):379-84. PubMed ID: 20627642
    [Abstract] [Full Text] [Related]

  • 9. Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.
    Qu J, Wang Y, Tong Y, Zhou X, Zhao F, Yang L, Zhang S, Zhang J, West CE, Guan MX.
    Invest Ophthalmol Vis Sci; 2010 Oct 18; 51(10):4906-12. PubMed ID: 20435583
    [Abstract] [Full Text] [Related]

  • 10. Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.
    Qu J, Zhou X, Zhao F, Liu X, Zhang M, Sun YH, Liang M, Yuan M, Liu Q, Tong Y, Wei QP, Yang L, Guan MX.
    Biochim Biophys Acta; 2010 Mar 18; 1800(3):305-12. PubMed ID: 19733221
    [Abstract] [Full Text] [Related]

  • 11. Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.
    Qian Y, Zhou X, Hu Y, Tong Y, Li R, Lu F, Yang H, Mo JQ, Qu J, Guan MX.
    Biochem Biophys Res Commun; 2005 Jul 01; 332(2):614-21. PubMed ID: 15896721
    [Abstract] [Full Text] [Related]

  • 12. Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation.
    Qu J, Li R, Tong Y, Hu Y, Zhou X, Qian Y, Lu F, Guan MX.
    Biochem Biophys Res Commun; 2005 Mar 25; 328(4):1139-45. PubMed ID: 15707996
    [Abstract] [Full Text] [Related]

  • 13. Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.
    Tong Y, Sun YH, Zhou X, Zhao F, Mao Y, Wei QP, Yang L, Qu J, Guan MX.
    Mol Genet Metab; 2010 Apr 25; 99(4):417-24. PubMed ID: 20053576
    [Abstract] [Full Text] [Related]

  • 14. Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.
    Kaewsutthi S, Phasukkijwatana N, Joyjinda Y, Chuenkongkaew W, Kunhapan B, Tun AW, Suktitipat B, Lertrit P.
    Invest Ophthalmol Vis Sci; 2011 Jul 01; 52(7):4742-8. PubMed ID: 21398275
    [Abstract] [Full Text] [Related]

  • 15. Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.
    Zhang M, Zhou X, Li C, Zhao F, Zhang J, Yuan M, Sun YH, Wang J, Tong Y, Liang M, Yang L, Cai W, Wang L, Qu J, Guan MX.
    Mol Genet Metab; 2010 Jul 01; 101(2-3):192-9. PubMed ID: 20728388
    [Abstract] [Full Text] [Related]

  • 16. Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
    Ji Y, Zhang AM, Jia X, Zhang YP, Xiao X, Li S, Guo X, Bandelt HJ, Zhang Q, Yao YG.
    Am J Hum Genet; 2008 Dec 01; 83(6):760-8. PubMed ID: 19026397
    [Abstract] [Full Text] [Related]

  • 17. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
    Sudoyo H, Suryadi H, Lertrit P, Pramoonjago P, Lyrawati D, Marzuki S.
    J Hum Genet; 2002 Dec 01; 47(11):594-604. PubMed ID: 12436196
    [Abstract] [Full Text] [Related]

  • 18. [The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].
    Zhou HH, Dai XN, Lin B, Mi H, Liu XL, Zhao FX, Zhang JJ, Zhou XT, Sun YH, Wei QP, Qu J, Guan MX.
    Yi Chuan; 2012 Aug 01; 34(8):1031-42. PubMed ID: 22917908
    [Abstract] [Full Text] [Related]

  • 19. Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients.
    Zhang AM, Jia X, Bi R, Salas A, Li S, Xiao X, Wang P, Guo X, Kong QP, Zhang Q, Yao YG.
    PLoS One; 2011 Aug 01; 6(11):e27750. PubMed ID: 22110754
    [Abstract] [Full Text] [Related]

  • 20. Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA.
    Qiao C, Wei T, Hu B, Peng C, Qiu X, Wei L, Yan M.
    Mol Med Rep; 2015 Aug 01; 12(2):3067-72. PubMed ID: 25936877
    [Abstract] [Full Text] [Related]

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