These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 18619472)

  • 1. 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; 643(1-2):48-53. PubMed ID: 18619472
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 100(4):379-84. PubMed ID: 20627642
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 116(3):558-564.e3. PubMed ID: 19167085
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 332(2):614-21. PubMed ID: 15896721
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 364(2):238-42. PubMed ID: 17942074
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 99(4):417-24. PubMed ID: 20053576
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 328(4):1139-45. PubMed ID: 15707996
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 58(10):3923-3930. PubMed ID: 28768321
    [TBL] [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; 51(10):4906-12. PubMed ID: 20435583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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; 34(8):1031-42. PubMed ID: 22917908
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 1800(3):305-12. PubMed ID: 19733221
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 26(4):264-7. PubMed ID: 17204919
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 101(2-3):192-9. PubMed ID: 20728388
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.
    Liu XL; Zhou X; Zhou J; Zhao F; Zhang J; Li C; Ji Y; Zhang Y; Wei QP; Sun YH; Yang L; Lin B; Yuan Y; Li Y; Qu J; Guan MX
    Ophthalmology; 2011 May; 118(5):978-85. PubMed ID: 21131053
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 12(2):3067-72. PubMed ID: 25936877
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber's hereditary optic neuropathy.
    Zhang AM; Jia X; Yao YG; Zhang Q
    Biochem Biophys Res Commun; 2008 Nov; 376(1):221-4. PubMed ID: 18775412
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Leber's hereditary optic neuropathy is associated with the mitochondrial G11696A mutation in two Chinese families].
    Zhao FX; Zhou XT; Qu J; Wei QP; Tong Y; Yang L; Lv JX; Guan MX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Oct; 24(5):556-9. PubMed ID: 17922426
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.
    Qu J; Li R; Zhou X; Tong Y; Lu F; Qian Y; Hu Y; Mo JQ; West CE; Guan MX
    Invest Ophthalmol Vis Sci; 2006 Feb; 47(2):475-83. PubMed ID: 16431939
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees.
    Xie S; Zhang J; Sun J; Zhang M; Zhao F; Wei QP; Tong Y; Liu X; Zhou X; Jiang P; Ji Y; Guan MX
    Mitochondrial DNA A DNA Mapp Seq Anal; 2017 May; 28(3):434-441. PubMed ID: 27159682
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background.
    Howell N; Herrnstadt C; Shults C; Mackey DA
    Am J Med Genet A; 2003 Jun; 119A(2):147-51. PubMed ID: 12749053
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.