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 *

284 related articles for article (PubMed ID: 19733221)

  • 1. 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]  

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

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss.
    Wei QP; Zhou X; Yang L; Sun YH; Zhou J; Li G; Jiang R; Lu F; Qu J; Guan MX
    Biochem Biophys Res Commun; 2007 Jun; 357(4):910-6. PubMed ID: 17452034
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
    Liang M; Jiang P; Li F; Zhang J; Ji Y; He Y; Xu M; Zhu J; Meng X; Zhao F; Tong Y; Liu X; Sun Y; Zhou X; Mo JQ; Qu J; Guan MX
    Invest Ophthalmol Vis Sci; 2014 Mar; 55(3):1321-31. PubMed ID: 24398099
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families.
    Ji Y; Liang M; Zhang J; Zhang M; Zhu J; Meng X; Zhang S; Gao M; Zhao F; Wei QP; Jiang P; Tong Y; Liu X; Qin Mo J; Guan MX
    J Hum Genet; 2014 Mar; 59(3):134-40. PubMed ID: 24430572
    [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. [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; 36(4):336-45. PubMed ID: 24846978
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families.
    Zhang J; Zhou X; Zhou J; Li C; Zhao F; Wang Y; Meng Y; Wang J; Yuan M; Cai W; Tong Y; Sun YH; Yang L; Qu J; Guan MX
    Biochem Biophys Res Commun; 2010 Sep; 399(4):647-53. PubMed ID: 20691156
    [TBL] [Abstract][Full Text] [Related]  

  • 16. T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.
    Zhang S; Wang L; Hao Y; Wang P; Hao P; Yin K; Wang QK; Liu M
    Mitochondrion; 2008 Jun; 8(3):205-10. PubMed ID: 18440284
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leber's hereditary optic neuropathy is associated with the mitochondrial ND6 T14484C mutation in three Chinese families.
    Sun YH; Wei QP; Zhou X; Qian Y; Zhou J; Lu F; Qu J; Guan MX
    Biochem Biophys Res Commun; 2006 Aug; 347(1):221-5. PubMed ID: 16806060
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ; Qu J; Guan MX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Leber's Hereditary Optic Neuropathy is Associated with Compound Primary Mutations of Mitochondrial ND1 m.3635G > A and ND6 m.14502 T > C.
    Jin X; Wang L; Gong Y; Chen B; Wang Y; Chen T; Wei S
    Ophthalmic Genet; 2015; 36(4):291-8. PubMed ID: 24417559
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.