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 *

180 related articles for article (PubMed ID: 33840063)

  • 1. Clinical and molecular features of two diabetes families carrying mitochondrial ND1 T3394C mutation.
    You X; Huang X; Bi L; Li R; Zheng L; Xin C
    Ir J Med Sci; 2022 Apr; 191(2):749-758. PubMed ID: 33840063
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy.
    Tong Y; Mao Y; Zhou X; Yang L; Zhang J; Cai W; Zhao F; Wang X; Lu F; Qu J; Guan MX
    Biochem Biophys Res Commun; 2007 Jun; 357(2):524-30. PubMed ID: 17434142
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation.
    Liang M; Guan M; Zhao F; Zhou X; Yuan M; Tong Y; Yang L; Wei QP; Sun YH; Lu F; Qu J; Guan MX
    Biochem Biophys Res Commun; 2009 Jun; 383(3):286-92. PubMed ID: 19324017
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variation of mitochondrial gene and the association with type 2 diabetes mellitus in a Chinese population.
    Tang DL; Zhou X; Li X; Zhao L; Liu F
    Diabetes Res Clin Pract; 2006 Jul; 73(1):77-82. PubMed ID: 16414144
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial
    Jiang Z; Teng L; Zhang S; Ding Y
    Mitochondrial DNA A DNA Mapp Seq Anal; 2021 Mar; 32(2):59-65. PubMed ID: 33284036
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Clinical and molecular features of a Han Chinese family with maternally transmitted hypertension.
    Shao J; Chen C; Lin W; Dong Z; Gao R; Chen C; Lin B; Chen J; Xu J
    Int J Clin Exp Pathol; 2017; 10(7):7384-7389. PubMed ID: 31966580
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial Diabetes Is Associated with the
    Ding Y; Zhang S; Guo Q; Leng J
    Biomolecules; 2023 May; 13(6):. PubMed ID: 37371486
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Major depressive disorder is correlated with the mitochondrial
    Jing P; Mei X; Zhang YY; Zheng FJ; Luo XM; Liu LJ; Yu HH; Zhang XB
    World J Psychiatry; 2023 Feb; 13(2):75-83. PubMed ID: 36925947
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Late onset of type 2 diabetes is associated with mitochondrial tRNA
    Yang L; Guo Q; Leng J; Wang K; Ding Y
    J Clin Lab Anal; 2022 Jan; 36(1):e24102. PubMed ID: 34811812
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial tRNAAla 5601C>T variant may affect the clinical expression of the LHON‑related ND4 11778G>A mutation in a family.
    Ding Y; Ye YF; Li MY; Xia BH; Leng JH
    Mol Med Rep; 2020 Jan; 21(1):201-208. PubMed ID: 31939618
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maternally transmitted diabetes mellitus may be associated with mitochondrial ND5 T12338C and tRNA
    Jiang Z; Cai X; Kong J; Zhang R; Ding Y
    Ir J Med Sci; 2022 Dec; 191(6):2625-2633. PubMed ID: 34993838
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family.
    Li Z; Liu Y; Yang L; Wang S; Guan MX
    Biochem Biophys Res Commun; 2008 Mar; 367(4):906-11. PubMed ID: 18177739
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Maternally Inherited Essential Hypertension May Be Associated with the Mutations in Mitochondrial tRNA
    Wang C; Deng X; Li L; Li M
    Pharmgenomics Pers Med; 2024; 17():13-26. PubMed ID: 38222291
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mutations found in mitochondrial diabetes in Chinese Han population.
    Liu SM; Zhou X; Zheng F; Li X; Liu F; Zhang HM; Xie Y
    Diabetes Res Clin Pract; 2007 Jun; 76(3):425-35. PubMed ID: 17125872
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The mitochondrial ND1 T3308C mutation in a Chinese family with the secondary hypertension.
    Liu Y; Li Z; Yang L; Wang S; Guan MX
    Biochem Biophys Res Commun; 2008 Mar; 368(1):18-22. PubMed ID: 18194667
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.