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 *

192 related articles for article (PubMed ID: 37371486)

  • 1. 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]  

  • 2. Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families.
    Zhou X; Wei Q; Yang L; Tong Y; Zhao F; Lu C; Qian Y; Sun Y; Lu F; Qu J; Guan MX
    Biochem Biophys Res Commun; 2006 Feb; 340(1):69-75. PubMed ID: 16364244
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family.
    Qu J; Li R; Zhou X; Tong Y; Yang L; Chen J; Zhao F; Lu C; Qian Y; Lu F; Guan MX
    Mitochondrion; 2007; 7(1-2):140-6. PubMed ID: 17300996
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Mitochondrial Diabetes is Associated with tRNA
    Ding Y; Zhang S; Guo Q; Zheng H
    Diabetes Metab Syndr Obes; 2022; 15():1687-1701. PubMed ID: 35685248
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [The mitochondrial ND5 T12338C mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families].
    Ji YC; Liu XL; Zhao FX; Zhang JJ; Zhang Y; Zhou XT; Qu J; Guan MX
    Yi Chuan; 2011 Apr; 33(4):322-8. PubMed ID: 21482521
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of a Novel Mitochondrial tRNA Mutation in Chinese Family with Type 2 Diabetes Mellitus.
    Li X; Shang J; Li S; Wang Y
    Pharmgenomics Pers Med; 2024; 17():149-161. PubMed ID: 38645701
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.
    Ji Y; Zhang J; Lu Y; Yi Q; Chen M; Xie S; Mao X; Xiao Y; Meng F; Zhang M; Yang R; Guan MX
    J Biol Chem; 2020 Sep; 295(38):13224-13238. PubMed ID: 32723871
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
    Jiang P; Jin X; Peng Y; Wang M; Liu H; Liu X; Zhang Z; Ji Y; Zhang J; Liang M; Zhao F; Sun YH; Zhang M; Zhou X; Chen Y; Mo JQ; Huang T; Qu J; Guan MX
    Hum Mol Genet; 2016 Feb; 25(3):584-96. PubMed ID: 26647310
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 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. 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. 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]  

  • 20. Molecular characterization of two Chinese pedigrees with maternally inherited hypertension.
    Ding Y; Yu J; Guo Q; Gao B; Huang J
    J Gene Med; 2021 Apr; 23(4):e3328. PubMed ID: 33625761
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.