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 *

128 related articles for article (PubMed ID: 34993838)

  • 1. 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]  

  • 2. 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]  

  • 3. Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.
    Chen B; Sun D; Yang L; Zhang C; Yang A; Zhu Y; Zhao J; Chen Y; Guan M; Wang X; Li R; Tang X; Wang J; Tao Z; Lu J; Guan MX
    Am J Med Genet A; 2008 May; 146A(10):1248-58. PubMed ID: 18386806
    [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. Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNA
    Yu X; Li S; Ding Y
    J Clin Lab Anal; 2022 Apr; 36(4):e24298. PubMed ID: 35218233
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus.
    Lin L; Zhang D; Jin Q; Teng Y; Yao X; Zhao T; Xu X; Jin Y
    Int J Gen Med; 2021; 14():5719-5735. PubMed ID: 34557026
    [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. Mitochondrial DNA associations with East Asian metabolic syndrome.
    Chalkia D; Chang YC; Derbeneva O; Lvova M; Wang P; Mishmar D; Liu X; Singh LN; Chuang LM; Wallace DC
    Biochim Biophys Acta Bioenerg; 2018 Sep; 1859(9):878-892. PubMed ID: 29997041
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial tRNA
    Yang P; Wu P; Liu X; Feng J; Zheng S; Wang Y; Fan Z
    Ir J Med Sci; 2020 May; 189(2):489-496. PubMed ID: 31776834
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Mitochondrial tRNA
    Ding Y; Xia BH; Zhang CJ; Zhuo GC
    Gene; 2018 Feb; 642():299-306. PubMed ID: 29155328
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The mitochondrial tRNAAsp T7561C, tRNAHis C12153T and A12172G mutations may be associated with essential hypertension in a Han Chinese pedigree.
    Fu H; Sun J; Xu X
    Hum Hered; 2022 Mar; ():. PubMed ID: 35344953
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family].
    Wu Y; Liang LZ; Xiao HL; Yang YL; Yu X; Zheng J; Fang F; Zheng BJ; Tang XW; Jin LJ; Guan MX
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Dec; 48(12):978-84. PubMed ID: 24506995
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic.
    Kong QP; Yao YG; Sun C; Zhu CL; Zhong L; Wang CY; Cai WW; Xu XM; Xu AL; Zhang YP
    J Hum Genet; 2004; 49(8):414-423. PubMed ID: 15278763
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Correlation of mitochondrial tRNA variants with coronary heart disease in a Chinese pedigree].
    Ding Y; Yu J; Gao B; Huang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jul; 40(7):807-814. PubMed ID: 37368381
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Complete mtDNA genomes reveal similar penetrances of maternally inherited type 2 diabetes in two Chinese families.
    Yang Y; Zhou T; Peng M; Liu Y; Li Y; Wang H; Irwin DM; Zhang Y
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 May; 27(3):2040-4. PubMed ID: 25469813
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese family.
    Lu J; Wang D; Li R; Li W; Ji J; Zhao J; Ye W; Yang L; Qian Y; Zhu Y; Guan MX
    Biochem Biophys Res Commun; 2006 Sep; 348(1):115-9. PubMed ID: 16876129
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber's hereditary optic neuropathy.
    Shuai J; Shi J; Liang Y; Ji F; Gu L; Yuan Z
    Ir J Med Sci; 2022 Apr; 191(2):865-876. PubMed ID: 34053002
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Maternally Inherited Diabetes Mellitus Associated with a Novel m.15897G>A Mutation in Mitochondrial tRNA
    Li K; Wu L; Liu J; Lin W; Qi Q; Zhao T
    J Diabetes Res; 2020; 2020():2057187. PubMed ID: 32083134
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.