BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

213 related articles for article (PubMed ID: 34012229)

  • 1. Whole mitochondrial genome analysis in Chinese patients with keratoconus.
    Xu L; Yang K; Fan Q; Zhao D; Pang C; Ren S
    Mol Vis; 2021; 27():270-282. PubMed ID: 34012229
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial DNA heteroplasmy analysis in keratoconus patients from China.
    Xu L; Yang K; Fan Q; Gu Y; Ren S
    Front Genet; 2023; 14():1251951. PubMed ID: 37790701
    [No Abstract]   [Full Text] [Related]  

  • 3. Identification of seven novel
    Yu X; Chen B; Zhang X; Shentu X
    Mol Vis; 2017; 23():296-305. PubMed ID: 28484309
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Exome sequencing identification of susceptibility genes in Chinese patients with keratoconus.
    Xu L; Yang K; Fan Q; Gu Y; Zhang B; Pang C; Ren S
    Ophthalmic Genet; 2020 Dec; 41(6):518-525. PubMed ID: 32744102
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial complex 1 gene analysis in keratoconus.
    Pathak D; Nayak B; Singh M; Sharma N; Tandon R; Sinha R; Titiyal JS; Dada R
    Mol Vis; 2011; 17():1514-25. PubMed ID: 21691575
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial DNA copy number, but not haplogroup is associated with keratoconus in Han Chinese population.
    Hao XD; Chen P; Wang Y; Li SX; Xie LX
    Exp Eye Res; 2015 Mar; 132():59-63. PubMed ID: 25613073
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of Novel Loci With Keratoconus Susceptibility in a Chinese Genome-Wide Association Study.
    Xu L; Zheng X; Yin S; Yang K; Fan Q; Gu Y; Yuan Y; Yin C; Zang Y; Pang C; Sun L; Ren S
    Invest Ophthalmol Vis Sci; 2024 May; 65(5):29. PubMed ID: 38767907
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis.
    Al-Kafaji G; Bakheit HF; AlAli F; Fattah M; Alhajeri S; Alharbi MA; Daif A; Alsabbagh MM; Alwehaidah MS; Bakhiet M
    PLoS One; 2022; 17(2):e0263606. PubMed ID: 35130313
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients.
    Zhang AM; Jia X; Guo X; Zhang Q; Yao YG
    J Transl Med; 2012 Mar; 10():43. PubMed ID: 22400981
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Mitochondrial tRNAHis G12192A Mutation May Modulate the Clinical Expression of Deafness-Associated tRNAThr G15927A Mutation in a Chinese Pedigree.
    Ding Y; Teng YS; Zhuo GC; Xia BH; Leng JH
    Curr Mol Med; 2019; 19(2):136-146. PubMed ID: 30854964
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Next-generation sequencing profiling of mitochondrial genomes in gout.
    Tseng CC; Chen CJ; Yen JH; Huang HY; Chang JG; Chang SJ; Liao WT
    Arthritis Res Ther; 2018 Jul; 20(1):137. PubMed ID: 29976239
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients.
    Xu X; Zhang X; Cui Y; Yang H; Ping X; Wu J; Yu X; Jin X; Huang X; Shentu X
    Sci Rep; 2020 Apr; 10(1):5844. PubMed ID: 32246022
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Association of Interleukin-1 Gene Single Nucleotide Polymorphisms with Keratoconus in Chinese Han Population.
    Wang Y; Wei W; Zhang C; Zhang X; Liu M; Zhu X; Xu K
    Curr Eye Res; 2016 May; 41(5):630-5. PubMed ID: 26200829
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.
    Alila OF; Rebai EM; Tabebi M; Tej A; Chamkha I; Tlili A; Bouguila J; Tilouche S; Soyah N; Boughamoura L; Fakhfakh F
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016 Jul; 27(4):2873-80. PubMed ID: 26258512
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel variant in
    Lin Q; Zheng L; Shen Z
    Ophthalmic Genet; 2022 Apr; 43(2):159-163. PubMed ID: 34895010
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel mitochondrial gene variants in Northwestern Chinese probands with non-syndromic hearing loss by whole mitochondrial genome screening.
    Chen X; Wang F; Maerhaba A; Li Q; Wang J; Liu X; Zheng J; Chen Y; Guo Y
    Gene; 2018 Apr; 652():59-65. PubMed ID: 29408584
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population.
    Hao XD; Chen P; Chen ZL; Li SX; Wang Y
    Ophthalmic Genet; 2015 Jun; 36(2):132-6. PubMed ID: 25675348
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial DNA variant spectrum and the association with chronic tic disorders.
    Jiang P; Zhu T; Liu J; Tao X; Xue Z; Tao Y; Chen H; Zeng X; Zhu W; Shu Q; Yu L
    Eur J Neurol; 2022 Nov; 29(11):3187-3196. PubMed ID: 35781907
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Germline and somatic mtDNA mutation spectrum of rheumatoid arthritis patients in the Taizhou area, China.
    Du J; Yu S; Wang D; Chen S; Chen S; Zheng Y; Wang N; Chen S; Li J; Shen B
    Rheumatology (Oxford); 2020 Oct; 59(10):2982-2991. PubMed ID: 32159782
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Differential Expression of Coding and Long Noncoding RNAs in Keratoconus-Affected Corneas.
    Khaled ML; Bykhovskaya Y; Yablonski SER; Li H; Drewry MD; Aboobakar IF; Estes A; Gao XR; Stamer WD; Xu H; Allingham RR; Hauser MA; Rabinowitz YS; Liu Y
    Invest Ophthalmol Vis Sci; 2018 Jun; 59(7):2717-2728. PubMed ID: 29860458
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.