BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

275 related articles for article (PubMed ID: 21694444)

  • 1. A simple oligonucleotide biochip capable of rapidly detecting known mitochondrial DNA mutations in Chinese patients with Leber's hereditary optic neuropathy (LHON).
    Du WD; Chen G; Cao HM; Jin QH; Liao RF; He XC; Chen DB; Huang SR; Zhao H; Lv YM; Tang HY; Tang XF; Wang YQ; Sun S; Zhao JL; Zhang XJ
    Dis Markers; 2011; 30(4):181-90. PubMed ID: 21694444
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNA.
    Catarino CB; Ahting U; Gusic M; Iuso A; Repp B; Peters K; Biskup S; von Livonius B; Prokisch H; Klopstock T
    Mitochondrion; 2017 Sep; 36():15-20. PubMed ID: 27721048
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pathogenic mitochondrial DNA mutations and associated clinical features in Korean patients with Leber's hereditary optic neuropathy.
    Yum HR; Chae H; Shin SY; Kim Y; Kim M; Park SH
    Invest Ophthalmol Vis Sci; 2014 Oct; 55(12):8095-101. PubMed ID: 25342614
    [TBL] [Abstract][Full Text] [Related]  

  • 5. ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.
    Behbehani R; Melhem M; Alghanim G; Behbehani K; Alsmadi O
    Br J Ophthalmol; 2014 Jun; 98(6):826-31. PubMed ID: 24568867
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.
    Jiang P; Liang M; Zhang J; Gao Y; He Z; Yu H; Zhao F; Ji Y; Liu X; Zhang M; Fu Q; Tong Y; Sun Y; Zhou X; Huang T; Qu J; Guan MX
    Invest Ophthalmol Vis Sci; 2015 Jul; 56(8):4778-88. PubMed ID: 26218905
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Applications of the method of high resolution melting analysis for diagnosis of Leber's disease and the three primary mutation spectrum of LHON in the Han Chinese population.
    Cui G; Ding H; Xu Y; Li B; Wang DW
    Gene; 2013 Jan; 512(1):108-12. PubMed ID: 23063736
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial DNA Variation of Leber's Hereditary Optic Neuropathy in Western Siberia.
    Starikovskaya E; Shalaurova S; Dryomov S; Nazhmidenova A; Volodko N; Bychkov I; Mazunin I; Sukernik R
    Cells; 2019 Dec; 8(12):. PubMed ID: 31817256
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Leber's hereditary optic neuropathy--the spectrum of mitochondrial DNA mutations in Chinese patients.
    Yen MY; Wang AG; Chang WL; Hsu WM; Liu JH; Wei YH
    Jpn J Ophthalmol; 2002; 46(1):45-51. PubMed ID: 11853713
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial tRNA variants in 811 Chinese probands with Leber's hereditary optic neuropathy.
    Ji Y; Zhang J; Liang M; Meng F; Zhang M; Mo JQ; Wang M; Guan MX
    Mitochondrion; 2022 Jul; 65():56-66. PubMed ID: 35623556
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Leber's hereditary optic neuropathy (LHON) in an Apulian cohort of subjects.
    Bianco A; Bisceglia L; Trerotoli P; Russo L; D'Agruma L; Guerriero S; Petruzzella V
    Acta Myol; 2017 Sep; 36(3):163-177. PubMed ID: 29774306
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia.
    Korkiamäki P; Kervinen M; Karjalainen K; Majamaa K; Uusimaa J; Remes AM
    Acta Ophthalmol; 2013 Nov; 91(7):630-4. PubMed ID: 22970697
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Study on five point mutations in mitochondrial DNA in patients with Leber's hereditary optic neuropathy].
    Du PJ; Zhou JW; Jin XM; Li XW; Wang P
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):675-8. PubMed ID: 16331570
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathy.
    Ji Y; Zhang J; Yu J; Wang Y; Lu Y; Liang M; Li Q; Jin X; Wei Y; Meng F; Gao Y; Cang X; Tong Y; Liu X; Zhang M; Jiang P; Zhu T; Mo JQ; Huang T; Jiang P; Guan MX
    Hum Mol Genet; 2019 May; 28(9):1515-1529. PubMed ID: 30597069
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondrial Genetic Heterogeneity in Leber's Hereditary Optic Neuropathy: Original Study with Meta-Analysis.
    Jha RK; Dawar C; Hasan Q; Pujar A; Gupta G; Vishnu VY; Kekunnaya R; Thangaraj K
    Genes (Basel); 2021 Aug; 12(9):. PubMed ID: 34573281
    [TBL] [Abstract][Full Text] [Related]  

  • 16. mtDNA m.3635G>A may be classified as a common primary mutation for Leber hereditary optic neuropathy in the Chinese population.
    Jia X; Li S; Wang P; Guo X; Zhang Q
    Biochem Biophys Res Commun; 2010 Dec; 403(2):237-41. PubMed ID: 21074518
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic and Clinical Analyses of DOA and LHON in 304 Chinese Patients with Suspected Childhood-Onset Hereditary Optic Neuropathy.
    Li Y; Li J; Jia X; Xiao X; Li S; Guo X
    PLoS One; 2017; 12(1):e0170090. PubMed ID: 28081242
    [TBL] [Abstract][Full Text] [Related]  

  • 18. In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber's hereditary optic neuropathy.
    Rovcanin B; Jancic J; Samardzic J; Rovcanin M; Nikolic B; Ivancevic N; Novakovic I; Kostic V
    Exp Eye Res; 2020 Dec; 201():108277. PubMed ID: 32991883
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A study of clinical and genetic characteristics of a Leber hereditary optic neuropathy family with the heteroplasmic m.14484T>C mutation].
    Sun Y; Lei K; Xu ZL; Geng Y
    Zhonghua Yan Ke Za Zhi; 2018 Jul; 54(7):526-534. PubMed ID: 29996615
    [No Abstract]   [Full Text] [Related]  

  • 20. Mitochondrial tRNAThr 15891C>G mutation was not associated with Leber's hereditary optic neuropathy in Han Chinese patients.
    Jiang Z; Yu J; Xia B; Zhuo G
    Mitochondrial DNA A DNA Mapp Seq Anal; 2016; 27(2):1564-6. PubMed ID: 25186221
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.