BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 24319328)

  • 1. Point mutations associated with Leber hereditary optic neuropathy in a Latvian population.
    Aitullina A; Baumane K; Zalite S; Ranka R; Zole E; Pole I; Sepetiene S; Laganovska G; Baumanis V; Pliss L
    Mol Vis; 2013; 19():2343-51. PubMed ID: 24319328
    [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. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy.
    Tharaphan P; Chuenkongkaew WL; Luangtrakool K; Sanpachudayan T; Suktitipat B; Suphavilai R; Srisawat C; Sura T; Lertrit P
    J Neuroophthalmol; 2006 Dec; 26(4):264-7. PubMed ID: 17204919
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Multiplex MALDI-TOF MS detection of mitochondrial variants in Brazilian patients with hereditary optic neuropathy.
    Miranda PM; Matilde da Silva-Costa S; Balieiro JC; Fernandes MS; Alves RM; Guerra AT; Marcondes AM; Sartorato EL
    Mol Vis; 2016; 22():1024-35. PubMed ID: 27582625
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy.
    Kumar M; Kaur P; Kumar M; Saxena R; Sharma P; Dada R
    Mol Vis; 2012; 18():2687-99. PubMed ID: 23170061
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
    Mashima Y; Nagano M; Funayama T; Zhang Q; Egashira T; Kudho J; Shimizu N; Oguchi Y
    Clin Biochem; 2004 Apr; 37(4):268-76. PubMed ID: 15003728
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Optimization of a genotyping screening based on hydrolysis probes to detect the main mutations related to Leber hereditary optic neuropathy (LHON).
    Martins FTA; Miranda PMDAD; Fernandes MSA; Maciel-Guerra AT; Sartorato EL
    Mol Vis; 2017; 23():495-503. PubMed ID: 28761322
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy.
    Kaewsutthi S; Phasukkijwatana N; Joyjinda Y; Chuenkongkaew W; Kunhapan B; Tun AW; Suktitipat B; Lertrit P
    Invest Ophthalmol Vis Sci; 2011 Jul; 52(7):4742-8. PubMed ID: 21398275
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Leber's hereditary optic neuropathy: the spectrum of mitochondrial DNA mutations in Iranian patients.
    Houshmand M; Sharifpanah F; Tabasi A; Sanati MH; Vakilian M; Lavasani SH; Joughehdoust S
    Ann N Y Acad Sci; 2004 Apr; 1011():345-9. PubMed ID: 15126312
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation.
    Ji Y; Zhang AM; Jia X; Zhang YP; Xiao X; Li S; Guo X; Bandelt HJ; Zhang Q; Yao YG
    Am J Hum Genet; 2008 Dec; 83(6):760-8. PubMed ID: 19026397
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].
    Zhou HH; Dai XN; Lin B; Mi H; Liu XL; Zhao FX; Zhang JJ; Zhou XT; Sun YH; Wei QP; Qu J; Guan MX
    Yi Chuan; 2012 Aug; 34(8):1031-42. PubMed ID: 22917908
    [TBL] [Abstract][Full Text] [Related]  

  • 15. mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation.
    Ji Y; Jia X; Zhang Q; Yao YG
    Biochem Biophys Res Commun; 2007 Dec; 364(2):238-42. PubMed ID: 17942074
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>A and Leber hereditary optic neuropathy.
    Bi R; Zhang AM; Jia X; Zhang Q; Yao YG
    Mol Vis; 2012; 18():3087-94. PubMed ID: 23304069
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA.
    Qiao C; Wei T; Hu B; Peng C; Qiu X; Wei L; Yan M
    Mol Med Rep; 2015 Aug; 12(2):3067-72. PubMed ID: 25936877
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial D-loop variation in leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors.
    Shafa Shariat Panahi M; Houshmand M; Tabassi AR
    Arch Med Res; 2006 Nov; 37(8):1028-33. PubMed ID: 17045122
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A family with 3460G>A and 11778G>A mutations and haplogroup analysis of Polish Leber hereditary optic neuropathy patients.
    Tonska K; Kurzawa M; Ambroziak AM; Korwin-Rujna M; Szaflik JP; Grabowska E; Szaflik J; Bartnik E
    Mitochondrion; 2008 Dec; 8(5-6):383-8. PubMed ID: 18801464
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.