BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

318 related articles for article (PubMed ID: 15126312)

  • 1. 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]  

  • 2. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
    Sudoyo H; Suryadi H; Lertrit P; Pramoonjago P; Lyrawati D; Marzuki S
    J Hum Genet; 2002; 47(11):594-604. PubMed ID: 12436196
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
    Martin-Kleiner I; Gabrilovac J; Bradvica M; Vidović T; Cerovski B; Fumić K; Boranić M
    Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The influence of mitochondrial haplogroup on Leber's hereditary optic neuropathy].
    Mao YJ; Qu J; Guan MX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Feb; 25(1):45-9. PubMed ID: 18247303
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.
    Liang M; Jiang P; Li F; Zhang J; Ji Y; He Y; Xu M; Zhu J; Meng X; Zhao F; Tong Y; Liu X; Sun Y; Zhou X; Mo JQ; Qu J; Guan MX
    Invest Ophthalmol Vis Sci; 2014 Mar; 55(3):1321-31. PubMed ID: 24398099
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. The epidemiology and mutation types of Leber's hereditary optic neuropathy in Thailand.
    Sathianvichitr K; Sigkaman B; Chirapapaisan N; Laowanapiban P; Padungkiatsagul T; Apinyawasisuk S; Witthayaweerasak J; Chuenkongkaew W
    Ann Med; 2022 Dec; 54(1):1601-1607. PubMed ID: 35723074
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON).
    Rezvani Z; Didari E; Arastehkani A; Ghodsinejad V; Aryani O; Kamalidehghan B; Houshmand M
    Mol Biol Rep; 2013 Dec; 40(12):6837-41. PubMed ID: 24158608
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation.
    Isashiki Y; Sonoda S; Izumo S; Sakamoto T; Tachikui H; Inoue I
    Ophthalmic Res; 2003; 35(4):224-31. PubMed ID: 12815198
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Rapid genetic screening of Leber's hereditary optic neuropathy with mtDNA G11778A mutation by AS-PCR with whole blood].
    Yang JH; Tong Y; Li BH; Chen YK
    Zhonghua Yan Ke Za Zhi; 2005 Mar; 41(3):243-5. PubMed ID: 15840367
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial DNA mutations with Leber's hereditary optic neuropathy in Japanese patients with open-angle glaucoma.
    Inagaki Y; Mashima Y; Fuse N; Ohtake Y; Fujimaki T; Fukuchi T;
    Jpn J Ophthalmol; 2006; 50(2):128-34. PubMed ID: 16604388
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole mitochondrial genome analysis in South Indian patients with Leber's hereditary optic neuropathy.
    Saikia BB; Dubey SK; Shanmugam MK; Sundaresan P
    Mitochondrion; 2017 Sep; 36():21-28. PubMed ID: 27989883
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population.
    Mishra A; Devi S; Saxena R; Gupta N; Kabra M; Chowdhury MR
    Indian J Ophthalmol; 2017 Nov; 65(11):1156-1160. PubMed ID: 29133642
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Spectrum of pathogenic mtDNA mutations in Leber hereditary optic neuropathy families from Siberia].
    Volod'ko NV; L'vova MA; Starikovskaia EB; Derbeneva OA; Bychkov IIu; Mikhaĭlovskaia IE; Pogozheva IV; Fedotov FF; Soyan GV; Procaccio V; Wallace DC; Sukernik RI
    Genetika; 2006 Jan; 42(1):89-97. PubMed ID: 16523671
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The pathological mechanisms and novel therapeutics for Leber's hereditary optic neuropathy.
    Yang YP; Foustine S; Hsiao YJ; Tsai ET; Tsai FT; Wang CL; Ko YL; Tai HY; Tsai YC; Yang CH; Fu YJ; Wang AG; Chien Y
    J Chin Med Assoc; 2023 Jun; 86(6):539-541. PubMed ID: 37027535
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Leber's hereditary optic neuropathy: a multifactorial disease.
    Yen MY; Wang AG; Wei YH
    Prog Retin Eye Res; 2006 Jul; 25(4):381-96. PubMed ID: 16829155
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.