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Journal Abstract Search

238 related items for PubMed ID: 27746671

  • 21. [Detection of mtDNA*LHON G11778A mutation by real-time polymerase chain reaction using TaqMan-MGB probe technology].
    Li YM, Wang JY, Chen Y, Shao JB, Wang J, Tong Y.
    Zhonghua Yan Ke Za Zhi; 2006 Aug; 42(8):728-32. PubMed ID: 17081446
    [Abstract] [Full Text] [Related]

  • 22. 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, Glaucoma Gene Research Group.
    Jpn J Ophthalmol; 2006 Aug; 50(2):128-34. PubMed ID: 16604388
    [Abstract] [Full Text] [Related]

  • 23. [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
    [Abstract] [Full Text] [Related]

  • 24. Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach.
    Genasetti A, Valentino ML, Carelli V, Vigetti D, Viola M, Karousou EG, Melzi d'Eril GV, De Luca G, Passi A, Pallotti F.
    J Mol Diagn; 2007 Sep; 9(4):538-45. PubMed ID: 17652639
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. Reduced frequency of known mutations in a cohort of LHON patients from India.
    Sundaresan P, Kumar SM, Thompson S, Fingert JH.
    Ophthalmic Genet; 2010 Dec; 31(4):196-9. PubMed ID: 20809775
    [Abstract] [Full Text] [Related]

  • 28. 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 Dec; 47(11):594-604. PubMed ID: 12436196
    [Abstract] [Full Text] [Related]

  • 29. Analysis of mitochondrial gene mutations in Chinese pedigrees of Leber's hereditary optic neuropathy.
    Lin L, Chen Y, Tong Y, Zheng Z, Lin J.
    Yan Ke Xue Bao; 2002 Sep; 18(3):147-50. PubMed ID: 15510743
    [Abstract] [Full Text] [Related]

  • 30. A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathy.
    Luberichs J, Leo-Kottler B, Besch D, Fauser S.
    Graefes Arch Clin Exp Ophthalmol; 2002 Feb; 240(2):96-100. PubMed ID: 11931086
    [Abstract] [Full Text] [Related]

  • 31. Mutations for Leber hereditary optic neuropathy in patients with alcohol and tobacco optic neuropathy.
    Amaral-Fernandes MS, Marcondes AM, do Amor Divino Miranda PM, Maciel-Guerra AT, Sartorato EL.
    Mol Vis; 2011 Feb; 17():3175-9. PubMed ID: 22194643
    [Abstract] [Full Text] [Related]

  • 32. Leber's Hereditary Optic Neuropathy with Mitochondrial DNA Mutation G11778A: A Systematic Literature Review and Meta-Analysis.
    Yuan J, Zhao J, Ye C, Pang L, Zhang X, Luk A, Du Y, Fan KY, Zhang X, Li B, Chen C.
    Biomed Res Int; 2023 Feb; 2023():1107866. PubMed ID: 36743514
    [Abstract] [Full Text] [Related]

  • 33. 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
    [Abstract] [Full Text] [Related]

  • 34. 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
    [Abstract] [Full Text] [Related]

  • 35. A hospital-based five-year prospective study on the prevalence of Leber's hereditary optic neuropathy with genetic confirmation.
    Gowri P, Kumar SM, Vanniarajan A, Bharanidharan D, Sundaresan P.
    Mol Vis; 2020 Nov; 26():789-796. PubMed ID: 33380779
    [Abstract] [Full Text] [Related]

  • 36. 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 Nov; 35(4):224-31. PubMed ID: 12815198
    [Abstract] [Full Text] [Related]

  • 37. Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathy.
    Fauser S, Leo-Kottler B, Besch D, Luberichs J.
    Ophthalmic Genet; 2002 Sep; 23(3):191-7. PubMed ID: 12324878
    [Abstract] [Full Text] [Related]

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  • 39. [Detection of mtDNA 11778 (G-->A) point mutation in a family with Leber's hereditary optic neuropathy by site-specific polymerase chain reaction].
    Niu SL, Zhang Y, Xu YF, Bu DF, Ren ZQ, Wang SY, Liu GH, Qi Y.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Apr; 25(2):153-5. PubMed ID: 12905709
    [Abstract] [Full Text] [Related]

  • 40. Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia.
    Nishioka T, Tasaki M, Soemantri A, Dyat M, Susanto JC, Tamam M, Sudarmanto B, Ishida T.
    J Hum Genet; 2003 Apr; 48(7):385-9. PubMed ID: 12827453
    [Abstract] [Full Text] [Related]

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