These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 15293268)

  • 41. LHON/MELAS overlap mutation in ND1 subunit of mitochondrial complex I affects ubiquinone binding as revealed by modeling in Escherichia coli NDH-1.
    Pätsi J; Maliniemi P; Pakanen S; Hinttala R; Uusimaa J; Majamaa K; Nyström T; Kervinen M; Hassinen IE
    Biochim Biophys Acta; 2012 Feb; 1817(2):312-8. PubMed ID: 22079202
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Gene Therapy for Leber Hereditary Optic Neuropathy: Is Vision Truly RESCUED?
    Chen JJ; Bhatti MT
    Ophthalmology; 2021 May; 128(5):661-662. PubMed ID: 33892900
    [No Abstract]   [Full Text] [Related]  

  • 43. Genetic variants of TP53 and EPHX1 in Leber's hereditary optic neuropathy and their relationship to age at onset.
    Ishikawa K; Funayama T; Ohde H; Inagaki Y; Mashima Y
    Jpn J Ophthalmol; 2005; 49(2):121-6. PubMed ID: 15838728
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. Gene Therapies for the Treatment of Leber Hereditary Optic Neuropathy.
    Sahel JA; Newman NJ; Yu-Wai-Man P; Vignal-Clermont C; Carelli V; Biousse V; Moster ML; Sergott R; Klopstock T; Sadun AA; Blouin L; Katz B; Taiel M
    Int Ophthalmol Clin; 2021 Oct; 61(4):195-208. PubMed ID: 34584057
    [No Abstract]   [Full Text] [Related]  

  • 46. [Research progress of Leber hereditary optic neuropathy].
    Zhang AM; Yao YG
    Yi Chuan; 2013 Feb; 35(2):123-35. PubMed ID: 23448924
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Progressive Bilateral Cecocentral Scotomata.
    Abalem MF; Johnson MW; Jayasundera T
    JAMA Ophthalmol; 2019 Jan; 137(1):107-108. PubMed ID: 30347014
    [No Abstract]   [Full Text] [Related]  

  • 48. Leber hereditary optic neuropathy due to a new ND1 mutation.
    Soldath P; Wegener M; Sander B; Rosenberg T; Duno M; Wibrand F; Vissing J
    Ophthalmic Genet; 2017; 38(5):480-485. PubMed ID: 28139165
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Loss of visual acuity].
    Maeda K; Terada M; Mitsunami K
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():526-9. PubMed ID: 12013932
    [No Abstract]   [Full Text] [Related]  

  • 50. Leber hereditary optic neuropathy: clinical and molecular genetic findings.
    Huoponen K
    Neurogenetics; 2001 Jul; 3(3):119-25. PubMed ID: 11523562
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.
    Zhang AM; Zou Y; Guo X; Jia X; Zhang Q; Yao YG
    Biochem Biophys Res Commun; 2009 Aug; 386(2):392-5. PubMed ID: 19527690
    [TBL] [Abstract][Full Text] [Related]  

  • 52. 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]  

  • 53. Leber hereditary optic neuropathy--a disease with a known molecular basis but a mysterious mechanism of pathology.
    Mroczek-Tońska K; Kisiel B; Piechota J; Bartnik E
    J Appl Genet; 2003; 44(4):529-38. PubMed ID: 14617834
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation.
    Yang J; Zhu Y; Tong Y; Chen L; Liu L; Zhang Z; Wang X; Huang D; Qiu W; Zhuang S; Ma X
    Biochem Biophys Res Commun; 2009 Aug; 386(1):50-4. PubMed ID: 19497304
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Restoring retinal function in a mouse model of hereditary blindness.
    Moore T
    PLoS Med; 2005 Nov; 2(11):e399. PubMed ID: 16288566
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Treatment of Leber's Hereditary Optic Neuropathy.
    Karanjia R; Chahal J; Ammar M; Sadun AA
    Curr Pharm Des; 2017; 23(4):624-628. PubMed ID: 28128056
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mitochondrial disorders: aetiologies, models systems, and candidate therapies.
    Farrar GJ; Chadderton N; Kenna PF; Millington-Ward S
    Trends Genet; 2013 Aug; 29(8):488-97. PubMed ID: 23756086
    [TBL] [Abstract][Full Text] [Related]  

  • 58. [A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis].
    Lubos L; Wajgt A; Maciejowski M; Mroczek-Tońska K; Bartnik E; Dziekanowska D
    Neurol Neurochir Pol; 2003; 37(1):229-34. PubMed ID: 12910843
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Leber's hereditary optic neuropathy with molecular characterization in two Indian families.
    Verma IC; Bijarnia S; Saxena R; Kohli S; Puri RD; Thomas E; Chowdhary D; Jha SN; Grover AK
    Indian J Ophthalmol; 2005 Sep; 53(3):167-71. PubMed ID: 16137960
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome.
    Carreño-Gago L; Gamez J; Cámara Y; Alvarez de la Campa E; Aller-Alvarez JS; Moncho D; Salvado M; Galan A; de la Cruz X; Pinós T; García-Arumí E
    Biochim Biophys Acta Mol Basis Dis; 2017 Jan; 1863(1):182-187. PubMed ID: 27613247
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.