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 *

173 related articles for article (PubMed ID: 12749053)

  • 1. Low penetrance of the 14484 LHON mutation when it arises in a non-haplogroup J mtDNA background.
    Howell N; Herrnstadt C; Shults C; Mackey DA
    Am J Med Genet A; 2003 Jun; 119A(2):147-51. PubMed ID: 12749053
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.
    Brown MD; Starikovskaya E; Derbeneva O; Hosseini S; Allen JC; Mikhailovskaya IE; Sukernik RI; Wallace DC
    Hum Genet; 2002 Feb; 110(2):130-8. PubMed ID: 11935318
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity.
    Ghelli A; Porcelli AM; Zanna C; Vidoni S; Mattioli S; Barbieri A; Iommarini L; Pala M; Achilli A; Torroni A; Rugolo M; Carelli V
    PLoS One; 2009 Nov; 4(11):e7922. PubMed ID: 19936068
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Strikingly different penetrance of LHON in two Chinese families with primary mutation G11778A is independent of mtDNA haplogroup background and secondary mutation G13708A.
    Wang HW; Jia X; Ji Y; Kong QP; Zhang Q; Yao YG; Zhang YP
    Mutat Res; 2008 Aug; 643(1-2):48-53. PubMed ID: 18619472
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.
    Tong Y; Sun YH; Zhou X; Zhao F; Mao Y; Wei QP; Yang L; Qu J; Guan MX
    Mol Genet Metab; 2010 Apr; 99(4):417-24. PubMed ID: 20053576
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.
    Howell N; Oostra RJ; Bolhuis PA; Spruijt L; Clarke LA; Mackey DA; Preston G; Herrnstadt C
    Am J Hum Genet; 2003 Jun; 72(6):1460-9. PubMed ID: 12736867
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
    Zhou X; Zhang H; Zhao F; Ji Y; Tong Y; Zhang J; Zhang Y; Yang L; Qian Y; Lu F; Qu J; Guan MX
    Mol Genet Metab; 2010 Aug; 100(4):379-84. PubMed ID: 20627642
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.
    Qu J; Zhou X; Zhao F; Liu X; Zhang M; Sun YH; Liang M; Yuan M; Liu Q; Tong Y; Wei QP; Yang L; Guan MX
    Biochim Biophys Acta; 2010 Mar; 1800(3):305-12. PubMed ID: 19733221
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.
    Khan NA; Govindaraj P; Soumittra N; Srilekha S; Ambika S; Vanniarajan A; Meena AK; Uppin MS; Sundaram C; Taly AB; Bindu PS; Gayathri N; Thangaraj K
    Invest Ophthalmol Vis Sci; 2013 Jun; 54(6):3999-4005. PubMed ID: 23674761
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees.
    Xie S; Zhang J; Sun J; Zhang M; Zhao F; Wei QP; Tong Y; Liu X; Zhou X; Jiang P; Ji Y; Guan MX
    Mitochondrial DNA A DNA Mapp Seq Anal; 2017 May; 28(3):434-441. PubMed ID: 27159682
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background.
    Hudson G; Carelli V; Spruijt L; Gerards M; Mowbray C; Achilli A; Pyle A; Elson J; Howell N; La Morgia C; Valentino ML; Huoponen K; Savontaus ML; Nikoskelainen E; Sadun AA; Salomao SR; Belfort R; Griffiths P; Yu-Wai-Man P; de Coo RF; Horvath R; Zeviani M; Smeets HJ; Torroni A; Chinnery PF
    Am J Hum Genet; 2007 Aug; 81(2):228-33. PubMed ID: 17668373
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers.
    Bianco A; Valletti A; Longo G; Bisceglia L; Montoya J; Emperador S; Guerriero S; Petruzzella V
    BMC Res Notes; 2018 Dec; 11(1):911. PubMed ID: 30572950
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.
    Dawod PGA; Jancic J; Marjanovic A; Brankovic M; Jankovic M; Samardzic J; Potkonjak D; Djuric V; Mesaros S; Novakovic I; Abdel Motaleb FI; Kostic VS; Nikolic D
    Genes (Basel); 2020 Sep; 11(9):. PubMed ID: 32887465
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.