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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

254 related items for PubMed ID: 23674761

  • 1. 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 10; 54(6):3999-4005. PubMed ID: 23674761
    [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 01; 58(10):3923-3930. PubMed ID: 28768321
    [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 01; 26(4):264-7. PubMed ID: 17204919
    [Abstract] [Full Text] [Related]

  • 4. [The analysis of mitochondrial DNA haplogroups and variants for Leber's hereditary optic neuropathy in Chinese families carrying the m.14484T >C mutation].
    Meng X, Zhu J, Gao M, Zhang S, Zhao F, Zhang J, Liu X, Wei Q, Tong Y, Zhang M, Qu J, Guan M.
    Yi Chuan; 2014 Apr 01; 36(4):336-45. PubMed ID: 24846978
    [Abstract] [Full Text] [Related]

  • 5. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families.
    Zhang J, Zhao F, Fu Q, Liang M, Tong Y, Liu X, Lin B, Mi H, Zhang M, Wei QP, Xue L, Jiang P, Zhou X, Mo JQ, Huang T, Qu J, Guan MX.
    Mitochondrion; 2013 Nov 01; 13(6):772-81. PubMed ID: 23665487
    [Abstract] [Full Text] [Related]

  • 6. 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 21; 386(2):392-5. PubMed ID: 19527690
    [Abstract] [Full Text] [Related]

  • 7. Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.
    Yu D, Jia X, Zhang AM, Li S, Zou Y, Zhang Q, Yao YG.
    PLoS One; 2010 Oct 18; 5(10):e13426. PubMed ID: 20976138
    [Abstract] [Full Text] [Related]

  • 8. 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 18; 110(2):130-8. PubMed ID: 11935318
    [Abstract] [Full Text] [Related]

  • 9. [A study of clinical and genetic characteristics of a Leber hereditary optic neuropathy family with the heteroplasmic m.14484T>C mutation].
    Sun Y, Lei K, Xu ZL, Geng Y.
    Zhonghua Yan Ke Za Zhi; 2018 Jul 11; 54(7):526-534. PubMed ID: 29996615
    [Abstract] [Full Text] [Related]

  • 10. m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
    Kodroń A, Krawczyński MR, Tońska K, Bartnik E.
    J Clin Pathol; 2014 Jul 11; 67(7):639-41. PubMed ID: 24747208
    [Abstract] [Full Text] [Related]

  • 11. 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 11; 56(8):4778-88. PubMed ID: 26218905
    [Abstract] [Full Text] [Related]

  • 12. Prevalence of the primary LHON mutations in Northern Finland associated with bilateral optic atrophy and tobacco-alcohol amblyopia.
    Korkiamäki P, Kervinen M, Karjalainen K, Majamaa K, Uusimaa J, Remes AM.
    Acta Ophthalmol; 2013 Nov 11; 91(7):630-4. PubMed ID: 22970697
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 52(7):4742-8. PubMed ID: 21398275
    [Abstract] [Full Text] [Related]

  • 14. 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 06; 55(3):1321-31. PubMed ID: 24398099
    [Abstract] [Full Text] [Related]

  • 15. ND4L gene concurrent 10609T>C and 10663T>C mutations are associated with Leber's hereditary optic neuropathy in a large pedigree from Kuwait.
    Behbehani R, Melhem M, Alghanim G, Behbehani K, Alsmadi O.
    Br J Ophthalmol; 2014 Jun 06; 98(6):826-31. PubMed ID: 24568867
    [Abstract] [Full Text] [Related]

  • 16. Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy.
    Khan NA, Govindaraj P, Jyothi V, Meena AK, Thangaraj K.
    Mol Vis; 2013 Jun 06; 19():1282-9. PubMed ID: 23805034
    [Abstract] [Full Text] [Related]

  • 17. 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 Jun 06; 47(11):594-604. PubMed ID: 12436196
    [Abstract] [Full Text] [Related]

  • 18. [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 06; 42(1):89-97. PubMed ID: 16523671
    [Abstract] [Full Text] [Related]

  • 19. 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 06; 81(2):228-33. PubMed ID: 17668373
    [Abstract] [Full Text] [Related]

  • 20. Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNA.
    Catarino CB, Ahting U, Gusic M, Iuso A, Repp B, Peters K, Biskup S, von Livonius B, Prokisch H, Klopstock T.
    Mitochondrion; 2017 Sep 06; 36():15-20. PubMed ID: 27721048
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.