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Journal Abstract Search

319 related items for PubMed ID: 20357205

  • 1. Characterization of retinal and blood mitochondrial DNA from age-related macular degeneration patients.
    Kenney MC, Atilano SR, Boyer D, Chwa M, Chak G, Chinichian S, Coskun P, Wallace DC, Nesburn AB, Udar NS.
    Invest Ophthalmol Vis Sci; 2010 Aug; 51(8):4289-97. PubMed ID: 20357205
    [Abstract] [Full Text] [Related]

  • 2. Mitochondrial DNA haplogroups associated with age-related macular degeneration.
    Udar N, Atilano SR, Memarzadeh M, Boyer DS, Chwa M, Lu S, Maguen B, Langberg J, Coskun P, Wallace DC, Nesburn AB, Khatibi N, Hertzog D, Le K, Hwang D, Kenney MC.
    Invest Ophthalmol Vis Sci; 2009 Jun; 50(6):2966-74. PubMed ID: 19151382
    [Abstract] [Full Text] [Related]

  • 3. Rapid quantification of the heteroplasmy of mutant mitochondrial DNAs in Leber's hereditary optic neuropathy using the Invader technology.
    Mashima Y, Nagano M, Funayama T, Zhang Q, Egashira T, Kudho J, Shimizu N, Oguchi Y.
    Clin Biochem; 2004 Apr; 37(4):268-76. PubMed ID: 15003728
    [Abstract] [Full Text] [Related]

  • 4. Low frequency mitochondrial DNA heteroplasmy SNPs in blood, retina, and [RPE+choroid] of age-related macular degeneration subjects.
    Atilano SR, Udar N, Satalich TA, Udar V, Chwa M, Kenney MC.
    PLoS One; 2021 Apr; 16(1):e0246114. PubMed ID: 33513185
    [Abstract] [Full Text] [Related]

  • 5. Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy.
    Jacobi FK, Leo-Kottler B, Mittelviefhaus K, Zrenner E, Meyer J, Pusch CM, Wissinger B.
    Invest Ophthalmol Vis Sci; 2001 May; 42(6):1208-14. PubMed ID: 11328729
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  • 7. Mitochondrial DNA mutations in breast cancer tissue and in matched nipple aspirate fluid.
    Zhu W, Qin W, Bradley P, Wessel A, Puckett CL, Sauter ER.
    Carcinogenesis; 2005 Jan; 26(1):145-52. PubMed ID: 15375011
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  • 10. 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 Jan; 47(11):594-604. PubMed ID: 12436196
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  • 11. [Leber's hereditary optic neuropathy].
    Konrádová V, Zeman J, Stratilová L, Hermanská J, Vseticka I, Misovicová N, Kurca E, Gerinec A, Houstĕk J.
    Cas Lek Cesk; 1999 Oct 20; 138(18):565-8. PubMed ID: 10596473
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  • 12. [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 20; 41(3):243-5. PubMed ID: 15840367
    [Abstract] [Full Text] [Related]

  • 13. A family with Leber's hereditary optic neuropathy with mitochondrial DNA heteroplasmy related to disease expression.
    Tanaka A, Kiyosawa M, Mashima Y, Tokoro T.
    J Neuroophthalmol; 1998 Jun 20; 18(2):81-3. PubMed ID: 9621260
    [Abstract] [Full Text] [Related]

  • 14. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.
    Rev Neurol (Paris); 2001 May 20; 157(5):537-41. PubMed ID: 11438773
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  • 15. Mitochondrial abnormalities in ageing macular photoreceptors.
    Barron MJ, Johnson MA, Andrews RM, Clarke MP, Griffiths PG, Bristow E, He LP, Durham S, Turnbull DM.
    Invest Ophthalmol Vis Sci; 2001 Nov 20; 42(12):3016-22. PubMed ID: 11687550
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  • 16. Identification of somatic and germline mitochondrial DNA sequence variants in prostate cancer patients.
    Gómez-Zaera M, Abril J, González L, Aguiló F, Condom E, Nadal M, Nunes V.
    Mutat Res; 2006 Mar 20; 595(1-2):42-51. PubMed ID: 16472830
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  • 17. [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 20; 42(8):728-32. PubMed ID: 17081446
    [Abstract] [Full Text] [Related]

  • 18. The iron carrier transferrin is upregulated in retinas from patients with age-related macular degeneration.
    Chowers I, Wong R, Dentchev T, Farkas RH, Iacovelli J, Gunatilaka TL, Medeiros NE, Presley JB, Campochiaro PA, Curcio CA, Dunaief JL, Zack DJ.
    Invest Ophthalmol Vis Sci; 2006 May 20; 47(5):2135-40. PubMed ID: 16639025
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  • 19. Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes.
    Hofmann S, Bezold R, Jaksch M, Obermaier-Kusser B, Mertens S, Kaufhold P, Rabl W, Hecker W, Gerbitz KD.
    Genomics; 1997 Jan 01; 39(1):8-18. PubMed ID: 9027481
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  • 20. Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathy.
    Zhu DP, Economou EP, Antonarakis SE, Maumenee IH.
    Am J Med Genet; 1992 Jan 15; 42(2):173-9. PubMed ID: 1346348
    [Abstract] [Full Text] [Related]

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