BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 22336116)

  • 1. [Mutation analysis in a family of Leber hereditary optic neuropathy].
    She CY; Gu H; Xu J; Ma K; Liu NP
    Zhonghua Yan Ke Za Zhi; 2011 Dec; 47(12):1080-3. PubMed ID: 22336116
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Clinical examination of Leber hereditary optic neuropathy in patients with the same gene mutation].
    Chelstowska J; Mroczek K; Niebudek D; Małecka-Idzikowska A; Bartnik E; Hanna Nizankowska M; Sasiadek M
    Przegl Lek; 2002; 59(10):777-9. PubMed ID: 12632910
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Leber's hereditary optic neuropathy: clinical and molecular profile of a Brazilian sample.
    Maciel-Guerra AT; Zanchetta LM; Amaral Fernandes MS; Andrade PB; do Amor Divino Miranda PM; Sartorato EL
    Ophthalmic Genet; 2010 Sep; 31(3):126-8. PubMed ID: 20565249
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A pedigree of Leber's hereditary optic neuropathy with mtDNA 14484 mutation].
    Tong Y; Wang Y; Jiang F; Liu B; Zhang S; Yang W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):531-3. PubMed ID: 18841565
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family.
    Kaplanová V; Zeman J; Hansíková H; Cerná L; Houst'ková H; Misovicová N; Houstek J
    J Neurol Sci; 2004 Aug; 223(2):149-55. PubMed ID: 15337616
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Leber's hereditary optic neuroretinopathy (LHON) associated with mitochondrial DNA point mutation G11778A in two Croatian families.
    Martin-Kleiner I; Gabrilovac J; Bradvica M; Vidović T; Cerovski B; Fumić K; Boranić M
    Coll Antropol; 2006 Mar; 30(1):171-4. PubMed ID: 16617593
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [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; 42(1):89-97. PubMed ID: 16523671
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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; 41(3):243-5. PubMed ID: 15840367
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Penetrance of Leber hereditary optic neuropathy individuals with mitochondrial DNA 11778 mutation in the Shanxi area].
    Zheng ML; Zhang GL; Hua AL; Zhang YL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):166-7. PubMed ID: 15079802
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Optimization of a genotyping screening based on hydrolysis probes to detect the main mutations related to Leber hereditary optic neuropathy (LHON).
    Martins FTA; Miranda PMDAD; Fernandes MSA; Maciel-Guerra AT; Sartorato EL
    Mol Vis; 2017; 23():495-503. PubMed ID: 28761322
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Penetrance of Leber hereditary optic neuropathy in Chinese individuals with mitochondrial DNA 11778 mutation].
    Zhang Q; Guo X; Jia X; Xiao X; Guo L; Li S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec; 18(6):441-3. PubMed ID: 11774211
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.
    Sadun AA; Carelli V; Salomao SR; Berezovsky A; Quiros P; Sadun F; DeNegri AM; Andrade R; Schein S; Belfort R
    Trans Am Ophthalmol Soc; 2002; 100():169-78; discussion 178-9. PubMed ID: 12545691
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A patient with two mitochondrial DNA mutations causing PEO and LHON.
    Melberg A; Moslemi AR; Palm O; Raininko R; Stålberg E; Oldfors A
    Eur J Med Genet; 2009; 52(1):47-8. PubMed ID: 19015050
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Influence of mutation type on clinical expression of Leber hereditary optic neuropathy.
    Spruijt L; Kolbach DN; de Coo RF; Plomp AS; Bauer NJ; Smeets HJ; de Die-Smulders CE
    Am J Ophthalmol; 2006 Apr; 141(4):676-82. PubMed ID: 16564802
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.