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 *

152 related articles for article (PubMed ID: 11175302)

  • 1. Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G.
    Moilanen JS; Majamaa K
    Eur J Hum Genet; 2001 Jan; 9(1):59-62. PubMed ID: 11175302
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
    Kärppä M; Herva R; Moslemi AR; Oldfors A; Kakko S; Majamaa K
    Brain; 2005 Aug; 128(Pt 8):1861-9. PubMed ID: 15857931
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Population prevalence of the MELAS A3243G mutation.
    Manwaring N; Jones MM; Wang JJ; Rochtchina E; Howard C; Mitchell P; Sue CM
    Mitochondrion; 2007 May; 7(3):230-3. PubMed ID: 17300999
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.
    Uusimaa J; Moilanen JS; Vainionpää L; Tapanainen P; Lindholm P; Nuutinen M; Löppönen T; Mäki-Torkko E; Rantala H; Majamaa K
    Ann Neurol; 2007 Sep; 62(3):278-87. PubMed ID: 17823937
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prevalence of A-to-G mutation at nucleotide 3243 of the mitochondrial tRNA(Leu(UUR)) gene in Japanese patients with diabetes mellitus and end stage renal disease.
    Iwasaki N; Babazono T; Tsuchiya K; Tomonaga O; Suzuki A; Togashi M; Ujihara N; Sakka Y; Yokokawa H; Ogata M; Nihei H; Iwamoto Y
    J Hum Genet; 2001; 46(6):330-4. PubMed ID: 11393536
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>G.
    Kärppä M; Mahjneh I; Karttunen A; Tolonen U; Majamaa K
    J Neurol; 2004 May; 251(5):556-63. PubMed ID: 15164188
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pigmentary retinopathy in patients with the MELAS mutation 3243A-->G in mitochondrial DNA.
    Latvala T; Mustonen E; Uusitalo R; Majamaa K
    Graefes Arch Clin Exp Ophthalmol; 2002 Oct; 240(10):795-801. PubMed ID: 12397426
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.
    Janssen AJ; Schuelke M; Smeitink JA; Trijbels FJ; Sengers RC; Lucke B; Wintjes LT; Morava E; van Engelen BG; Smits BW; Hol FA; Siers MH; Ter Laak H; van der Knaap MS; Van Spronsen FJ; Rodenburg RJ; van den Heuvel LP
    Ann Neurol; 2008 Apr; 63(4):473-81. PubMed ID: 18306232
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA.
    Azevedo O; Vilarinho L; Almeida F; Ferreira F; Guardado J; Ferreira M; Lourenço A; Medeiros R; Almeida J
    Cardiology; 2010; 115(1):71-4. PubMed ID: 19864902
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection.
    Marotta R; Reardon K; McKelvie PA; Chiotis M; Chin J; Cook M; Collins SJ
    J Clin Neurosci; 2009 Sep; 16(9):1223-5. PubMed ID: 19502062
    [TBL] [Abstract][Full Text] [Related]  

  • 11. New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndrome.
    Maassen JA; Jahangir Tafrechi RS; Janssen GM; Raap AK; Lemkes HH; 't Hart LM
    Endocrinol Metab Clin North Am; 2006 Jun; 35(2):385-96, x-xi. PubMed ID: 16632100
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.
    Munakata K; Iwamoto K; Bundo M; Kato T
    Biol Psychiatry; 2005 Mar; 57(5):525-32. PubMed ID: 15737668
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Peripheral neuropathy in patients with the 3243A>G mutation in mitochondrial DNA.
    Kärppä M; Syrjälä P; Tolonen U; Majamaa K
    J Neurol; 2003 Feb; 250(2):216-21. PubMed ID: 12574954
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Muscle phenotype and mutation load in 51 persons with the 3243A>G mitochondrial DNA mutation.
    Jeppesen TD; Schwartz M; Frederiksen AL; Wibrand F; Olsen DB; Vissing J
    Arch Neurol; 2006 Dec; 63(12):1701-6. PubMed ID: 17172609
    [TBL] [Abstract][Full Text] [Related]  

  • 15. High prevalence of impaired glucose homeostasis and myopathy in asymptomatic and oligosymptomatic 3243A>G mitochondrial DNA mutation-positive subjects.
    Frederiksen AL; Jeppesen TD; Vissing J; Schwartz M; Kyvik KO; Schmitz O; Poulsen PL; Andersen PH
    J Clin Endocrinol Metab; 2009 Aug; 94(8):2872-9. PubMed ID: 19470628
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.
    Mimaki M; Hatakeyama H; Ichiyama T; Isumi H; Furukawa S; Akasaka M; Kamei A; Komaki H; Nishino I; Nonaka I; Goto Y
    Mitochondrion; 2009 Apr; 9(2):115-22. PubMed ID: 19460299
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Termination of damaged protein repair defines the occurrence of symptoms in carriers of the m.3243A > G tRNA(Leu) mutation.
    van Eijsden RG; Eijssen LM; Lindsey PJ; van den Burg CM; de Wit LE; Rubio-Gozalbo ME; de Die CE; Ayoubi T; Sluiter W; de Coo IF; Smeets HJ
    J Med Genet; 2008 Aug; 45(8):525-34. PubMed ID: 18456717
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment.
    Lehtonen MS; Uimonen S; Hassinen IE; Majamaa K
    Eur J Hum Genet; 2000 Apr; 8(4):315-8. PubMed ID: 10854117
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS.
    Wang Z; Liu S; Yang Y; Yuan Y; Wu L; Qi Y; Chen Q
    Chin Med J (Engl); 2002 Jul; 115(7):995-7. PubMed ID: 12150728
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiac involvement in adults with m.3243A>G MELAS gene mutation.
    Vydt TC; de Coo RF; Soliman OI; Ten Cate FJ; van Geuns RJ; Vletter WB; Schoonderwoerd K; van den Bosch BJ; Smeets HJ; Geleijnse ML
    Am J Cardiol; 2007 Jan; 99(2):264-9. PubMed ID: 17223431
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.