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 *

217 related articles for article (PubMed ID: 30089816)

  • 1. Mitochondrial DNA m.3243A > G heteroplasmy affects multiple aging phenotypes and risk of mortality.
    Tranah GJ; Katzman SM; Lauterjung K; Yaffe K; Manini TM; Kritchevsky S; Newman AB; Harris TB; Cummings SR
    Sci Rep; 2018 Aug; 8(1):11887. PubMed ID: 30089816
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial DNA mutation m.3243A>G is associated with altered mitochondrial function in peripheral blood mononuclear cells, with heteroplasmy levels and with clinical phenotypes.
    Geng X; Zhang Y; Yan J; Chu C; Gao F; Jiang Z; Zhang X; Chen Y; Wei X; Feng Y; Lu H; Wang C; Zeng F; Jia W
    Diabet Med; 2019 Jun; 36(6):776-783. PubMed ID: 30536471
    [TBL] [Abstract][Full Text] [Related]  

  • 3. mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease.
    Grady JP; Pickett SJ; Ng YS; Alston CL; Blakely EL; Hardy SA; Feeney CL; Bright AA; Schaefer AM; Gorman GS; McNally RJ; Taylor RW; Turnbull DM; McFarland R
    EMBO Mol Med; 2018 Jun; 10(6):. PubMed ID: 29735722
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Determining Mitochondrial 3243A>G Heteroplasmy Using an ARMS-ddPCR Strategy.
    Xu P; Jia M; Yan J; Yuan X; Yu W; Zhou Z; Fang H; Gao F; Shen L
    Am J Clin Pathol; 2022 May; 157(5):664-677. PubMed ID: 34698344
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heteroplasmy and phenotype spectrum of the mitochondrial tRNA
    Liu G; Shen X; Sun Y; Lv Q; Li Y; Du A
    J Neurol Sci; 2020 Jan; 408():116562. PubMed ID: 31722256
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Mitochondrial DNA heteroplasmy of the m.3243A>G mutation in maternally inherited diabetes and deafness].
    Cataldo LR; Olmos P; Valerie Smalley S; Díez A; Parada A; Gejman R; Fadic R; Santos JL
    Rev Med Chil; 2013 Mar; 141(3):305-12. PubMed ID: 23900320
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Heteroplasmy and Copy Number in the Common m.3243A>G Mutation-A Post-Mortem Genotype-Phenotype Analysis.
    Scholle LM; Zierz S; Mawrin C; Wickenhauser C; Urban DL
    Genes (Basel); 2020 Feb; 11(2):. PubMed ID: 32085658
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lecocytes mutation load declines with age in carriers of the m.3243A>G mutation: A 10-year Prospective Cohort.
    Langdahl JH; Larsen M; Frost M; Andersen PH; Yderstraede KB; Vissing J; Dunø M; Thomassen M; Frederiksen AL
    Clin Genet; 2018 Apr; 93(4):925-928. PubMed ID: 29266179
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Negative correlation between organ heteroplasmy, particularly hepatic heteroplasmy, and age at death revealed by post-mortem studies of m.3243A > G cases.
    Yagi K; Okazaki S; Ohbatake A; Nakaya M; Liu J; Arite E; Miyamoto Y; Ito N; Nakano K; Yamaaki N; Honoki H; Fujisaka S; Chujo D; Tsunoda SI; Yanagimoto K; Nozue T; Yamada M; Ooe K; Araki T; Nakashima A; Azami Y; Sodemoto Y; Tadokoro K; Nagano M; Noguchi T; Nohara A; Origasa H; Niida Y; Tada H
    Mol Genet Metab; 2023 Nov; 140(3):107691. PubMed ID: 37660570
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Droplet digital polymerase chain reaction to measure heteroplasmic m.3243A>G mitochondrial mutations.
    Matsumoto S; Uchiumi T; Noda N; Ueyanagi Y; Hotta T; Kang D
    Lab Med; 2024 Mar; 55(2):227-233. PubMed ID: 37478467
    [TBL] [Abstract][Full Text] [Related]  

  • 11. ATF5, a putative therapeutic target for the mitochondrial DNA 3243A > G mutation-related disease.
    Gao X; Jiang Z; Yan X; Liu J; Li F; Liu P; Li J; Wei Y; Sun YE; Zhang Y; Wang C
    Cell Death Dis; 2021 Jul; 12(7):701. PubMed ID: 34262025
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutation.
    Pyle A; Taylor RW; Durham SE; Deschauer M; Schaefer AM; Samuels DC; Chinnery PF
    J Med Genet; 2007 Jan; 44(1):69-74. PubMed ID: 16950816
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial DNA m.13514G>A heteroplasmy is associated with depressive symptoms in the elderly.
    Tranah GJ; Maglione JE; Yaffe K; Katzman SM; Manini TM; Kritchevsky S; Newman AB; Harris TB; Cummings SR;
    Int J Geriatr Psychiatry; 2018 Oct; 33(10):1319-1326. PubMed ID: 29984425
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial DNA Heteroplasmy Associations With Neurosensory and Mobility Function in Elderly Adults.
    Tranah GJ; Yaffe K; Katzman SM; Lam ET; Pawlikowska L; Kwok PY; Schork NJ; Manini TM; Kritchevsky S; Thomas F; Newman AB; Harris TB; Coleman AL; Gorin MB; Helzner EP; Rowbotham MC; Browner WS; Cummings SR;
    J Gerontol A Biol Sci Med Sci; 2015 Nov; 70(11):1418-24. PubMed ID: 26328603
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation.
    de Laat P; Koene S; van den Heuvel LP; Rodenburg RJ; Janssen MC; Smeitink JA
    J Inherit Metab Dis; 2012 Nov; 35(6):1059-69. PubMed ID: 22403016
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Intra-patient variability of heteroplasmy levels in urinary epithelial cells in carriers of the m.3243A>G mutation.
    de Laat P; Rodenburg RJ; Smeitink JAM; Janssen MCH
    Mol Genet Genomic Med; 2019 Feb; 7(2):e00523. PubMed ID: 30516030
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study.
    Shi Y; Chen G; Sun D; Hu C; Liu Z; Shen D; Wang J; Song T; Zhang W; Li J; Ren X; Han T; Ding C; Wang Y; Fang F
    Mitochondrion; 2022 Jan; 62():139-150. PubMed ID: 34800692
    [TBL] [Abstract][Full Text] [Related]  

  • 18. De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome.
    Jiang Z; Zhang Y; Yan J; Li F; Geng X; Lu H; Wei X; Feng Y; Wang C; Jia W
    J Diabetes Res; 2019; 2019():5184647. PubMed ID: 31143779
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical Characteristics of Diabetes in People with Mitochondrial DNA 3243A>G Mutation in Korea.
    Rho EH; Baek SI; Lee H; Seong MW; Chae JH; Park KS; Kwak SH
    Diabetes Metab J; 2024 May; 48(3):482-486. PubMed ID: 38311059
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Phenotypic Heterogeneity in 5 Family Members with the Mitochondrial Variant m.3243A>G.
    Finsterer J; Laccone F
    Am J Case Rep; 2020 Nov; 21():e927938. PubMed ID: 33237887
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.