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 *

136 related articles for article (PubMed ID: 31261379)

  • 1. G-quadruplex-mediated reduction of a pathogenic mitochondrial heteroplasmy.
    Naeem MM; Maheshan R; Costford SR; Wahedi A; Trajkovski M; Plavec J; Yatsunyk LA; Ciesielski GL; Kaufman BA; Sondheimer N
    Hum Mol Genet; 2019 Oct; 28(19):3163-3174. PubMed ID: 31261379
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heteroplasmy Shifting as Therapy for Mitochondrial Disorders.
    Naeem MM; Sondheimer N
    Adv Exp Med Biol; 2019; 1158():257-267. PubMed ID: 31452145
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mitochondrial DNA heteroplasmy in disease and targeted nuclease-based therapeutic approaches.
    Nissanka N; Moraes CT
    EMBO Rep; 2020 Mar; 21(3):e49612. PubMed ID: 32073748
    [TBL] [Abstract][Full Text] [Related]  

  • 4. LONP-1 and ATFS-1 sustain deleterious heteroplasmy by promoting mtDNA replication in dysfunctional mitochondria.
    Yang Q; Liu P; Anderson NS; Shpilka T; Du Y; Naresh NU; Li R; Zhu LJ; Luk K; Lavelle J; Zeinert RD; Chien P; Wolfe SA; Haynes CM
    Nat Cell Biol; 2022 Feb; 24(2):181-193. PubMed ID: 35165413
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Nuclear genetic control of mtDNA copy number and heteroplasmy in humans.
    Gupta R; Kanai M; Durham TJ; Tsuo K; McCoy JG; Kotrys AV; Zhou W; Chinnery PF; Karczewski KJ; Calvo SE; Neale BM; Mootha VK
    Nature; 2023 Aug; 620(7975):839-848. PubMed ID: 37587338
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Extensive pathogenicity of mitochondrial heteroplasmy in healthy human individuals.
    Ye K; Lu J; Ma F; Keinan A; Gu Z
    Proc Natl Acad Sci U S A; 2014 Jul; 111(29):10654-9. PubMed ID: 25002485
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial DNA Variation and Heteroplasmy in Monozygotic Twins Clinically Discordant for Multiple Sclerosis.
    Souren NY; Gerdes LA; Kümpfel T; Lutsik P; Klopstock T; Hohlfeld R; Walter J
    Hum Mutat; 2016 Aug; 37(8):765-75. PubMed ID: 27119776
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heteroplasmy and stoichiometric complexity of plant mitochondrial genomes--though this be madness, yet there's method in't.
    Woloszynska M
    J Exp Bot; 2010 Mar; 61(3):657-71. PubMed ID: 19995826
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints.
    Dong DW; Pereira F; Barrett SP; Kolesar JE; Cao K; Damas J; Yatsunyk LA; Johnson FB; Kaufman BA
    BMC Genomics; 2014 Aug; 15(1):677. PubMed ID: 25124333
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The 8993 mtDNA mutation: heteroplasmy and clinical presentation in three families.
    Tatuch Y; Pagon RA; Vlcek B; Roberts R; Korson M; Robinson BH
    Eur J Hum Genet; 1994; 2(1):35-43. PubMed ID: 8044652
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Intracellular heteroplasmy for disease-associated point mutations in mtDNA: implications for disease expression and evidence for mitotic segregation of heteroplasmic units of mtDNA.
    Matthews PM; Brown RM; Morten K; Marchington D; Poulton J; Brown G
    Hum Genet; 1995 Sep; 96(3):261-8. PubMed ID: 7649539
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Presence and transmission of mitochondrial heteroplasmic mutations in human populations of European and African ancestry.
    Liu C; Fetterman JL; Qian Y; Sun X; Blackwell TW; Pitsillides A; Cade BE; Wang H; Raffield LM; Lange LA; Anugu P; Abecasis G; Adrienne Cupples L; Redline S; Correa A; Vasan RS; Wilson JG; Ding J; Levy D;
    Mitochondrion; 2021 Sep; 60():33-42. PubMed ID: 34303007
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Quantitative and qualitative profiling of mitochondrial DNA length heteroplasmy.
    Lee HY; Chung U; Yoo JE; Park MJ; Shin KJ
    Electrophoresis; 2004 Jan; 25(1):28-34. PubMed ID: 14730565
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography.
    van Den Bosch BJ; de Coo RF; Scholte HR; Nijland JG; van Den Bogaard R; de Visser M; de Die-Smulders CE; Smeets HJ
    Nucleic Acids Res; 2000 Oct; 28(20):E89. PubMed ID: 11024191
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nuclear genome-wide associations with mitochondrial heteroplasmy.
    Nandakumar P; Tian C; O'Connell J; ; Hinds D; Paterson AD; Sondheimer N
    Sci Adv; 2021 Mar; 7(12):. PubMed ID: 33731350
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Evaluating the Bioenergetics Health Index Ratio in Leigh Syndrome Fibroblasts to Understand Disease Severity.
    Bakare AB; Dean J; Chen Q; Thorat V; Huang Y; LaFramboise T; Lesnefsky EJ; Iyer S
    Int J Mol Sci; 2021 Sep; 22(19):. PubMed ID: 34638685
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Natural Aromatic Compounds as Scaffolds to Develop Selective G-Quadruplex Ligands: From Previously Reported Berberine Derivatives to New Palmatine Analogues.
    Franceschin M; Cianni L; Pitorri M; Micheli E; Cacchione S; Frezza C; Serafini M; Hu MH; Su H; Huang Z; Gu L; Bianco A
    Molecules; 2018 Jun; 23(6):. PubMed ID: 29895786
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Polymerase γ efficiently replicates through many natural template barriers but stalls at the HSP1 quadruplex.
    Sullivan ED; Longley MJ; Copeland WC
    J Biol Chem; 2020 Dec; 295(51):17802-17815. PubMed ID: 33454015
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel insights into the functional metabolic impact of an apparent de novo m.8993T>G variant in the MT-ATP6 gene associated with maternally inherited form of Leigh Syndrome.
    Uittenbogaard M; Brantner CA; Fang Z; Wong LC; Gropman A; Chiaramello A
    Mol Genet Metab; 2018 May; 124(1):71-81. PubMed ID: 29602698
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assessing heteroplasmic variant drift in the mtDNA control region of human hairs using an MPS approach.
    Gallimore JM; McElhoe JA; Holland MM
    Forensic Sci Int Genet; 2018 Jan; 32():7-17. PubMed ID: 29024924
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.