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 *

768 related articles for article (PubMed ID: 26281784)

  • 1. The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease.
    Stewart JB; Chinnery PF
    Nat Rev Genet; 2015 Sep; 16(9):530-42. PubMed ID: 26281784
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Modulating mitochondrial DNA mutations: factors shaping heteroplasmy in the germ line and somatic cells.
    Chiaratti MR; Chinnery PF
    Pharmacol Res; 2022 Nov; 185():106466. PubMed ID: 36174964
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Universal heteroplasmy of human mitochondrial DNA.
    Payne BA; Wilson IJ; Yu-Wai-Man P; Coxhead J; Deehan D; Horvath R; Taylor RW; Samuels DC; Santibanez-Koref M; Chinnery PF
    Hum Mol Genet; 2013 Jan; 22(2):384-90. PubMed ID: 23077218
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Bottleneck and selection in the germline and maternal age influence transmission of mitochondrial DNA in human pedigrees.
    Zaidi AA; Wilton PR; Su MS; Paul IM; Arbeithuber B; Anthony K; Nekrutenko A; Nielsen R; Makova KD
    Proc Natl Acad Sci U S A; 2019 Dec; 116(50):25172-25178. PubMed ID: 31757848
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission.
    Freyer C; Cree LM; Mourier A; Stewart JB; Koolmeister C; Milenkovic D; Wai T; Floros VI; Hagström E; Chatzidaki EE; Wiesner RJ; Samuels DC; Larsson NG; Chinnery PF
    Nat Genet; 2012 Nov; 44(11):1282-5. PubMed ID: 23042113
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Age-related accumulation of de novo mitochondrial mutations in mammalian oocytes and somatic tissues.
    Arbeithuber B; Hester J; Cremona MA; Stoler N; Zaidi A; Higgins B; Anthony K; Chiaromonte F; Diaz FJ; Makova KD
    PLoS Biol; 2020 Jul; 18(7):e3000745. PubMed ID: 32667908
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos.
    Floros VI; Pyle A; Dietmann S; Wei W; Tang WCW; Irie N; Payne B; Capalbo A; Noli L; Coxhead J; Hudson G; Crosier M; Strahl H; Khalaf Y; Saitou M; Ilic D; Surani MA; Chinnery PF
    Nat Cell Biol; 2018 Feb; 20(2):144-151. PubMed ID: 29335530
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Maternal age effect and severe germ-line bottleneck in the inheritance of human mitochondrial DNA.
    Rebolledo-Jaramillo B; Su MS; Stoler N; McElhoe JA; Dickins B; Blankenberg D; Korneliussen TS; Chiaromonte F; Nielsen R; Holland MM; Paul IM; Nekrutenko A; Makova KD
    Proc Natl Acad Sci U S A; 2014 Oct; 111(43):15474-9. PubMed ID: 25313049
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inheritance of mitochondrial DNA in humans: implications for rare and common diseases.
    Wei W; Chinnery PF
    J Intern Med; 2020 Jun; 287(6):634-644. PubMed ID: 32187761
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation-specific effects in germline transmission of pathogenic mtDNA variants.
    Otten ABC; Sallevelt SCEH; Carling PJ; Dreesen JCFM; Drüsedau M; Spierts S; Paulussen ADC; de Die-Smulders CEM; Herbert M; Chinnery PF; Samuels DC; Lindsey P; Smeets HJM
    Hum Reprod; 2018 Jul; 33(7):1331-1341. PubMed ID: 29850888
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial Network State Scales mtDNA Genetic Dynamics.
    Aryaman J; Bowles C; Jones NS; Johnston IG
    Genetics; 2019 Aug; 212(4):1429-1443. PubMed ID: 31253641
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Significance of Mitochondria DNA Mutations in Diseases.
    Zhu Z; Wang X
    Adv Exp Med Biol; 2017; 1038():219-230. PubMed ID: 29178079
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The role of mitochondrial DNA mutations in mammalian aging.
    Kujoth GC; Bradshaw PC; Haroon S; Prolla TA
    PLoS Genet; 2007 Feb; 3(2):e24. PubMed ID: 17319745
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mitochondria and Their Role in Human Reproduction.
    Zou W; Slone J; Cao Y; Huang T
    DNA Cell Biol; 2020 Aug; 39(8):1370-1378. PubMed ID: 31603716
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing.
    Greaves LC; Nooteboom M; Elson JL; Tuppen HA; Taylor GA; Commane DM; Arasaradnam RP; Khrapko K; Taylor RW; Kirkwood TB; Mathers JC; Turnbull DM
    PLoS Genet; 2014 Sep; 10(9):e1004620. PubMed ID: 25232829
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The contribution of mitochondrial DNA alterations to aging, cancer, and neurodegeneration.
    Picca A; Guerra F; Calvani R; Coelho-Júnior HJ; Leeuwenburgh C; Bucci C; Marzetti E
    Exp Gerontol; 2023 Jul; 178():112203. PubMed ID: 37172915
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Preventing the transmission of pathogenic mitochondrial DNA mutations: Can we achieve long-term benefits from germ-line gene transfer?
    Samuels DC; Wonnapinij P; Chinnery PF
    Hum Reprod; 2013 Mar; 28(3):554-9. PubMed ID: 23297368
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mitochondrial DNA mutations in disease and ageing.
    Cottrell DA; Blakely EL; Johnson MA; Borthwick GM; Ince PI; Turnbull DM
    Novartis Found Symp; 2001; 235():234-43; discussion 243-6. PubMed ID: 11280028
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial DNA mutation and the ageing process: bioenergy and pharmacological intervention.
    Linnane AW; Zhang C; Baumer A; Nagley P
    Mutat Res; 1992 Sep; 275(3-6):195-208. PubMed ID: 1383761
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 39.