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 *

137 related articles for article (PubMed ID: 32066781)

  • 1. The role of control region mitochondrial DNA mutations in cardiovascular disease: stroke and myocardial infarction.
    Umbria M; Ramos A; Aluja MP; Santos C
    Sci Rep; 2020 Feb; 10(1):2766. PubMed ID: 32066781
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Involvement of mitochondrial haplogroups in myocardial infarction and stroke: A case-control study in Castile and Leon (Spain) population.
    Umbria M; Ramos A; Caner J; Vega T; Lozano JE; Santos C; Aluja MP
    Mitochondrion; 2019 Jan; 44():1-6. PubMed ID: 29258787
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Complete mitochondrial DNA profile in stroke: A geographical matched case-control study in Spanish population.
    Onieva A; Martin J; R Cuesta-Aguirre D; Planells V; Coronado-Zamora M; Beyer K; Vega T; Lozano JE; Santos C; Aluja MP
    Mitochondrion; 2023 Nov; 73():51-61. PubMed ID: 37793469
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication.
    Coskun PE; Beal MF; Wallace DC
    Proc Natl Acad Sci U S A; 2004 Jul; 101(29):10726-31. PubMed ID: 15247418
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Platelet mitochondrial DNA methylation: A novel biomarker for myocardial infarction - A preliminary study.
    Peng N; Guo L; Wei Z; Wang X; Zhao L; Kang L; Wang K; Zhou W; Cheng S; Yin S; Xu B; Bao X
    Int J Cardiol; 2024 Mar; 398():131606. PubMed ID: 37996014
    [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. Genetic variants of arachidonate 5-lipoxygenase-activating protein, and risk of incident myocardial infarction and ischemic stroke: a nested case-control approach.
    Zee RY; Cheng S; Hegener HH; Erlich HA; Ridker PM
    Stroke; 2006 Aug; 37(8):2007-11. PubMed ID: 16778124
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy.
    Arbustini E; Diegoli M; Fasani R; Grasso M; Morbini P; Banchieri N; Bellini O; Dal Bello B; Pilotto A; Magrini G; Campana C; Fortina P; Gavazzi A; Narula J; Viganò M
    Am J Pathol; 1998 Nov; 153(5):1501-10. PubMed ID: 9811342
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.
    Palacín M; Alvarez V; Martín M; Díaz M; Corao AI; Alonso B; Díaz-Molina B; Lozano I; Avanzas P; Morís C; Reguero JR; Rodríguez I; López-Larrea C; Cannata-Andía J; Batalla A; Ruiz-Ortega M; Martínez-Camblor P; Coto E
    Mitochondrion; 2011 Jan; 11(1):176-81. PubMed ID: 20863902
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evaluating length heteroplasmy in the human mitochondrial DNA control region.
    Forster L; Forster P; Gurney SM; Spencer M; Huang C; Röhl A; Brinkmann B
    Int J Legal Med; 2010 Mar; 124(2):133-42. PubMed ID: 19937256
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Overexpression of mitochondrial transcription factor a ameliorates mitochondrial deficiencies and cardiac failure after myocardial infarction.
    Ikeuchi M; Matsusaka H; Kang D; Matsushima S; Ide T; Kubota T; Fujiwara T; Hamasaki N; Takeshita A; Sunagawa K; Tsutsui H
    Circulation; 2005 Aug; 112(5):683-90. PubMed ID: 16043643
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prognostic value of mitochondrial DNA
    Vecoli C; Borghini A; Pulignani S; Mercuri A; Turchi S; Carpeggiani C; Picano E; Andreassi MG
    Atherosclerosis; 2018 Sep; 276():91-97. PubMed ID: 30053637
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Associations of mitochondrial DNA 3777-4679 region mutations with maternally inherited essential hypertensive subjects in China.
    Zhu Y; You J; Xu C; Gu X
    BMC Med Genet; 2020 May; 21(1):105. PubMed ID: 32414374
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Homozygous R627W mutations in POLG cause mitochondrial DNA depletion leading to encephalopathy, seizures and stroke-like episodes.
    Paramasivam A; Venkatapathi C; Sandeep G; Meena AK; Uppin MS; Mohapatra S; Pitceathly RDS; Thangaraj K
    Mitochondrion; 2019 Sep; 48():78-83. PubMed ID: 31425757
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Control region mutations and the 'common deletion' are frequent in the mitochondrial DNA of patients with esophageal squamous cell carcinoma.
    Abnet CC; Huppi K; Carrera A; Armistead D; McKenney K; Hu N; Tang ZZ; Taylor PR; Dawsey SM
    BMC Cancer; 2004 Jul; 4():30. PubMed ID: 15230979
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Repetitive sequences in Eurasian lynx (Lynx lynx L.) mitochondrial DNA control region.
    Sindičić M; Gomerčić T; Galov A; Polanc P; Huber D; Slavica A
    Mitochondrial DNA; 2012 Jun; 23(3):201-7. PubMed ID: 22515208
    [TBL] [Abstract][Full Text] [Related]  

  • 18. TALEN-mediated shift of mitochondrial DNA heteroplasmy in MELAS-iPSCs with m.13513G>A mutation.
    Yahata N; Matsumoto Y; Omi M; Yamamoto N; Hata R
    Sci Rep; 2017 Nov; 7(1):15557. PubMed ID: 29138463
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of Mitochondrial DNA Copy Number With Cardiovascular Disease.
    Ashar FN; Zhang Y; Longchamps RJ; Lane J; Moes A; Grove ML; Mychaleckyj JC; Taylor KD; Coresh J; Rotter JI; Boerwinkle E; Pankratz N; Guallar E; Arking DE
    JAMA Cardiol; 2017 Nov; 2(11):1247-1255. PubMed ID: 29049454
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial Genome Mutations Associated with Myocardial Infarction.
    Sazonova MA; Ryzhkova AI; Sinyov VV; Galitsyna EV; Melnichenko AA; Demakova NA; Sobenin IA; Shkurat TP; Orekhov AN
    Dis Markers; 2018; 2018():9749457. PubMed ID: 29670672
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.