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 *

174 related articles for article (PubMed ID: 31757988)

  • 1. A simple method for sequencing the whole human mitochondrial genome directly from samples and its application to genetic testing.
    Yao Y; Nishimura M; Murayama K; Kuranobu N; Tojo S; Beppu M; Ishige T; Itoga S; Tsuchida S; Mori M; Takayanagi M; Yokoyama M; Yamagata K; Kishita Y; Okazaki Y; Nomura F; Matsushita K; Tanaka T
    Sci Rep; 2019 Nov; 9(1):17411. PubMed ID: 31757988
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial and nuclear disease panel (Mito-aND-Panel): Combined sequencing of mitochondrial and nuclear DNA by a cost-effective and sensitive NGS-based method.
    Abicht A; Scharf F; Kleinle S; Schön U; Holinski-Feder E; Horvath R; Benet-Pagès A; Diebold I
    Mol Genet Genomic Med; 2018 Nov; 6(6):1188-1198. PubMed ID: 30406974
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Impact of the sequencing method on the detection and interpretation of mitochondrial DNA length heteroplasmy.
    Sturk-Andreaggi K; Parson W; Allen M; Marshall C
    Forensic Sci Int Genet; 2020 Jan; 44():102205. PubMed ID: 31783338
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Whole Genome Sequencing of Human mtDNA Based on Ion Torrent PGM™ Platform].
    Cao Y; Zou KN; Huang JP; Ma K; Ping Y
    Fa Yi Xue Za Zhi; 2017 Aug; 33(4):368-373. PubMed ID: 29219266
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comprehensive Mitochondrial Genome Analysis by Massively Parallel Sequencing.
    Palculict ME; Zhang VW; Wong LJ; Wang J
    Methods Mol Biol; 2016; 1351():3-17. PubMed ID: 26530670
    [TBL] [Abstract][Full Text] [Related]  

  • 6. MitoRS, a method for high throughput, sensitive, and accurate detection of mitochondrial DNA heteroplasmy.
    Marquis J; Lefebvre G; Kourmpetis YAI; Kassam M; Ronga F; De Marchi U; Wiederkehr A; Descombes P
    BMC Genomics; 2017 Apr; 18(1):326. PubMed ID: 28441938
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects.
    Tang S; Wang J; Zhang VW; Li FY; Landsverk M; Cui H; Truong CK; Wang G; Chen LC; Graham B; Scaglia F; Schmitt ES; Craigen WJ; Wong LJ
    Hum Mutat; 2013 Jun; 34(6):882-93. PubMed ID: 23463613
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial DNA variant discovery and evaluation in human Cardiomyopathies through next-generation sequencing.
    Zaragoza MV; Fass J; Diegoli M; Lin D; Arbustini E
    PLoS One; 2010 Aug; 5(8):e12295. PubMed ID: 20808834
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Advanced approach for comprehensive mtDNA genome testing in mitochondrial disease.
    Wang J; Balciuniene J; Diaz-Miranda MA; McCormick EM; Aref-Eshghi E; Muir AM; Cao K; Troiani J; Moseley A; Fan Z; Zolkipli-Cunningham Z; Goldstein A; Ganetzky RD; Muraresku CC; Peterson JT; Spinner NB; Wallace DC; Dulik MC; Falk MJ
    Mol Genet Metab; 2022 Jan; 135(1):93-101. PubMed ID: 34969639
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel economical, accurate, sensitive, single-cell analytical method for mitochondrial DNA quantification in mtDNA mutation carriers.
    Zou W; Zong K; Zhang Z; Shen L; Wang X; Su X; Wang X; Yin T; Liang C; Liu Y; Liang D; Hu C; Cao Y; Ji D
    J Assist Reprod Genet; 2023 Sep; 40(9):2197-2209. PubMed ID: 37462790
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genome.
    Falk MJ; Pierce EA; Consugar M; Xie MH; Guadalupe M; Hardy O; Rappaport EF; Wallace DC; LeProust E; Gai X
    Discov Med; 2012 Dec; 14(79):389-99. PubMed ID: 23272691
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dynamics of mitochondrial heteroplasmy in three families investigated via a repeatable re-sequencing study.
    Goto H; Dickins B; Afgan E; Paul IM; Taylor J; Makova KD; Nekrutenko A
    Genome Biol; 2011; 12(6):R59. PubMed ID: 21699709
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The development of next-generation sequencing assays for the mitochondrial genome and 108 nuclear genes associated with mitochondrial disorders.
    Dames S; Chou LS; Xiao Y; Wayman T; Stocks J; Singleton M; Eilbeck K; Mao R
    J Mol Diagn; 2013 Jul; 15(4):526-34. PubMed ID: 23665194
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Plasma-derived cell-free mitochondrial DNA: A novel non-invasive methodology to identify mitochondrial DNA haplogroups in humans.
    Newell C; Hume S; Greenway SC; Podemski L; Shearer J; Khan A
    Mol Genet Metab; 2018 Dec; 125(4):332-337. PubMed ID: 30361042
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders.
    Cui H; Li F; Chen D; Wang G; Truong CK; Enns GM; Graham B; Milone M; Landsverk ML; Wang J; Zhang W; Wong LJ
    Genet Med; 2013 May; 15(5):388-94. PubMed ID: 23288206
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of mitochondrial DNA variants at low level heteroplasmy in pediatric CNS and extra-CNS solid tumors with three different enrichment methods.
    Kaneva K; Merkurjev D; Ostrow D; Ryutov A; Triska P; Stachelek K; Cobrinik D; Biegel JA; Gai X
    Mitochondrion; 2020 Mar; 51():97-103. PubMed ID: 31972374
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Concordance and reproducibility of a next generation mtGenome sequencing method for high-quality samples using the Illumina MiSeq.
    Peck MA; Brandhagen MD; Marshall C; Diegoli TM; Irwin JA; Sturk-Andreaggi K
    Forensic Sci Int Genet; 2016 Sep; 24():103-111. PubMed ID: 27368088
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Differential mitochondrial genome in patients with Rheumatoid Arthritis.
    Jaiswal KS; Khanna S; Ghosh A; Padhan P; Raghav SK; Gupta B
    Autoimmunity; 2021 Feb; 54(1):1-12. PubMed ID: 33191792
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Challenges of bringing next generation sequencing technologies to clinical molecular diagnostic laboratories.
    Wong LJ
    Neurotherapeutics; 2013 Apr; 10(2):262-72. PubMed ID: 23269496
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sensitivity of mitochondrial DNA heteroplasmy detection using Next Generation Sequencing.
    González MDM; Ramos A; Aluja MP; Santos C
    Mitochondrion; 2020 Jan; 50():88-93. PubMed ID: 31669622
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.