BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

373 related articles for article (PubMed ID: 23272691)

  • 21. 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]  

  • 22. Mitochondrial diseases: a cross-talk between mitochondrial and nuclear genomes.
    Spinazzola A; Zeviani M
    Adv Exp Med Biol; 2009; 652():69-84. PubMed ID: 20225020
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evaluating heteroplasmic variations of the mitochondrial genome from whole genome sequencing data.
    Duan M; Chen L; Ge Q; Lu N; Li J; Pan X; Qiao Y; Tu J; Lu Z
    Gene; 2019 May; 699():145-154. PubMed ID: 30876822
    [TBL] [Abstract][Full Text] [Related]  

  • 24. High throughput exome coverage of clinically relevant cardiac genes.
    Manase D; D'Alessandro LC; Manickaraj AK; Al Turki S; Hurles ME; Mital S
    BMC Med Genomics; 2014 Dec; 7():67. PubMed ID: 25496018
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling.
    Zhang G; Wang J; Yang J; Li W; Deng Y; Li J; Huang J; Hu S; Zhang B
    BMC Genomics; 2015 Aug; 16(1):581. PubMed ID: 26242175
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Evaluation of the precision ID mtDNA whole genome panel on two massively parallel sequencing systems.
    Woerner AE; Ambers A; Wendt FR; King JL; Moura-Neto RS; Silva R; Budowle B
    Forensic Sci Int Genet; 2018 Sep; 36():213-224. PubMed ID: 30059903
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.
    Falk MJ; Shen L; Gonzalez M; Leipzig J; Lott MT; Stassen AP; Diroma MA; Navarro-Gomez D; Yeske P; Bai R; Boles RG; Brilhante V; Ralph D; DaRe JT; Shelton R; Terry SF; Zhang Z; Copeland WC; van Oven M; Prokisch H; Wallace DC; Attimonelli M; Krotoski D; Zuchner S; Gai X; ; ; ; ; ;
    Mol Genet Metab; 2015 Mar; 114(3):388-96. PubMed ID: 25542617
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Whole exome sequencing is an alternative method in the diagnosis of mitochondrial DNA diseases.
    Sun C; Wu S; Chen R; Liu J; Wang J; Ma Y; Yuan Z; Li Y
    Mol Genet Genomic Med; 2022 Jun; 10(6):e1943. PubMed ID: 35388601
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The Value of Whole-Genome Sequencing for Mitochondrial DNA Population Studies: Strategies and Criteria for Extracting High-Quality Mitogenome Haplotypes.
    Sturk-Andreaggi K; Ring JD; Ameur A; Gyllensten U; Bodner M; Parson W; Marshall C; Allen M
    Int J Mol Sci; 2022 Feb; 23(4):. PubMed ID: 35216360
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Comparison of Mendeliome exome capture kits for use in clinical diagnostics.
    Pengelly RJ; Ward D; Hunt D; Mattocks C; Ennis S
    Sci Rep; 2020 Feb; 10(1):3235. PubMed ID: 32094380
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Identification of Mitochondrial DNA (NUMTs) in the Nuclear Genome of
    Kowal K; Tkaczyk A; Pierzchała M; Bownik A; Ślaska B
    Int J Mol Sci; 2020 Nov; 21(22):. PubMed ID: 33218217
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Diagnostic challenges of mitochondrial disorders: complexities of two genomes.
    Graham BH
    Methods Mol Biol; 2012; 837():35-46. PubMed ID: 22215539
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Targeted multiplex next-generation sequencing: advances in techniques of mitochondrial and nuclear DNA sequencing for population genomics.
    Hancock-Hanser BL; Frey A; Leslie MS; Dutton PH; Archer FI; Morin PA
    Mol Ecol Resour; 2013 Mar; 13(2):254-68. PubMed ID: 23351075
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Quantitative assessment of heteroplasmy of mitochondrial genome: perspectives in diagnostics and methodological pitfalls.
    Sobenin IA; Mitrofanov KY; Zhelankin AV; Sazonova MA; Postnov AY; Revin VV; Bobryshev YV; Orekhov AN
    Biomed Res Int; 2014; 2014():292017. PubMed ID: 24818137
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular genetics of mitochondrial disorders.
    Wong LJ
    Dev Disabil Res Rev; 2010; 16(2):154-62. PubMed ID: 20818730
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mitochondria sequence mapping strategies and practicability of mitochondria variant detection from exome and RNA sequencing data.
    Zhang P; Samuels DC; Lehmann B; Stricker T; Pietenpol J; Shyr Y; Guo Y
    Brief Bioinform; 2016 Mar; 17(2):224-32. PubMed ID: 26249222
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: a population-based exome-wide association study.
    Li Z; Zhu M; Du J; Ma H; Jin G; Dai J
    BMC Genomics; 2018 Oct; 19(1):752. PubMed ID: 30326835
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Advances in methods for reducing mitochondrial DNA disease by replacing or manipulating the mitochondrial genome.
    Rai PK; Craven L; Hoogewijs K; Russell OM; Lightowlers RN
    Essays Biochem; 2018 Jul; 62(3):455-465. PubMed ID: 29950320
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.