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 *

148 related articles for article (PubMed ID: 21249378)

  • 1. Factors affecting the detection and quantification of mitochondrial point heteroplasmy using Sanger sequencing and SNaPshot minisequencing.
    Naue J; Sänger T; Schmidt U; Klein R; Lutz-Bonengel S
    Int J Legal Med; 2011 May; 125(3):427-36. PubMed ID: 21249378
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Damage patterns observed in mtDNA control region MPS data for a range of template concentrations and when using different amplification approaches.
    Holland CA; McElhoe JA; Gaston-Sanchez S; Holland MM
    Int J Legal Med; 2021 Jan; 135(1):91-106. PubMed ID: 32940843
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Massively parallel pyrosequencing of the mitochondrial genome with the 454 methodology in forensic genetics.
    Mikkelsen M; Frank-Hansen R; Hansen AJ; Morling N
    Forensic Sci Int Genet; 2014 Sep; 12():30-7. PubMed ID: 24879032
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Evidence for frequent and tissue-specific sequence heteroplasmy in human mitochondrial DNA.
    Naue J; Hörer S; Sänger T; Strobl C; Hatzer-Grubwieser P; Parson W; Lutz-Bonengel S
    Mitochondrion; 2015 Jan; 20():82-94. PubMed ID: 25526677
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Single lymphocytes from two healthy individuals with mitochondrial point heteroplasmy are mainly homoplasmic.
    Lutz-Bonengel S; Sänger T; Parson W; Müller H; Ellwart JW; Follo M; Bonengel B; Niederstätter H; Heinrich M; Schmidt U
    Int J Legal Med; 2008 May; 122(3):189-97. PubMed ID: 17922134
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Quantification of mtDNA mixtures in forensic evidence material using pyrosequencing.
    Andréasson H; Nilsson M; Budowle B; Frisk S; Allen M
    Int J Legal Med; 2006 Nov; 120(6):383-90. PubMed ID: 16453148
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Problems in Mitochondrial DNA forensics: while interpreting length heteroplasmy conundrum of various Sindhi and Baluchi ethnic groups of Pakistan.
    Bhatti S; Aslam Khan M; Abbas S; Attimonelli M; Gonzalez GR; Aydin HH; de Souza EMS
    Mitochondrial DNA A DNA Mapp Seq Anal; 2018 May; 29(4):501-510. PubMed ID: 28391756
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Assessment of mitochondrial DNA heteroplasmy detected on commercial panel using MPS system with artificial mixture samples.
    Cho S; Kim MY; Lee JH; Lee SD
    Int J Legal Med; 2018 Jul; 132(4):1049-1056. PubMed ID: 29279961
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Reducing the Number of Mismatches between Hairs and Buccal References When Analysing mtDNA Heteroplasmic Variation by Massively Parallel Sequencing.
    Gaag KJV; Desmyter S; Smit S; Prieto L; Sijen T
    Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33207560
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Quantitative analysis of human DNA sequences by PCR and solid-phase minisequencing.
    Suomalainen A; Syvänen AC
    Mol Biotechnol; 2000 Jun; 15(2):123-31. PubMed ID: 10949825
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A single multiplex PCR and SNaPshot minisequencing reaction of 42 SNPs to classify admixture populations into mitochondrial DNA haplogroups.
    Paneto GG; Köhnemann S; Martins JA; Cicarelli RM; Pfeiffer H
    Mitochondrion; 2011 Mar; 11(2):296-302. PubMed ID: 21172459
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial DNA heteroplasmy in the emerging field of massively parallel sequencing.
    Just RS; Irwin JA; Parson W
    Forensic Sci Int Genet; 2015 Sep; 18():131-9. PubMed ID: 26009256
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing.
    Juvonen V; Huoponen K; Syvänen AC; Nikoskelainen E; Savontaus ML
    Hum Genet; 1994 Jan; 93(1):16-20. PubMed ID: 8270249
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pyrosequencing-based strategy for a successful SNP detection in two hypervariable regions: HV-I/HV-II of the human mitochondrial displacement loop.
    Anjum GM; Du W; Klein R; Amara U; Huber-Lang M; Schneider EM; Wiegand P
    Electrophoresis; 2010 Jan; 31(2):309-14. PubMed ID: 20084631
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.