BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 36574763)

  • 1. Noninvasive Prenatal Diagnosis of Beta-Thalassemia Disease by Using Digital PCR Analysis of Cell-Free Fetal DNA in Maternal Plasma.
    Charoenkwan P; Traisrisilp K; Sirichotiyakul S; Phusua A; Sanguansermsri T; Tongsong T
    Fetal Diagn Ther; 2022; 49(11-12):468-478. PubMed ID: 36574763
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Noninvasive prenatal testing of beta-thalassemia for common Pakistani mutations: a comparative study using cell-free fetal DNA from maternal plasma and chorionic villus sampling.
    Afzal M; Naeem MA; Ahmed S; Amin N; Rahim A; Munawar M; Ishaq M; Rathore A; Maria K
    Hematology; 2022 Dec; 27(1):353-359. PubMed ID: 35287566
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: an accuracy assessment.
    Ramezanzadeh M; Salehi M; Farajzadegan Z; Kamali S; Salehi R
    J Matern Fetal Neonatal Med; 2016; 29(16):2645-9. PubMed ID: 26553322
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diagnostic Value of Non-Invasive Prenatal Screening of β-thalassemia by Cell Free Fetal DNA and Fetal NRBC.
    Shafei N; Hakhamaneshi MS; Houshmand M; Gerayeshnejad S; Fathi F; Sharifzadeh S
    Curr Mol Med; 2019; 19(2):105-111. PubMed ID: 30813874
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Noninvasive prenatal diagnosis experience in the Çukurova Region of Southern Turkey: detecting paternal mutations of sickle cell anemia and β-thalassemia in cell-free fetal DNA using high-resolution melting analysis.
    Yenilmez ED; Tuli A; Evrüke IC
    Prenat Diagn; 2013 Nov; 33(11):1054-62. PubMed ID: 23836351
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Non-invasive prenatal testing for fetal inheritance of maternal β-thalassaemia mutations using targeted sequencing and relative mutation dosage: a feasibility study.
    Xiong L; Barrett AN; Hua R; Ho S; Jun L; Chan K; Mei Z; Choolani M
    BJOG; 2018 Mar; 125(4):461-468. PubMed ID: 29211324
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Non-invasive prenatal screening & diagnosis of β-thalassaemia in an affected foetus.
    Suwannakhon N; Hemvuthiphan J; Pangeson T; Mahingsa K; Pingyod A; Bumrungpakdee W; Sanguansermsri T
    Indian J Med Res; 2023 May; 157(5):447-452. PubMed ID: 37322635
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Non-invasive prenatal diagnosis using fetal DNA in maternal plasma: a preliminary study for identification of paternally-inherited alleles using single nucleotide polymorphisms.
    Chen JJ; Tan JA; Chua KH; Tan PC; George E
    BMJ Open; 2015 Jul; 5(7):e007648. PubMed ID: 26201722
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma.
    Li Y; Di Naro E; Vitucci A; Zimmermann B; Holzgreve W; Hahn S
    JAMA; 2005 Feb; 293(7):843-9. PubMed ID: 15713774
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Prenatal gene diagnosis of paternally inherited alpha-thalassemia by detecting fetal DNA in maternal plasma].
    Chen P; Li MJ; Li MQ; Li SQ; Zhou LY; Lin WX
    Zhonghua Yi Xue Za Zhi; 2007 Jun; 87(22):1540-4. PubMed ID: 17785106
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fast Temperature-Gradient COLD PCR for the enrichment of the paternally inherited SNPs in cell free fetal DNA; an application to non-invasive prenatal diagnosis of β-thalassaemia.
    Byrou S; Makrigiorgos GM; Christofides A; Kallikas I; Papasavva T; Kleanthous M
    PLoS One; 2018; 13(7):e0200348. PubMed ID: 30044883
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Non-invasive prenatal diagnosis for beta-thalassemia by detecting paternal CD41-42 mutation in cell-free DNA derived from maternal plasma with droplet digital PCR].
    Zhang Y; Gong X; He Y; Huang L; Zhang Q; Liu Y; Li J; Chen Y; Zhou W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):787-790. PubMed ID: 30512146
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Optimized Droplet Digital PCR Assay on Cell-Free DNA Samples for Non-Invasive Prenatal Diagnosis: Application to Beta-Thalassemia.
    Constantinou CG; Karitzi E; Byrou S; Stephanou C; Michailidou K; Makariou C; Hadjilambi G; Christofides A; Kleanthous M; Papasavva T
    Clin Chem; 2022 Jul; 68(8):1053-1063. PubMed ID: 35652459
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Droplet Digital PCR for Non-Invasive Prenatal Detection of Fetal Single-Gene Point Mutations in Maternal Plasma.
    D'Aversa E; Breveglieri G; Boutou E; Balassopoulou A; Voskaridou E; Pellegatti P; Guerra G; Scapoli C; Gambari R; Borgatti M
    Int J Mol Sci; 2022 Mar; 23(5):. PubMed ID: 35269962
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detection of Paternal IVS-II-1 (G>A) (
    Mortazavipour MM; Shahbazi S; Mahdian R
    Hemoglobin; 2020 May; 44(3):168-173. PubMed ID: 32703054
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma.
    Lun FM; Tsui NB; Chan KC; Leung TY; Lau TK; Charoenkwan P; Chow KC; Lo WY; Wanapirak C; Sanguansermsri T; Cantor CR; Chiu RW; Lo YM
    Proc Natl Acad Sci U S A; 2008 Dec; 105(50):19920-5. PubMed ID: 19060211
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Prenatal diagnosis of β-thalassaemia using cell-free fetal DNA in maternal plasma].
    Li GH; Rong KB; Luo YF; Chen D; Gong CP; Wu J; DI YW; Ge YF
    Nan Fang Yi Ke Da Xue Xue Bao; 2011 Aug; 31(8):1437-9. PubMed ID: 21868341
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evaluation of beta-thalassemia in the fetus through cffDNA with multiple polymorphisms as a haplotype in the beta-globin gene.
    Mirzaei Gisomi N; Javadi G; Zare Karizi S; Miryounesi M; Keshavarz P
    Transfus Clin Biol; 2020 Nov; 27(4):243-252. PubMed ID: 32798758
    [TBL] [Abstract][Full Text] [Related]  

  • 20. COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.
    Galbiati S; Monguzzi A; Damin F; Soriani N; Passiu M; Castellani C; Natacci F; Curcio C; Seia M; Lalatta F; Chiari M; Ferrari M; Cremonesi L
    J Med Genet; 2016 Jul; 53(7):481-7. PubMed ID: 26912453
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.