BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

273 related articles for article (PubMed ID: 32111191)

  • 1. Molecular epidemiology and hematologic characterization of δβ-thalassemia and hereditary persistence of fetal hemoglobin in 125,661 families of greater Guangzhou area, the metropolis of southern China.
    Jiang F; Zuo L; Li D; Li J; Tang X; Chen G; Zhou J; Lu H; Liao C
    BMC Med Genet; 2020 Feb; 21(1):43. PubMed ID: 32111191
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The prevalence and molecular characterization of (δβ)
    He S; Wei Y; Lin L; Chen Q; Yi S; Zuo Y; Wei H; Zheng C; Chen B; Qiu X
    J Clin Lab Anal; 2018 Mar; 32(3):. PubMed ID: 28763119
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic research and clinical analysis of β-globin gene cluster deletions in the Chinese population of Fujian province: A 14-year single-center experience.
    Chen M; Zhang M; Chen L; Lin N; Wang Y; Xu L; Huang H
    J Clin Lab Anal; 2022 Feb; 36(2):e24181. PubMed ID: 34951062
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotypic-phenotypic heterogeneity of δβ-thalassemia and hereditary persistence of fetal hemoglobin (HPFH) in India.
    Hariharan P; Kishnani P; Sawant P; Gorivale M; Mehta P; Kargutkar N; Colah R; Nadkarni A
    Ann Hematol; 2020 Jul; 99(7):1475-1483. PubMed ID: 32524201
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Screening for common β-globin gene cluster deletions in Chinese individuals with increased hemoglobin F.
    Cai WJ; Li J; Xie XM; Li DZ
    Int J Lab Hematol; 2015 Dec; 37(6):752-7. PubMed ID: 26179971
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Molecular Epidemiological Characteristics and Differential Diagnosis of Common δβ-Thalassemia/HPFH].
    Ju AP; Li N; Lin K; Huang HH; Liu SX; Jiang F
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2022 Aug; 30(4):1182-1187. PubMed ID: 35981381
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic research and clinical analysis of deletional Chinese
    Wu Y; Yao Q; Zhong M; Wu J; Xie L; Su L; Yu F
    Ann Hematol; 2020 Dec; 99(12):2747-2753. PubMed ID: 32930850
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Contrasting co-inheritance of alpha and beta mutations in delta beta thalassemia and hereditary persistence of fetal hemoglobin: a study from India.
    Pandey H; Ranjan R; Singh K; Sharma A; Kishor K; Seth T; Saxena R
    Hematology; 2018 Oct; 23(9):692-696. PubMed ID: 29621931
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.
    Fornari TA; Lanaro C; Albuquerque DM; Ferreira R; Costa FF
    Exp Biol Med (Maywood); 2017 Feb; 242(3):267-274. PubMed ID: 27591578
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection and characterisation of beta-globin gene cluster deletions in Chinese using multiplex ligation-dependent probe amplification.
    So CC; So AC; Chan AY; Tsang ST; Ma ES; Chan LC
    J Clin Pathol; 2009 Dec; 62(12):1107-11. PubMed ID: 19946097
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical variability and molecular characterization of Hbs/Gγ (Aγδβ)0-thal and Hbs/HPFH in Indian sickle cell disease patients: AIIMS experience.
    Pandey H; Singh K; Ranjan R; Pandey SK; Sharma A; Kishor K; Seth T; Mahapatra M; Saxena R
    Hematology; 2019 Dec; 24(1):349-352. PubMed ID: 30777489
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of deletional hereditary persistence of fetal hemoglobin/δβ-thalassemia and δ-globin gene mutations in Southerwestern China.
    Zhang J; Yang Y; Li P; Yan Y; Lv T; Zhao T; Zeng X; Li D; Zhou X; Chen H; Su J; Yang T; He J; Zhu B
    Mol Genet Genomic Med; 2019 Jun; 7(6):e706. PubMed ID: 31044540
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of HPFH and δβ-thalassemia mutations in a Brazilian group with high Hb F levels.
    Carrocini GC; Ondei LS; Zamaro PJ; Bonini-Domingos CR
    Genet Mol Res; 2011 Dec; 10(4):3213-9. PubMed ID: 22194178
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening of Iranian thalassemic families for the most common deletions of the beta-globin gene cluster.
    Esteghamat F; Imanian H; Azarkeivan A; Pourfarzad F; Almadani N; Najmabadi H
    Hemoglobin; 2007; 31(4):463-9. PubMed ID: 17994380
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.
    Prakobkaew N; Fucharoen S; Fuchareon G; Siriratmanawong N
    Eur J Haematol; 2014 Jan; 92(1):73-9. PubMed ID: 24112054
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular characterization of a novel homozygous deletion in β-globin cluster causing (δβ)
    Kalai M; Moumni I; Ouragini H; Ben Fraj I; Mellouli F; Ouederni M; Chaouachi D; Boudriga I; Menif S
    Ann Clin Biochem; 2023 Mar; 60(2):81-85. PubMed ID: 36214153
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.
    Panyasai S; Fucharoen S; Surapot S; Fucharoen G; Sanchaisuriya K
    Haematologica; 2004 Jul; 89(7):777-81. PubMed ID: 15257928
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Application of multiplex ligation-dependent probe amplification to screen for β-globin cluster deletions: detection of two novel deletions in a multi ethnic population.
    Cui J; Azimi M; Baysdorfer C; Vichinsky EP; Hoppe CC
    Hemoglobin; 2013; 37(3):241-56. PubMed ID: 23577918
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation.
    Singha K; Tepakhan W; Yamsri S; Chaibunruang A; Srivorakun H; Pansuwan A; Fucharoen G; Fucharoen S
    Clin Chim Acta; 2023 Nov; 551():117615. PubMed ID: 37884119
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A single-tube multiplex gap-polymerase chain reaction for the detection of eight β-globin gene cluster deletions common in Southeast Asia.
    Tritipsombut J; Phylipsen M; Viprakasit V; Chalaow N; Sanchaisuriya K; Giordano PC; Fucharoen S; Harteveld CL
    Hemoglobin; 2012; 36(6):571-80. PubMed ID: 23181748
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.