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 *

207 related articles for article (PubMed ID: 28763119)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Molecular characterization of delta beta-thalassemia and hereditary persistence of fetal hemoglobin in the Indian population.
    Nadkarni A; Wadia M; Gorakshakar A; Kiyama R; Colah RB; Mohanty D
    Hemoglobin; 2008; 32(5):425-33. PubMed ID: 18932066
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.
    Patel DK; Patel M; Mashon RS; Patel S; Dash PM; Das BS
    Hemoglobin; 2010; 34(6):604-9. PubMed ID: 21077771
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Misdiagnosis of β-Thalassemia Major Due to Chinese
    Zheng LH; Liang L; Bai JP; Liao HX; Li YQ
    Hemoglobin; 2024 Jan; 48(1):24-29. PubMed ID: 38240123
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.