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 *

313 related articles for article (PubMed ID: 18343225)

  • 1. Molecular basis of deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia in Indian patients.
    Bhattacharya G; Banerjee D; Chandra S; Ghosh M; Chaudhuri U; Das M; Dasgupta UB
    Clin Chim Acta; 2008 Jun; 392(1-2):69-70. PubMed ID: 18343225
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia.
    Kalamaras A; Chassanidis C; Samara M; Papadakis MN; Vagena A; Aleporou-Marinou V; Patrinos GP; Kollia P
    Am J Hematol; 2008 Sep; 83(9):760. PubMed ID: 18615450
    [No Abstract]   [Full Text] [Related]  

  • 4. Compound heterozygote state for GgammaAgamma(deltabeta) degrees -thalassemia and hereditary persistence of fetal hemoglobin.
    Fucharoen S; Panyasai S; Surapot S; Fucharoen G; Sanchaisuriya K
    Am J Hematol; 2005 Oct; 80(2):119-23. PubMed ID: 16184575
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. High frequency of deletional alpha-thalassemia in beta-thalassemia trait: implications for genetic counseling.
    Panigrahi I; Rafeeq PH; Choudhry VP; Saxena R
    Am J Hematol; 2004 Jul; 76(3):297-9. PubMed ID: 15224373
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Compound heterozygosity for the Cretan type of non-deletional hereditary persistence of fetal hemoglobin and beta-thalassemia or Hb Sabine confirms the functional role of the Agamma -158 C>T mutation in gamma-globin gene transcription.
    Kollia P; Kalamaras A; Chassanidis C; Samara M; Vamvakopoulos NK; Radmilovic M; Pavlovic S; Papadakis MN; Patrinos GP
    Blood Cells Mol Dis; 2008; 41(3):263-4. PubMed ID: 18718799
    [No Abstract]   [Full Text] [Related]  

  • 8. Somatic deletion of the normal beta-globin gene leading to thalassaemia intermedia in heterozygous beta-thalassaemic patients.
    Galanello R; Perseu L; Perra C; Maccioni L; Barella S; Longinotti M; Cao A; Cazzola M
    Br J Haematol; 2004 Dec; 127(5):604-6. PubMed ID: 15566365
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Ggamma(Agammadeltabeta)0-thalassemia and Ggamma(Agammadeltabeta)0-thalassemia/HbE in Thai patients.
    Fucharoen S; Pengjam Y; Surapot S; Fucharoen G; Sanchaisuriya K
    Am J Hematol; 2002 Oct; 71(2):109-13. PubMed ID: 12353310
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.
    Feriotto G; Salvatori F; Finotti A; Breveglieri G; Venturi M; Zuccato C; Bianchi N; Borgatti M; Lampronti I; Mancini I; Massei F; Favre C; Gambari R
    Acta Haematol; 2008; 119(1):28-37. PubMed ID: 18230963
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular characterization of deletional forms of beta-thalassemia in Taiwan.
    Peng CT; Liu SC; Chiou SS; Kuo PL; Shih MC; Chang JY; Chang JG
    Ann Hematol; 2003 Jan; 82(1):33-6. PubMed ID: 12574962
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Lack of association of G779A ZHX-2 gene variant with HbF levels in β-thalassemia major.
    Munshi A; Dadheech S; Jain S; Joseph J; Al-Hazzani A; Alshatwi AA; Sai Babu M; Rajeshwar K; Jyothy A
    Eur J Haematol; 2011 Jun; 86(6):502-6. PubMed ID: 21443521
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. XmnI Ggamma-polymorphism in six unrelated Pakistani families with Inv/Del Ggamma(Agammadeltabeta) degrees deltabeta-thalassemia.
    Ahmed S; Anwar M
    Am J Hematol; 2005 Dec; 80(4):303-5. PubMed ID: 16315258
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Hereditary persistence of foetal haemoglobin in northwest India.
    Ghosh K; Hasan SW; Kumar S
    Trop Geogr Med; 1988 Jul; 40(3):209-12. PubMed ID: 2460980
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 16.