BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

886 related articles for article (PubMed ID: 12185510)

  • 21. Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects.
    Chaibunruang A; Fucharoen G; Jetsrisuparb A; Fucharoen S
    Ann Hematol; 2011 Nov; 90(11):1337-40. PubMed ID: 21302111
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Interactions of hemoglobin Lepore (deltabeta hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis.
    Chaibunruang A; Srivorakun H; Fucharoen S; Fucharoen G; Sae-ung N; Sanchaisuriya K
    Blood Cells Mol Dis; 2010 Mar; 44(3):140-5. PubMed ID: 20022270
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Compound heterozygous Hb Tak/Hb E causes secondary erythrocytosis in a Thai family.
    Teawtrakul N; Sirijirachai C; Chansung G; Fucharoen G
    Hemoglobin; 2010 Jan; 34(2):165-8. PubMed ID: 20353353
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular and hematological characterization of Hb Tak and Hb Pyrgos in Thailand.
    Fucharoen S; Fucharoen G; Sae-ung N; Sanchaisuriya K; Fukumaki Y
    Southeast Asian J Trop Med Public Health; 1997; 28 Suppl 3():110-4. PubMed ID: 9640611
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α(0)-thalassemia: molecular and hematological features and differential diagnosis.
    Singha K; Srivorakun H; Fucharoen G; Changtrakul Y; Komwilaisak P; Jetsrisuparb A; Puangplruk R; Fucharoen S
    Hemoglobin; 2013; 37(1):37-47. PubMed ID: 23215800
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical phenotypes and molecular characterization of Hb H-Paksé disease.
    Viprakasit V; Tanphaichitr VS; Pung-Amritt P; Petrarat S; Suwantol L; Fisher C; Higgs DR
    Haematologica; 2002 Feb; 87(2):117-25. PubMed ID: 11836160
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular Characterization and Hematological Aspects of Hb E-Myanmar [β26(B8)Glu→Lys and β65(E9)Lys→Asn,
    Satthakarn S; Boonmee S; Panyasai S
    Hemoglobin; 2020 Nov; 44(6):385-390. PubMed ID: 33222574
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Interaction of hemoglobin E and several forms of alpha-thalassemia in Cambodian families.
    Fucharoen S; Sanchaisuriya K; Fucharoen G; Panyasai S; Devenish R; Luy L
    Haematologica; 2003 Oct; 88(10):1092-8. PubMed ID: 14555303
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The first compound heterozygosity for HKalpha alpha allele and Southeast Asian deletion allele.
    Li Z; Cai S; Rong K; Song G; Li Y; Guo R
    Clin Biochem; 2007 Mar; 40(5-6):407-10. PubMed ID: 17306786
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The prevalence and molecular basis of hemoglobinopathies in Cambodia.
    Carnley BP; Prior JF; Gilbert A; Lim E; Devenish R; Sing H; Sarin E; Guhadasan R; Sullivan SG; Wise CA; Bittles AH; Chan K; Wong MS; Chan V; Erber WN
    Hemoglobin; 2006; 30(4):463-70. PubMed ID: 16987801
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H; Fucharoen G; Sae-Ung N; Sanchaisuriya K; Ratanasiri T; Fucharoen S
    Eur J Haematol; 2009 Jul; 83(1):57-65. PubMed ID: 19226360
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Further identification of Hb G-Coushatta [beta22(B4)Glu-->Ala (GAA-->GCA)] in Thailand by the polymerase chain reaction-single-strand conformation polymorphism technique and by amplification refractory mutation system-polymerase chain reaction.
    Chinchang W; Viprakasit V
    Hemoglobin; 2007; 31(1):93-9. PubMed ID: 17365010
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular and clinical features of Hb H disease in northern Thailand.
    Charoenkwan P; Taweephon R; Sae-Tung R; Thanarattanakorn P; Sanguansermsri T
    Hemoglobin; 2005; 29(2):133-40. PubMed ID: 15921165
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method.
    Sura T; Trachoo O; Viprakasit V; Vathesatogkit P; Tunteeratum A; Busabaratana M; Wisedpanichkij R; Isarangkura P
    Ann Hematol; 2007 Sep; 86(9):659-63. PubMed ID: 17503046
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Molecular and hematological profiles of hemoglobin EE disease with different forms of alpha-thalassemia.
    Fucharoen G; Trithipsombat J; Sirithawee S; Yamsri S; Changtrakul Y; Sanchaisuriya K; Fucharoen S
    Ann Hematol; 2006 Jul; 85(7):450-4. PubMed ID: 16565831
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease.
    Sura T; Busabaratana M; Youngcharoen S; Wisedpanichkij R; Viprakasit V; Trachoo O
    Eur J Haematol; 2007 Sep; 79(3):251-4. PubMed ID: 17655700
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
    Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR
    Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The molecular basis of alpha-thalassemia in Thailand.
    Winichagoon P; Fucharoen S; Wasi P
    Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():7-13. PubMed ID: 1298997
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutational spectrum of delta-globin gene in the Portuguese population.
    Morgado A; Picanço I; Gomes S; Miranda A; Coucelo M; Seuanes F; Seixas MT; Romão L; Faustino P
    Eur J Haematol; 2007 Nov; 79(5):422-8. PubMed ID: 17916081
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Compound heterozygosity of Hb D(Iran) (beta(22) Glu-->Gln) and beta(0)-thalassemia (619 bp-deletion) in India.
    Agrawal MG; Bhanushali AA; Dedhia P; Jeswani KD; Dayanand S; Dasgupta A; Das BR
    Eur J Haematol; 2007 Sep; 79(3):248-50. PubMed ID: 17655708
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 45.