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 *

102 related articles for article (PubMed ID: 15813858)

  • 1. Co-inheritance of the Hb Sun Prairie mutation with a point mutation at 5'-UTR in the eastern Indian population.
    Sarkar AA; Mukhopadhyay C; Chandra S; Banerjee S; Das MK; Dasgupta UB
    Br J Haematol; 2005 Apr; 129(2):282-6. PubMed ID: 15813858
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Polymerase chain reaction-based search for two alpha-globin gene mutations in India.
    Bhattacharya G; Sarkar AA; Banerjee D; Chandra S; Das M; Dasgupta UB
    Hemoglobin; 2008; 32(5):485-90. PubMed ID: 18932074
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala --> Pro and Hb Caserta alpha2 26 Ala --> Thr) in a single HBA2 gene.
    Passarello C; Giambona A; Prossomariti L; Ammirabile M; Pucci P; Renda D; Pagano L; Maggio A
    Br J Haematol; 2008 Oct; 143(1):138-42. PubMed ID: 18691171
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hb Southern Italy: coexistence of two missence mutations (the Hb Sun Prairie alpha2 130 Ala > Pro and Hb Caserta alpha2 26 Ala > Thr) in a single HBA2 gene.
    Lacerra G; Carestia C
    Br J Haematol; 2009 Jun; 145(6):843-4. PubMed ID: 19344421
    [No Abstract]   [Full Text] [Related]  

  • 5. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
    Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
    Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two new alpha-thalassemia point mutations that are undetectable by biochemical techniques.
    Joly P; Pégourie B; Courby S; Barro C; Besson G; Cohen L; Garcia C; Francina A
    Hemoglobin; 2008; 32(4):411-7. PubMed ID: 18654892
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hb Sallanches [alpha104(G11)Cys-->Tyr, TGC>TAC] occurs frequently on the Indian subcontinent.
    Roy P; Bhattacharya G; Banerjee D; Chandra S; Ghosh M; Choudhuri U; Das M; Dasgupta UB
    Hemoglobin; 2009; 33(6):486-91. PubMed ID: 19958194
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hb Hekinan in a Taiwanese subject: a G-->T substitution at codon 27 of the alpha1-globin gene abolishes an HaeIII site.
    Shih HC; Shih MC; Chang YC; Peng CT; Chang TJ; Chang JG
    Hemoglobin; 2007; 31(4):495-8. PubMed ID: 17994385
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
    Martin G; Villegas A; González FA; Ropero P; Hojas R; Polo M; Mateo M; Salvador M; Benavente C
    Hemoglobin; 2005; 29(2):113-7. PubMed ID: 15921163
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Two new hemoglobin variants: Hb Brem-sur-Mer [beta9(A6)Ser-->Tyr] and Hb Passy [alpha81(F2)Ser-->Pro (alpha2)].
    Lacan P; Moreau M; Becchi M; Zanella-Cleon I; Aubry M; Louis JJ; Couprie N; Francina A
    Hemoglobin; 2005; 29(1):69-75. PubMed ID: 15768558
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further identification of the hyperunstable alpha-globin chain variant Hb Heraklion [codons 36/37 (-CCC); Pro-->0 (alpha1)] in Greek cases with co-inherited alpha+-thalassemia mutations.
    Douna V; Papassotiriou I; Metaxotou-Mavrommati A; Stamoulakatou A; Liapi D; Kampourakis D; Tsilimigaki A; Kanavakis E; Traeger-Synodinos J
    Hemoglobin; 2008; 32(4):379-85. PubMed ID: 18654888
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Thalassemias and other hemoglobinopathies in the Republic of Macedonia.
    Efremov GD
    Hemoglobin; 2007; 31(1):1-15. PubMed ID: 17365000
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hb Showa-Yakushiji [beta110(G12)Leu-->Pro] in four unrelated patients from west Bengal.
    Edison ES; Shaji RV; Devi SG; Kumar SS; Srivastava A; Chandy M
    Hemoglobin; 2005; 29(1):19-25. PubMed ID: 15768552
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. First observation of Hb Taybe [Codons 38/39 (-Acc) Thr-->0 (alpha1)] in Greece: clinical and hematological findings in patients with co-inherited alpha+-thalassemia mutations.
    Douna V; Liapi D; Kampourakis D; Repapinou Z; Papassotiriou I; Stamoulakatou A; Poziopoulos C; Kanavakis E; Traeger-Synodinos J
    Hemoglobin; 2008; 32(4):371-8. PubMed ID: 18654887
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype.
    Harteveld CL; van Helden WC; Boxma GL; van Delft P; Bakker-Verweij M; Wajcman H; Zanella-Cleon I; Becchi M; Giordano PC
    Hemoglobin; 2007; 31(3):325-32. PubMed ID: 17654069
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies.
    Ho PJ; Rochette J; Rees DC; Fisher CA; Huehns ER; Will AM; Thein SL
    Hemoglobin; 1996 May; 20(2):103-12. PubMed ID: 8811313
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype.
    Harteveld CL; Steen G; Vlasveld LT; van Delft P; Giordano PC
    Haematologica; 2006 Apr; 91(4):570-1. PubMed ID: 16533721
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.