BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

150 related articles for article (PubMed ID: 8195011)

  • 1. Alpha 2-globin gene mutation Hb G-Waimanalo: occurrence in combination with alpha-thalassemia-1.
    Landin B; Berg P
    Hemoglobin; 1994 Jan; 18(1):71-2. PubMed ID: 8195011
    [No Abstract]   [Full Text] [Related]  

  • 2. A new highly unstable alpha chain variant causing alpha(+)-thalassemia: Hb Zurich Albisrieden [alpha59(E8)Gly-->Arg (alpha2)].
    Dutly F; Fehr J; Goede JS; Morf M; Troxler H; Frischknecht H
    Hemoglobin; 2004; 28(4):347-51. PubMed ID: 15658192
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Hb Questembert is due to a base substitution (T-->C) in codon 131 of the alpha 2-globin gene and has an alpha-thalassemia biosynthetic ratio.
    Rochette J; Barnetson R; Thein SL; Varet B; Valensi F
    Am J Hematol; 1995 Apr; 48(4):289-90. PubMed ID: 7717382
    [No Abstract]   [Full Text] [Related]  

  • 5. The alpha / beta and alpha 2 / alpha 1-globin mRNA ratios in different forms of alpha-thalassemia.
    Smetanina NS; Leonova JY; Levy N; Huisman TH
    Biochim Biophys Acta; 1996 Apr; 1315(3):188-92. PubMed ID: 8611658
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotes.
    Molchanova TP; Pobedimskaya DD; Huisman TH
    Br J Haematol; 1994 Oct; 88(2):300-6. PubMed ID: 7803274
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Hb Prato [alpha31(B12)Arg --> Ser (A2)] and alpha-thalassemia in a Taiwanese.
    Shih MC; Peng CT; Chang JY; Liu SC; Kuo PL; Chang JG
    Hemoglobin; 2003 Feb; 27(1):45-7. PubMed ID: 12603094
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Rapid detection of chain termination mutations in the alpha 2 globin gene.
    Makonkawkeyoon L; Sanguansermsri T; Asato T; Nakashima Y; Takei H
    Blood; 1993 Dec; 82(11):3503-4. PubMed ID: 8241518
    [No Abstract]   [Full Text] [Related]  

  • 12. Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients.
    Cürük MA; Dimovski AJ; Baysal E; Gu LH; Kutlar F; Molchanova TP; Webber BB; Altay C; Gürgey A; Huisman TH
    Am J Hematol; 1993 Dec; 44(4):270-5. PubMed ID: 8237999
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hb Utrecht [alpha 2 129(H12)Leu-->Pro], a new unstable alpha 2-chain variant associated with a mild alpha-thalassaemic phenotype.
    Harteveld CL; Giordano PC; Losekoot M; Heister JG; Batelaan D; van Delft P; Bruin MC; Bernini LF
    Br J Haematol; 1996 Sep; 94(3):483-5. PubMed ID: 8790146
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haemoglobin Tunis-Bizerte: a new alpha 1 globin 129 Leu-->Pro unstable variant with thalassaemic phenotype.
    Darbellay R; Mach-Pascual S; Rose K; Graf J; Beris P
    Br J Haematol; 1995 May; 90(1):71-6. PubMed ID: 7786798
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant.
    Traeger-Synodinos J; Metaxotou-Mavromati A; Kanavakis E; Vrettou C; Papassotiriou I; Michael T; Kattamis C
    Hemoglobin; 1998 May; 22(3):209-15. PubMed ID: 9629496
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hb Douala [alpha3(A1)Ser --> Phe]: a new alpha1 gene mutation in a Cameroonian woman heterozygous for Hb S and a 3.7 kb deletional alpha-thalassemia.
    Préhu C; Hanichi A; Yapo AP; Claparols C; Promé D; Riou J; Wajcman H
    Hemoglobin; 2001 Aug; 25(3):323-9. PubMed ID: 11570726
    [No Abstract]   [Full Text] [Related]  

  • 17. Hb H disease in association with the silent beta chain variant Hb Hamilton or alpha 2 beta 2(11)(A8)Val----Ile.
    Su CW; Liang S; Liang R; Wen XJ; Tang CN
    Hemoglobin; 1992; 16(5):403-8. PubMed ID: 1428944
    [No Abstract]   [Full Text] [Related]  

  • 18. Molecular spectrum of alpha-thalassemia in the Iranian population of Hormozgan: three novel point mutation defects.
    Harteveld CL; Yavarian M; Zorai A; Quakkelaar ED; van Delft P; Giordano PC
    Am J Hematol; 2003 Oct; 74(2):99-103. PubMed ID: 14508795
    [TBL] [Abstract][Full Text] [Related]  

  • 19. First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population.
    Canatan D; Bilgen T; Çiftçi V; Yazıcı G; Delibaş S; Keser İ
    Turk J Haematol; 2016 Mar; 33(1):71-2. PubMed ID: 27020723
    [No Abstract]   [Full Text] [Related]  

  • 20. Hb G-Waimanalo: occurrence in combination with alpha-thalassemia-1 Southeast Asian deletion.
    Lin M; Wu JR; Yang LY; Chen H; Wang PP; Wang Q; Zheng L
    Blood Cells Mol Dis; 2009; 42(1):36-7. PubMed ID: 19010698
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.