BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

250 related articles for article (PubMed ID: 21797708)

  • 1. A new α1-globin mutation, Hb Brugg [α20(B1)His→Gln].
    Rizzi M; Zurbriggen K; Schmid M; Goede JS; Nardi MA; Schmugge M; Speer O
    Hemoglobin; 2011; 35(4):417-22. PubMed ID: 21797708
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A new alpha-globin variant with increased oxygen affinity in a Swiss family: Hb Frauenfeld [alpha 138(H21)Ser-->Phe, TCC>TTC (alpha 2)].
    Hochuli M; Zurbriggen K; Schmid M; Speer O; Rochat P; Frauchiger B; Kleinert P; Schmugge M; Troxler H
    Hemoglobin; 2009; 33(1):54-8. PubMed ID: 19205974
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hb Nile[A1] and Hb Nile[A2]: novel identical [alpha77(EF6)Pro-->Ser] variants found in either the alpha1- or alpha2-globin genes.
    van Zwieten R; Kaufmann JO; Vuil H; Kouwenberg J; Verhoeven AJ; Fogelberg K; Harteveld CL; Giordano PC
    Hemoglobin; 2009; 33(3):188-95. PubMed ID: 19657832
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hb Gerland [alpha 55(E4)Val-->Ala]: a mutation found on the alpha1-globin gene.
    Moradkhani K; Riou J; Francina A; Wajcman H; Prehu C
    Hemoglobin; 2008; 32(5):478-84. PubMed ID: 18932073
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hb Bakersfield (HBA1: c.151_152insGGAGCC): The Insertion of Arg-His Between Codons 49 and 50 of the α1-Globin Chain Leads to Increased Oxygen Affinity.
    Brunner-Agten S; von Känel T; Röthlisberger B; Broquet C; Huber AR
    Hemoglobin; 2017 Jan; 41(1):1-5. PubMed ID: 28532286
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hb G-Waimanalo [A1] [α64(E13)Asp→Asn; HBA1: c.193 G > A] with Decreased Oxygen Affinity.
    Karow A; Eekels JJ; Zurbriggen K; Schmid M; Schmugge M; Speer O
    Hemoglobin; 2015; 39(6):432-4. PubMed ID: 26291968
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hb Alperton [beta135(H13)Ala-->Val] shows decreased oxygen affinity.
    Zurbriggen K; Schmid M; Schmugge M; Troxler H; Speer O
    Hemoglobin; 2009; 33(6):498-502. PubMed ID: 19958196
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype.
    Joly P; Szymanowicz A; Neyron MJ; Zine A; Wajcman H; Francina A
    Hemoglobin; 2010; 34(4):366-73. PubMed ID: 20642334
    [TBL] [Abstract][Full Text] [Related]  

  • 9. HB Hillingdon [alpha46(CE4)Phe-->Val (alpha1 Or alpha2)]: a new alpha chain hemoglobin variant.
    Babb A; Solaiman S; Green BN; Mantio D; Patel K
    Hemoglobin; 2009; 33(6):503-6. PubMed ID: 19958197
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hb St. Truiden [α68(E17)Asn→His] and Hb Westeinde [α125(H8)Leu→Gln]: two new abnormalities of the α2-globin gene.
    Kaufmann JO; Phylipsen M; Neven C; Huisman W; van Delft P; Bakker-Verweij M; Arkesteijn SG; Harteveld CL; Giordano PC
    Hemoglobin; 2010; 34(5):439-44. PubMed ID: 20854117
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel base change leading to Hb Vanderbilt [β89(F5)Ser→Arg, AGT>AGA].
    Goodyer MJ; Elhassadi EI; Percy MJ; McMullin MF
    Hemoglobin; 2011; 35(4):428-9. PubMed ID: 21797710
    [TBL] [Abstract][Full Text] [Related]  

  • 12. First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child.
    Paglietti ME; Sollaino MC; Loi D; Barella S; Desogus MF; Galanello R
    Hemoglobin; 2012; 36(3):299-304. PubMed ID: 22428534
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hb Hubei [α114(GH2)Pro→His, HBA1: c.344C>A]: A Novel Hemoglobin Variant of the α1-Globin Chain.
    Xu AP; Li J; Chen WD; Zhou Y; Ji L
    Hemoglobin; 2018 May; 42(3):206-208. PubMed ID: 30277418
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Further studies on Hb Canebière [β12(G4)Asn→His], a low affinity hemoglobin variant.
    Froelund U; Sandbakken E; Szecsi P; Birgens H
    Hemoglobin; 2010; 34(5):495-9. PubMed ID: 20854124
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.
    Azma RZ; Othman A; Azman N; Alauddin H; Ithnin A; Yusof N; Razak NF; Sardi NH; Hussin NH
    Malays J Pathol; 2012 Jun; 34(1):57-62. PubMed ID: 22870600
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy.
    Sanchaisuriya K; Chunpanich S; Fucharoen S; Fucharoen G; Sanchaisuriya P; Changtrakun Y
    Eur J Haematol; 2005 Mar; 74(3):221-7. PubMed ID: 15693792
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocket.
    Giambona A; Vinciguerra M; Cassarà F; Li Muli R; Leto F; Passarello C; Wajcman H; Maggio A
    Hemoglobin; 2006; 30(2):139-48. PubMed ID: 16798637
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hb Geldrop St. Anna [beta94(FG1)Asp --> Tyr]: a new hemoglobin variant observed in a diabetic patient.
    Harteveld CL; Thelen MH; Rutten JJ; Leuverman J; Akkermans N; van Delft P; Arkesteijn S; Giordano PC
    Hemoglobin; 2005; 29(2):107-12. PubMed ID: 15921162
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia.
    Srivorakun H; Fucharoen G; Puangplruk R; Kheawon N; Fucharoen S
    Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular and hematological characteristics of a novel form of α-globin gene triplication: the hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2.
    Singha K; Fucharoen G; Jetsrisuparb A; Fucharoen S
    Clin Biochem; 2013 May; 46(7-8):675-80. PubMed ID: 23395770
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.