BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 1983218)

  • 1. Hb Hekinan observed in three Chinese from Macau; identification of the GAG----GAT mutation in the alpha 1-globin gene.
    Zhao W; Wilson JB; Webber BB; Kutlar A; Tamagnini GP; Kuam B; Huisman TH
    Hemoglobin; 1990; 14(6):627-35. PubMed ID: 1983218
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family.
    Fucharoen S; Changtrakun Y; Ratanasiri T; Fucharoen G; Sanchaisuriya K
    Eur J Haematol; 2003 May; 70(5):304-9. PubMed ID: 12694166
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two cases of compound heterozygosity for Hb Hekinan [alpha27(B8)Glu-->Asp (alpha1)] and alpha-thalassemia in Thailand.
    Ngiwsara L; Srisomsap C; Winichagoon P; Fucharoen S; Svasti J
    Hemoglobin; 2004 May; 28(2):145-50. PubMed ID: 15182057
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hb Coimbra or alpha 2 beta (2)99(G1)Asp----Glu, a newly discovered highoxygen affinity variant.
    Tamagnini GP; Ribeiro ML; Valente V; Ramachandran M; Wilson JB; Baysal E; Gu LH; Huisman TH
    Hemoglobin; 1991; 15(6):487-96. PubMed ID: 1814856
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hb Karlskoga or alpha 2 beta (2)21(B3) Asp-->His: a new slow-moving variant found in Sweden.
    Landin B
    Hemoglobin; 1993 Jun; 17(3):201-8. PubMed ID: 8330972
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hb Catonsville (glutamic acid inserted between Pro-37(C2)alpha and Thr-38(C3)alpha). Nonallelic gene conversion in the globin system?
    Moo-Penn WF; Swan DC; Hine TK; Baine RM; Jue DL; Benson JM; Johnson MH; Virshup DM; Zinkham WH
    J Biol Chem; 1989 Dec; 264(36):21454-7. PubMed ID: 2574721
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Hb Trollhättan [beta 20(B2)Val-->Glu]--a new haemoglobin variant with increased oxygen affinity causing erythrocytosis.
    Landin B; Berglund S; Lindoff B
    Eur J Haematol; 1994 Jul; 53(1):21-5. PubMed ID: 7914875
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hb Costa Rica or alpha 2 beta 2 77(EF1)His --> Arg: the first example of a somatic cell mutation in a globin gene.
    Rodriguez Romero WE; Castillo M; Chaves MA; Saenz GF; Gu LH; Wilson JB; Baysal E; Smetanina NS; Leonova JY; Huisman TH
    Hum Genet; 1996 Jun; 97(6):829-33. PubMed ID: 8641705
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in Thailand.
    Chunpanich S; Ayukarn K; Sanchaisuriya K; Fucharoen G; Fucharoen S
    Clin Lab Haematol; 2004 Oct; 26(5):355-8. PubMed ID: 15485467
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Hb Kurosaki [alpha7(A5)Lys -->Glu (AAG --> GAG)]: an alpha2-globin gene mutation found in Thailand.
    Ngiwsara L; Srisomsap C; Winichagoon P; Fucharoen S; Sae-Ngow B; Svasti J
    Hemoglobin; 2005; 29(2):155-9. PubMed ID: 15921168
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemia.
    Wilson JB; Webber BB; Kutlar A; Reese AL; McKie VC; Lutcher CL; Felice AE; Huisman TH
    Hemoglobin; 1989; 13(6):557-66. PubMed ID: 2606724
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140.
    Jogessar VB; Westermeyer K; Webber BB; Wilson JB; Hu H; Gonzalez-Redondo JM; Kutlar A; Huisman TH
    Biochim Biophys Acta; 1988 Nov; 951(1):36-41. PubMed ID: 3191134
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hb A2-Wrens or alpha 2 delta 2 98(FG5) Val----Met, an unstable delta chain variant identified by sequence analysis of amplified DNA.
    Codrington JF; Kutlar F; Harris HF; Wilson JB; Stoming TA; Huisman TH
    Biochim Biophys Acta; 1989 Sep; 1009(1):87-9. PubMed ID: 2477064
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hb Watts [alpha 74(EF3) or alpha 75(EF4)Asp-->0]: a shortened alpha chain variant due to the deletion of three nucleotides in exon 2 of the alpha 2-globin gene.
    Rahbar S; Lee C; Fáirbanks VF; McCormick DJ; Kubik K; Madden BJ; Nozari G
    Hemoglobin; 1997 Jul; 21(4):321-30. PubMed ID: 9255611
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comparison of the protein and DNA approaches for the characterization of a beta-globin chain variant, hemoglobin Cocody [beta 21 (B3) Asp--->Asn], in a Caucasian patient.
    Aguilar-Martinez P; Galacteros F; Schved JF; Blouquit Y; Gris JC; Demaille J; Claustres M
    Ann Hematol; 1993 May; 66(5):269-72. PubMed ID: 8507722
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Compound heterozygosity for Hb Korle-Bu (beta(73); Asp-Asn) and Hb E (beta(26); Glu-Lys) with a 3.7-kb deletional alpha-thalassemia in Thai patients.
    Changtrakun Y; Fucharoen S; Ayukarn K; Siriratmanawong N; Fucharoen G; Sanchaisuriya K
    Ann Hematol; 2002 Jul; 81(7):389-93. PubMed ID: 12185510
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The mutation of Hb Turriff [alpha99(G6)Lys --> Glu (AAG --> GAG)] is carried by the alpha1-globin gene in a Japanese (Hb Turriff-I).
    Harano T; Harano K; Hong YF; Than AM; Suetsugu Y; Ohba K
    Hemoglobin; 2003 May; 27(2):123-7. PubMed ID: 12779275
    [No Abstract]   [Full Text] [Related]  

  • 20. Hb Sassari [alpha 126(H9)Asp-->His] results from a GAC-->CAC mutation in the alpha 1-globin gene.
    Paglietti E; Barella S; Satta S; Perra C; Cao A; Galanello R
    Hemoglobin; 1998 Jan; 22(1):65-7. PubMed ID: 9494049
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.