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Volumn 36, Issue 3, 2012, Pages 293-298

Nondeletional Hb Queens Park [α32(B13)Met→Lys]/Hb H (β4) disease

Author keywords

Thalassemia ( thal); Hb H disease; Hb Queens Park

Indexed keywords

CHAPERONE;

EID: 84860786091     PISSN: 03630269     EISSN: 1532432X     Source Type: Journal    
DOI: 10.3109/03630269.2012.658939     Document Type: Article
Times cited : (6)

References (20)
  • 3
    • 34547597988 scopus 로고    scopus 로고
    • Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations
    • Singsanan S, Fucharoen G, Savongsy O, Sanchaisuriya K, Fucharoen S. Molecular characterization and origins of Hb Constant Spring and Hb Paksé in Southeast Asian populations. Ann Hematol. 2007;86(9):665-669.
    • (2007) Ann. Hematol. , vol.86 , Issue.9 , pp. 665-669
    • Singsanan, S.1    Fucharoen, G.2    Savongsy, O.3    Sanchaisuriya, K.4    Fucharoen, S.5
  • 4
    • 79952162877 scopus 로고    scopus 로고
    • Molecular screening of the Hbs Constant Spring (codon 142 TAA>CAA a2) and Paksé (codon 142 TAA>TAT a2) mutations in Thailand
    • Pichanun D, Munkongdee T, Klamchuen S, et al. Molecular screening of the Hbs Constant Spring (codon 142, TAA>CAA, a2) and Paksé (codon 142, TAA>TAT, a2) mutations in Thailand. Hemoglobin. 2010;34(6):582-586.
    • (2010) Hemoglobin , vol.34 , Issue.6 , pp. 582-586
    • Pichanun, D.1    Munkongdee, T.2    Klamchuen, S.3
  • 5
    • 0035543926 scopus 로고    scopus 로고
    • Interaction of the a2 polyadenylation signal mutation (AATAAA?AATA-) and a0-thalassemia (-SEA), resulting in Hb H disease in a Thai patient
    • Laosombat V, Fucharoen S, Wiriyasateinkul A. Interaction of the a2 polyadenylation signal mutation (AATAAA?AATA-) and a0-thalassemia (-SEA), resulting in Hb H disease in a Thai patient. Hemoglobin. 2001;25(4):383-389.
    • (2001) Hemoglobin , vol.25 , Issue.4 , pp. 383-389
    • Laosombat, V.1    Fucharoen, S.2    Wiriyasateinkul, A.3
  • 6
    • 23244456639 scopus 로고    scopus 로고
    • A rare association of a0-thalassemia (-SEA) and an initiation codon mutation (ATG?A-G) of the a2 gene causes Hb H disease in Thailand
    • Viprakasit V, Chinchang W, Glomglao W, Tanphaichitr VS. A rare association of a0-thalassemia (-SEA) and an initiation codon mutation (ATG?A-G) of the a2 gene causes Hb H disease in Thailand. Hemoglobin. 2005;29(3):235-240.
    • (2005) Hemoglobin , vol.29 , Issue.3 , pp. 235-240
    • Viprakasit, V.1    Chinchang, W.2    Glomglao, W.3    Tanphaichitr, V.S.4
  • 7
    • 47949122211 scopus 로고    scopus 로고
    • An a0-thalassemia-like mutation: Hb Suan-Dok [a109(G16)Leu?Arg] carried by a recombinant -A3.7 gene
    • Moradkhani K, Mazurier E, Giordano PC, Wajcman H, Prehu C. An a0-thalassemia-like mutation: Hb Suan-Dok [a109(G16)Leu?Arg] carried by a recombinant -A3.7 gene. Hemoglobin. 2008;32(4):419-424.
    • (2008) Hemoglobin , vol.32 , Issue.4 , pp. 419-424
    • Moradkhani, K.1    Mazurier, E.2    Giordano, P.C.3    Wajcman, H.4    Prehu, C.5
  • 8
    • 34547559606 scopus 로고    scopus 로고
    • 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, et al. 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. Ann Hematol. 2007;86(9):659-663.
    • (2007) Ann. Hematol. , vol.86 , Issue.9 , pp. 659-663
    • Sura, T.1    Trachoo, O.2    Viprakasit, V.3
  • 10
    • 1342302434 scopus 로고    scopus 로고
    • Co-inheritance of Hb Pak Num Po, a novel a1 gene mutation, and a0 thalassemia associated with transfusion-dependent Hb H disease
    • Viprakasit V, Tanphaichitr VS, Veerakul G, et al. Co-inheritance of Hb Pak Num Po, a novel a1 gene mutation, and a0 thalassemia associated with transfusion-dependent Hb H disease. Am J Hematol. 2004;75(3):157-163.
    • (2004) Am. J. Hematol. , vol.75 , Issue.3 , pp. 157-163
    • Viprakasit, V.1    Tanphaichitr, V.S.2    Veerakul, G.3
  • 11
    • 0033774960 scopus 로고    scopus 로고
    • Simplified multiplex-PCR diagnosis of common Southeast Asian deletional determinants of a-thalassemia
    • Chong SS, Boehm CD, Cutting GR, Higgs DR. Simplified multiplex-PCR diagnosis of common Southeast Asian deletional determinants of a-thalassemia. Clin Chem. 2000;46(10):1692-1695.
    • (2000) Clin. Chem. , vol.46 , Issue.10 , pp. 1692-1695
    • Chong, S.S.1    Boehm, C.D.2    Cutting, G.R.3    Higgs, D.R.4
  • 12
    • 0033983971 scopus 로고    scopus 로고
    • Single-tube multiplex-PCR screen for common deletional determinants of a-thalassemia
    • Chong SS, Boehm CD, Higgs DR, Cutting GR. Single-tube multiplex-PCR screen for common deletional determinants of a-thalassemia. Blood. 2000;95(1):360-362.
    • (2000) Blood , vol.95 , Issue.1 , pp. 360-362
    • Chong, S.S.1    Boehm, C.D.2    Higgs, D.R.3    Cutting, G.R.4
  • 13
    • 0025310064 scopus 로고
    • Simple non-radioactive method for detecting Haemoglobin Constant Spring gene
    • Fucharoen S, Fucharoen G, Fukumaki Y. Simple non-radioactive method for detecting Haemoglobin Constant Spring gene. Lancet. 1990;335(8704):1527.
    • (1990) Lancet , vol.335 , Issue.8704 , pp. 1527
    • Fucharoen, S.1    Fucharoen, G.2    Fukumaki, Y.3
  • 15
    • 77950545115 scopus 로고    scopus 로고
    • Two new a1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [a28(B9 Ala? Val] andHb Queens Park (HBA1:c.98T>A) [a32(B13)Met?Lys]
    • Phylipsen M, Prior JF, Lim E, et al. Two new a1-globin gene point mutations: Hb Nedlands (HBA1:c.86C>T) [a28(B9)Ala?Val] andHb Queens Park (HBA1:c.98T>A) [a32(B13)Met?Lys]. Hemoglobin. 2010;34(2):123-126.
    • (2010) Hemoglobin , vol.34 , Issue.2 , pp. 123-126
    • Phylipsen, M.1    Prior, J.F.2    Lim, E.3
  • 16
    • 77951212077 scopus 로고    scopus 로고
    • A-Hemoglobin stabilizing protein: Molecular function and clinical correlation
    • Turbpaiboon C, Wilairat P. a-Hemoglobin stabilizing protein: molecular function and clinical correlation. Front Biosci. 2010;15:1-11.
    • (2010) Front Biosci. , vol.15 , pp. 1-11
    • Turbpaiboon, C.1    Wilairat, P.2
  • 17
    • 47949117716 scopus 로고    scopus 로고
    • Unstable and thalassemic a chain hemoglobin variants: A cause of Hb H disease and thalassemia intermedia
    • Wajcman H, Traeger-Synodinos J, Papassotiriou I, et al. Unstable and thalassemic a chain hemoglobin variants: A cause of Hb H disease and thalassemia intermedia. Hemoglobin. 2008;32(4):327-349.
    • (2008) Hemoglobin , vol.32 , Issue.4 , pp. 327-349
    • Wajcman, H.1    Traeger-Synodinos, J.2    Papassotiriou, I.3
  • 18
    • 28844462795 scopus 로고    scopus 로고
    • Hb Amsterdam [a32(B13 Met?Ile a2)]: A new unstable variant associated with an a-thalassemia phenotype and a new African polymorphism
    • Harteveld CL, Vervloet M, Zweegman S, et al. Hb Amsterdam [a32(B13)Met?Ile (a2)]: A new unstable variant associated with an a-thalassemia phenotype and a new African polymorphism. Hemoglobin. 2005;29(4):257-262.
    • (2005) Hemoglobin. , vol.29 , Issue.4 , pp. 257-262
    • Harteveld, C.L.1    Vervloet, M.2    Zweegman, S.3
  • 19
    • 77954854335 scopus 로고    scopus 로고
    • Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): Two novel a2 gene mutations associated with mild a-thalassemia found in the same family after newborn screening
    • Giordano PC, Cnossen MH, Joosten AM, et al. Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): Two novel a2 gene mutations associated with mild a-thalassemia found in the same family after newborn screening. Hemoglobin. 2010;34(4):354-365.
    • (2010) Hemoglobin , vol.34 , Issue.4 , pp. 354-365
    • Giordano, P.C.1    Cnossen, M.H.2    Joosten, A.M.3
  • 20
    • 0026652315 scopus 로고
    • Developmental switch in the relative expression of the a1- and a2-globin genes in humans and in transgenic mice
    • Albitar M, Cash FE, Peschle C, Liebhaber SA. Developmental switch in the relative expression of the a1- and a2-globin genes in humans and in transgenic mice. Blood. 1992;79(9):2471-2474.
    • (1992) Blood , vol.79 , Issue.9 , pp. 2471-2474
    • Albitar, M.1    Cash, F.E.2    Peschle, C.3    Liebhaber, S.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.