메뉴 건너뛰기




Volumn 8, Issue 3, 2016, Pages 37-41

GBT440 inhibits sickling of sickle cell trait blood under in vitro conditions mimicking strenuous exercise

Author keywords

Exertional sickling; Hemoglobin oxygen affinity; Rhabdomylosis; Sickle cell disease; Sickle cell trait

Indexed keywords

ANTISICKLING AGENT; GBT 440; HEMOGLOBIN A; HEMOGLOBIN S; UNCLASSIFIED DRUG;

EID: 84990852355     PISSN: 20388322     EISSN: 20388330     Source Type: Journal    
DOI: 10.4081/hr.2016.6637     Document Type: Article
Times cited : (16)

References (23)
  • 1
    • 66449103072 scopus 로고    scopus 로고
    • Complications associated with sickle cell trait: A brief narrative review
    • Tsaras G, Owusu-Ansah A, Boateng FO, Amoateng-Adjepong Y. Complications associated with sickle cell trait: a brief narrative review. Am J Med 2009;122:507-12.
    • (2009) Am J Med , vol.122 , pp. 507-512
    • Tsaras, G.1    Owusu-Ansah, A.2    Boateng, F.O.3    Amoateng-Adjepong, Y.4
  • 2
    • 13644260897 scopus 로고    scopus 로고
    • Vascular obstruction in sickle cell disease
    • Kaul DK. Vascular obstruction in sickle cell disease. J Biol Med 2001;156-63.
    • (2001) J Biol Med , pp. 156-163
    • Kaul, D.K.1
  • 3
    • 84900448631 scopus 로고    scopus 로고
    • A review of clinical profile in sick le cell traits
    • John N. A review of clinical profile in sick le cell traits. Oman Med J 2010;25:3-8.
    • (2010) Oman Med J , vol.25 , pp. 3-8
    • John, N.1
  • 4
    • 84874713831 scopus 로고    scopus 로고
    • Pathophysiology of exertional death associated with sickle cell trait: Can we make a parallel with vaso-occlusion mechanisms in sickle cell disease?
    • Connes P, Harmon KG, Bergeron MF. Pathophysiology of exertional death associated with sickle cell trait: can we make a parallel with vaso-occlusion mechanisms in sickle cell disease? Br J Sports Med 2013;47:190.
    • (2013) Br J Sports Med , vol.47 , pp. 190
    • Connes, P.1    Harmon, K.G.2    Bergeron, M.F.3
  • 5
    • 84857045310 scopus 로고    scopus 로고
    • Framing the research agenda for sickle cell trait: Building on the current understanding of clinical events and their potential implications
    • Goldsmith JC, Bonham VL, Joiner CH, et al. Framing the research agenda for sickle cell trait: building on the current understanding of clinical events and their potential implications. Am J Hematol 2012;87: 340-6.
    • (2012) Am J Hematol , vol.87 , pp. 340-346
    • Goldsmith, J.C.1    Bonham, V.L.2    Joiner, C.H.3
  • 6
    • 0023195612 scopus 로고
    • Delay time of hemoglobin S polymerization prevents most cells from sickling in vivo
    • Mozzarelli A, Hofrichter J, Eaton WA. Delay time of hemoglobin S polymerization prevents most cells from sickling in vivo. Science 1987;237:500-6.
    • (1987) Science , vol.237 , pp. 500-506
    • Mozzarelli, A.1    Hofrichter, J.2    Eaton, W.A.3
  • 8
    • 0024375070 scopus 로고
    • Exercise and hypoxia increase sickling in venous blood from an exercising limb in individuals with sickle cell trait
    • Martin TW, Weisman IM, Zeballos RJ, Stephenson SR. Exercise and hypoxia increase sickling in venous blood from an exercising limb in individuals with sickle cell trait. Am J Med 1989;87:48-56.
    • (1989) Am J Med , vol.87 , pp. 48-56
    • Martin, T.W.1    Weisman, I.M.2    Zeballos, R.J.3    Stephenson, S.R.4
  • 10
    • 33947153000 scopus 로고    scopus 로고
    • Sickle cell trait and sudden death-bringing it home
    • Mitchell BL. Sickle cell trait and sudden death-bringing it home. J Natl Med Assoc 2007;99:300-5.
    • (2007) J Natl Med Assoc , vol.99 , pp. 300-305
    • Mitchell, B.L.1
  • 11
    • 0029067861 scopus 로고
    • Nontraumatic sports death in high school and college athletes
    • Van Camp SP, Bloor CM, Mueller FO, et al. Nontraumatic sports death in high school and college athletes. Med Sci Sports Exerc 1995;27:641-7.
    • (1995) Med Sci Sports Exerc , vol.27 , pp. 641-647
    • Van Camp, S.P.1    Bloor, C.M.2    Mueller, F.O.3
  • 12
    • 0028328614 scopus 로고
    • Fatal rhabdomyolysis presenting as mild heat illness in military training
    • Gardner JW, Kark JA. Fatal rhabdomyolysis presenting as mild heat illness in military training. Mil Med 1994;159:160-3.
    • (1994) Mil Med , vol.159 , pp. 160-163
    • Gardner, J.W.1    Kark, J.A.2
  • 13
    • 84866732907 scopus 로고    scopus 로고
    • Sickle cell trait associated with sudden death in competitive athletes
    • Harris KM, Haas TS, Eichner ER, Maron BJ. Sickle cell trait associated with sudden death in competitive athletes. Am J Cardiol 2012;110:1185-8.
    • (2012) Am J Cardiol , vol.110 , pp. 1185-1188
    • Harris, K.M.1    Haas, T.S.2    Eichner, E.R.3    Maron, B.J.4
  • 14
    • 84982893749 scopus 로고    scopus 로고
    • GBT440 increases haemoglobin oxygen affinity, reduces sickling and prolongs RBC half-life in a murine model of sickle cell disease
    • [Epub ahead of print]
    • Oksenberg D, Dufu K, Patel MP, et al. GBT440 increases haemoglobin oxygen affinity, reduces sickling and prolongs RBC half-life in a murine model of sickle cell disease. Br J Haematol 2016. [Epub ahead of print]
    • Br J Haematol 2016.
    • Oksenberg, D.1    Dufu, K.2    Patel, M.P.3
  • 15
    • 0017641722 scopus 로고
    • Participation of hemoglobins A and F in polymerization of sickle hemoglobin
    • Goldberg MA, Husson MA, Bunn HF. Participation of hemoglobins A and F in polymerization of sickle hemoglobin. J Biol Chem 1977;252:3414-21.
    • (1977) J Biol Chem , vol.252 , pp. 3414-3421
    • Goldberg, M.A.1    Husson, M.A.2    Bunn, H.F.3
  • 17
    • 84928279234 scopus 로고    scopus 로고
    • The delay time in sickle cell disease after 40 years: A paradigm assessed
    • Ferrone FA. The delay time in sickle cell disease after 40 years: a paradigm assessed. Am J Hematol 2015;90:438-45.
    • (2015) Am J Hematol , vol.90 , pp. 438-445
    • Ferrone, F.A.1
  • 18
    • 0016369152 scopus 로고
    • Kinetics and mechanism of deoxyhemoglobin S gelation: A new approach to understanding sickle cell disease
    • Hofrichter J, Ross PD, Eaton WA. Kinetics and mechanism of deoxyhemoglobin S gelation: a new approach to understanding sickle cell disease. Proc Natl Acad Sci USA 1974;71:4864-8.
    • (1974) Proc Natl Acad Sci USA , vol.71 , pp. 4864-4868
    • Hofrichter, J.1    Ross, P.D.2    Eaton, W.A.3
  • 19
    • 0016294907 scopus 로고
    • The rates of polymerization and depolymerization of sickle cell hemoglobin
    • Moffat K, Gibson QH. The rates of polymerization and depolymerization of sickle cell hemoglobin. Biochem Biophys Res Commun 1974;61:237-42.
    • (1974) Biochem Biophys Res Commun , vol.61 , pp. 237-242
    • Moffat, K.1    Gibson, Q.H.2
  • 20
    • 0018565753 scopus 로고
    • Gelation of sickle cell hemoglobin in mixtures with normal adult and fetal hemoglobins
    • Sunshine HR, Hofrichter J, Eaton WA. Gelation of sickle cell hemoglobin in mixtures with normal adult and fetal hemoglobins. J Mol Biol 1979;133:435-67.
    • (1979) J Mol Biol , vol.133 , pp. 435-467
    • Sunshine, H.R.1    Hofrichter, J.2    Eaton, W.A.3
  • 21
    • 7944237674 scopus 로고    scopus 로고
    • Red blood cell pH, the Bohr effect, and other oxygenation-linked phenomena in blood O2 and CO2 transport
    • Jensen FB. Red blood cell pH, the Bohr effect, and other oxygenation-linked phenomena in blood O2 and CO2 transport. Acta Physiol Scand 2004;182:215-27.
    • (2004) Acta Physiol Scand , vol.182 , pp. 215-227
    • Jensen, F.B.1
  • 22
    • 0023572225 scopus 로고
    • Hemoglobin S gelation and sickle cell disease
    • Eaton W, Hofrichter J. Hemoglobin S gelation and sickle cell disease. Blood 1987;70:1245-66.
    • (1987) Blood , vol.70 , pp. 1245-1266
    • Eaton, W.1    Hofrichter, J.2
  • 23
    • 84919484933 scopus 로고    scopus 로고
    • Exertional sickling: Questions and controversy
    • Blinde MA, Russel S. Exertional sickling: questions and controversy. Hematol Rep 2014;6:66-70.
    • (2014) Hematol Rep , vol.6 , pp. 66-70
    • Blinde, M.A.1    Russel, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.