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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 4
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Original Article

Unstable Hb Newcastle [β92(F8)His→Pro], First Case Discovered in a Russian Patient

T. P. Molchanova The Sickle Cell Anemia Foundation, Augusta, GA, 30912, USACorrespondence[email protected]
,
S. V. Kolledey Hematological Scientific Center, Moscow, 125167, Russia
,
L. Ch. Pronina Hematological Scientific Center, Moscow, 125167, Russia
,
O. A. Mirgorodskaya Hematological Scientific Center, Moscow, 125167, Russia
,
A. Ch. Musolyamov Institute of Molecular Biology, Moscow, 117984, Russia
,
L. V. Abaturov Institute of Molecular Biology, Moscow, 117984, Russia
&
T. H. J. Huisman The Sickle Cell Anemia Foundation, Augusta, GA, 30912, USA
 show all
Pages 373-378 | Received 27 May 1998, Accepted 08 Jul 1999, Published online: 07 Jul 2009

References

  • Finney R., Casey R., Lehmann H., Walker W. Hb Newcastle: β92 (F8) His←Pro. FEBS Lett. 1975; 60: 435–438
  • Wajcman H., Blouquit Y., Vasseur C., Le Querrec A., Laniece M, Melevendi C., Rasore A., Galacteros F. Two new human hemoglobin variants caused by unusual mutational events: Hb Zäire contains a five residue repetition within the α-chain and Hb Duino has two residues substituted in the β-chain. Hum. Genet. 1992; 78: 676–680
  • Huisman T. H.J, Jonxis J. H.P. The Hemoglobinopathies Techniques of Identification. Clinical and Biochemical Analysis. Marcel Dekker Inc, New York, NYUSA 1977; Vol. 6
  • Molchanova T. P. A new screening test for unstable hemoglobins using n-butanol and red blood cells. Hemoglobin 1993; 17: 81–84
  • Huisman T. H.J. Introduction and review of standard methodology for the detection of hemoglobin abnormalities. The Hemoglobinopathies, edited by T.H.J., Methods in Hematology. Churchill Livingstone, EdinburghScotland 1986; Vol. 15: 1–31
  • Molchanova T. P., Mirgorodskaya O. A, Abaturov L. V., Podtelezhnikov A. V., Tokarev Yu. N., Grachev S. K. Localization of amino acid substitutions in human hemoglobin. Mass-spectral approximate analysis of tryptic peptides. Mol. Biol. 1989; 23: 225–239, (translated into English from Russian)
  • Wilson J. B., Lam H., Pravatmuang P., Huisman T. H.J. Separation of tryptic peptides of normal and abnormal α, β-, γ-, and δ-globin chains by high-performance liquid chromatography. J. Chromatogr. 1979; 179: 271–290
  • Bunn H. F., Jandl J. H. Exchange of heme among hemoglobins and between hemoglobin and albumin. J. Biol. Chem. 1968; 243: 465–475
  • Rachmilewitz E. A. Denaturation of the normal and abnormal hemoglobin molecule. Semin. Hematol. 1974; 11: 441–462
  • Molchanova T. P., Tokarev Yu. N. Abnormal hemoglobins in the USSR. Hematology Reviews, O. K. Gavrilov. Harvard Academy Press, Boston, MAUSA 1990; Vol. 2B: 1–31
  • Huisman T. H.J., Carver M. F.H., Efremov G. D. A Syllabus of Human Hemoglobin Variants 1996. The Sickle Cell Anemia Foundation, Augusta, GAUSA 1996; 230–233, http://www.plobin.cse.psu.edu/globin/html/
  • Ohba Y., Miyaji T., Hattori Y., Fuyuno K., Matsuoka M. Unstable hemoglobins in Japan. Hemoglobin 1980; 4: 307–312
  • Ohba Y., Imanaka M., Matsuoka M., Hattori Y., Miyaji T., Funaki C., Shibata K., Shimokata H., Kuzuya F., Miwa S. A new unstable, high oxygen affinity hemoglobin: Hb Nagoya or β97 (FG4) His←Pro. Hemoglobin 1985; 9: 11–24
  • Wajcman H., Behnken L. J., Riou J., Galacteros F. Hb Mainz [β98(FG5) Val←Glu]: a new unstable variant carrying a structural modification at the same position as Hb Köln. Abstract 258. Br. J. Haematol. 1994; 87(66), Suppl. 1

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