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Hemoglobin
international journal for hemoglobin research
Volume 11, 1987 - Issue 3
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Original Article

IHIC Variants List

Pages 243-308 | Published online: 07 Jul 2009

References

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  • XIII Meeting Gruppo di Studio Dell'Entrocita, Torino, 12 June, 1977
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  • 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: 11–21
  • Wilson J. B., Webber B. B., Huisman T. H.J. Annotation: Hb Leslie is the same as Hb Shelby or α2β2 131 (H9) Glrr → Lys. Hemogobin 1981; 8: 595–596
  • Chen S. S., Wilson J. B., Webber B. B., Huisman T. H.J., Miwa S., Amenomori Y. Hb F-Tokyo or α Gγ2 34 (B16) Val → lIe, a silent chain variant detected by reverse pTiase high performance liquid chromatography. Hemoglobin 1985; 9: 25–32
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  • Como P. F., Hockey D., Trent R. J., Kronenberg H. Hb Geelong: β2 139 (H17) Asn → Asp. A new hemoglobin with thalassemia-like characteristics. Presented as Abstract at February meeting of N.S.W. Thalassemia Society. February, 1985
  • Barwick R. C., Jones R. T., Head C. G., Shih M. F-C, Prchal J. T., Shih D. T-B. Hb Long Island: A hemoglobin variant with a methionyl extension at the NH2 terminus and a prolyl substitution for the normal histidyl residue 2 Of the β chain. Proc. Natl. Acad. Sci., USA 1985; 82: 4602–4605
  • Blouquit Y., Arous N., Lena D., Delanoe-Garin J., Lacombe C, Bardakdjian J., Vovan L., Orsini A., Rosa J., Galacteros F. Hb Marseille [α2β2 N methionyl-2 (NA2) His → Pro]: a new β chain variant having an extended N-terminus. FEBS Lett. 1984; 178: 315–318
  • Shelton J. B., Shelton J. R., Schroeder W. A., Powars D. R. Hb Aztec or α276 (EF5) MET → THR β2 detection of a silent mutant by high performance liquid chromatography. Hemoglobin 1985; 9: 325–332
  • Harano T., Harano K., Ueda S. Hb Owari [αc121 (H4) Val → Met]: a new hemoglobin variant with a neutral-to-neutral amino acid substitution detected by isoelectric focusing. Hemoglobin 1986; 10: 127–134
  • Bowman J. E., Bloom R., Chen S-S., Webber B. B., Wilson J. B., Kutlar F., Kutlar A., Huisman T. H.J. Hb Chicago or α2136 (H19) Leu → Met β2. Hemoglobin 1986; 10: 495–505
  • Rahbar S., Louis J., Lee T., Asmerom Y. Hemoglobin North Chicago (β36 [C2] Proline → Serine): A new high affinity hemoglobin. Hemoglobin 1985; 9: 559–576
  • Huisman T. H.J., Wilson J. B., Kutlar A., Yang K-G., Chen S-S., Webber B. B., Altay C, Martinez Villegas A. Hb J-Antakya or α2β2 65 (E9) Lys → Met in a Turkish family and Hb Complutense or α2β2 127 (H5) Glrn → Glu in a Spanish family; correction of a previously published identification. Biochim. Biophys. Acta 1986; 871: 229–231
  • Harano T., Harano K., Ueda S., Imai N., Kitazumi T. A new electrophoretically-silent hemoglobin variant: Hemoglobin Kofu or α2β2 84 (EF8) Thr → lle. Hemoglobin 1986; 10h: 417–420
  • Ohba Y., Miyaji T., Murakami M., Kadowaki S., Fujita T., Oimomi M., Hatanaka H., Ishikawa K., Baba S., Hitaka K., Imai K. Hb Himeji or β140 (H18) Ala → Asp a slightly unstable hemoglobin with increased N-terminal glycation. Hemoglobin 1986; 10: 109–125
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  • Ohba Y., Igarashi M., Tsukahara M., Nakashima M., Sanada C., Ami M., Arai Y., Miyaji T. Hb A2 Yokoshima, α2δ225 (B7) GLY → ASP, a new δ chain variant found in a Japanese Family. Hemoglobin 1985; 9: 613–615
  • Fujita S., Ohta Y., Saito S., Kobayashi Y., Naritomi Y., Kawaguchi T., Imamura T., Wada Y., Hayashi A. Hemoglobin A2 Honai (α2β290 (F6) Glu → Val): A new delta chain variant. Hemoglobin 1985; 9: 597–607
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  • Barwick R. C., Head C. G., Shih M. F-C, Block S. H., Jones R. T. Hb T-Cambodia [Beta 26 (B8) Glu → Lys, Beta 121 (CH4) Glu → GIn]: a new doubly substituted beta globin variant found in a Cambodian family. Blood 1985; 66(Suppl. 1)68a
  • Moo-Penn W. F., McGuffey J. E., Jue D. L., Johnson M. H., Schum T. Hemoglobin New Mexico: β100 (G2) Pro → Arg. A variant hemoglobin associated with erythrocytosis (BBA 32356). Biochim. Biophys. Acta 1985; 832: 192–196
  • Lacombe C, Craescu C. T., Blouquit Y., Kister J., Poyart C, Delanoe-Garin J., Arous N., Bardakdjian J., Riou J., Rosa J., Schaeffer C, Galacteros F. Structural and functional studies of hemoglobin Poissy α2β256 (D7) Gly → Arg and 86 (F2) Ala → Pro. Eur. J. Biochem. 1985; 153: 655–662
  • Como P. F., Raven J. L., Wilkinson T., Kronenberg H. Comparison of the six hemoglobin variants occurring at the α6 (A4) position with particular reference to the α6 Asp → Gly substitution found in Perth, Western Australia. Haematology Society of Australia. Perth, Western Australia October, 1984
  • Chen S. s., Webber B. B.A, Wilson J. B., Huisman T. H.J. Hb F-Forest Park, a new γ variant with two amino acid substitutions, 75(E19) lle → Thr and 73(E17) Asp → Asn, which can be identified in adults by gene-mapping analysis. Biochim. Biophys. Acta 1985; 832: 242–247
  • Hayashi A., Wada Y., Matsuo T., Katakuse I., Matsuda H. Neonatal screening and mass spectrometric analysis of haemoglobin variants in Japan. Haemoglobin Research and Applications Symposium, England, Sept. 8–10, 1986
  • Monplaisir N., Merault G., Poyart C, Rhoda M. D., Craescu C. T., Vidaud M., Galacteros F., Blouquit Y., Rosa J. Hb S Antilles (α2β2 6 Glu →-Val, 23 Val → lleu): A new variant with lower solubility than Hb S and producing sickle cell disease in heterozygotes. Proc. Natl. Acad. Sci., USA 1986; 83: 9363–9367
  • Jones R. T., Head C, Shih M. F-C, Shih D. T-B., Dana B., Jones M. B., Koler R. D. Hemoglobin Linkoping [β36 (C2) Pro → Thr] in a large Finnish family from Astoria, Oregon, USA. Hemoglobin 1986; 10: 455–467
  • Ogata K., Ito T., Okazaki T., Dan K., Nomura T., Nozawa Y., Kajita A. Hemoglobin Sendagi (β42 Phe → Val): a new unstable hemoglobin variant having an amino acid substitution at CD1 of the β-chain. Hemoglobin 1986; 10: 469–481
  • Baiget M., Gomez Pereira C, Jue D. L., Johnson M. H., McGuffey J. E., Moo-Penn W. F. A case of Hemoglobin Indianapolis [β112(G14) Cys → Arg] in an individual from Cordoba, Spain. Hemoglobin 1986; 10: 483–494
  • De Pablos J. M., Wilson J. B., Kutlar A., Chen S. S., Huisman T. H.J. Hb F-Albaicin or Gγ8(A5)Lys → Glu or Gin. Hemoglobin 1986; 10: 655–659
  • Kutlar A., Kutlar F., Wilson J. B., Webber B. B., Gonzalez Redondo J. M., Huisman T. H.J. Hb F-Clarke or α2Gγ265(E9)Lys → Asn-Hemoglobin, in press
  • Kleman K., Lubin B., Wilson J. B., Kutlar A., Webber B. B., Huisman T. H.J. Hb F-Oakland or α2GγI226(B8)Glu-Lys. Hemoglobin, in press
  • Indrak K., Wiedermann B. F., Batek F., Wilson J. B., Webber B. B., Kutlar A., Huisman T. H.J. Hb Olomouc or α2β286(5p86(F2) Ala →Asp, a new high oxygen affinity variant. Hemoglobin, in press
  • Jen P. C., Liu Y. Hemoglobin Guangzhou, α64(E13)Asp → Gly, a new abnormal hemoglobin found in Guangzhou, China. Hemoglobin 1987; 11: 25–30
  • Zhou Z-q., Chen L-c., Chen P-f., Zhang K-q., Wang Y-h. Hemoglobin Hangznou, α64(E13)Asp → Gly, a new variant found in China. Hemoglobin 1987; 11: 31–33
  • Ohba Y., Yamamoto K., Kawata R., Miyaji T. Hyperunstable Hemoglobin Toyama α2l36 (H19) Leu → Arg β2 detection and identification by in vitro biosynthesis with radioactive amino acids. Hemoglobin, in press
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