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Hemoglobin
international journal for hemoglobin research
Volume 23, 1999 - Issue 1
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Original Article

Two hemoglobin variants with an alteration of the oxygen-linked chloride binding: Hb antananarivo [α1(NA1)Val→Gly] and Hb barbizon [β144(HC1)Lys→Met]

J. Kister INSERM U473, 94276 Le, Kremlin-Bicětre, FranceCorrespondence[email protected]
,
C. Préhu Department of Biochemistry, Créteil, France; INSERM U468, Créteil, France
,
J. Riou Department of Biochemistry, Créteil, France
,
C. Godart Department of Biochemistry, Créteil, FranceView further author information
,
J. Bardakdjian Department of Biochemistry, Créteil, France; INSERM U474 Hôpital Henri Mondor, 94010, Créteil, France
,
D. Promé Institut de Pharmacologic et de Biologie Structurale, CNRS, 31077, Toulouse, France
,
F. Galactéros Department of Biochemistry, Créteil, France; INSERM U474 Hôpital Henri Mondor, 94010, Créteil, France
&
H. Wajcman INSERM U468, Créteil, France
 show all
Pages 21-32 | Received 23 Jul 1998, Accepted 28 Sep 1998, Published online: 05 Aug 2009

Citations (9)

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Read on this site (6)

Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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Yan Li, Jin-Mei Yan, Jian-Ying Zhou, Yue-Cheng Lu & Dong-Zhi Li. (2017) Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β0-Thalassemia in a Chinese Patient with β-Thalassemia Intermedia. Hemoglobin 41:1, pages 47-49.
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Margherita Vinciguerra, Cristina Passarello, Filippo Cassarà, Filippo Leto, Monica Cannata, Anna Crivello, Veronica Di Salvo, Aurelio Maggio & Antonino Giambona. (2016) Hb San Cataldo [β144(HC1)Lys→Thr; HBB: C.434A > C]: A New Hemoglobin Variant with Increased Affinity for Oxygen. Hemoglobin 40:4, pages 223-227.
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Cornelis L. Harteveld, Florens G.A. Versteegh, Eduard H.G. van Leer, Jaap S. Starreveld, Peter J.M.J. Kok, Irene van Rooijen-Nijdam, Peter van Delft, Isabelle Zanella-Cleon, Michel Becchi, Henri Wajcman & Piero C. Giordano. (2007) Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Gene in Cis with a −α3.7 Thalassemia Deletion. Hemoglobin 31:3, pages 313-323.
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C. Fisher, J. Hanslip, B. N. Green, V. Gupta, J. M. Old & D. C. Rees. (2000) HB Watford [βl(NA1)VAL→GLY]: A new, Clinically Silent Hemoglobin Variant in Linkage with a new Neutral Mutation [CAP +36 (G→A)]. Hemoglobin 24:4, pages 347-353.
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Georgi D. Efremov, Henri Wajcman & Marianne F.H. Carver. (1999) International Hemoglobin Information Center. Hemoglobin 23:3, pages 303-315.
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Articles from other publishers (3)

Chandrasekhar Natarajan, Anthony V. SignoreVikas KumarRoy E. Weber, Angela Fago & Jay F. Storz. (2020) Effect of NH2-terminal acetylation on the oxygenation properties of vertebrate haemoglobin. Biochemical Journal 477:19, pages 3839-3850.
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Isabelle Zanella-Cleon, Philippe Joly, Michel Becchi & Alain Francina. (2009) Phenotype determination of hemoglobinopathies by mass spectrometry. Clinical Biochemistry 42:18, pages 1807-1817.
Crossref
P. Lacan, G. Souillet, M. Aubry, D. Promé, S. Richelme‐David, J. Kister, H. Wajcman & A. Francina. (2002) New α2 globin chain variant with low oxygen affinity affecting the N‐terminal residue and leading to N‐acetylation [Hb Lyon‐Bron α 1(NA1)Val→Ac‐Ala]. American Journal of Hematology 69:3, pages 214-218.
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