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Hemoglobin
international journal for hemoglobin research
Volume 12, 1988 - Issue 4
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Original Article

Hemoglobin Saverne: A New Variant with Elongated β Chains: Structural and Functional Properties

J. Delanoe-Garin INSERM, U. 91, Hopital Henri Mondor, 91010, Creteil, France
,
Y. Blouquit INSERM, U. 91, Hopital Henri Mondor, 91010, Creteil, France
,
N. Arous INSERM, U. 91, Hopital Henri Mondor, 91010, Creteil, France
,
J. Kister INSERM, U. 299, Hopital de Bicětre, 91275, Le Kremlin-Bicětre, France
,
C. Poyart INSERM, U. 299, Hopital de Bicětre, 91275, Le Kremlin-Bicětre, France
,
M. L. North Centre de Transfusion Sanguine, 67000, Strasbourg, France
,
J. Bardakdjian INSERM, U. 91, Hopital Henri Mondor, 91010, Creteil, France
,
C. Lacombe INSERM, U. 91, Hopital Henri Mondor, 91010, Creteil, France
,
J. Rosa INSERM, U. 91, Hopital Henri Mondor, 91010, Creteil, France
&
F. Galacteros INSERM, U. 91, Hopital Henri Mondor, 91010, Creteil, France
 show all
Pages 337-352 | Received 09 Feb 1988, Accepted 09 May 1988, Published online: 07 Jul 2009

Citations (23)

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Ekaterina Demidova, Valentina Salomashkina, Daria Selivanova, Evgeny Litvin, Natalia Karamyan, Svetlana Mann, Valentina Dvirnyk, Salia Maryina, Natal’ya Petrova, Lana Gorgidze, Anastasiya Peredel’skaya, Nina Tsvetaeva, Nataliya Smetanina & Vadim Surin. (2023) Hb Ryazan: An Elongated C‐Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25. Hemoglobin 47:2, pages 97-101.
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Manit Nuinoon, Orapan Thipthara & Suthat Fucharoen. (2019) Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2. Hemoglobin 43:1, pages 52-55.
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Pierre Chagnon, Luigina Mollica, Claude Belisle, Céline Deveaux, Giovanni D. Angelo, Denis-Claude Roy, Denis Soulières & Lambert Busque. (2008) Hb Montreal II: A Novel Elongated β-Globin Variant Caused by a Frameshift Mutation [β142 (−C)]. Hemoglobin 32:4, pages 351-359.
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Philippe Lacan, Martine Aubry, Nicole Couprie & Alain Francina. (2007) Two New β0-Thalassemic Mutations: A Deletion (−CC) at Codon 142 or Overlapping Codons 142-143, and an Insertion (+T) at Codon 45 or Overlapping Codons 44-45/45-46 of the β-Globin Gene. Hemoglobin 31:2, pages 159-165.
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Yong Jiang, Xiang-Sheng Xu & J. Eric Russell. (2006) A Nucleolin-Binding 3′ Untranslated Region Element Stabilizes β-Globin mRNA In Vivo. Molecular and Cellular Biology 26:6, pages 2419-2429.
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Claude Préhu, Serge Pissard, Maha Al-Sheikh, Catherine Le Niger, Dora Bachir, Fréderic Galactéros & Henri Wajcman. (2005) Two French Caucasian Families with Dominant Thalassemia-Like Phenotypes Due to Hyper Unstable Hemoglobin Variants: Hb Sainte Seve [Codon 118 (− T)] and Codon 127 [CAG→TAG (Gln→Stop]). Hemoglobin 29:3, pages 229-233.
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Giovanni Ivaldi, Onorata David, Maria Baffico, Daniela Leone, Maurizia Baldi, Maria Isola Parodi, Valeria Scimè‐Degani, Antonio Piga, Paola Scagni, Emma Rabino‐Massa & Giuseppe Ricco. (2003) Hb Trento: An Elongated C‐Terminal β Chain Due to a New Frameshift Mutation [β144 (−A)]. Hemoglobin 27:1, pages 15-25.
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Jia Yu & J. Eric Russell. (2001) Structural and Functional Analysis of an mRNP Complex That Mediates the High Stability of Human β-Globin mRNA. Molecular and Cellular Biology 21:17, pages 5879-5888.
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M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
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. (1993) Variants of the Alpea Chain. Hemoglobin 17:2, pages 89-177.
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. (1992) Variants of the Alpha Chain. Hemoglobin 16:3, pages 127-213.
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. (1991) International hemoglobin information center: Variants of the alpha chain. Hemoglobin 15:3, pages 139-217.
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. (1990) International Hemoglobin Information Center. Hemoglobin 14:3, pages 249-325.
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. (1989) Variants of the Alpha Chain. Hemoglobin 13:3, pages 223-297.
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Articles from other publishers (7)

Wanying Lin, Qianqian Zhang, Zongrui Shen, Xiang Qu, Qi Wang, Liuyuan Wei, Yuhao Qiu, Jie Yang, Xiangmin Xu & Jinquan Lao. (2021) Molecular and phenotype characterization of an elongated β‐globin variant produced by HBB:C.313delA. International Journal of Laboratory Hematology 43:6, pages 1620-1627.
Crossref
Berndt Zur. (2016) Hemoglobin variants – pathomechanism, symptoms and diagnosis. LaboratoriumsMedizin 39:s1.
Crossref
Berndt Zur. (2015) Hämoglobinvarianten – Pathomechanismus, Symptome und Diagnostik. LaboratoriumsMedizin 39:5, pages 311-324.
Crossref
B. Gulbis, F. Cotton & F. Vertongen. (2006) Hémoglobines anormales rares. EMC - Hématologie 1:1, pages 1-6.
Crossref
B. Gulbis, F. Cotton & F. Vertongen. (2004) Hémoglobines anormales rares. EMC - Hématologie 1:4, pages 106-114.
Crossref
Onur Bilenoglu, A. Nazli Basak & J. Eric Russell. (2002) A 3′UTR mutation affects β‐globin expression without altering the stability of its fully processed mRNA. British Journal of Haematology 119:4, pages 1106-1114.
Crossref
J. Eric Russell, Julia Morales & Stephen A. Liebhaber. 1997. 249 287 .

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