Literature DB >> 19815833

Chronic hemolytic anemia due to novel alpha-globin chain variants: critical location of the mutation within the gene sequence for a dominant effect.

Claude Préhu, Kamran Moradkhani, Jean Riou, Michel Bahuau, Pierre Launay, Natacha Martin, Henri Wajcman, Michel Goossens, Frédéric Galactéros.   

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Year:  2009        PMID： 19815833      PMCID： PMC2770978          DOI： 10.3324/haematol.2009.012971

Source DB:  PubMed          Journal:  Haematologica        ISSN： 0390-6078            Impact factor:   9.941


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  8 in total

1.  HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server.

Authors:  Ross C Hardison; David H K Chui; Belinda Giardine; Cathy Riemer; George P Patrinos; Nicholas Anagnou; Webb Miller; Henri Wajcman
Journal:  Hum Mutat       Date:  2002-03       Impact factor: 4.878

2.  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]).

Authors:  Claude Préhu; Serge Pissard; Maha Al-Sheikh; Catherine Le Niger; Dora Bachir; Fréderic Galactéros; Henri Wajcman
Journal:  Hemoglobin       Date:  2005       Impact factor: 0.849

3.  HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.

Authors:  Belinda Giardine; Sjozef van Baal; Polynikis Kaimakis; Cathy Riemer; Webb Miller; Maria Samara; Panagoula Kollia; Nicholas P Anagnou; David H K Chui; Henri Wajcman; Ross C Hardison; George P Patrinos
Journal:  Hum Mutat       Date:  2007-02       Impact factor: 4.878

4.  An alpha0-thalassemia-like mutation: Hb Suan-Dok [alpha109(G16)Leu-->Arg] carried by a recombinant -alpha(3.7) gene.

Authors:  Kamran Moradkhani; Elodie Mazurier; Piero C Giordano; Henri Wajcman; Claude Préhu
Journal:  Hemoglobin       Date:  2008       Impact factor: 0.849

5.  Haemoglobin Tak: a variant with additional residues at the end of the beta-chains.

Authors:  G Flatz; J L Kinderlerer; J V Kilmartin; H Lehmann
Journal:  Lancet       Date:  1971-04-10       Impact factor: 79.321

6.  Molecular mechanism of AHSP-mediated stabilization of alpha-hemoglobin.

Authors:  Liang Feng; David A Gell; Suiping Zhou; Lichuan Gu; Yi Kong; Jianqing Li; Min Hu; Nieng Yan; Christopher Lee; Anne M Rich; Robert S Armstrong; Peter A Lay; Andrew J Gow; Mitchell J Weiss; Joel P Mackay; Yigong Shi
Journal:  Cell       Date:  2004-11-24       Impact factor: 41.582

7.  Hemoglobin Wayne: a frameshift mutation detected in human hemoglobin alpha chains.

Authors:  M Seid-Akhavan; W P Winter; R K Abramson; D L Rucknagel
Journal:  Proc Natl Acad Sci U S A       Date:  1976-03       Impact factor: 11.205

Review 8.  Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia.

Authors:  Henri Wajcman; Jan Traeger-Synodinos; Ioannis Papassotiriou; Piero C Giordano; Cornelis L Harteveld; Véronique Baudin-Creuza; John Old
Journal:  Hemoglobin       Date:  2008       Impact factor: 0.849
  8 in total

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