Citations (16)
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Kathryn E. Plant, Michael J. Dye, Celina Lafaille & Nick J. Proudfoot. (2005) Strong Polyadenylation and Weak Pausing Combine To Cause Efficient Termination of Transcription in the Human Gγ-Globin Gene. Molecular and Cellular Biology 25:8, pages 3276-3285.
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Henri Wajcman, Jean Riou & Angoué P. Yapo. (2002) GLOBIN CHAIN ANALYSIS BY REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY: RECENT DEVELOPMENTS. Hemoglobin 26:3, pages 271-283.
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Henri Wajcman, Claude Préhu, Josiane Bardakdjian-Michau, Danielle Promé, Jean Riou, Christian Godart, Mireille Mathis, Didier Hurtrel & Frederic Galactéros. (2001) ABNORMAL HEMOGLOBINS: LABORATORY METHODS. Hemoglobin 25:2, pages 169-181.
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Ioannis Papassotiriou, Joanne Traeger-Synodinos, Danielle Promé, Jean Kister, Christina Vrettou, Athina Xaidara, Michael Marden, Alexandra Stamoulakatou, Henri Wajcman & Emmanuel Kanavakis. (2001) Hb SITIA [β128(H6)Ala→Val]: AN UNSTABLE VARIANT WITH A SUBSTITUTION IN THE α1β1 INTERFACE. Hemoglobin 25:1, pages 45-56.
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C. Préhu, J. Riou, C. Godart, M. Bost, C. Barro, D. Promé, J. Kister, F. Galactéros & H. Wajcman. (2000) Hb Diamant [α119(H2)Pro→Leu]: A New Variant with a Modification at the α1β1 Interface. Hemoglobin 24:3, pages 249-252.
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Articles from other publishers (11)
Hooshang Nemati, Gholamreza Bahrami & Zohreh Rahimi. (2010) Rapid separation of human globin chains in normal and thalassemia patients by RP-HPLC. Molecular Biology Reports 38:5, pages 3213-3218.
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Andrea Mosca, Renata Paleari, Daniela Leone & Giovanni Ivaldi. (2009) The relevance of hemoglobin F measurement in the diagnosis of thalassemias and related hemoglobinopathies. Clinical Biochemistry 42:18, pages 1797-1801.
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Henri Wajcman & Jean Riou. (2009) Globin chain analysis: An important tool in phenotype study of hemoglobin disorders. Clinical Biochemistry 42:18, pages 1802-1806.
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg, Mary Fabry & John M. Old. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallMartin H. Steinberg. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin
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Ioannis Papassotiriou, Joanne Traeger-Synodinos, Michael C. Marden, Jean Kister, Dimitra Liapi, Danielle Prome, Alexandra Stamoulakatou, Henri Wajcman & Emmanuel Kanavakis. (2005) The homozygous state for Hb Crete [β129 (H7) Ala→Pro] is associated with a complex phenotype including erythrocytosis and functional anemia. Blood Cells, Molecules, and Diseases 34:3, pages 229-234.
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Marie-Catherine Giarratana, Ladan Kobari, Hélène Lapillonne, David Chalmers, Laurent Kiger, Thérèse Cynober, Michael C Marden, Henri Wajcman & Luc Douay. (2004) Ex vivo generation of fully mature human red blood cells from hematopoietic stem cells. Nature Biotechnology 23:1, pages 69-74.
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Thi My Anh Neildez-Nguyen, Henri Wajcman, Michael C. Marden, Morad Bensidhoum, Vincent Moncollin, Marie-Catherine Giarratana, Ladan Kobari, Dominique Thierry & Luc Douay. (2002) Human erythroid cells produced ex vivo at large scale differentiate into red blood cells in vivo. Nature Biotechnology 20:5, pages 467-472.
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Henri Wajcman, Frédéric Galactéros, Ahmed Hanichi, Angoue Yapo & Claude Préhu. (2000) HbF in the adult: could its composition discriminate normal from abnormal foetal globin gene expression?. Comptes Rendus de l'Académie des Sciences - Series III - Sciences de la Vie 323:11, pages 975-981.
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Joanne Traeger-Synodinos, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Christina Vrettou, Alexandra Stamoulakatou & Emmanuel Kanavakis. (2000) Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic Hemoglobinopathies. Blood Cells, Molecules, and Diseases 26:4, pages 276-284.
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Robert T. Kennedy, Igor German, Jonathan E. Thompson & Steven R. Witowski. (1999) Fast Analytical-Scale Separations by Capillary Electrophoresis and Liquid Chromatography. Chemical Reviews 99:10, pages 3081-3132.
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