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Hemoglobin
international journal for hemoglobin research
Volume 17, 1993 - Issue 3
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Original Article

HB Alesha or α2 β267(E11)VAL →MET: A New Unstable Hemoglobin Variant Identified Through Sequencing of, Amplified DNA

T. P. Molchanova Laboratory of Protein Chemistry and Department of Biochemistry, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
Yu. V. Postnikov Laboratory of Protein Chemistry and Department of Biochemistry, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
D. D. Pobedimskaya Laboratory of Protein Chemistry and Department of Biochemistry, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
N. S. Smetanina Research Institute of Pediatric Hematology, Moscow, 117513, Russia
,
A. A. Moschan Research Institute of Pediatric Hematology, Moscow, 117513, Russia
,
E. G. Kazanetz Research Institute of Pediatric Hematology, Moscow, 117513, Russia
,
Yu. N. Tokarev Research Institute of Pediatric Hematology, Moscow, 117513, Russia
&
T. H. J. Huisman Research Institute of Pediatric Hematology, Moscow, 117513, Russia
 show all
Pages 217-225 | Received 25 Nov 1992, Accepted 15 Feb 1993, Published online: 07 Jul 2009

Citations (17)

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Read on this site (11)

Jordyn A. Moore, Beverley M. Pullon, Darrell Wang, Julie Monaghan & Helen Moore. (2022) Hb Kirikiriroa [α57(E6)Gly→Cys; HBA1: c.172G>T]: A Novel Unstable α-Globin Variant with Oxidized Derivatives Interfering with Hb A1c. Hemoglobin 46:2, pages 81-86.
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Qiong Su, Shiping Chen, Liusong Wu, Runmei Tian, Xiaoqin Yang, Xiaoyan Huang, Yan Chen, Zhiyu Peng & Jindong Chen. (2019) Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene. Hemoglobin 43:1, pages 7-11.
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Gisele A. Pedroso, Elza M. Kimura, Magnun N. N. Santos, Dulcinéia M. Albuquerque, Jucilane L. H. Ferruzzi, Susan E. Jorge, Fernando F. Costa, Sara T. O. Saad & Maria F. Sonati. (2017) Coinheritance of Hb Bristol-Alesha [β67(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia. Hemoglobin 41:3, pages 203-208.
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Hua Jiang, Jin-Mei Yan, Jian-Ying Zhou & Dong-Zhi Li. (2016) Hb Alesha [β67(E11)Val→Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese Girl. Hemoglobin 40:6, pages 420-421.
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Silvia Eandi Eberle, Nélida I. Noguera, Gabriela Sciuccati, Mariana Bonduel, Lilian Díaz, Raquel Staciuk, Héctor M. Targovnik & Aurora Feliu-Torres. (2007) Hb Alesha [β67(E11)Val→Met, GTG→ATG] in an Argentinean Girl. Hemoglobin 31:3, pages 379-382.
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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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D. Urabe, W. Li, Y. Hattori & Y. Ohba. (1996) A New Case of Hb F-M-Osaka [Gγ63(E7)HIS → TYR] Showed Only Benign Neonatal Cyanosis. Hemoglobin 20:2, pages 169-173.
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D. R. Miller, N. S. Smetanina, L-H. Gu, J. Ye. Leonova & T. H. J. Huisman. (1996) HB Sögn or α2β214(A11)LEU → ARG in Combination with an α-Thalassemia Heterozygosity. Hemoglobin 20:2, pages 131-134.
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. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
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D. D. Pobedimskaya, T. P. Molchanova, R. Amernick, M. S. Druskin, B. B. Webber, J. B. Wilson & T. H. J. Huisman. (1993) HB Sinai-Baltimore or α2β218(A15)VAL→GLY, a Silent, Mildly Unstable β Chain Variant Detected by Isoelectrofocusing and High Performance Liquid Chromatography. Hemoglobin 17:6, pages 505-512.
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Articles from other publishers (6)

Michael Brad Strader, Wayne A. Hicks, Tigist Kassa, Eileen Singleton, Jayashree Soman, John S. Olson, Mitchell J. Weiss, Todd L. Mollan, Michael T. Wilson & Abdu I. Alayash. (2014) Post-translational Transformation of Methionine to Aspartate Is Catalyzed by Heme Iron and Driven by Peroxide. Journal of Biological Chemistry 289:32, pages 22342-22357.
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Moira A. Crowley, Todd L. Mollan, Osheisa Y. Abdulmalik, Andrew D. Butler, Emily F. Goodwin, Arindam Sarkar, Catherine A. Stolle, Andrew J. Gow, John S. Olson & Mitchell J. Weiss. (2011) A Hemoglobin Variant Associated with Neonatal Cyanosis and Anemia. New England Journal of Medicine 364:19, pages 1837-1843.
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ANITA RACK, SILVIA STOJANOV, BERND H. BELOHRADSKY & PETER LOHSE. (2006) A new low-penetrance TNFRSF1A mutation causing atypical periodic fever. Pediatrics International 48:2, pages 169-171.
Crossref
Knut Brockmann, Stephan Stolpe, Carsten Fels, Nadia Khan, Andreas E Kulozik & Arnulf Pekrun. (2005) Moyamoya Syndrome Associated With Hemolytic Anemia Due to Hb Alesha. Journal of Pediatric Hematology/Oncology 27:8, pages 436-440.
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Claude Préhu, Christian Godart, Claude Vigneron & Henri Wajcman. (1998) Hb Nancy and Hb Osler: two distinct genetic variants with identical clinical and hemoglobin phenotype. Comptes Rendus de l'Académie des Sciences - Series III - Sciences de la Vie 321:5, pages 373-376.
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M. A.çürük, T. P. Molchanova, Yu. V. Postnikov, D. D. Pobedimskaya, R. Liang, E. Baysal, S. Kolodey, N. S. Smetanina, Yu. N. Tokarev, A. G. Rumyantsev & T. H. J. Huisman. (1994) β-thalassemia alleles and unstable hemoglobin types among russian pediatric patients. American Journal of Hematology 46:4, pages 329-332.
Crossref

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