Citations (12)
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Sima Alkilani & Tuba Sevimoglu. (2023) In silico analysis of substitution mutations in the β-globin gene in Turkish population of β-thalassemia. Journal of Biomolecular Structure and Dynamics 0:0, pages 1-8.
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Shao-Min Wu, Fan Jiang, Chan Li, Zhen-Tian Guo, Su-Ran Huang & Dong-Zhi Li. (2022) Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (HBB: c.255_264delinsTTTTTCTCAG). Hemoglobin 46:2, pages 129-131.
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Ibrahim Al Nabhani, John C. Aneke, Madeleine Verhovsek, Barry Eng, Kevin H.M. Kuo, Leona C. Rudinskas & John S. Waye. (2020) Novel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TTT>TTG); HBB: c.258T>G]. Hemoglobin 44:1, pages 10-12.
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Anderson B. Collier$suffix/text()$suffix/text(), Lea M. Coon, Philip Monteleone, Samuel Umaru, Kenneth C. Swanson, James D. Hoyer & Jennifer L. Oliveira. (2016) A Novel β-Globin Chain Hemoglobin Variant, Hb Allentown [β137(H15)Val→Trp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Intermittent Aplastic Crises and Splenomegaly. Hemoglobin 40:2, pages 130-133.
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Céline Renoux, Cécile Feray, Philippe Joly, Isabelle Zanella-Cleon, Caroline Garcia, Philippe Lacan, Nicole Couprie & Alain Francina. (2015) A New Hemoglobin Variant: Hb Meylan [β73(E17)Asp → Phe; HBB: c.220G>T; c.221A>T] with a Double Base Mutation at the Same Codon. Hemoglobin 39:1, pages 46-48.
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Philippe Joly, Philippe Lacan, Caroline Garcia, Aurélie Desbrée, Nicole Couprie & Alain Francina. (2013) Two New δ-Globin Gene Variants: Hb A2-Saint-Etienne [δ14(A11)Leu→Pro (HBD: c.44T>C)] and Hb A2-Marseille [δ22(B4) Ala→Lys (HBD: c.67G>A;68C>A)]. Hemoglobin 37:1, pages 80-84.
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Aydan Çelebiler, Derya Aksoy, Serkan Ocakcı & Baysal Karaca. (2012) A New Hemoglobin Variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T]. Hemoglobin 36:5, pages 474-479.
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Articles from other publishers (5)
Leah S. Heidenreich, Jennifer L. Oliveira, Peter J. Holmberg & Vilmarie Rodriguez. (2020) Hemoglobin Sunshine Seth: A Case Report of Low-Oxygen-Affinity Hemoglobinopathy. Case Reports in Pediatrics 2020, pages 1-4.
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John R. A. Shepherd, Paolo B. Dominelli, Tuhin K. Roy, Timothy W. Secomb, James D. Hoyer, Jennifer L. Oliveira & Michael J. Joyner. (2019) Modelling the relationships between haemoglobin oxygen affinity and the oxygen cascade in humans. The Journal of Physiology 597:16, pages 4193-4202.
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Jennifer L. Oliveira, Lea M. Coon, Lori A. Frederick, Molly Hein, Kenneth C. Swanson, Michelle E. Savedra, Tavanna R. Porter, Mrinal M. Patnaik, Ayalew Tefferi, Animesh Pardanani, Stefan K. Grebe, David S. Viswanatha & James D. Hoyer. (2018) Genotype-phenotype correlation of hereditary erythrocytosis mutations, a single center experience. American Journal of Hematology 93:8, pages 1029-1041.
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Jennifer L. Oliveira. (2018) Diagnostic Strategies in Hemoglobinopathy Testing, the Role of a Reference Laboratory in the USA. Thalassemia Reports 8:1, pages 7476.
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Chandrasekhar Natarajan, Joana Projecto-Garcia, Hideaki Moriyama, Roy E. Weber, Violeta Muñoz-Fuentes, Andy J. Green, Cecilia Kopuchian, Pablo L. Tubaro, Luis Alza, Mariana Bulgarella, Matthew M. Smith, Robert E. Wilson, Angela Fago, Kevin G. McCracken & Jay F. Storz. (2015) Convergent Evolution of Hemoglobin Function in High-Altitude Andean Waterfowl Involves Limited Parallelism at the Molecular Sequence Level. PLOS Genetics 11:12, pages e1005681.
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