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Worrawut Chinchang & Vip Viprakasit. (2007) Further Identification of Hb G-Coushatta [β22(B4)Glu→Ala (GAA→GCA)] in Thailand by the Polymerase Chain Reaction-Single-Strand Conformation Polymorphism Technique and by Amplification Refractory Mutation System-Polymerase Chain Reaction. Hemoglobin 31:1, pages 93-99.
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Articles from other publishers (15)
Ezalia Esa, Ahmad Sabry Mohamad, Roszymah Hamzah, Faidatul Syazlin Abdul Hamid, Nur Aisyah Aziz, Veena Sevaratnam, Jameela Sathar, Guo Chen & Norafiza Mohd Yasin. (2023) Clinical and haematological characteristics of 38 individuals with Hb G‐Makassar in Malaysia. eJHaem 4:4, pages 940-948.
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Giulia Hardouin, Elisa MagrinAlice Corsia, Marina Cavazzana, Annarita MiccioMichaela Semeraro. (2023) Sickle Cell Disease: From Genetics to Curative Approaches. Annual Review of Genomics and Human Genetics 24:1, pages 255-275.
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Himanshu Garg, Kristina J. Tatiossian, Karsten Peppel, Gregory J. Kato & Eva Herzog. (2022) Gene Therapy as the New Frontier for Sickle Cell Disease. Current Medicinal Chemistry 29:3, pages 453-466.
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Dibyajyoti Maity & Debnath Pal. (2021) Molecular Dynamics of Hemoglobin Reveals Structural Alterations and Explains the Interactions Driving Sickle Cell Fibrillation. The Journal of Physical Chemistry B 125:35, pages 9921-9933.
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Gregory A. Newby, Jonathan S. Yen, Kaitly J. Woodard, Thiyagaraj Mayuranathan, Cicera R. Lazzarotto, Yichao Li, Heather Sheppard-Tillman, Shaina N. Porter, Yu Yao, Kalin Mayberry, Kelcee A. Everette, Yoonjeong Jang, Christopher J. Podracky, Elizabeth Thaman, Christophe Lechauve, Akshay Sharma, Jordana M. Henderson, Michelle F. Richter, Kevin T. Zhao, Shannon M. Miller, Tina Wang, Luke W. Koblan, Anton P. McCaffrey, John F. Tisdale, Theodosia A. Kalfa, Shondra M. Pruett-Miller, Shengdar Q. Tsai, Mitchell J. Weiss & David R. Liu. (2021) Base editing of haematopoietic stem cells rescues sickle cell disease in mice. Nature 595:7866, pages 295-302.
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Phillip A. Doerfler, Akshay Sharma, Jerlym S. Porter, Yan Zheng, John F. Tisdale & Mitchell J. Weiss. (2021) Genetic therapies for the first molecular disease. Journal of Clinical Investigation 131:8.
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Giacomo Frati & Annarita Miccio. (2021) Genome Editing for β-Hemoglobinopathies: Advances and Challenges. Journal of Clinical Medicine 10:3, pages 482.
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Panagiotis Antoniou, Annarita Miccio & Mégane Brusson. (2021) Base and Prime Editing Technologies for Blood Disorders. Frontiers in Genome Editing 3.
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James B. Papizan, Shaina N. Porter, Akshay Sharma & Shondra M. Pruett-Miller. (2021) Therapeutic gene editing strategies using CRISPR-Cas9 for the β-hemoglobinopathies. The Journal of Biomedical Research 35:2, pages 115.
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Mégane Brusson & Annarita Miccio. 2021. Curing Genetic Diseases Through Genome Reprogramming. Curing Genetic Diseases Through Genome Reprogramming
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Vannarat Saechan, Chawadee Nopparatana, Chamnong Nopparatana & Suthat Fucharoen. (2010) Molecular basis and hematological features of hemoglobin variants in Southern Thailand. International Journal of Hematology 92:3, pages 445-450.
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Vip Viprakasit, Worrawut Chinchang & Pipat Chotimarat. (2006) Hb Woodville, a rare alpha-globin variant, caused by codon 6 mutation of the alpha1 gene. European Journal of Haematology 76:1, pages 79-82.
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Kanokwan Sanchaisuriya, Sunisa Chunpanich, Supan Fucharoen, Goonnapa Fucharoen, Pattara Sanchaisuriya & Yossombat Changtrakun. (2005) Association of Hb Q-Thailand with homozygous Hb E and heterozygous Hb Constant Spring in pregnancy. European Journal of Haematology 74:3, pages 221-227.
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Kanokwan Sanchaisuriya, Sunisa Chunpanich, Goonnapa Fucharoen & Supan Fucharoen. (2004) Multiplex allele-specific PCR assay for differential diagnosis of Hb S, Hb D-Punjab and Hb Tak. Clinica Chimica Acta 343:1-2, pages 129-134.
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