Generation and characterization of induced pluripotent stem cell line (IGIBi001-A) from a sickle cell anemia patient with homozygous β-globin mutation
Author:
Funder
Council for Scientific and Industrial Research
Ramalingaswami Fellowship, Department of Biotechnology
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,General Medicine
Reference5 articles.
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2. Genereation of three spinocerebellar ataxia type-12 patients derived induced pluripotent stem cell lines (IGIBi002-A, IGIBi003-A and IGIBi004-A);Kumar;Stem Cell Res.,2018
3. Pharmacological and molecular approaches for the treatment of β-hemoglobin disorders;Lohani;J of Cell Physiol,2017
4. Consequences and management of iron overload in sickle cell disease;Porter;Hematology,2013
5. In situ genetic correction of the Sickle cell anemia mutation in human induced pluripotent stem cells using engineered zinc finger nucleases;Sebastiano;Stem cells,2011
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