Systems and methods for treating hemoglobinopathies
Genome editing systems, guide RNA and CRISPR-mediated methods are provided for altering portions of HBG1 and HBG2 loci in a cell and increasing expression of fetal hemoglobin. 提供了基因组编辑系统、向导RNA和CRISPR介导的方法,用于改变细胞中的HBG1和HBG2基因座的部分并且增加胎儿血红蛋白的表达。...
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Format | Patent |
Language | Chinese English |
Published |
26.04.2024
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Abstract | Genome editing systems, guide RNA and CRISPR-mediated methods are provided for altering portions of HBG1 and HBG2 loci in a cell and increasing expression of fetal hemoglobin.
提供了基因组编辑系统、向导RNA和CRISPR介导的方法,用于改变细胞中的HBG1和HBG2基因座的部分并且增加胎儿血红蛋白的表达。 |
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AbstractList | Genome editing systems, guide RNA and CRISPR-mediated methods are provided for altering portions of HBG1 and HBG2 loci in a cell and increasing expression of fetal hemoglobin.
提供了基因组编辑系统、向导RNA和CRISPR介导的方法,用于改变细胞中的HBG1和HBG2基因座的部分并且增加胎儿血红蛋白的表达。 |
Author | CHANG KWANHO |
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DocumentTitleAlternate | 用于治疗血红蛋白病的系统和方法 |
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Title | Systems and methods for treating hemoglobinopathies |
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