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Title
Correction of β-thalassemia mutant by base editor in human embryos
Authors
Keywords
β-thalassemia, <em class=EmphasisTypeItalic >HBB</em> −28 (A>G), base editor, human embryo
Journal
Protein & Cell
Volume 8, Issue 11, Pages 811-822
Publisher
Springer Nature
Online
2017-09-23
DOI
10.1007/s13238-017-0475-6
References
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Related references
Note: Only part of the references are listed.- Editor’s comment on “CRISPR/Cas9-mediated gene editing in human zygotes using Cas9 protein”
- (2017) Stefan Hohmann MOLECULAR GENETICS AND GENOMICS
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- (2017) Y Bill Kim et al. NATURE BIOTECHNOLOGY
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- (2017) Daesik Kim et al. NATURE BIOTECHNOLOGY
- A CRISPR/Cas9 toolkit for efficient targeted base editing to induce genetic variations in rice
- (2017) Bin Ren et al. Science China-Life Sciences
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- (2017) Changyang Zhou et al. Protein & Cell
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- (2017) Puping Liang et al. Protein & Cell
- Electroporation of Cas9 protein/sgRNA into early pronuclear zygotes generates non-mosaic mutants in the mouse
- (2016) Masakazu Hashimoto et al. DEVELOPMENTAL BIOLOGY
- Introducing precise genetic modifications into human 3PN embryos by CRISPR/Cas-mediated genome editing
- (2016) Xiangjin Kang et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- CRISPR/Cas9 β-globin gene targeting in human haematopoietic stem cells
- (2016) Daniel P. Dever et al. NATURE
- Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
- (2016) Alexis C. Komor et al. NATURE
- Survival and complication rates in patients with thalassemia major in Taiwan
- (2016) Han-Ping Wu et al. PEDIATRIC BLOOD & CANCER
- Efficient Production of Gene-Modified Mice using Staphylococcus aureus Cas9
- (2016) Xiya Zhang et al. Scientific Reports
- Derivation of a Homozygous Human Androgenetic Embryonic Stem Cell Line
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- (2015) Puping Liang et al. Protein & Cell
- The inherited diseases of hemoglobin are an emerging global health burden
- (2010) D. J. Weatherall BLOOD
- Beta-thalassemia
- (2010) Antonio Cao et al. GENETICS IN MEDICINE
- Beta-thalassemia
- (2010) Renzo Galanello et al. Orphanet Journal of Rare Diseases
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