Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia
about
CRISPR-based strategies for studying regulatory elements and chromatin structure in mammalian gene control.Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.Body iron status of children and adolescents with transfusion dependent β-thalassaemia: trends of serum ferritin and associations of optimal body iron control
P2860
Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for β-thalassemia
description
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2017年論文
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2017年論文
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name
Editing an α-globin enhancer i ...... a treatment for β-thalassemia
@en
type
label
Editing an α-globin enhancer i ...... a treatment for β-thalassemia
@en
prefLabel
Editing an α-globin enhancer i ...... a treatment for β-thalassemia
@en
P2093
P2860
P50
P1476
Editing an α-globin enhancer i ...... a treatment for β-thalassemia
@en
P2093
Andreia Coelho
Batchimeg Usukhbayar
Chris A Fisher
Deborah Hay
Jackie A Sloane-Stanley
Jacqueline A Sharpe
Jessica Doondeea
Kevin Clark
P2860
P2888
P356
10.1038/S41467-017-00479-7
P407
P50
P577
2017-09-04T00:00:00Z