ASXL1 mutation correction by CRISPR/Cas9 restores gene function in leukemia cells and increases survival in mouse xenografts.
about
P1343
The CRISPR/Cas9 system efficiently reverts the tumorigenic ability of BCR/ABL in vitro and in a xenograft model of chronic myeloid leukemia.Hepatitis B Virus X Protein Stimulates Proliferation, Wound Closure and Inhibits Apoptosis of HuH-7 Cells via CDC42.COL7A1 Editing via CRISPR/Cas9 in Recessive Dystrophic Epidermolysis Bullosa.The Application of CRISPR/Cas Technology to Efficiently Model Complex Cancer Genomes in Stem Cells.CRISPR-Cas9 technology and its application in haematological disorders.The Role of Additional Sex Combs-Like Proteins in Cancer.Therapeutic gene editing: delivery and regulatory perspectivesSelective disruption of an oncogenic mutant allele by CRISPR/Cas9 induces efficient tumor regressionAddressing challenges in the clinical applications associated with CRISPR/Cas9 technology and ethical questions to prevent its misuse.CRISPR/Cas9-mediated ASXL1 mutations in U937 cells disrupt myeloid differentiation.Oncolytic Virus-Mediated RAS Targeting in Rhabdomyosarcoma
P2860
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P2860
ASXL1 mutation correction by CRISPR/Cas9 restores gene function in leukemia cells and increases survival in mouse xenografts.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
ASXL1 mutation correction by C ...... survival in mouse xenografts.
@en
type
label
ASXL1 mutation correction by C ...... survival in mouse xenografts.
@en
prefLabel
ASXL1 mutation correction by C ...... survival in mouse xenografts.
@en
P2093
P2860
P356
P1433
P1476
ASXL1 mutation correction by C ...... s survival in mouse xenografts
@en
P2093
Amit Verma
Andrea Pellagatti
Anna Schuh
Bon Ham Yip
Erica Bello
Hamid Dolatshad
Jacqueline Boultwood
Jacqueline Shaw
Laura Scifo
Shanisha Gordon
P2860
P304
44061-44071
P356
10.18632/ONCOTARGET.6392
P407
P577
2015-12-01T00:00:00Z