CRISPR/Cas9-mediated mutation of PHEX in rabbit recapitulates human X-linked hypophosphatemia (XLH).
about
Rabbit models for biomedical research revisited via genome editing approaches.Principles and Applications of Rabbit Models for Atherosclerosis Research.Production of Wilson Disease Model Rabbits with Homology-Directed Precision Point Mutations in the ATP7B Gene Using the CRISPR/Cas9 System.Truncated C-terminus of fibrillin-1 induces Marfanoid-progeroid-lipodystrophy (MPL) syndrome in rabbit.Development of muscular dystrophy in a CRISPR-engineered mutant rabbit model with frame-disrupting ANO5 mutations.A novel rabbit model of Duchenne muscular dystrophy generated by CRISPR/Cas9.Highly efficient RNA-guided base editing in rabbit.CRISPR-induced exon skipping is dependent on premature termination codon mutations
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P2860
CRISPR/Cas9-mediated mutation of PHEX in rabbit recapitulates human X-linked hypophosphatemia (XLH).
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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name
CRISPR/Cas9-mediated mutation ...... linked hypophosphatemia (XLH).
@en
CRISPR/Cas9-mediated mutation ...... uman X-linked hypophosphatemia
@nl
type
label
CRISPR/Cas9-mediated mutation ...... linked hypophosphatemia (XLH).
@en
CRISPR/Cas9-mediated mutation ...... uman X-linked hypophosphatemia
@nl
prefLabel
CRISPR/Cas9-mediated mutation ...... linked hypophosphatemia (XLH).
@en
CRISPR/Cas9-mediated mutation ...... uman X-linked hypophosphatemia
@nl
P2093
P2860
P356
P1476
CRISPR/Cas9-mediated mutation ...... linked hypophosphatemia (XLH).
@en
P2093
Jichao Deng
Liangxue Lai
Tingting Sui
Zhanjun Li
P2860
P304
P356
10.1093/HMG/DDW125
P577
2016-04-28T00:00:00Z