Optimising CRISPR for targeting of primary haematopoietic stem cells
<p>CRISPR (clustered regularly interspaced short palindromic repeats) offers an unprecedented array of genetic tools for treating and modelling haematological disorders. However, there are concerns about its safety. CRISPR-based editing can induce upregulation of TP53 associated pathways, a f...
المؤلف الرئيسي: | Field, L |
---|---|
مؤلفون آخرون: | Mead, A |
التنسيق: | أطروحة |
اللغة: | English |
منشور في: |
2021
|
الموضوعات: |
مواد مشابهة
-
Fluorescent tagging of endogenous proteins with CRISPR/Cas9 in primary mouse neural stem cells
حسب: Christopher S. Morrow, وآخرون
منشور في: (2021-09-01) -
Notch signalling in Xenopus laevis haematopoietic stem cell programming
حسب: Stephenson, RA
منشور في: (2013) -
Protocol for in vivo CRISPR screening targeting murine testicular cells
حسب: Yuki Noguchi, وآخرون
منشور في: (2024-09-01) -
The emergence and early fate decisions of stem and progenitor cells in the haematopoietic system
حسب: Lutteropp, M
منشور في: (2012) -
Efficient isolation of mouse deletion mutant embryonic stem cells by CRISPR
حسب: Yuhan Liu, وآخرون
منشور في: (2022-06-01)