[HTML][HTML] CRISPR medicine for blood disorders: progress and challenges in delivery
T Mohammadian Gol, G Ureña-Bailén… - Frontiers in Genome …, 2023 - frontiersin.org
Blood disorders are a group of diseases including hematological neoplasms, clotting
disorders and orphan immune deficiency diseases that affects human health. Current …
disorders and orphan immune deficiency diseases that affects human health. Current …
Mini review: genome and transcriptome editing using CRISPR-cas systems for haematological malignancy gene therapy
EK Elliott, LM Haupt, LR Griffiths - Transgenic Research, 2021 - Springer
The recent introduction of clustered regularly interspaced short palindromic repeats
(CRISPR) and CRISPR associated protein (Cas) systems, offer an array of genome and …
(CRISPR) and CRISPR associated protein (Cas) systems, offer an array of genome and …
Genome editing for blood disorders: state of the art and recent advances
M Romito, R Rai, AJ Thrasher… - Emerging Topics in Life …, 2019 - portlandpress.com
In recent years, tremendous advances have been made in the use of gene editing to
precisely engineer the genome. This technology relies on the activity of a wide range of …
precisely engineer the genome. This technology relies on the activity of a wide range of …
[HTML][HTML] CRISPR-Based Gene Therapies: From Preclinical to Clinical Treatments
In recent years, clustered regularly interspaced short palindromic repeats (CRISPRs) and
CRISPR-associated (Cas) protein have emerged as a revolutionary gene editing tool to treat …
CRISPR-associated (Cas) protein have emerged as a revolutionary gene editing tool to treat …
[PDF][PDF] Comprehensive update on applications of CRISPR/Cas9 for hematological diseases
H Shi, M Jiang, Z Wang - Int J Clin Exp Med, 2017 - e-century.us
There have been significant advances in understanding the genetics and molecular basis of
a number of hematological disorders in recent years, but clinical interventions, such as …
a number of hematological disorders in recent years, but clinical interventions, such as …
[HTML][HTML] CRISPR–Cas9 gene editing induced complex on-target outcomes in human cells
W Wen, XB Zhang - Experimental Hematology, 2022 - Elsevier
Highlights•Unwanted on-target mutation occurs after CRISPR–Cas9 cleavage.•Assessment
of comprehensive on-target outcomes is necessary.•Clinical genomic engineering requires …
of comprehensive on-target outcomes is necessary.•Clinical genomic engineering requires …
CRISPR/Cas9 system: A promising technology for the treatment of inherited and neoplastic hematological diseases
JS Antony, AKMA Haque… - Advances in Cell …, 2018 - Wiley Online Library
The ongoing advent of genome editing with programmable nucleases, including zinc‐finger
nuclease (ZFN), TAL effector nuclease (TALEN), and Clustered Regularly Interspaced Short …
nuclease (ZFN), TAL effector nuclease (TALEN), and Clustered Regularly Interspaced Short …
[HTML][HTML] Current advances of CRISPR-Cas technology in cell therapy
HY Qiu, RJ Ji, Y Zhang - Cell Insight, 2022 - Elsevier
CRISPR-Cas is a versatile genome editing technology that has been broadly applied in both
basic research and translation medicine. Ever since its discovery, the bacterial derived …
basic research and translation medicine. Ever since its discovery, the bacterial derived …
[HTML][HTML] CRISPR–Cas9: New Heights, New Hesitations
K Rich, SF Terry - Genetic Testing and Molecular Biomarkers, 2018 - liebertpub.com
Though the dust is still settling on the contentious CRISPR–Cas9 patent battle, the
conversation surrounding this revolutionary technology has only just begun. Since the …
conversation surrounding this revolutionary technology has only just begun. Since the …
[HTML][HTML] The CRISPR-Cas System and Clinical Applications of CRISPR-Based Gene Editing in Hematology with a Focus on Inherited Germline Predisposition to …
R Kansal - Genes, 2024 - mdpi.com
Clustered regularly interspaced short palindromic repeats (CRISPR)-based gene editing
has begun to transform the treatment landscape of genetic diseases. The history of the …
has begun to transform the treatment landscape of genetic diseases. The history of the …