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Crispr Gene Editing — Hindsite — Hindsite

Event

Crispr Gene Editing

707 sources spanning 2022–2025

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Overview

CRISPR gene editing (; pronounced like "crisper"; an abbreviation for "clustered regularly interspaced short palindromic repeats") is a genetic engineering technique in molecular biology by which the genomes of living organisms may be modified. It is based on a simplified version of the bacterial CRISPR-Cas9 antiviral defense system. By delivering the Cas9 nuclease complexed with a synthetic guide RNA (gRNA) into a cell, the cell's genome can be cut at a desired location, allowing existing...

2025

Precisely defining disease variant effects in CRISPR-edited single cells.GOV23 Jul 2025

Epigenetic editing at individual age-associated CpGs affects the genome-wide epigenetic aging landscape.24 Mar 2025

Congratulations, #Bahrain, on successfully administering first CRISPR-based sickle cell treatment. Thank you for your continued investment in science to ensure all people in 🇧🇭 have the best possible care and to help the world advance medical treatment17 Feb 2025

Bahrain conducts 1st CRISPR-based sickle cell treatment outside U.S.17 Feb 2025

HRH the Crown Prince and Prime Minister visits the world's first sickle cell disease patient outside of the United States to successfully complete treatment with Casgevy16 Feb 2025

2024

Gene editing for allergen amelioration in plants – A review12 Dec 2024

CRISPR en agricultura: 2024 en revisión10 Dec 2024

Roll out of revolutionary gene-editing therapy is 'an historic moment8 Aug 2024

Seven diseases CRISPR technology could cure4 Apr 2024

Epigenetic modification: A novel insight into diabetic wound healingGOV30 Mar 2024

Scientists say they can cut HIV out of cells20 Mar 2024

2023

FDA Approves First Gene Therapies to Treat Patients with Sickle Cell DiseaseGOV11 Dec 2023

CASGEVY receives Bahrain approval for treatment, marking it the second country in the world2 Dec 2023

Casgevy: UK approves gene-editing drug for sickle cell16 Nov 2023

MHRA authorises world-first gene therapy that aims to cure sickle-cell disease and transfusion-dependent β-thalassemia16 Nov 2023

Casgevy: UK approves gene-editing drug for sickle cell16 Nov 2023

Efficient high-precision homology-directed repair-dependent genome editing by HDRobust12 Sep 2023

Efficient high-precision homology-directed repair-dependent genome editing by HDRobustGOV12 Sep 2023

Efficient high-precision homology-directed repair-dependent genome editing by HDRobustGOV20 Jul 2023

Modulating mutational outcomes and improving precise gene editing at CRISPR-Cas9-induced breaks by chemical inhibition of end-joining pathwaysGOV12 Jul 2023

Loss-function mutants of OsCKX gene family based on CRISPR-Cas systems revealed their diversified roles in rice12 Jun 2023

Drag-and-drop genome insertion of large sequences without double-strand DNA cleavage using CRISPR-directed integrases12 Apr 2023

Modulating mutational outcomes and improving precise gene editing at CRISPR-Cas9-induced breaks by chemical inhibition of end-joining pathways12 Feb 2023

Modulating mutational outcomes and improving precise gene editing at CRISPR-Cas9-induced breaks by chemical inhibition of end-joining pathways12 Feb 2023

2022

Base editing: Revolutionary therapy clears girl's incurable cancer11 Dec 2022

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