We narrowed to 126 results for: Cre

#234855

A CRISPRi library for inducible, genome-wide gene repression in Pseudomonas aeruginosa PA14.

Xue Liu

Zhang et al Nat Commun. 2025 Jul 1;16(1):5870. doi:

June 5, 2025

Academic Institutions and Nonprofits only

#232068

The CRASP-Seq backbone is designed to accommodate the cloning of diverse gRNA libraries. It includes a cell barcode (CBC), which enhances its functionality by enabling library preparation.

Thomas Gonatopoulos-Pournatzis

Behera et al Mol Cell. 2026 Jan 8;86(1):41-59.e15. do

Oct. 28, 2025

Academic Institutions and Nonprofits only

#227708

CRISPR guide RNA library for prime editing

Brittany Adamson

Cirincione et al Nat Methods. 2024 Nov 19. doi: 10.1038/s

Jan. 23, 2025

Academic Institutions and Nonprofits only

#232070

Tiling library to conduct CRASP-Seq experiments combined with high-throughput base editing for precise and scalable investigations into protein regions that affect splicing regulation.

Thomas Gonatopoulos-Pournatzis

Behera et al Mol Cell. 2026 Jan 8;86(1):41-59.e15. do

Oct. 28, 2025

Academic Institutions and Nonprofits only

#183825

Paired gRNA library targeting genes related to B-cell to macrophage transdifferentiation.

Roderic Guigo

Arnan et al BMC Genomics. 2022 May 26;23(1):402. doi

Aug. 25, 2022

Academic Institutions and Nonprofits only

#236783

A genome-wide loss-of-function CRISPR base editing library designed to introduce STOP codons within the first 50% of coding sequences in the genome of Leishmania mexicana.

Tom Beneke

Arias del Angel et al bioRxiv 2025.06.16.659792

April 1, 2026

Academic Institutions and Nonprofits only