We narrowed to 175 results for: ELL

#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

#200011

Knockout library targeting a comprehensive set of mouse genes with annotated function as chromatin regulators.

Bradley Bernstein, Gabriel Griffin, Robert Manguso

Griffin et al Nature. 2021 Jul;595(7866):309-314. doi:

Dec. 15, 2023

Academic Institutions and Nonprofits only

#174296

This library contains mutations to SARS-CoV-2 Spike RBD N501Y variant in which all surface exposed residues on S RBD (Tile 2, positions 437-527) were mutated to every other amino acid.

Timothy Whitehead

Francino-Urdaniz et al Cell Rep. 2021 Aug 31;36(9):109627. doi:

Sept. 13, 2021

Academic Institutions and Nonprofits only

#174295

This library contains mutations to SARS-CoV-2 Spike RBD N501Y variant in which all surface exposed residues on S RBD (Tile 1, positions 333-436) were mutated to every other amino acid.

Timothy Whitehead

Francino-Urdaniz et al Cell Rep. 2021 Aug 31;36(9):109627. doi:

Sept. 13, 2021

Academic Institutions and Nonprofits only

#174294

This library contains mutations to SARS-CoV-2 Spike RBD E484K variant in which all surface exposed residues on S RBD (Tile 2, positions 437-527) were mutated to every other amino acid.

Timothy Whitehead

Francino-Urdaniz et al Cell Rep. 2021 Aug 31;36(9):109627. doi:

Sept. 13, 2021

Academic Institutions and Nonprofits only

#174293

This library contains mutations to SARS-CoV-2 Spike RBD E484K variant in which all surface exposed residues on S RBD (Tile 1, positions 333-436) were mutated to every other amino acid.

Timothy Whitehead

Francino-Urdaniz et al Cell Rep. 2021 Aug 31;36(9):109627. doi:

Sept. 13, 2021

Academic Institutions and Nonprofits only

#140961

Knockout library targeting human genes involved in cellular glycosylation.

Sriram Neelamegham

Zhu et al Glycobiology. 2020 Aug 8. pii: 5889976.

Sept. 9, 2020

Academic Institutions and Nonprofits only

#213927

Uses lentivirus to deliver the library into hard-to-transduce cells

Wenfang Spring Tan

Tan et al PLoS Pathog. 2023 Dec 6;19(12):e1011822.

April 9, 2024

Academic Institutions and Nonprofits only

#213928

Uses the PiggyBac transposon system to deliver the library into hard to transduce cells

Wenfang Spring Tan

Tan et al PLoS Pathog. 2023 Dec 6;19(12):e1011822.

April 9, 2024

Academic Institutions and Nonprofits only

#174163

Cytosine base editors for genome-scale knockout screens in human cells. Targets gene start codons, splice sites, or introduces premature termination codons.

Wensheng Wei

Xu et al Nat Biotechnol. 2021 Jun 21. pii: 10.103

Aug. 31, 2021

Academic Institutions and Nonprofits only

#229137

Donor vector library to introduce TP53 mutations into the endogenous gene locus at exon 5 of human cells via CRISPR-HDR.

Thorsten Stiewe

Funk et al Nat Genet. 2025 Jan;57(1):140-153. doi:

Feb. 24, 2025

Industry, Academic Institutions, and Nonprofits

#229138

Donor vector library to introduce TP53 mutations into the endogenous gene locus at exon 6 of human cells via CRISPR-HDR.

Thorsten Stiewe

Funk et al Nat Genet. 2025 Jan;57(1):140-153. doi:

Feb. 24, 2025

Industry, Academic Institutions, and Nonprofits

#229139

Donor vector library to introduce TP53 mutations into the endogenous gene locus at exon 7 of human cells via CRISPR-HDR.

Thorsten Stiewe

Funk et al Nat Genet. 2025 Jan;57(1):140-153. doi:

Feb. 24, 2025

Industry, Academic Institutions, and Nonprofits

#229140

Donor vector library to introduce TP53 mutations into the endogenous gene locus at exon 8 of human cells via CRISPR-HDR.

Thorsten Stiewe

Funk et al Nat Genet. 2025 Jan;57(1):140-153. doi:

Feb. 24, 2025

Industry, Academic Institutions, and Nonprofits

#248187

The SpeckSeq library is a pooled lentiviral plasmid library containing 229 distinct variants of the MEFV gene, each linked to a unique barcode.

Thomas Henry

Bronnec et al J Exp Med. 2026 Feb 2;223(2):e20251065.

Feb. 6, 2026

Academic Institutions and Nonprofits only