mRNA Display in Cell Lysates Enables Identification of Cyclic Peptides Targeting the BRD3 Extraterminal Domain.

Hurd, Catherine A et al.·Angewandte Chemie (International ed. in English)·2024·
RPEP-084192024RETHINKTHC RESEARCH DATABASErethinkthc.com/research

Quick Facts

Study Type
Not classified
Evidence
Not graded
Sample
Not reported

What This Study Found

Key Numbers

How They Did This

Why This Research Matters

What This Study Doesn't Tell Us

Trust & Context

Original Title:
mRNA Display in Cell Lysates Enables Identification of Cyclic Peptides Targeting the BRD3 Extraterminal Domain.
Published In:
Angewandte Chemie (International ed. in English), 63(38), e202406414 (2024)
Database ID:
RPEP-08419

Evidence Hierarchy

Meta-Analysis / Systematic Review
Randomized Controlled Trial
Cohort / Case-Control
Cross-Sectional / ObservationalSnapshot without intervening
This study
Case Report / Animal Study
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Cite This Study

RPEP-08419·https://rethinkpeptides.com/research/RPEP-08419

APA

Hurd, Catherine A; Bush, Jacob T; Powell, Andrew J; Walport, Louise J. (2024). mRNA Display in Cell Lysates Enables Identification of Cyclic Peptides Targeting the BRD3 Extraterminal Domain.. Angewandte Chemie (International ed. in English), 63(38), e202406414. https://doi.org/10.1002/anie.202406414

MLA

Hurd, Catherine A, et al. "mRNA Display in Cell Lysates Enables Identification of Cyclic Peptides Targeting the BRD3 Extraterminal Domain.." Angewandte Chemie (International ed. in English), 2024. https://doi.org/10.1002/anie.202406414

RethinkPeptides

RethinkPeptides Research Database. "mRNA Display in Cell Lysates Enables Identification of Cycli..." RPEP-08419. Retrieved from https://rethinkpeptides.com/research/hurd-2024-mrna-display-in-cell

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Study data sourced from PubMed, a service of the U.S. National Library of Medicine, National Institutes of Health.

This study breakdown was produced by the RethinkPeptides research team. We analyze and report published research findings without making health recommendations. All interpretations are based solely on the published abstract and study data.