H. Rees
Molecular Biology · 2017–2020
A researcher in the Science corpus: 5 papers; trusts 9 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 170 citations into it; #16,355 of 17,773 by trust here, #4,806 by citations
- Oncology — 8 citations into it
Whom H. Rees trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts H. Rees overall
Papers from H. Rees's perspective
Ordered by how strongly the researchers H. Rees trusts endorse each paper. Same corpus, a different order for every researcher.
- Comparison of non-canonical PAMs for CRISPR/Cas9-mediated DNA cleavage in human cells
- Rationally engineered Cas9 nucleases with improved specificity
- Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
- Identifying DNA sequences recognized by a transcription factor using a bacterial one-hybrid system
- Activation of prokaryotic transcription through arbitrary protein–protein contacts
- Directed evolution converts subtilisin E into a functional equivalent of thermitase.
- Twenty years of the MEROPS database of proteolytic enzymes, their substrates and inhibitors
- Highly-efficient Cas9-mediated transcriptional programming
- Continuous directed evolution of aminoacyl-tRNA synthetases
- Cytosine base editor generates substantial off-target single-nucleotide variants in mouse embryos (Science)
Their papers
- Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage (2017) — 5,379 citations
- Evolved Cas9 variants with broad PAM compatibility and high DNA specificity (2018) — 1,381 citations
- Cytosine base editors with minimized unguided DNA and RNA off-target events and high on-target activity (2020) — 115 citations
- Base editing: precision chemistry on the genome and transcriptome of living cells (2018) — 1,428 citations
- Phage-assisted continuous evolution of proteases with altered substrate specificity (2017) — 114 citations