Paper · 41365890
Efficient high-precision transgene knock-in by Recombinases (Redα/β)-enhanced DNA integration-CRISPR-Cas9 (RED-CRISPR).
Li W and 17 others. Nat Commun, 2025. Cited by 6 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. Efficient high-precision transgene knock-in by Recombinases (Redα/β)-enhanced DNA integration-CRISPR-Cas9 (RED-CRISPR). Papers, record 41365890. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41365890
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Efficient high-precision transgene knock-in by Recombinases (Redα/β)-enhanced DNA integration-CRISPR-Cas9 (RED-CRISPR).
- PubMed
Topics11
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| CRISPR-Cas Systems | Major topic |
| Gene Knock-In Techniques | Major topic |
| Transgenes | Major topic |
| Gene Editing | Major topic |
| Recombinases | Major topic |
| Animals | |
| Mice | |
| Humans | |
| Recombinational DNA Repair | |
| DNA | |
| HEK293 Cells |
Source PubMed
Grants0
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None in this release.
Trials0
The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.
None in this release.
Comments and corrections0
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References101
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 18,230,724 | Identification and analysis of recombineering functions from Gram-negative and Gram-positive bacteria and their phages. | Proc Natl Acad Sci U S A | 2008 | https://conductscience.org/library/papers/18230724 | PubMed |
| 2 | 35,534,455 | Targeting double-strand break indel byproducts with secondary guide RNAs improves Cas9 HDR-mediated genome editing efficiencies. | Nat Commun | 2022 | https://conductscience.org/library/papers/35534455 | PubMed |
| 3 | 10,585,965 | Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda. | Microbiol Mol Biol Rev | 1999 | https://conductscience.org/library/papers/10585965 | PubMed |
| 4 | 36,153,319 | Comprehensive assessment of miniature CRISPR-Cas12f nucleases for gene disruption. | Nat Commun | 2022 | https://conductscience.org/library/papers/36153319 | PubMed |
| 5 | 10,921,910 | RecE/RecT and Redalpha/Redbeta initiate double-stranded break repair by specifically interacting with their respective partners. | Genes Dev | 2000 | https://conductscience.org/library/papers/10921910 | PubMed |
| 6 | 31,147,612 | The next generation of CRISPR-Cas technologies and applications. | Nat Rev Mol Cell Biol | 2019 | https://conductscience.org/library/papers/31147612 | PubMed |
| 7 | 26,923,600 | Improved Genome Editing Efficiency and Flexibility Using Modified Oligonucleotides with TALEN and CRISPR-Cas9 Nucleases. | Cell Rep | 2016 | https://conductscience.org/library/papers/26923600 | PubMed |
| 8 | 36,639,728 | Assessing and advancing the safety of CRISPR-Cas tools: from DNA to RNA editing. | Nat Commun | 2023 | https://conductscience.org/library/papers/36639728 | PubMed |
| 9 | 5,553,408 | The role of exonuclease and beta protein of phage lambda in genetic recombination. 3. Binding to deoxyribonucleic acid. | J Biol Chem | 1971 | https://conductscience.org/library/papers/5553408 | PubMed |
| 10 | 21,243,013 | Efficient human iPS cell derivation by a non-integrating plasmid from blood cells with unique epigenetic and gene expression signatures. | Cell Res | 2011 | https://conductscience.org/library/papers/21243013 | PubMed |
1 to 10 of 101
See all 101 referencesCited by6
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 6 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,891,351 | Strategies and mechanisms of precision genome engineering: From gene editing to genome writing. | IMetaOmics | 2026 | https://conductscience.org/library/papers/42891351 | PubMed |
| 42,755,359 | Large serine recombinase-mediated gene insertion for high-throughput screens: advantages, design principles, and applications. | Nucleic Acids Res | 2026 | https://conductscience.org/library/papers/42755359 | PubMed |
| 42,464,282 | Establishment of SRLC: a multiplex genome editing technology for Saccharomyces cerevisiae and its application in metabolic engineering of malonyl-CoA pathway. | Microb Cell Fact | 2026 | https://conductscience.org/library/papers/42464282 | PubMed |
| 42,373,632 | Development of efficient genetic toolkits and heterologous chassis for bioprospecting of myxobacteria. | Nat Commun | 2026 | https://conductscience.org/library/papers/42373632 | PubMed |
| 41,993,426 | Ultra-large targeted DNA integrations in primary human cells. | bioRxiv | 2026 | https://conductscience.org/library/papers/41993426 | PubMed |
| 41,914,500 | Enhancement of single-stranded template annealing activity by Rad52 during repair of CRISPR-induced dsDNA breaks. | Nucleic Acids Res | 2026 | https://conductscience.org/library/papers/41914500 | PubMed |
Genes0
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
None in this release.
Drugs0
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None in this release.
Data0
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None in this release.
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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