Paper · 41279409
Adapting CRISPR-associated transposons for rapid and high-throughput reverse genetics.
Basta DW and 5 others. bioRxiv, 2025. Cited by 0 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. Adapting CRISPR-associated transposons for rapid and high-throughput reverse genetics. Papers, record 41279409. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41279409
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Paper
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Topics0
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Grants2
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| Grant, as the record writes it | Agency | Country | NIH project | Stated by | Source |
|---|---|---|---|---|---|
| R01 AI042347 | NIAID NIH HHS | United States | R01AI042347 | PubMed and NIH | NIH RePORTER |
| T32 AI007061 | NIAID NIH HHS | United States | T32AI007061 | PubMed and NIH | NIH RePORTER |
Trials0
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None in this release.
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References50
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 | 36,304,290 | ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program. | Front Bioinform | 2022 | https://conductscience.org/library/papers/36304290 | PubMed |
| 2 | 39,631,148 | The promise of CRISPR-associated transposons for bacterial functional genomics. | Curr Opin Microbiol | 2025 | https://conductscience.org/library/papers/39631148 | PubMed |
| 3 | 28,811,374 | Recruitment of CRISPR-Cas systems by Tn7-like transposons. | Proc Natl Acad Sci U S A | 2017 | https://conductscience.org/library/papers/28811374 | PubMed |
| 4 | 33,271,061 | Guide RNA Categorization Enables Target Site Choice in Tn7-CRISPR-Cas Transposons. | Cell | 2020 | https://conductscience.org/library/papers/33271061 | PubMed |
| 5 | 36,384,163 | Functional characterization of diverse type I-F CRISPR-associated transposons. | Nucleic Acids Res | 2022 | https://conductscience.org/library/papers/36384163 | PubMed |
| 6 | 20,659,289 | H-NS-mediated repression of CRISPR-based immunity in Escherichia coli K12 can be relieved by the transcription activator LeuO. | Mol Microbiol | 2010 | https://conductscience.org/library/papers/20659289 | PubMed |
| 7 | 35,051,352 | Evolutionary and mechanistic diversity of Type I-F CRISPR-associated transposons. | Mol Cell | 2022 | https://conductscience.org/library/papers/35051352 | PubMed |
| 8 | 32,994,326 | Gene Dispensability in Escherichia coli Grown in Thirty Different Carbon Environments. | mBio | 2020 | https://conductscience.org/library/papers/32994326 | PubMed |
| 9 | 27,578,758 | The Nucleoid Binding Protein H-NS Biases Genome-Wide Transposon Insertion Landscapes. | mBio | 2016 | https://conductscience.org/library/papers/27578758 | PubMed |
| 10 | 34,478,496 | Orthogonal CRISPR-associated transposases for parallel and multiplexed chromosomal integration. | Nucleic Acids Res | 2021 | https://conductscience.org/library/papers/34478496 | PubMed |
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Drugs0
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None in this release.
Data0
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None in this release.
Data dates
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- 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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