Modular cloning in plant cells.
By M. Karimi, Björn De Meyer, P. Hilson. Trends in Plant Science, 2005
621 citations recorded by the source corpus.
Subfields: Biotechnology, Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/8bd1ee973059e0117751f7ed9496c5d79fb7ad15
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- T. Beeckman
- M. B. Bitonti
- Malcolm J. Bennett
- Maria Greco
- Craig S. Pikaard
- O. Pontes
- J. Haag
- A. Chiappetta
In Plant Science
- T. Beeckman
- M. B. Bitonti
- Malcolm J. Bennett
- Maria Greco
- A. Séguin
- Craig S. Pikaard
- O. Pontes
- J. Haag
Citations in the corpus
- A Heat-Inducible Transcription Factor, HsfA2, Is Required for Extension of Acquired Thermotolerance in Arabidopsis1[W][OA] (2006, methodology): “The cloned HsfA2 genomic DNA was then subcloned into pBGW,0 (Karimi et al., 2005) by an in vitro recombinase method to yield the binary vector pYC112, which was then transferred into Agrobacterium tumefaciens LBA4404 strain for Arabidopsis (Col-0) transformation by the floral dip method (Clough and…”
- Gateway-compatible vectors for plant functional genomics and proteomics. (2006, background): “…Inducible RNAi Rubio et al. (2005) TAP protein purification Protein A IgG binding domain, cMyc-His Tzfira et al. (2005) Protein localization GFP Karimi et al. (2005) Multicomponent recombination http://www.psb.ugent.be/gateway/ Albrecht von Arnim (University of Tennessee, Knoxville, TN, USA,…”
- A novel sensor to map auxin response and distribution at high spatio-temporal resolution (2012, methodology): “1 ) and put under the control of the strong constitutive CaMV 35S promoter, using a 35S promoter cloned in pDONR P4-P1R and recombination into the gateway-compatible pH7m34GW binary vecto”
- Molecular characterization of EgMYB1, a putative transcriptional repressor of the lignin biosynthetic pathway (2007, methodology): “LR recombination reaction with the GATEWAY1 binary expression vector pH7CWG2 [20] generated the expression vector EgMyb1-CFP.”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, positive): “PCR products were cloned using the Gateway® system (Invitrogen) with TOPO isomerase mix into the pENTRTM/DTOPO® entry, followed by LR clonase recombination with pKGWFS7 (VIB, Gent, Belgium) (Karimi et al., 2005).”