Arabidopsis : a laboratory manual

By Detlef Weigel, Jane Glazebrook. 2002

1,037 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/2de391bbe6978e6a6209e923b287898c5543e8c5

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

Citations in the corpus

A Downstream Mediator in the Growth Repression Limb of the Jasmonate Pathway[W][OA] (2007, background): “Each of the eight cDNAs (representing seven genes) were then cloned under the control of the 35S promoter and transformed into Arabidopsis (Weigel and Glazebrook, 2002).”
Antagonistic Interaction between Abscisic Acid and Jasmonate-Ethylene Signaling Pathways Modulates Defense Gene Expression and Disease Resistance in Arabidopsis (2004, methodology): “Protoplasts were produced from leaf segments and transformations performed according to Weigel and Glazebrook (2001).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, unknown): “Flowers and siliques were removed from 6-week-old soil-grown plants and stained for GUS expression (Weigel and Glazebrook, 2002).”
Cadmium and arsenic affect root development in Oryza sativa L. negatively interacting with auxin. (2018, methodology): “Samples were cleared with chloral hydrate solution (Weigel and Glazebrook, 2002), mounted on microscope slides, and observed with Nomarski optics applied to a Leica DMRB optical microscope equipped with a Leica DC 500 camera.”
Highly Specific Gene Silencing by Artificial MicroRNAs in Arabidopsis[W][OA] (2006, methodology): “Transgenic plants were generated by Agrobacterium tumefaciens– mediated transformation (Weigel and Glazebrook, 2002).”
Genetic Transformation and Hybridization (2002, unknown): “Agrobacterium cells harboring the binary vector were grown for 24 h in Luria Butani (LB) medium (Weigel and Glazebrook 2002) supplemented with 50 mg/l rifampicin, 50 mg/l kanamycin, and 50 mg/l gentamycin on an orbital shaker at 28◦C and 250 rpm.”
Repression of AUXIN RESPONSE FACTOR10 by microRNA160 is critical for seed germination and post-germination stages. (2007, methodology): “GUS staining of seeds and seedlings was performed as previously described (Weigel and Glazebrook, 2002) using 100 mM sodium phosphate buffer (pH 7.”