Naturally occurring genetic variation in Arabidopsis thaliana.
By M. Koornneef, C. Alonso‐Blanco, D. Vreugdenhil. Annual Review of Plant Biology, 2004
735 citations recorded by the source corpus.
Subfields: Genetics, Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/a253ccd671ae4a1930fc0fa5ee5af3ca5d98aa08
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Genetics
- Edward S. Buckler
- C. Richards
- S. Tonsor
- O. Bossdorf
- T. Rocheford
- Jim Holland
- M. Koornneef
- C. Alonso‐Blanco
In Molecular Biology
In Plant Science
- Edward S. Buckler
- W. Finch‐Savage
- M. Koornneef
- L. Bentsink
- G. Leubner‐Metzger
- S. Tonsor
- M. B. Bitonti
- Maria Greco
Citations in the corpus
- Gene function beyond the single trait: natural variation, gene effects, and evolutionary ecology in Arabidopsis thaliana (2005, methodology): “The functional genomics of flowering time has been reviewed elsewhere (Simpson & Dean 2002; Mouradov, Cremer & Coupland 2002; Koornneef et al. 2004), and natural variation has been a key element of flowering time research (Koornneef et al. 2004).”
- Genome-wide association study of leaf architecture in the maize nested association mapping population (2011, result): “, in contrast with the larger effects observed in self-pollinated plant specie”
- On the Relevance and Control of Leaf Angle (2010, background): “Moreover, it has been introduced in other parts of the Northern hemisphere, including North America, Japan, and Korea (Hoffmann 2002; Koornneef et al., 2004).”
- Evolution of metal hyperaccumulation required cis-regulatory changes and triplication of HMA4 (2008, background): “formed, (2) regenerated from tissue culture following mock transformation and”
- Leaf Responses to Mild Drought Stress in Natural Variants of Arabidopsis1[OPEN] (2015, neutral): “Arabidopsis ( Arabidopsis thaliana ) is found all around the northern hemisphere, with some small patches along the African coast (Hoffmann, 2002; Koornneef et al., 2004), comprising many different habitats, each with speci fi c environmental conditions, and therefore leading to differences in…”
- Natural phenological variation in aspen (Populus tremula): the SwAsp collection (2008, neutral): “The multigenic and quantitative nature of much of the variation in natural populations makes it difficult to identify the genes underlying these traits (Koornneef et al. 2004).”
- New insights into plant responses to the attack from insect herbivores. (2010, background): “Owing to its abundant genetic and genomic resources, Arabidopsis has been intensively studied for its diversity in many phenotypic traits (53).”
- Progress in the genetic understanding of plant iron and zinc nutrition (2006, background): “This analysis is based on the genetic variationwhich exists between accessions of one species and is generally performed on genetic segregating populations like F2s or recombinant inbred line (RIL) populations (Koornneef et al. 2004).”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, positive): “The transcript abundance was normalized against peanut Ubiquitin (Luo et al. , 2005) transcript levels.”
- Seed dormancy and the control of germination. (2006, background): “thaliana (Alonso-Blanco et al., 2003; Clerkx et al., 2004; Koornneef et al., 2004), Brassica oleracea (Bettey et al.”
- The advantages and limitations of trait analysis with GWAS: a review (2013, background): “The key components of the flowering time pathway in Arabidopsis have been dissected in this way [1-3]; for a review of natural variation and QTL mapping in Arabidopsis see [4].”
- Experimental alteration of DNA methylation affects the phenotypic plasticity of ecologically relevant traits in Arabidopsis thaliana (2010, background): “However, because of the growing body of knowledge about its physiology, development and molecular biology, the logistic advantages it affords, and the availability of a broad array of molecular tools, the species is now also frequently used as a model for addressing basic questions at the interface ”
- Sucrose-Specific Induction of Anthocyanin Biosynthesis in Arabidopsis Requires the MYB75/PAP1 Gene1 (2005, background): “…that generate single amino acid substitutions, small deletions that produce truncated protein or altered expression level, large deletions eliminating the complete gene, and large transposon-related insertions in noncoding regulatory regions that alter the expression level (Koornneef et al., 2004).”