2010
DOI: 10.1007/s11032-010-9442-0
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Genome-wide association mapping of Fusarium head blight resistance in contemporary barley breeding germplasm

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Cited by 145 publications
(139 citation statements)
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“…The developments of numerous molecular markers for various plant species, high throughput sequencing techniques (Metzker, 2009), and modern analytical tools (Yu et al, 2005;Kang et al, 2008;Kang and Sul, 2010;Zhang et al, 2010) have led to new initiatives for utilizing AM to identify causal variants for diverse traits (Zhu et al, 2008) such as flowering time, kernel composition, and kernel color in maize Palaisa et al, 2004;Wilson et al, 2004); developmental and floweringrelated traits in Arabidopsis (Atwell et al, 2010); multiple agronomic traits in sugar beet (Würschum et al, 2011); quality traits in potato (D′Hoop et al, 2008); disease resistance in sugarcane (Wei et al, 2006); wood property traits in Pinus taeda (González-Martínez et al, 2007); disease resistance in barley (Massman et al, 2011); and flowering time in ryegrass (Skøt et al, 2007).…”
Section: Introductionmentioning
confidence: 99%
“…The developments of numerous molecular markers for various plant species, high throughput sequencing techniques (Metzker, 2009), and modern analytical tools (Yu et al, 2005;Kang et al, 2008;Kang and Sul, 2010;Zhang et al, 2010) have led to new initiatives for utilizing AM to identify causal variants for diverse traits (Zhu et al, 2008) such as flowering time, kernel composition, and kernel color in maize Palaisa et al, 2004;Wilson et al, 2004); developmental and floweringrelated traits in Arabidopsis (Atwell et al, 2010); multiple agronomic traits in sugar beet (Würschum et al, 2011); quality traits in potato (D′Hoop et al, 2008); disease resistance in sugarcane (Wei et al, 2006); wood property traits in Pinus taeda (González-Martínez et al, 2007); disease resistance in barley (Massman et al, 2011); and flowering time in ryegrass (Skøt et al, 2007).…”
Section: Introductionmentioning
confidence: 99%
“…In addition, DON content and Fusarium-damaged kernels (FDK) are also used in Canadian barley grading system (Clear et al 1996;Tekauz et al 2000), corresponding to Type III and Type IV resistance in wheat, respectively (Mesterhazy et al 2005). Agronomic and morphological traits have been found to be associated with FHB resistance in barley, which has been elucidated by genetic studies to be derived from either pleiotropic effects or tight linkages (de la Pena et al 1999;Zhu et al 1999;Massman et al 2011). Generally, high stature, late heading, two-row, lack of laterals, lax and nodding spike, hulless, and lodging resistance are often associated with FHB resistance (Steffenson et al 2003;Choo 2006).…”
mentioning
confidence: 99%
“…While, in the past the qualitative resistance, based on monogenetic inheritance, has been successfully used to elite cultivars to improve resistance, the quantitative resistance, which is presumed to be durable, non-race-specific, and effective against a large bouquet of pathogens, is mainly unknown [10]. However, a huge number of quantitative trait loci (QTLs) associated with qualitative resistance against pathogen-associated molecular patterns (PAMs), found for example in soy beans (Glycine max), and with quantitative resistance, found for blast in barley (Hordeum vulgare), or powdery mildew in wheat have already been identified for biotic stress challenges [10,[48][49][50]. But both, the mechanisms of resistance and the metabolites up-regulated during plant stress controlled by the QTLs are mainly unexplored [48].…”
Section: From Biotic Stress Metabolomics To Metabolic Responsementioning
confidence: 99%