The introgressed segment carrying rust resistance genes Yr17, Lr37 and Sr38 in wheat can be assayed by a cloned disease resistance gene-like sequence
By S. Seah, H. Bariana, J. Jahier, K. Sivasithamparam, E. Lagudah. Theoretical and Applied Genetics, 2001
96 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/a1d52c963bc86f63cccd8b7557e97dee5833b2e6
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Citations in the corpus
- An RGA – like marker detects all known Lr21 leaf rust resistance gene family members in Aegilops tauschii and wheat (2001, background): “However, tightly linked PCR-based markers have been developed only for Lr1 (Feuillet et al. 1995), Lr10 (Feuillet et al. 1997), Lr25 and Lr29 (Procunier et al. 1995), Lr28 (Naik et al. 1998), Lr35 (Seyfarth et al. 1999) and Lr37 ( Seah et al. 2000 ).”
- PCR assays for the Lr37-Yr17-Sr38 cluster of rust resistance genes and their use to develop isogenic hard red spring wheat lines (2003, background): “Seah et al. (2001) Diploid species with genomes related to A, B, and developed a PCR marker from the sequence of a nucleo-D genomes from bread wheat offer a pool of traits tide-binding-site leucine-rich repeat disease resistance that can be used to increase genetic diversity in wheat. gene located…”
- Molecular-genetic characterisation of a new nematode resistance gene in wheat (2001, background): “Several clones that hybridised to DNA probes derived from the Cre3 CCN resistant locus were isolated from the Ae. ventricosa #11 genomic DNA library in bacteriophage lambda ( Seah et al. 2001a ).”
- Trends in genetic and genome analyses in wheat: a review (2001, methodology): “Through the pioneering work of Sears (1954), a series of lines was generated, based on the variety Chinese Spring, where individual pairs of chromosomes were deleted and replaced by an extra chromosome pair from the homoeologous group.”
- Epidemiology and control of stripe rust [Puccinia striiformis f. sp. tritici] on wheat (2005, methodology): “Most of the markers were identified using RAPD, SSR, and AFLP techniques, while the markers for Yr17 were identified using the clone of a gene-like sequence for resistance to disease (Seah et al. 2001).”