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No study with regard to IPT and ZOG genes has yet been reported for wheat.
The high transferability among Triticeae species and genera has also been reported for wheat EST-SSR markers.
To our knowledge, this is the first time that such microstructural observations have been reported for wheat endosperm digested in the upper gastrointestinal tract of humans.
Although numerous miRNAs have been identified in many plant species, only 42 sequences have been reported for wheat in the miRBase registry (miRBase release 20).
A number of centromere-specific sequences have been reported for wheat and its relatives, including 15 Ty3/ gypsy-type centromeric retrotransposons in wheat (CRW) [ 50], one centromeric satellite-like repeat (contig310431) in wheat [ 51], one Ty3/ gypsy retrotransposon CCS1-R11H-2 CCS1-R11H-2 CCS1-R11H-2, and one DNA marker sequence (KF719092) in rye.
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Similar redundancy estimates, including lower redundancy in un-subtracted libraries, are reported for wheat [11], tomato, sorghum and sugarcane (DArT P/L, unpublished).
For rice, 516 Sr measurements and 513 Cs measurements were reported; for wheat, 363 Sr measurements and 355 Cs measurements.
Quite poor cross-population predictions were reported for wheat [ 31], in the presence of partly related populations evaluated under the same phenotyping conditions.
The homeologous forms in oat show similar or even a higher percentage of identity among them than was reported for wheat, with 90-99% identity at the nucleotide level and often identical at the amino acid level [ 9].
Investigations of the accuracy of GEBV predictions using empirical data have been reported for maize, barley, wheat and Arabidopsis thaliana (Table 2).
Comparable treatment parameter trends have been reported for alkali pretreatment of wheat straws [ 19].
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