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In spite of considerable efforts in developing molecular markers in maize, the number of SSRs publicly available is still limited.
In typical association mapping studies in maize, the number of genotypes in a population ranges between around 100 and 500 individuals [ 58].
In maize, the number of nonadditively expressed genes and the degree of their expression increase from duplex to quadruplex hybrids (Riddle et al. 2010).
In maize, the number of gene fragments acquired per exemplar is reported to range from 1 to 9 (Du et al. 2009; Yang and Bennetzen 2009a), where as in M. lucifugus, it is 1 2.
Of the 1831 identified lincRNAs in maize, the number of lincRNAs that had the inferred function (34 lincRNAs as miRNA target, 86 lincRNAs as miRNA decoys) was still limited, which is consistent with the diverse mechanism of action of lincRNAs [ 15, 22].
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**For reasons of ongoing annotating and unexpected complexity in maize, the numbers here may not reflect the integrated UPS profile for maize.
Nevertheless in both plant species a high loading 7 mg L−1 FLT significantly reduced both growth (total length by 95% in pea, 94% in maize) and the number of lateral roots (by 78% in pea, 94% in maize).
The smaller number of SNPs reported here reflects a number of important limitations, including: the reduced nucleotide diversity of sorghum compared with maize; the reduced number of families compared with NAM (5 vs. 25); the use of partially isogenic families rather than a reference design; and the genotyping method used (GBS vs. whole genome resequencing).
Since the first RF was sequenced and identified in maize, the increasing numbers of RF genes have provided an ongoing challenge in their clear identification and logical classification across species.
The variability of maize sold determined the number of vendors interviewed at each market.
Hsfs were distributed in every chromosome of the maize genome, however, the number of Hsf genes on each chromosome varied widely.
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