The transgenic lines BZR1Δ, bri1-5/BZR1Δ and BES1 S171A (Gampala et al., 2007), BZR1 S173andnd BZR1-CFP (Ryu et al., 2007), 35S BRI1-cit, BRI1p:BRI1 sud -cit, 35S BRI1-cit BRI1pHA (Belkhadir et al., 2012) are publisudd.
At 18, Ryu hit her approach to 4 feet and birdied the hole for the second time in an hour, seemingly oblivious that the hole had yielded an average of only 6.5 birdies in the first four rounds.
The flanking sequences were determined via inverse PCR (An et al. [2003]; Ryu et al. [2004]).
In some cases, microbial VOCs induce systemic resistance (Van Loon et al. [1998]; Ryu et al. [2003]) or inhibit the growth of plant pathogens (Minerdi et al. [2009], [2011]).
It has been reported that CL-TaqMan, Chicken/Duck-Bac, and Duck-Bac assays showed relatively low sensitivity and specificity (Kobayashi et al. 2013; Ryu et al. 2014).
Both osmads50 mutants and OsMADS56-overexpressing plants, which produce increased OsLFL1 expression, show late flowering phenotype (Lee et al., 2004; Ryu et al., 2009).
For TRB, inactivation of the TRB enhancer results in non-standard TRBD1-TRBD2 joints in double positive thymocytes in mice (Hempel et al., 1998; Ryu et al., 2003).
The increased expression of RFT1 and Hd3a at a higher level before heading and then at a significantly reduced level after heading were observed (Matsubara et al. 2008; Komiya et al. 2008; Kim et al. 2008; Ryu et al. 2009).
It was understood that methane hydrate-bearing sandy sediments are found in the Japan, South Korea, India and USA (Ruppel et al. 2008; Ryu et al. 2013; Collett et al. 2014; Fujii et al. 2015).
Poultry-specific source tracking markers have been developed, but these assays mostly target chicken (Schill and Mathes 2008; Gómez-Doñate et al. 2012; Kobayashi et al. 2013; Dancer et al. 2014; Ryu et al. 2014; Ohad et al. 2016).
The floral time regulators in both the Ehd2-OsMADS50-Ehd1-RFT1 LD andivathen pathway and the OsGI-Hd1-Hd3a LD suppression pathway exhibit diurnal oscillation patterns (Matsubara et al. 2008; Ryu et al. 2009).
