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SZ, PM, LG, OR, GS and PA carried out the DNA extraction and sample quantification.
JMA, VB, SM, OR, GS, VA, FA, CS and PW analysed data.
To isolate germline-conditioned flies, heterozygous tud 1 bw 1 sp1 1 /CyO or gs(1) N441 /femalesales were crossed to tud 1 bw 1 sp 1 /CyO or gs(1) N441 /Y males respectively which gave germline-conditioned homozygous mutant females.
Furthermore, the selected descriptors in the list can also be changed from the visible nodes on Gp or Gs.
The NH4+-induced OsAS1 expression was inhibited when GS1 2 was missing or GS activity was inhibited by MSX treatment (Figs. 4, 5, Additional file 2: Figure S2).
The responses of Pnm, Pna and gs to salinity could be further described by a general model of log y) = a1 + a2x + a3x2, where y represents either Pnm, Pna, or gs; a1, a2 and a3, empirical constants; x, salinity.
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Then linear maps preserving lgw-majorization or gs-majorization and linear maps, preserving rgw-majorization are characterized.
As shown in Fig. 5, the cell viability is above 80%% for GS, GS-PEG-Apt, or GS-PEG/HA2-Apt NP groups within the tested concentration range, and the cytotoxicity appeared dose-dependent.
Fusion of V5-His or GS-SBP-His tags to the rsβ3 integrins resulted in high-yield expression.
Quantification was performed by densitometric analysis (GS-700 or GS-800, BioRad) of autoradiography films (Amersham Hyperfilm) using the Quantity One software (BioRad).
For the determination of SEAP levels, cells were treated with DMSO or GS-E for 48 hours.
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