User contributions
- 14:47, 8 June 2014 (diff | hist) . . (+1,526) . . GW5 (current)
- 14:37, 8 June 2014 (diff | hist) . . (+787) . . GW5
- 14:32, 8 June 2014 (diff | hist) . . (+546) . . GW5
- 14:25, 8 June 2014 (diff | hist) . . (+680) . . GW5
- 14:22, 8 June 2014 (diff | hist) . . (+943) . . GW5
- 14:17, 8 June 2014 (diff | hist) . . (+787) . . GW5
- 14:10, 8 June 2014 (diff | hist) . . (+89) . . N File:Ma207.jpg (Figure 7.—Physical-to-genetic distance ratios in 10 marker intervals near the GW5 gene.) (current)
- 14:09, 8 June 2014 (diff | hist) . . (+1,125) . . N File:Ma206.jpg (Figure 6.—Genetic and physical maps of the gw-5 gene on rice chromosome 5. (A) QTL mapping of the qGW-5 locus. (B) Six BAC/PAC contigs around the gw-5 locus. (C) Fine mapping of gw-5 using newly developed SSR markers. The red superscript a indicates tha) (current)
- 14:05, 8 June 2014 (diff | hist) . . (+357) . . N File:Ma205.jpg (Figure 5.—The ratios of three genotypes of SSR markers and frequency distributions of grain width in 300 BC4F2 individuals across four environments (E9–E12). A1–D1 represent the ratios of three genotypes of 12 SSR markers in E9–E12, respectively; ) (current)
- 14:02, 8 June 2014 (diff | hist) . . (+301) . . N File:Ma204.jpg (Figure 4.—Frequency distributions of grain width of paddy rice in the CSSL28/Asominori F2 populations grown in E10, E11, and E12. (A) Grain width of paddy rice in E10 (1248 individuals); (B) grain width of paddy rice in E11 (2465 individuals); (C) grain) (current)
- 14:00, 8 June 2014 (diff | hist) . . (+363) . . N File:Ma203.jpg (Figure 3.—Frequency distributions of grain width, grain length, and length–width ratio in the CSSL28/Asominori BC4F2 population (2171 individuals) in E9. (A) Grain width of paddy rice; (B) grain width of brown rice; (C) grain length of paddy rice; (D)) (current)
- 13:59, 8 June 2014 (diff | hist) . . (+403) . . N File:Ma202.jpg (Figure 2.—Grain width of the milled rice in Asominori and target CSSLs carrying qGW-5 or qGW-9 alleles in eight environments (E1–E8). * and ** indicate significance levels of 5 and 1%, respectively; ns, nonsignificant difference. The open and shaded b) (current)
- 13:57, 8 June 2014 (diff | hist) . . (+135) . . N File:Ma201.jpg (Figure 1.—Phenotypic distributions of rice grain width in the Asominori/IR24 recombinant inbred lines in four environments (E1–E4).) (current)
- 13:55, 8 June 2014 (diff | hist) . . (+344) . . N File:Ma6.jpg (Figure 6 GW5 interacts with polyubiquitin in yeast two-hybrid assay. (A) AH109 yeast cells expressing pGBKT7-GW5/pGADT7(top), pGBKT7/pGADT7-polyubiquitin (middle) and pGBKT7-GW5/pGADT7-polyubiquitin (bottom) were selected on synthetic growth medium withou) (current)
- 13:52, 8 June 2014 (diff | hist) . . (+260) . . N File:Ma5.jpg (Figure 5 Sub-cellular localization of GW5. (A) and (C) Bright field images of onion epidermal cells. (B) GFP by itself (pCAMBIA 1302 vector) localizes to both cytoplasm and nucleus. (D) GW5-GFP fusion protein is localized only to the nucleus. Scale bars:5) (current)
- 13:50, 8 June 2014 (diff | hist) . . (+572) . . N File:Ma4.jpg (Figure 4 GW5 expression analyses. (A) The sequence of the predicted ORF2. The primers (F6, R2 and R3) used for RT-PCR analysis and the predicted NLS are denoted by arrows and a line, respectively. In addition, amino-acid residues 20-71 formed an arginine-) (current)
- 13:49, 8 June 2014 (diff | hist) . . (+378) . . N File:Ma3.jpg (Figure 3 Genotyping analyses in 46 rice cultivars. (A) PCR products of the Indel1 marker in 23 narrow-grain rice lines; (B) PCR products of the Indel1 marker in 23 wide-grain rice varieties; (C) PCR products of the Indel2 marker in 23 narrow-grain rice li) (current)
- 13:47, 8 June 2014 (diff | hist) . . (+771) . . N File:Ma2.jpg (Figure 2 Fine mapping of GW5. This map was constructed on the basis of publicly available rice sequences. The CAPS and Indel markers developed in this work are indicated. (A) GW5 was mapped to a region between markers RM3328 and RMW513 in 805 recessive in) (current)
- 13:26, 8 June 2014 (diff | hist) . . (+348) . . GW5
- 13:23, 8 June 2014 (diff | hist) . . (-1) . . GW5
- 13:21, 8 June 2014 (diff | hist) . . (+106) . . GW5
- 13:12, 8 June 2014 (diff | hist) . . (+416) . . N File:Ma1.jpg (Figure 1 qGW5 controls grain width and weight in CSSL28. (A) Genotype of the narrow grain line, CSSL28 (a segment substitution between the RFLP markers C263 and R2289 on chromosome 5). The black bar indicates the fragment from IR24 in the Asominori genomi) (current)
- 13:00, 8 June 2014 (diff | hist) . . (-35) . . GW5
- 12:59, 8 June 2014 (diff | hist) . . (+32) . . GW5
- 12:56, 8 June 2014 (diff | hist) . . (-3) . . GW5
- 12:53, 8 June 2014 (diff | hist) . . (0) . . GW5
- 12:52, 8 June 2014 (diff | hist) . . (-2) . . GW5
- 12:39, 8 June 2014 (diff | hist) . . (+98) . . GW5
- 12:34, 8 June 2014 (diff | hist) . . (-48) . . GW5
- 12:31, 8 June 2014 (diff | hist) . . (+55) . . GW5
- 12:26, 8 June 2014 (diff | hist) . . (+18,853) . . GW5
- 12:25, 8 June 2014 (diff | hist) . . (+1,264) . . GW5
- 12:14, 8 June 2014 (diff | hist) . . (-29) . . GW5
- 12:12, 8 June 2014 (diff | hist) . . (+2,435) . . GW5
