Rice cultivar \u27Banks\u27

A rice cultivar designated ‘Banks’ is disclosed. The invention relates to the seeds of rice cultivar ‘Banks’, to the plants of rice ‘Banks’ and to methods for producing a rice plant produced by crossing the cultivar ‘Banks’ with itself or another rice variety. The invention further relates to hybrid rice seeds and plants produced by crossing the cultivar ‘Banks’ with another rice cultivar

Rice cultivar \u27Francis\u27

A novel rice cultivar, designated ‘Francis’, is disclosed. The invention relates to the seeds of rice cultivar ‘Francis’, to the plants of rice ‘Francis’ and to methods for producing a rice plant produced by crossing the cultivar ‘Francis’ with itself or another rice variety. The invention further relates to hybrid rice seeds and plants produced by crossing the cultivar ‘Francis’ with another rice cultivar

Rice cultivar ‘Ahrent’

A novel rice cultivar, designated ‘Ahrent’, is disclosed. The invention relates to the seeds of rice cultivar ‘Ahrent’, to the plants of rice ‘Ahrent’ and to methods for producing a rice plant produced by crossing the cultivar ‘Ahrent’ with itself or another rice variety. The invention further relates to hybrid rice seeds and plants produced by crossing the cultivar ‘Ahrent’ with another rice cultivar

Rice cultivar \u27Ahrent\u27

A novel rice cultivar, designated ‘Ahrent’, is disclosed. The invention relates to the seeds of rice cultivar ‘Ahrent’, to the plants of rice ‘Ahrent’ and to methods for producing a rice plant produced by crossing the cultivar ‘Ahrent’ with itself or another rice variety. The invention further relates to hybrid rice seeds and plants produced by crossing the cultivar ‘Ahrent’ with another rice cultivar

Rice cultivar \u27Spring\u27

A rice cultivar designated ‘Spring’ is disclosed. The invention relates to the seeds of rice cultivar ‘Spring’, to the plants of rice ‘Spring’ and to methods for producing a rice plant produced by crossing the cultivar ‘Spring’ with itself or another rice variety. The invention further relates to hybrid rice seeds and plants produced by crossing the cultivar ‘Spring’ with another rice cultivar

Linear filtering precedes nonlinear processing in early vision

Background: Nonlinearities play a significant role in early visual processing. They are central to the perception of spatial contrast variations, multiplicative transparencies and texture boundaries. This article concerns the stage of processing at which nonlinearities first become significant. Results: Subjects were adapted to a high contrast sinusoidal grating followed by a brief presentation of a contrast modulated test (plaid) pattern. Thresholds for the detection of the contrast modulation (the beat) were measured. Results show that threshold elevation is greatest when the orientation and spatial frequency of the adapting grating are close to the principal Fourier frequency (the carrier) of the test pattern. Adaptation to sinewave-gratings near the frequency of the contrast modulation has relatively little effect. The data also show that the processing of contrast is frequency selective, with a peak tuning frequency near 0.4 cycles per degree. Conclusions: The data are consistent with a model in which the contrast beats are processed in a frequency- specific manner, after an initial stage of frequency-specific and orientation-specific linear filtering

2-De­oxy-2,3-O-isopropyl­idene-2,4-di-C-methyl-β-l-arabinose

X-ray crystallography unequivocally confirmed the stereochemistry of the C atom at position 2 in the carbon scaffold of the title mol­ecule, C10H18O4. The pyran­ose ring exists in a chair conformation with the methyl group on the C atom in the 2 position in an equatorial configuration. The absolute stereochemistry was determined from the starting material. The crystal structure consists of O—H⋯O hydrogen-bonded chains of mol­ecules running parallel to the b axis

1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1

<p>Abstract</p> <p>Background</p> <p>Prostate cancer is the second leading cause of cancer mortality among US men. Epidemiological evidence suggests that high vitamin D status protects men from prostate cancer and the active form of vitamin D, 1α,25 dihydroxyvitamin D₃(1,25(OH)₂D) has anti-cancer effects in cultured prostate cells. Still, the molecular mechanisms and the gene targets for vitamin D-mediated prostate cancer prevention are unknown.</p> <p>Results</p> <p>We examined the effect of 1,25(OH)₂D (+/- 100 nM, 6, 24, 48 h) on the transcript profile of proliferating RWPE1 cells, an immortalized, non-tumorigenic prostate epithelial cell line that is growth arrested by 1,25(OH)₂D (Affymetrix U133 Plus 2.0, n = 4/treatment per time and dose). Our analysis revealed many transcript level changes at a 5% false detection rate: 6 h, 1571 (61% up), 24 h, 1816 (60% up), 48 h, 3566 (38% up). 288 transcripts were regulated similarly at all time points (182 up, 80 down) and many of the promoters for these transcripts contained putative vitamin D response elements. Functional analysis by pathway or Gene Set Analysis revealed early suppression of WNT, Notch, NF-kB, and IGF1 signaling. Transcripts related to inflammation were suppressed at 6 h (e.g. IL-1 pathway) and suppression of proinflammatory pathways continued at later time points (e.g. IL-17 and IL-6 pathways). There was also evidence for induction of anti-angiogenic pathways and induction of transcripts for protection from oxidative stress or maintenance of cell redox homeostasis at 6 h.</p> <p>Conclusions</p> <p>Our data reveal of large number of potential new, direct vitamin D target genes relevant to prostate cancer prevention. In addition, our data suggests that rather than having a single strong regulatory effect, vitamin D orchestrates a pattern of changes within prostate epithelial cells that limit or slow carcinogenesis.</p