The oxidation power of the TiO2
-
x
N
x
powders with low nitrogen concentrations (<0.02) was evaluated by
the decomposition of gaseous 2-propanol (IPA) under the same absorbed photon number, 1.4 × 1014
quanta·cm-2·s-1, of visible (Vis) or ultraviolet (UV) light. Regardless of the x value, the quantum yield
values from irradiating with Vis light was lower than with UV light, which suggests that the isolated narrow
band formed above the valence band is responsible for the Vis light response in the present nitrogen doped
TiO2. In addition, increasing the nitrogen concentration when irradiating with UV light lowered the quantum
yields, indicating that the doping sites could also serve as recombination sites.
Carbon-doped TiO2 powders in an anatase phase colored yellow were fabricated by oxidative annealing of TiC. Carbons were located at oxygen sites. The carbon substitution caused the absorbance edge of TiO2 to be shifted to the higher wavelength region. Carbon-doped TiO2 showed photocatalytic activities for the decomposition of IPA to CO2 via acetone under visible light (400–530 nm) irradiation.
Only a small proportion of the mouse genome is transcribed into mature messenger RNA transcripts. There is an international collaborative effort to identify all full-length mRNA transcripts from the mouse, and to ensure that each is represented in a physical collection of clones. Here we report the manual annotation of 60,770 full-length mouse complementary DNA sequences. These are clustered into 33,409 'transcriptional units', contributing 90.1% of a newly established mouse transcriptome database. Of these transcriptional units, 4,258 are new protein-coding and 11,665 are new non-coding messages, indicating that non-coding RNA is a major component of the transcriptome. 41% of all transcriptional units showed evidence of alternative splicing. In protein-coding transcripts, 79% of splice variations altered the protein product. Whole-transcriptome analyses resulted in the identification of 2,431 sense-antisense pairs. The present work, completely supported by physical clones, provides the most comprehensive survey of a mammalian transcriptome so far, and is a valuable resource for functional genomics.
Recent studies have provided evidence for a positive association between migraine and restless legs syndrome (RLS), although the exact mechanisms and contributing factors remain unclear. A cross-sectional, case-control study was conducted, including patients with migraine (n = 262) and headache-free control subjects (n = 163). Migraine was diagnosed according to International Classification of Headache Disorders II criteria. RLS diagnosis was made based on four essential criteria as described by the International Restless Legs Syndrome Study Group. All patients completed the Migraine Disability Assessment (MIDAS) questionnaire, Beck Depression Inventory (BDI)-II scores, Pittsburgh Sleep Quality Index (PSQI), and Epworth Sleepiness Scale (ESS). A total of 210 blood samples were collected to correlate various parameters with RLS. RLS frequency was significantly greater in patients with migraine than in controls (13.7 vs. 1.8%). Migraine patients with RLS had high scores for MIDAS, BDI-II, PSQI, and ESS compared with those without RLS. In addition, migraine patients with RLS had a high rate of smoking and RLS family history, as well as increased levels of serum phosphorus and urea nitrogen compared with those without RLS. However, there was no difference in serum iron and ferritin levels between the groups. In migraine patients, logistic regression analysis revealed that positive RLS family history, BDI-II, ESS, and serum phosphorus levels were significant RLS predictors. Our study confirmed a positive association between RLS and migraine. RLS comorbidity in migraine patients was associated with insomnia, daytime sleepiness, depressive symptoms, headache-related disability, and increased serum phosphorus levels. These findings may provide a better understanding of RLS pathogenesis in migraine.
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