Rosafuningensis (Rosaceae), a new species from Yunnan, China.

A new species Rosafuningensis and its variant R.funingensisf.rosea, both collected from Yunnan Province, China, are, for the first time, documented and illustrated in this study. Morphological analysis in comparison with two related species in the wild, R.gigantea and R.rubus, presents distinguishable features through leaf surfaces, inflorescences and the shape of styles. R.funingensis leaf surfaces are abaxially villous, purple-red, pale green when mature, adaxially glabrous, dark green; inflorescences solitary or 2-5(7) in corymbose cyme; and styles connate into a column or not, exserted.

Precise analysis of the effect of basal core promoter/precore mutations on the main phenotype of chronic hepatitis B in mouse models.

High replication and mutation rates of hepatitis B virus (HBV) often lead to reduced or suppressed hepatitis B e antigen expression. The most common mutations are genomic variations in the basal core promoter (BCP) and pre-core (PC) regions. However, the effect of BCP/PC mutations on HBV phenotype in vivo remains unclear. We compared and analyzed BCP/PC mutations and BCP/PC reverse mutations in mouse models. In addition to terminating the expression of HBeAg, BCP/PC mutations also resulted in a significant decrease in HBsAg, HBV DNA, and cccDNA in the early stage, and an obvious increase in serum alanine aminotransferase throughout the transfection period. In both groups, serum HBV DNA was positively correlated with intracellular HBV DNA and cccDNA. Further, we found that interleukin-4 (IL-4) and L-10 levels were significantly lower in the BCP/PC(M) group than in the BCP/PC(R) group at 4 weeks post-injection. However, IL-1ß was significantly lower in the BCP/PC(M) group than in the BCP/PC(R) group at 26 weeks post-injection. In summary, we precisely analyzed the effect of BCP/PC mutations on the phenotype in vivo, which is important to evaluating disease progression and treatment responses of variable chronic hepatitis B patients.

Fast and fully automatic calibration of frequency offset for balanced steady-state free precession cardiovascular magnetic resonance at 3.0 Tesla.

BACKGROUND: This study proposed a fast and fully automatic calibration system to suppress the dark banding artifacts in balanced steady-state free precession (bSSFP) cardiovascular magnetic resonance (CMR) at 3.0 T. METHODS: Twenty-one healthy volunteers (18 men, 3 women; mean age 24.9 years) participated in this study after providing institutionally approved consent. The optimal frequency was obtained using sweep scans of transition-band low flip-angle bSSFP (bSSFP-L), performed with three conditions: breath-hold plus electrocardiography (ECG) triggering (BH + ECG), breath-hold only (BH), and free breathing (FB). A real-time feedback system was implemented to allow the performing of bSSFP-L calibration scanning and conventional cine bSSFP within one breath-hold. For each scan condition, the optimal phase was estimated using 20-point and 10-point spline fitting. RESULTS: Linear regression analysis indicated high correlation between the optimal phases obtained using BH and FB and those obtained using BH + ECG (R2 = 0.91 to 0.98, n = 21). The optimal phases obtained using 10-point datasets showed high correlation with the 20-point BH + ECG datasets (R2 = 0.92 to 0.99, n = 21); although the within-subject coefficient of variation (wsCV) was larger using 10-point fitting. The variation of repeated measurements was largest with FB acquisition and smallest with BH + ECG acquisition. The optimal frequency obtained by offline calculation and by real-time feedback calibration significantly reduced dark-band artifacts in cine bSSFP images (both p < .01). CONCLUSIONS: The proposed real-time feedback calibration method for bSSFP imaging is rapid and fully automatic. This method could greatly reduce dark-band artifacts in bSSFP images and facilitate clinical CMR at 3.0 T.

Optimization of PROPELLER reconstruction for free-breathing T1-weighted cardiac imaging.

PURPOSE: Clinical cardiac MR imaging techniques generally require patients to hold their breath during the scanning process to minimize respiratory motion-related artifacts. However, some patients cannot hold their breath because of illness or limited breath-hold capacity. This study aims to optimize the PROPELLER reconstruction for free-breathing myocardial T1-weighted imaging. METHODS: Eight healthy volunteers (8 men; mean age 26.4 years) participated in this study after providing institutionally approved consent. The PROPELLER encoding method can reconstruct a low-resolution image from every blade because of k-space center oversampling. This study investigated the feasibility of extracting a respiratory trace from the PROPELLER blades by implementing a fully automatic region of interest selection and introducing a best template index to account for the property of the human respiration cycle. RESULTS: Results demonstrated that the proposed algorithm significantly improves the contrast-to-noise ratio and the image sharpness (p < 0.05). CONCLUSIONS: The PROPELLER method is expected to provide a robust tool for clinical application in free-breathing myocardial T1-weighted imaging. It could greatly facilitate the acquisition procedures during such a routine examination.

Accelerating image registration of MRI by GPU-based parallel computation.

Automatic image registration for MRI applications generally requires many iteration loops and is, therefore, a time-consuming task. This drawback prolongs data analysis and delays the workflow of clinical routines. Recent advances in the massively parallel computation of graphic processing units (GPUs) may be a solution to this problem. This study proposes a method to accelerate registration calculations, especially for the popular statistical parametric mapping (SPM) system. This study reimplemented the image registration of SPM system to achieve an approximately 14-fold increase in speed in registering single-modality intrasubject data sets. The proposed program is fully compatible with SPM, allowing the user to simply replace the original image registration library of SPM to gain the benefit of the computation power provided by commodity graphic processors. In conclusion, the GPU computation method is a practical way to accelerate automatic image registration. This technology promises a broader scope of application in the field of image registration.

Real-time feedback optimization of z-shim gradient for automatic compensation of susceptibility-induced signal loss in EPI.

Signal loss in gradient-echo echo planar imaging (GE-EPI) due to susceptibility-induced magnetic field inhomogeneity makes it difficult to assess the blood oxygenation level-dependent (BOLD) effect in fMRI investigations. The z-shim method that applies an additional gradient moment is one of the more popular methods of compensating for GE-EPI signal loss. However, this method requires a calibration sweep scan and post-processing to identify the optimal z-shim gradients, which slows down fMRI experiments. This study attempts to decrease the calibration time by introducing a real-time feedback framework. Creating a feedback loop between the image processing and the GE-EPI pulse sequence converts the calibration of z-shim gradients to an optimization problem, which can be accelerated by local search methods. This study proposes an interleaved scan that allows the simultaneous optimization of two z-shim gradient moments and allocates sufficient processing time for networking and computation. The z-shim compensated images obtained by the proposed real-time method are comparable to those created by the sweep method. The optimization procedure for obtaining negative and positive gradient moments generally requires about twenty GE-EPI repetitions. In conclusion, the proposed z-shim method includes an automated real-time framework to achieve a significant reduction in susceptibility-induced signal loss in GE-EPI with a minimal increase in calibration time. The proposed procedure is fully automatic and compatible with conventional GE-EPI and can thus serve as a pre-adjustment module in EPI-based fMRI researches.

Synthesis and antitumor activity of sulfur-containing 9-anilinoacridines.

A series of sulfur-containing 9-anilinoacridines related to amsacrine were synthesized and evaluated for their anticancer potential. Among the compounds, both diol-containing compounds, 2a and 3, were the most cytotoxic of the sulfide series against V-79 cells in vitro (IC(90) = 2.1 microM and 1.9 microM, respectively). Among the non-alkyl-substituted compounds (7-9), compounds with electron-donating substitution para to the sulfide (7 and 9) were more cytotoxic than the electron-withdrawing nitro-substituted compound 8. The limited SAR suggested the importance of hydroxyl functionality along with its location for the cytotoxicity in the series. A preliminary anticancer screening against P388 leukemia showed that 2a is highly active in vivo as well. Topoisomerase II inhibitory activity appeared to be involved in the cytotoxicity of compound 2a. Sulfoxide compound 2b, which is 6-7-fold less cytotoxic than its sulfide 2a, appears to be a potential bioreductive anticancer prodrug on the basis of its bioreductive metabolism findings.