Background: The bimodal balance-recovery model predicts that corticospinal tract (CST) integrity in the affected hemisphere influences the partterns of brain recovery after stroke. Repetitive transcranial magnetic stimulation (rTMS) has been used to promote functional recovery of stroke patients by modulating motor cortical excitability and inducing reorganization of neural networks. This study aimed to explore how to optimize the efficiency of repetitive transcranial magnetic stimulation to promote upper limb functional recovery after stroke according to bimodal balance-recovery model. Methods: 60 patients who met the inclusion criteria were enrolled to high CST integrity group (n = 30) or low CST integrity group (n = 30), and further assigned randomly to receive high-frequency rTMS (HF-rTMS), low-frequency rTMS (LF-rTMS) or sham rTMS in addition to routine rehabilitation, with 10 patients in each group. Outcome measures included Fugl-Meyer scale for upper extremity (FMA-UE), Wolf Motor Function (WMFT) scale and Modified Barthel Index (MBI) scale which were evaluated at baseline and after 21 days of treatment. Results: For patients with high CST integrity, the LF group achieved higher FMA-UE, WMFT and MBI scores improvements after treatment when compared to the HF group and sham group. For patients with low CST integrity, after 21 days treatment, only the HF group showed significant improvements in FMA-UE and WMFT scores. For MBI assessment, the HF group revealed significantly better improvements than the LF group and sham group. Conclusions: For stroke patients with high CST integrity, low-frequency rTMS is superior to high-frequency rTMS in promoting upper limb motor function recovery. However, only high-frequency rTMS can improve upper limb motor function of stroke patients with low CST integrity.
We described a facile method for distance-based detection of aluminum on a thread based on the adsorption of formed complex onto thread. Chrome azurol S (CAS) containing Cetyltrimethylammonium Bromide (CTMAB) were used as chromogenic reagent, which reacts with aluminum to form AL-CAS-CTMAB complex on a thread. The complex was adsorbed onto thread to generate a colored band. Aluminum contents could be quantified by measuring the length of colored band on the thread using a ruler, thereby eliminating the need for electronic readout devices and trained personnel. This instrument-free method has features of low cost, easy to operation, fast analysis speed, disposability and low reagents/sample consumption. Moreover, considering that the thread fiber has adsorption capability to various molecules such as metal-ligand complexes and biomolecules, we believe that this technique holds the potentials to be widely adaptable to distance-based chemical and biochemical analysis.
Due to the rapidly growth of multimedia communication, video image deblurring has become a hot issue in image processing. As the image size increases, it is difficult to perform the large size image deblurring computation on a single computer in a limited time. One of the most efficient solving methods is parallel computing. In this paper, we first introduce a variational equation for the blurred image, analyze its computing scheme and improve the discretization, then detail the parallel implemenation with multithreads programming using OpenMP and MPI on a dual core cluster. Some experimental results show that this method can produce the large size video image deblurring.
In this paper a new method for the silica gel H phase-diffuse reflectance spectrophotometric determination of iron(III) with piperonal fluorine (PIF) has been developed. In the presence of cetyltrimethyl ammonium bromide and in a NH4 Cl-NH3.H2O medium at pH 9.6-10.3, iron(III) reacts with PIF to form a stable blue complex which is absorbed by silica gel H with a diffuse reflectance absorption peak at 640 nm. The calibration curve is linear over the concentration range 0-25 ng of iron(III) in 1 mL. The linear regression equation is AR = 0.022 1c-0.005,5(r = 0.999,7), where c is expressed as ng per 1 mL. The method has high analytical speed and sensitivity. The effect of a number of foreign ions has been studied by carrying out determining of 200 ng.(10 mL)-1 of iron (III), 1 mg K+, Na+, F-, Cl-, NO3-, PO(4)3-, 0.6 mg Ca2+, Mg2+, 35 micrograms Sr2+, 20 micrograms Cr(III), 6 micrograms Mn2+, 4 micrograms Pb2+, 3.5 micrograms Cd2+, 2.5 micrograms Cu2+, Ag+, 1.5 micrograms Cr(VI), 1 microgram Ni2+, 0.75 microgram Zn2+, Sn4+ et al don't interfere with the measurement. The method has been applied to the determination of microamount iron in magnesium oxide with satisfactory results.
We describe a simple and cost-effective strategy for rapid fabrication of microfluidic paper-based analytical devices and valves by inkjet printing. NaOH aqueous solution was printed onto a hydrophobic filter paper, which was previously obtained by soaking in a trimethoxyoctadecylsilane-heptane solution, allowing selective wet etching of hydrophobic cellulose to create hydrophilic-hydrophobic contrast with a relatively good resolution. Hexadecyltrimethylammonium bromide (CTMAB)-ethanol solution was printed onto hydrophobic paper to fabricate temperature-controlled valves. At low temperature, CTMAB deposited on the paper is insoluble in aqueous fluid, thus the paper remains hydrophobic. At high temperature, CTMAB becomes soluble so the CTMAB-deposited channel becomes hydrophilic, allowing the wicking of aqueous solution through the valve. We believe that this strategy will be very attractive for the development of simple micro analytical devices for point-of-care applications, including diagnostic testing, food safety control, and environmental monitoring.
Abstract Acute lymphoblastic leukemia (ALL) is the most common pediatric cancer, affecting the lymphoid cells of both B and T lineages. Most ALL cells are auxotrophic for asparagine, a nonessential amino acid for protein synthesis, due to the low expression of asparagine synthetase (ASNS), a rate limiting enzyme for de novo biosynthesis of asparagine. As a result, standard ALL treatment takes advantage of this vulnerability by giving patients L-asparaginase, a bacterial enzyme that depletes the circulating asparagine. However, previous work from our lab and others have shown that some ALL cells become resistance to L-asparaginase treatment through the induction of ASNS expression. Mechanistically, amino acid starvation actives the general control nonderepressible 2 (GCN2) kinase, leading to the accumulation of ATF4 transcriptional factor. ATF4, in turn, is recruited to the promoter of the ASNS gene to activate its transcription. However, the role of GCN2 kinase in the process of leukemogenesis under nutrient limiting environment has not been established. In this study, our goal is to use a mouse model of T-ALL driven by mutant KRas to determine the role of GCN2 in leukemogenesis and the therapeutic response to L-asparaginase treatment. Citation Format: Ji Zhang, Rodney Claude, Sankalp Srivastava, Sandeep Batra, Minghua Zhong, Utpal Dave, Ronald C. Wek. Exploring the role of adaptive amino acid responses in Ras-driven leukemia progression and therapy [abstract]. In: Proceedings of the AACR Special Conference: Targeting RAS; 2023 Mar 5-8; Philadelphia, PA. Philadelphia (PA): AACR; Mol Cancer Res 2023;21(5_Suppl):Abstract nr A012.
Treatment of aryl alkyl ketones with poly[4-(diacetoxyiodo)styrene] and trimethyl orthoformate in the presence of sulfuric acid followed by hydrolysis afforded methyl 2-arylalkanoates in good yields. The polymeric reagent can be regenerated and reused as an environmentally benign reagent.
We described a strategy to perform multistep operations on a simple laminated paper-based separation device by using electrokinetic flow to manipulate the fluids. A laminated crossed-channel paper-based separation device was fabricated by cutting a filter paper sheet followed by lamination. Multiple function units including sample loading, sample injection, and electrophoretic separation were integrated on a single paper based analytical device for the first time, by applying potential at different reservoirs for sample, sample waste, buffer, and buffer waste. As a proof-of-concept demonstration, mixed sample solution containing carmine and sunset yellow were loaded in the sampling channel, and then injected into separation channel followed by electrophoretic separation, by adjusting the potentials applied at the four terminals of sampling and separation channel. The effects of buffer pH, buffer concentration, channel width, and separation time on resolution of electrophoretic separation were studied. This strategy may be used to perform multistep operations such as reagent dilution, sample injection, mixing, reaction, and separation on a single microfluidic paper based analytical device, which is very attractive for building micro total analysis systems on microfluidic paper based analytical devices.
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