212 research outputs found
A baseband residual vector quantization algorithm for voiceband data signals
Journal ArticleAbstract-In this paper, we present a new approach to the digitization and compression of a class of voiceband modem signals. Our approach, which we call baseband residual vector quantization (BRVQ), relies heavily upon the simple structure present in a modem signal. After the signal is converted to baseband, the magnitude sequence and the sequence of residuals obtained when the phase within each baud of the baseband signal is modeled by a straight line are separately vector quantized. In order to carry out these operations, we developed the new carrier-frequency estimation and baud-rate classification schemes described in the paper. Experimental results show that the performance of the BRVQ system at and below 16 kbits/s is better than that of a previously developed vector quantization scheme that has itself been shown to outperform traditional speech-compression techniques such as adaptive predictive coding, adaptive transform coding, and subband coding when these techniques are used to compress modem signals
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Complete Genomic Sequences of Three Salmonella enterica subsp. enterica Serovar Muenchen Strains from an Orchard in San Joaquin County, California.
We present here the complete genome sequences of three Salmonella enterica subsp. enterica serovar Muenchen strains, LG24, LG25, and LG26. All three strains were isolated from almond drupes grown in an orchard in San Joaquin County, California, in 2016. These genomic sequences are nonidentical and will contribute to our understanding of S. enterica genomics
Synthesis and cytotoxic activity of madecassic acid–silybin conjugate compounds in liver cancer cells
A series of 14 conjugates of 2α,3β,23-triacetyl-madecassic acid and silybin were designed and synthesized. The madecassic acid unit was linked to silybin either directly at position C-7 or C-3; or through an amino acid linker (glycine, β-alanine, or 11-aminoundecanoic acid) at position C-3. The conjugates were tested in vitro for their cytotoxic effect on HepG2 cells using the MTT assay. The results confirmed that the conjugated compounds demonstrated a stronger cytotoxic effect compared to the parent compounds. Of these compounds, the most promising conjugate, compound 8, was evaluated for cytotoxic activity in the additional Hep3B, Huh7, and Huh7R human hepatocellular carcinoma cell lines and also for cell cycle changes and induction of apoptosis in HepG2 cells. This compound caused a rapid and significant induction of caspase 3 activity and induced cell cycle arrest in the S phase – effects distinct from the activity of madecassic acid. This is the first study on the synthesis and cytotoxicity of madecassic acid–silybin conjugates, and of their testing against liver cancer cell lines and provides evidence for a distinct biological profile versus madecassic acid alone
Theoretical predictions of melting behaviors of hcp iron up to 4000 GPa
The high-pressure melting diagram of iron is a vital ingredient for the
geodynamic modeling of planetary interiors. Nonetheless, available data for
molten iron show an alarming discrepancy. Herein, we propose an efficient
one-phase approach to capture the solid-liquid transition of iron under extreme
conditions. Our basic idea is to extend the statistical moment method to
determine the density of iron in the TPa region. On that basis, we adapt the
work-heat equivalence principle to appropriately link equation-of-state
parameters with melting properties. This strategy allows explaining
cutting-edge experimental and ab initio results without massive computational
workloads. Our theoretical calculations would be helpful to constrain the
chemical composition, internal dynamics, and thermal evolution of the Earth and
super-Earths
Bibliografía
Reaction of the anion-deficient,
cation-ordered perovskite phase
Ba<sub>2</sub>YFeO<sub>5</sub> with 80 atm of oxygen pressure at 410
°C results in the formation of the Fe<sup>4+</sup> phase Ba<sub>2</sub>YFeO<sub>5.5</sub>. The topochemical insertion of oxide ions
lifts the inversion symmetry of the centrosymmetric host phase, Ba<sub>2</sub>YFeO<sub>5</sub> (space group <i>P</i>2<sub>1</sub>/<i>n</i>), to yield a noncentrosymmetric (NCS) phase Ba<sub>2</sub>YFeO<sub>5.5</sub> (space group <i>Pb</i>2<sub>1</sub><i>m</i> (No. 26), <i>a</i> = 12.1320(2) Å, <i>b</i> = 6.0606(1) Å, <i>c</i> = 8.0956(1) Å, <i>V</i> = 595.257(2) Å<sup>3</sup>) confirmed by the observation
of second-harmonic generation. Dielectric and PUND ferroelectric measurements,
however, show no evidence for a switchable ferroelectric polarization,
limiting the material to pyroelectric behavior. Magnetization and
low-temperature neutron diffraction data indicate that Ba<sub>2</sub>YFeO<sub>5.5</sub> undergoes a magnetic transition at 20 K to adopt
a state which exhibits a combination of ferromagnetic and antiferromagnetic
order. The symmetry breaking from centrosymmetric to polar noncentrosymmetric,
which occurs during the topochemical oxidation process is discussed
on the basis of induced lattice strain and an electronic instability
and represents a new strategy for the preparation of NCS materials
that readily incorporate paramagnetic transition metal centers
Synthesis and cytotoxic activity of madecassic acid–silybin conjugate compounds in liver cancer cells
A series of 14 conjugates of 2α,3β,23-triacetyl-madecassic acid and silybin were designed and synthesized. The madecassic acid unit was linked to silybin either directly at position C-7 or C-3; or through an amino acid linker (glycine, β-alanine, or 11-aminoundecanoic acid) at position C-3. The conjugates were tested in vitro for their cytotoxic effect on HepG2 cells using the MTT assay. The results confirmed that the conjugated compounds demonstrated a stronger cytotoxic effect compared to the parent compounds. Of these compounds, the most promising conjugate, compound 8, was evaluated for cytotoxic activity in the additional Hep3B, Huh7, and Huh7R human hepatocellular carcinoma cell lines and also for cell cycle changes and induction of apoptosis in HepG2 cells. This compound caused a rapid and significant induction of caspase 3 activity and induced cell cycle arrest in the S phase – effects distinct from the activity of madecassic acid. This is the first study on the synthesis and cytotoxicity of madecassic acid–silybin conjugates, and of their testing against liver cancer cell lines and provides evidence for a distinct biological profile versus madecassic acid alone
A randomized controlled trial of a pharmacist-led intervention to enhance knowledge of Vietnamese patients with type 2 diabetes mellitus
OBJECTIVES: We aimed to assess whether a pharmacist-led intervention enhances knowledge, medication adherence and glycemic control in patients with type 2 diabetes mellitus (T2DM). METHODS: We conducted a single-blinded randomized controlled trial in Vietnam. Individuals with T2DM were recruited from a general hospital and randomly allocated to intervention and routine care. The intervention group received routine care plus counselling intervention by a pharmacist, including providing drug information and answering individual patients' queries relating to T2DM and medications, which had not been done in routine care. We assessed the outcomes: knowledge score as measured by the Diabetes Knowledge Questionnaire, self-reported adherence and fasting blood glucose (FBG) at the 1-month follow-up. KEY FINDINGS: A total of 165 patients (83 intervention, 82 control) completed the study; their mean age was 63.33 years, and 49.1% were males. The baseline characteristics of the patients were similar between the groups. At 1-month follow-up, the pharmacist's intervention resulted in an improvement in all three outcomes: knowledge score [B = 5.527; 95% confidence intervals (CI): 3.982 to 7.072; P < 0.001], adherence [odds ratio (OR) = 9.813; 95% CI: 2.456 to 39.205; P = 0.001] and attainment of target FBG (OR = 1.979; 95% CI: 1.029 to 3.806; P = 0.041). CONCLUSIONS: The pharmacist-led intervention enhanced disease knowledge, medication adherence and glycemic control in patients with T2DM. This study provides evidence of the benefits of pharmacist counselling in addition to routine care for T2DM outpatients in a Vietnam population
Live attenuated virus vaccine protects against SARS-CoV-2 variants of concern B.1.1.7 (Alpha) and B.1.351 (Beta).
[Figure: see text]
Appropriate Antibiotic Use and Associated Factors in Vietnamese Outpatients
Background: Inappropriate antibiotic use among outpatients is recognized as the primary driver of antibiotic resistance. A proper understanding of appropriate antibiotic usage and associated factors helps to determine and limit inappropriateness. We aimed to identify the rate of appropriate use of antibiotics and identify factors associated with the inappropriate prescriptions. Methods: We conducted a cross-sectional descriptive study in outpatient antibiotic use at a hospital in Can Tho City, Vietnam, from August 1, 2019, to January 31, 2020. Data were extracted from all outpatient prescriptions at the Medical Examination Department and analyzed by SPSS 18 and Chi-squared tests, with 95% confidence intervals. The rationale for antibiotic use was evaluated through antibiotic selection, dose, dosing frequency, dosing time, interactions between antibiotics and other drugs, and general appropriate usage. Results: A total of 420 prescriptions were 51.7% for females, 61.7% with health insurance, and 44.0% for patients with one comorbid condition. The general appropriate antibiotic usage rate was 86.7%. Prescriptions showed that 11.0% and 9.5% had a higher dosing frequency and dose than recommended, respectively; 10.2% had an inappropriate dosing time; 3.1% had drug interactions; and only 1.7% had been prescribed inappropriate antibiotics. The risk of inappropriate antibiotic use increased in patients with comorbidities and antibiotic treatment lasting >7 days (p < 0.05). Conclusions: The study indicated a need for more consideration when prescribing antibiotics to patients with comorbidities or using more than 7 days of treatment
Leukotriene A4 Hydrolase Genotype and HIV Infection Influence Intracerebral Inflammation and Survival From Tuberculous Meningitis.
BACKGROUND: Tuberculous meningitis (TBM) is the most devastating form of tuberculosis, yet very little is known about the pathophysiology. We hypothesized that the genotype of leukotriene A4 hydrolase (encoded by LTA4H), which determines inflammatory eicosanoid expression, influences intracerebral inflammation, and predicts survival from TBM. METHODS: We characterized the pretreatment clinical and intracerebral inflammatory phenotype and 9-month survival of 764 adults with TBM. All were genotyped for single-nucleotide polymorphism rs17525495, and inflammatory phenotype was defined by cerebrospinal fluid (CSF) leukocyte and cytokine concentrations. RESULTS: LTA4H genotype predicted survival of human immunodeficiency virus (HIV)-uninfected patients, with TT-genotype patients significantly more likely to survive TBM than CC-genotype patients, according to Cox regression analysis (univariate P = .040 and multivariable P = .037). HIV-uninfected, TT-genotype patients had high CSF proinflammatory cytokine concentrations, with intermediate and lower concentrations in those with CT and CC genotypes. Increased CSF cytokine concentrations correlated with more-severe disease, but patients with low CSF leukocytes and cytokine concentrations were more likely to die from TBM. HIV infection independently predicted death due to TBM (hazard ratio, 3.94; 95% confidence interval, 2.79-5.56) and was associated with globally increased CSF cytokine concentrations, independent of LTA4H genotype. CONCLUSIONS: LTA4H genotype and HIV infection influence pretreatment inflammatory phenotype and survival from TBM. LTA4H genotype may predict adjunctive corticosteroid responsiveness in HIV-uninfected individuals
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