A new method for the design of energy transfer filters

This paper is concerned with the development of a new method for the design of Energy Transfer Filters (ETFs). ETFs are a new class of nonlinear filters recently proposed by the authors, which employ nonlinear effects to transfer signal energy from one frequency band to a different frequency location. The new method uses the powerful Orthogonal Least Squares (OLS) algorithm to solve the Least Squares problem associated with the design and compared with previous methods achieves much better filtering performance

Finite impulse response filter design using a forward orthogonal least squares algorithm

This paper is concerned with the application of forward Orthogonal Least Squares (OLS) algorithm to the design of Finite Impulse Response (FIR) filters. The focus of this study is a new FIR filter design procedure and to compare this with traditional methods known as the fir2() routine, provided by MATLAB

Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: A case report

Background: Sixty mutations of claudin 16 coding gene have been reported in familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) patients. Recent investigations revealed that a highly conserved glycine-leucine-tryptophan (115G-L-W117) motif in the first extracellular segment (ESC1) of claudin 16 might be essential for stabilization of the appropriately folded ECS1 structure and conservation of normal claudin 16 function. However, neither missense nor nonsense mutation has ever been described in this motif. Our study aimed at identifying mutations in a Chinese patient with FHHNC and exploring the association between genotype and phenotype. Case presentation: A 33-year-old female presented with 4 years history of recurrent acute pyelonephritis without other notable past medical history. Her healthy parents, who aged 56 and 53 respectively, were second cousins, and her only sibling died from renal failure without definite cause at age 25. Renal ultrasound imaging demonstrated atrophic kidneys and bilateral nephrocalcinosis. The laboratory workup revealed impaired renal function (Stage CKD IV), hypocalcemia and mild hypomagnesemia, accompanied with marked renal loss of magnesium and hypercalciuria. During the follow-up, treatment with calcitriol and calcium but not with magnesium was difficult to achieve normal serum calcium levels, whereas her serum magnesium concentration fluctuated within normal ranges. In the end, the patient unavoidably reached ESRD at 36 years old. The clinical features and family history suggested the diagnosis of FHHNC. To make a definite diagnosis, we use whole-exome sequencing to identify the disease-causing mutations and Sanger sequencing to confirm the mutation co-segregation in the family. As a result, a novel homozygous mutation (c.346C > G, p.Leu116Val) in115G-L-W117motif of claudin 16 was identified. Her parents, grandmother and one of her cousins carried heterozygous p.Leu116Val, whereas 200 unrelated controls did not carry this mutation. Conclusions: We described a delayed diagnosis patient with FHHNC in the Chinese population and identified a novel missense mutation in the highly conserved115G-L-W117motif of claudin 16 for the first time. According to the reported data and the information deduced from 3D modeling, we speculate that this mutation probably reserve partial residual function which might be related to the slight phenotype of the patient

Diffusion in simple fluids

Computed self diffusion coefficients for the Lennard-Jones and hard sphere fluids are related by Dej = DNs(aB) exp (--e/2kB T) where σB=σLJ(2/[1+ii(1+2kBT/ε)])1/6, the effective hard sphere diameter, is the (average) distance of closest approach in collisions between molecules which interact with the positive part of the LJ potential, and the Arrhenius term reflects the influence of the negative part. σLJ and ε are the size and well depth parameters. Measured diffusion coefficients of the halomethane liquids are reproduced by the equation over wide ranges of temperature and density and do not reveal any influence of the inelastic effects associated with molecular anisotropy

Isospin effect on nuclear stopping in intermediate energy Heavy Ion Collisions

By using the Isospin Dependent Quantum Molecular Dynamics Model (IQMD), we study the dependence of nuclear stopping Q_{ZZ}/A and R in intermediate energy heavy ion collisions on system size, initial N/Z, isospin symmetry potential and the medium correction of two-body cross sections. We find the effect of initial N/Z ratio, isospin symmetry potential on stopping is weak. The excitation function of Q_{ZZ}/A and R depends on the form of medium correction of two-body cross sections, the equation of state of nuclear matter (EOS). Our results show the behavior of the excitation function of Q_{ZZ}/A and R can provide clearer information of the isospin dependence of the medium correction of two-body cross sections.Comment: 3 pages including 4 figure

Identification of a novel TSC2 c.3610G > A, p.G1204R mutation contribute to aberrant splicing in a patient with classical tuberous sclerosis complex: a case report

Background: Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by hamartomas in any organ systems. Mutations in the TSC1 or TSC2 gene lead to the dysfunction of hamartin or tuberin proteins, which cause tuberous sclerosis complex. Case presentation: We describe the clinical characteristics of patients from a Chinese family with tuberous sclerosis complex and analyze the functional consequences of their causal genetic mutations. A novel heterozygous mutation (c.3610G > A) at the last nucleotide of exon 29 in TSC2 was identified. On the protein level, this variant was presumed to be a missense mutation (p.Gly1204Arg). However, the splicing assay revealed that this mutation also leads to the whole TSC2 exon 29 skipping, besides the wild-type transcript. The mutated transcript results in an in-frame deletion of 71 amino acids (p.Gly1133_Thr1203del) and its ratio with the normal splice product is of about 44:56. Conclusions: The novel c.3610G > A TSC2 mutation was identified in association with tuberous sclerosis complex. And it was proven to code both for a missense-carrying transcript (56%), and for an isoform lacking exon 29 (44%)

Universal behavior of giant electroresistance in epitaxial La0.67Ca0.33MnO3 thin films

We report a giant resistance drop induced by dc electrical currents in La0.67Ca0.33MnO3 epitaxial thin films. Resistance of the patterned thin films decreases exponentially with increasing current and a maximum drop shows at the temperature of resistance peak Tp. Variation of resistance with current densities can be scaled below and above Tp, respectively. This work can be useful for the future applications of electroresistance.Comment: 13 pages, 4 figure