Political Competition, Welfare Outcomes and Expenditures on Human Development: The Experience of a Democracy

There is a growing literature on the effect of electoral competition and democratic participation on issues such as corruption and government policy. The theoretical and empirical literature suggests that electoral competition has a beneficial impact on policies. This paper studies the effects of political competition and democratic participation on welfare outcomes. We develop a model to assess the effects of electoral competition on human developmental outcomes and empirically test the key predictions using data on infant mortality rates (IMR) in India. The empirical results provide strong support for the theoretical conjectures, which suggest that high electoral competition and high citizen participation in elections can explain much of the variation in IMR across different states in a democratic country like India.human development, electoral competition

On Higher-Order Fourier Analysis over Non-Prime Fields

The celebrated Weil bound for character sums says that for any low-degree polynomial P and any additive character chi, either chi(P) is a constant function or it is distributed close to uniform. The goal of higher-order Fourier analysis is to understand the connection between the algebraic and analytic properties of polynomials (and functions, generally) at a more detailed level. For instance, what is the tradeoff between the equidistribution of chi(P) and its "structure"? Previously, most of the work in this area was over fields of prime order. We extend the tools of higher-order Fourier analysis to analyze functions over general finite fields. Let K be a field extension of a prime finite field F_p. Our technical results are: 1. If P: K^n -> K is a polynomial of degree |K|^{-s} for some s > 0 and non-trivial additive character chi, then P is a function of O_{d, s}(1) many non-classical polynomials of weight degree < d. The definition of non-classical polynomials over non-prime fields is one of the contributions of this work. 2. Suppose K and F are of bounded order, and let H be an affine subspace of K^n. Then, if P: K^n -> K is a polynomial of degree d that is sufficiently regular, then (P(x): x in H) is distributed almost as uniformly as possible subject to constraints imposed by the degree of P. Such a theorem was previously known for H an affine subspace over a prime field. The tools of higher-order Fourier analysis have found use in different areas of computer science, including list decoding, algorithmic decomposition and testing. Using our new results, we revisit some of these areas. (i) For any fixed finite field K, we show that the list decoding radius of the generalized Reed Muller code over K equals the minimum distance of the code. (ii) For any fixed finite field K, we give a polynomial time algorithm to decide whether a given polynomial P: K^n -> K can be decomposed as a particular composition of lesser degree polynomials. (iii) For any fixed finite field K, we prove that all locally characterized affine-invariant properties of functions f: K^n -> K are testable with one-sided error

Probing the Fermi surface and magnetotransport properties in MoAs2_{2}

Transition metal dipnictides (TMDs) have recently been identified as possible candidates to host topology protected electronic band structure. These materials belong to an isostructural family and show several exotic transport properties. Especially, the large values of magnetoresistance (MR) and carrier mobility have drawn significant attention from the perspective of technological applications. In this report, we have investigated the magnetotransport and Fermi surface properties of single crystalline MoAs$_{2}$, another member of this group of compounds. Field induced resistivity plateau and a large MR have been observed, which are comparable to several topological systems. Interestingly, in contrast to other isostructural materials, the carrier density in MoAs$_{2}$ is quite high and shows single-band dominated transport. The Fermi pockets, which have been identified from the quantum oscillation, are largest among the members of this group and have significant anisotropy with crystallographic direction. Our first-principles calculations reveal a substantial difference between the band structures of MoAs$_{2}$ and other TMDs. The calculated Fermi surface consists of one electron pocket and another 'open-orbit' hole pocket, which has not been observed in TMDs so far.Comment: 8 pages, 9 figure

Treating cutaneous T-cell lymphoma with highly irregular surfaces with photon irradiation using rice as tissue compensator.

PurposeCutaneous T-cell lymphoma (CTCL) is known to have an excellent response to radiotherapy, an important treatment modality for this disease. In patients with extremity and digit involvement, the irregular surface and depth variations create difficulty in delivering a homogenous dose using electrons. We sought to evaluate photon irradiation with rice packing as tissue equivalence and determine clinical tolerance and response.Materials and methodsThree consecutive CTCL patients with extensive lower extremity involvement including the digits were treated using external beam photon therapy with rice packing for tissue compensation. The entire foot was treated to 30-40 Gy in 2-3 Gy per fraction using 6 MV photons prescribed to the mid-plane of an indexed box filled with rice in which the foot was placed. Treatment tolerance and response were monitored with clinical evaluation.ResultsAll patients tolerated the treatment without treatment breaks. Toxicities included grade 3 erythema and desquamation with resolution within 4 weeks. No late toxicities were observed. All patients had a partial response by 4 weeks after therapy with two patients achieving a complete response. Patients reported improved functionality after treatment. No local recurrence has been observed.ConclusionTissue compensation with rice packing offers a convenient, inexpensive, and reproducible method for the treatment of CTCL with highly irregular surfaces

Matrix Metalloproteinase-1 (MMP-1) Promoter Polymorphisms are Well Linked with Lower Stomach Tumor Formation in Eastern Indian Population

Expression of matrix metalloproteinase-1 (MMP-1), an interstitial collagenase, plays a major role in cellular invasion during development of gastric cancer, a leading cause of death worldwide. A single-nucleotide polymorphism (SNP) 21607 1G/2G site of the MMP-1 gene promoter has been reported to alter transcription level. While the importance’s of other SNPs in the MMP-1 promoter have not yet been studied in gastric cancer, our aim was to investigate MMP-1 gene promoter polymorphisms and gastric cancer susceptibility in eastern Indian population. A total of 145 gastric cancer patients and 145 healthy controls were genotyped for MMP-1 21607 1G/2G (rs1799750) by PCR-restriction fragment length polymorphism (RFLP), while MMP-1 2519 A/G (rs1144393), MMP-1 2422 T/A (rs475007), MMP-1 2340 T/C (rs514921) and MMP-1 2320 T/C (rs494379) were genotyped by DNA sequencing. A positive association was found with MMP-1 2422 T/A SNP that showed significant risk for regional lymph node metastasis (P = 0.021, Odd’s ratio (OR) = 3.044, Confidence intervals (CI) = 1.187– 7.807). In addition, we found a significant association with lower stomach tumor formation among gastric cancer patients for three adjacent polymorphisms near the transcriptional start sites of [MMP-1 2422 T/A (P = 0.043, OR = 2.182, CI = 1.03– 4.643), MMP-1 2340 T/C (P = 0.075, OR = 1.97, CI = 0.94–4.158) and MMP-1 2320 T/C (P = 0.034, OR = 2.224, CI = 1.064– 40731)]. MMP-1 level in patients’ serum was correlated with MMP-1 promoter haplotypes conferring these three SNPs to evaluate the functional importance of these polymorphisms in lower stomach tumor formation and significant correlation was observed. Furthermore, MMP-1 2519 A/G polymorphism displayed poor cellular differentiation (P = 0.024, OR = 3.8, CI = 1.69–8.56) attributing a higher risk of cancer progression.In conclusion, MMP-1 proximal promoter SNPs are associated with the risk of lower stomach tumor formation and node metastasis in eastern Indian population

DNA linkage based diagnosis of Wilson disease in asymptomatic siblings

Wilson disease (WD) is an autosomal recessive disorder caused by defects in ATP7B gene located in chromosome 13q14, and manifested as hepatolenticular degeneration as a result of accumulation of copper. No information on the mutation in the ATP7B gene and haplotypes using linked markers is available for WD patients in India. Hence, the present study was undetaken to identify, by a PCR-based molecular diagnostic test, presymptomatic siblings of WD affected individuals in families with multiple offspring. Methods: Genomic DNA was prepared from the peripheral blood of the patients, siblings and his/her first degree relatives. The repeat-markers flanking WD locus were amplified by PCR using fluorescent labeled primers. Amplified DNA fragments were analyzed by polyacrylamide gel electrophoresis in ABI 377 DNA sequencing system. Genotypes of the samples were determined using Genescan software. Haplotypes were determined based on segregation of the alleles in the families under study. Results: Among 15 WD affected families with multiple children, 4 cases were identified where younger siblings shared same genotype as the patient at all three markers analyzed. Further, eight different haplotypes were detected in the four patients. Interpretation & conclusion: The siblings of the WD patients carrying the same genotype at the markers linked to WD locus were presymptomatically diagnosed individuals. Presence of eight different haplotypes in the four patients suggested mutational heterogeneity at the WD locus. The test helps clinicians for therapeutic intervention in suspect WD cases by copper chelating agents prior to manifestation of overt clinical symptoms. Key words ATP7B - genotype - haplotype - microsatellite - Wilson disease (WD) is a genetic disorder, which manifests as hepatolenticular degeneration as a result of accumulation of copper in the brain, liver, kidney and cornea due to its deranged biliary excretion1. In 1912, a WD was described as a familial syndrome of progressive lenticular degeneration associated with cirrhosis of the liver2. The etiological role of copper in the pathogenesis of WD was recognized much late