From exotic phases to microscopic Hamiltonians

We report recent analytical progress in the quest for spin models realising exotic phases. We focus on the question of `reverse-engineering' a local, SU(2) invariant S=1/2 Hamiltonian to exhibit phases predicted on the basis of effective models, such as large-N or quantum dimer models. This aim is to provide a point-of-principle demonstration of the possibility of constructing such microscopic lattice Hamiltonians, as well as to complement and guide numerical (and experimental) approaches to the same question. In particular, we demonstrate how to utilise peturbed Klein Hamiltonians to generate effective quantum dimer models. These models use local multi-spin interactions and, to obtain a controlled theory, a decoration procedure involving the insertion of Majumdar-Ghosh chainlets on the bonds of the lattice. The phases we thus realise include deconfined resonating valence bond liquids, a devil's staircase of interleaved phases which exhibits Cantor deconfinement, as well as a three-dimensional U(1) liquid phase exhibiting photonic excitations.Comment: Invited talk at Peyresq Workshop on "Effective models for low-dimensional strongly correlated systems". Proceedings to be published by AIP. v2: references adde

MTHFR A1298C polymorphism and idiopathic male infertility

Background: DNA methylation is an important epigenetic feature of DNA that plays a pivotal role in gene expression regulation during spermatogenesis. The enzyme methylenetetrahydrofolate reductase (MTHFR) catalyses the formation of folate intermediates that are vital for DNA synthesis and methylation reactions. C677T and A1298C variants of MTHFR result in reduced plasma folate and increase the susceptibility to various multifactorial disorders. We have already shown that homozygosity for 677 (C ®T) mutation in the MTHFR gene, is a risk factor for idiopathic male infertility in an Indian population. Aim: Recently, we showed that homozygosity for the 677(C;T) mutation in the MTHFR gene is a risk factor for idiopathic male infertility and now we aim to assess whether the A1298C mutation in the same gene is an additional risk factor for idiopathic male infertility in an Indian population. Setting and Designs : In a case-control study 151 idiopathic male infertile patients and 140 healthy fertile control individuals were recruited from the University hospital and infertility clinics in Varanasi city, India. Materials and Methods: Genotyping for A1298C change of the MTHFR gene was done by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Statistical Analysis : Allele frequencies were calculated using Fisher's exact test. Odds ratio was calculated as the measure of the association between the MTHFR genotype and idiopathic male infertility. Results : The homozygous (C/C) A1298C polymorphism of the MTHFR gene was present at a statistically high significance in idiopathic azoospermic infertile men (OR=3.4494, CI: 1.0092 to 11.7899, P<0.05). Conclusion : The MTHFR 1298CC genotype is an additional genetic risk factor for idiopathic male infertility in an Indian population

Acute Burkitt\u27s Leukemia: Case Report and Literature Review

The occurrence of leukemia in Burkitt\u27s lymphoma, with or without visceral or nodal tumefaction is uncommon, and its initial presentation as leukemia is even more unusual. Because it has a poor chemotherapeutic response and a grave prognosis, it is important to recognize this unusual leukemia correctly. Our report describes the clinical and pathologic findings of Burkitt\u27s lymphoma cell leukemia in a five-year-old white boy who presented with abdominal distension, hepatosplenomegaly, and lymphadenopathy. Blood examination revealed normocytic normochromic anemia, erythroblastosis, slight leukocytosis, and the presence of numerous (24%) blasts. A diagnosis of Burkitt\u27s lymphoma was established on the basis of morphologic, cytochemical, and immunologic studies performed on the blasts. When the chemotherapy protocol for the lymphoma was administered, the patient responded well initially but suffered uric acid nephropathy, which was successfully treated. However, within two weeks he had a rapid relapse of leukemia and died four months after admission

Comparison of two ultra-widefield cameras with high image resolution and wider view for identifying diabetic retinopathy lesions

Purpose: To compare the effectiveness of the Optos P200dTx and Zeiss Clarus 50fundus cameras in detecting diabetic retinopathy (DR) lesions. Methods: A cross-sectional study was conducted among 243 patients with clinically diagnoseddiabetesmellituswhowerereferredforaneyeexaminationfromtwotertiary eye care centers in Chennai, India. Patients underwent DR screening based on mydriatic fundal images acquired by both fundal cameras. Fundal images from the two separate devices for each eye were compared based on accurately identified pathological retinal lesions with respect to type and location. Results: When studying lesions of the central retina, they were better identified by the Zeiss Clarus compared with the Optos P200dTx, with six out of eight being statistically significant (P < 0.05). However, lesions of the mid-peripheral retina and peripheral retina were better identified by the Optos P200dTx than the Zeiss Clarus, with three out of eight lesions and five out of eight lesions being statistically significant (P < 0.05), respectively. Based on the color and size of lesions, the Optos P200dTx had a higher chance (59.6%) of missing white lesions than did the Zeiss Clarus (17%) (P < 0.0001). Consequently, small-and medium-sized lesions were missed more by the Optos P200dTx (30.72% and 32.63%, respectively) than the Zeiss Clarus (22.3% and 19.30%, respectively). Conclusions: The capability of detecting or missing a particular DR lesion among diabetics differed between the two cameras based on effective field of view, resolution, and the retinal zone being imaged. Translational Relevance: The choice of which ultra-widefield camera to be used for screening DR can be based on the greater prevalence of central versus peripheral retinal lesions noted in the patient population seen in a clinical practice

Metal based pharmacologically active agents: Synthesis, structural elucidation, DNA interaction, in vitro antimicrobial and in vitro cytotoxic screening of copper(II) and zinc(II) complexes derived from amino acid based pyrazolone derivatives

AbstractThe paper presents the synthesis of complex combinations of Cu(II) and Zn(II) with Schiff base obtained by the condensation reaction of 4-aminoantipyrine with benzaldehyde and 2-amino-3-methyl-butanoicacid. Structural features of synthesized compounds were determined by analytical and spectral techniques. Binding of synthesized complexes with calf thymus DNA (CT DNA) was studied by spectroscopic methods and viscosity measurements. Experimental results indicated the ability of the complexes to form adducts with DNA and to distort the double helix by changing the base stacking. Oxidative DNA cleavage activities of the complexes were studied with supercoiled (SC) pUC19 DNA using gel electrophoresis. The in vitro antimicrobial screening effects of the investigated compounds were monitored by the disk diffusion method. The synthesized Schiff base complexes exhibited higher antimicrobial activity than the respective free Schiff base. The in vitro cytotoxicity of synthesized complexes against Ehrlich ascites carcinoma (EAC) tumor model was investigated using trypan blue dye exclusion assay. The complexes possessed significant cytotoxic activity

SU(2)-invariant spin-1/2 Hamiltonians with RVB and other valence bond phases

We construct a family of rotationally invariant, local, S=1/2 Klein Hamiltonians on various lattices that exhibit ground state manifolds spanned by nearest-neighbor valence bond states. We show that with selected perturbations such models can be driven into phases modeled by well understood quantum dimer models on the corresponding lattices. Specifically, we show that the perturbation procedure is arbitrarily well controlled by a new parameter which is the extent of decoration of the reference lattice. This strategy leads to Hamiltonians that exhibit i) $Z_2$ RVB phases in two dimensions, ii) U(1) RVB phases with a gapless ``photon'' in three dimensions, and iii) a Cantor deconfined region in two dimensions. We also construct two models on the pyrochlore lattice, one model exhibiting a $Z_2$ RVB phase and the other a U(1) RVB phase.Comment: 16 pages, 15 figures; 1 figure and some references added; some minor typos fixe

Supersymmetric Model of Spin-1/2 Fermions on a Chain

In recent work, N=2 supersymmetry has been proposed as a tool for the analysis of itinerant, correlated fermions on a lattice. In this paper we extend these considerations to the case of lattice fermions with spin 1/2 . We introduce a model for correlated spin-1/2 fermions with a manifest N=4 supersymmetry, and analyze its properties. The supersymmetric ground states that we find represent holes in an anti-ferromagnetic background.Comment: 15 pages, 10 eps figure

Extended Quantum Dimer Model and novel valence-bond phases

We extend the quantum dimer model (QDM) introduced by Rokhsar and Kivelson so as to construct a concrete example of the model which exhibits the first-order phase transition between different valence-bond solids suggested recently by Batista and Trugman and look for the possibility of other exotic dimer states. We show that our model contains three exotic valence-bond phases (herringbone, checkerboard and dimer smectic) in the ground-state phase diagram and that it realizes the phase transition from the staggered valence-bond solid to the herringbone one. The checkerboard phase has four-fold rotational symmetry, while the dimer smectic, in the absence of quantum fluctuations, has massive degeneracy originating from partial ordering only in one of the two spatial directions. A resonance process involving three dimers resolves this massive degeneracy and dimer smectic gets ordered (order from disorder).Comment: 20 pages, 13 figures, accepted for publication in J. Stat. Mec

Diagnostic circulating biomarkers to detect vision-threatening diabetic retinopathy: Potential screening tool of the future?

With the increasing prevalence of diabetes in developing and developed countries, the socio-economic burden of diabetic retinopathy (DR), the leading complication of diabetes, is growing. Diabetic retinopathy (DR) is currently one of the leading causes of blindness in working-age adults worldwide. Robust methodologies exist to detect and monitor DR; however, these rely on specialist imaging techniques and qualified practitioners. This makes detecting and monitoring DR expensive and time-consuming, which is particularly problematic in developing countries where many patients will be remote and have little contact with specialist medical centres. Diabetic retinopathy (DR) is largely asymptomatic until late in the pathology. Therefore, early identification and stratification of vision-threatening DR (VTDR) is highly desirable and will ameliorate the global impact of this disease. A simple, reliable and more cost-effective test would greatly assist in decreasing the burden of DR around the world. Here, we evaluate and review data on circulating protein biomarkers, which have been verified in the context of DR. We also discuss the challenges and developments necessary to translate these promising data into clinically useful assays, to detect VTDR, and their potential integration into simple point-of-care testing devices