392 research outputs found

    A Problem of Relative, Constrained Motion

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    We develop a new method to determine the acceleration of a block sliding down along the face of a moving wedge. We have been able to link the solution of this problem to that of the inclined plane problem of elementary physics, thus providing a simpler solution to it.Comment: 4 pages, 3 figure

    Critical phenomena and quantum phase transition in long range Heisenberg antiferromagnetic chains

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    Antiferromagnetic Hamiltonians with short-range, non-frustrating interactions are well-known to exhibit long range magnetic order in dimensions, d2d\geq 2 but exhibit only quasi long range order, with power law decay of correlations, in d=1 (for half-integer spin). On the other hand, non-frustrating long range interactions can induce long range order in d=1. We study Hamiltonians in which the long range interactions have an adjustable amplitude lambda, as well as an adjustable power-law 1/xα1/|x|^\alpha, using a combination of quantum Monte Carlo and analytic methods: spin-wave, large-N non-linear sigma model, and renormalization group methods. We map out the phase diagram in the lambda-alpha plane and study the nature of the critical line separating the phases with long range and quasi long range order. We find that this corresponds to a novel line of critical points with continuously varying critical exponents and a dynamical exponent, z<1.Comment: 27 pages, 12 figures. RG flow added. Final version to appear in JSTA

    Natural polymorphisms of HIV type 2 pol sequences from drug-naive individuals

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    Until today, the susceptibility of human immunodeficiency virus type 2 (HIV-2) to protease and nucleosidic reverse-transcriptase inhibitors (PI and NRTI, respectively) has not been clearly documented. In this report we studied HIV-2 proviral sequences (n = 30) from drug-naive patients. Our results revealed that several amino acid positions in the protease and reverse transcriptase coding sequence harbored residues that have been associated with drug resistance in HIV-1-infected patients. In particular, the M46I substitution in the protease was detected in 90% of the sequences analyzed, which, together with the other substitutions identified, may indicate a reduced susceptibility of HIV-2-infected drug-naive patients to PI. Furthermore, interpretation of genotypic data with four available algorithms, developed for interpretation of HIV-1 sequence data, suggested nonoverlapping profiles of drug resistance

    Whole exome sequencing of patients with diffuse idiopathic skeletal hyperostosis and calcium pyrophosphate crystal chondrocalcinosis

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    Objectives: DISH/CC is a poorly understood phenotype characterised by peripheral and axial enthesopathic calcifications, frequently fulfilling the radiological criteria for Diffuse Idiopathic Skeletal Hyperostosis (DISH, MIM 106400), and in some cases associated with Calcium Pyrophosphate Dihydrate (CPPD) Chondrocalcinosis (CC). The concurrence of DISH and CC suggests a shared pathogenic mechanism. In order to identify genetic variants for susceptibility we performed whole exome sequencing in four patients showing this phenotype. Materials and methods: Exome data were filtered in order to find a variant or a group of variants that could be associated with the DISH/CC phenotype. Variants of interest were subsequently confirmed by Sanger sequencing. Selected variants were screened in a cohort of 65 DISH/CC patients vs 118 controls from Azores. The statistical analysis was performed using PLINK V1.07. Results:We identified 21 genetic variants in 17 genes that were directly or indirectly related to mineralization, several are predicted to have a strong effect at a protein level. Phylogenetic analysis of altered amino acids indicates that these are either highly conserved in vertebrates or conserved in mammals. In case-control analyses, variant rs34473884 in PPP2R2D was significantly associated with the DISH/CC phenotype (p=0.028; OR=1.789, 95% CI= 1.060 - 3.021)). Conclusion: The results of the present and preceding studies with the DISH/CC families suggests that the phenotype has a polygenic basis. The PPP2R2D gene could be involved in this phenotype in an as yet unknown way.FRCT: M3.1.2/F/023/2011info:eu-repo/semantics/publishedVersio

    LINFOMA DE CÉLULAS B LOCALIZADO NA CAVIDADE ORAL NUM FELÍDEO – CASO CLÍNICO

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    Um felídeo de 14 anos europeu comum foi apresentado à consulta com história clínica de 1 mês de diminuição de apetite, halitose e deformação facial. O seu estado imunitário foi negativo para FIV e FELV. Os resultados hematológicos e bioquímicos revelaram apenas um aumento de globulinas séricas e a punção aspirativa de agulha fina revelou linfoma localizado sem sinais de envolvimento sistémico nos exames complementares. A cirurgia foi recomendada e consistiu em maxilectomia rostral unilateral, excisão labial, enxerto labial de avanço e colocação de tubo esofágico. O resultado histopatológico revelou linfoma de baixo índice mitótico e os exames imunohistoquímicos revelaram positividade ao marcador CD79a, um marcador de células B. O tumor foi classificado em Estádio I pelo sistema de estadiamento de linfoma felino. Apesar dos resultados histopatológicos sugerirem uma resposta pobre à quimioterapia, iniciou-se um protocolo terapêutico com ciclofosfamida, vincristina e prednisolona. Dois meses após o diagnóstico e seis semanas após início de quimioterapia o animal revelou anorexia e no exame ecográfico de controlo foram detectadas metástases. O gato foi hospitalizado e morreu uma semana depois. O prognóstico de linfoma localizado no gato é desconhecido devido à sua rara ocorrência. Está recomendado o controlo local do tumor com cirurgia ou radioterapia combinadas ou não com quimioterapia. Apesar da sobrevivência do animal ter sido breve após o tratamento cirúrgico os proprietários ficaram satisfeitos com o aumento de qualidade de vida após cirurgia
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