Influence of the host related factors in the development of the hepatosplenic form of schistosomiasis mansoni

The frequency of hepatosplenomegaly in endemic areas is not proportional to the fecal ova count. This may be explained by epidemiological genetic. The occurrence of two or more cases of schistosomal hepatosplenomegaly in nuclear family is much higher than expected. The concentration is higher among siblings than it is among mothers and children of further and children. It is not significant between father and mother. If the mother, instead of the father has hepatosplenic schistosomiasis the relative risk for the child to acquire hepatosplenomegaly is at least five times (the maternal affect). The inbreeding is highler in the hepatosplenic than in the hepatointestinal patients. In some areas in Brazil the hepatosplenic form of the schistosomiasis mansoni occurs with much higher frequency in whites than in blacks. After treatment, reversion of hepatosplenic schistosomiasis occurs more frequently in non-whithers. It seems that the resistance of blacks to the hepatosplenic form of schistosomiasis may be related to the glyoxalase system , perhaps associated to another genetic marker. The hepatosplenic schistosomiasis is less frequent in longilineal individuals. In some areas the hepatosplenic form of schistosomiasis is more frequent in A blood group of ABO sistem. The family heredograms do not suggest a single mendelian inheritance, but probably a multifactorial and possibility poligenic one.

Is the Spanish Inheritance and Gift Tax incompatible with the free movement of workers and capital?: The reasoned opinion of the EU Commission IP/10/513

The aim of my speech is answering to the question if the Spanish Inheritance and Gift Tax is incompatible with the free movement of workers and capital. We are going to pay special attention to the European Commission’s request to Spain to change its Inheritance and Gift Tax provisions for Non-Residents or Assets held abroad. In order to answer to the question mentioned above five points will be explained. At first place I am going to describe the infrengement procedure established in the Article 258 that the EU Commission can follow when a Member State doesn’t comply with Community Law. At second place, we are going to explain what is the content of the EU Commission delivered on 5th of may 2010 regarding the spanish Inheritance and Gift Tax. Then, we will analise what establishes the Community Law regarding the freedom of workers and capital and how they are understood by the EU Court of Justice in similar cases. Finally, we are going to provide possible amendments that Spain could undertake.

On estimation and identifiability issues of sex-linked inheritance with a case study of pigmentation in Swiss barn owl (Tyto alba)

Genetic evaluation using animal models or pedigree-based models generally assume only autosomal inheritance. Bayesian animal models provide a flexible framework for genetic evaluation, and we show how the model readily can accommodate situations where the trait of interest is influenced by both autosomal and sex-linked inheritance. This allows for simultaneous calculation of autosomal and sex-chromosomal additive genetic effects. Inferences were performed using integrated nested Laplace approximations (INLA), a nonsampling-based Bayesian inference methodology. We provide a detailed description of how to calculate the inverse of the X- or Z-chromosomal additive genetic relationship matrix, needed for inference. The case study of eumelanic spot diameter in a Swiss barn owl (Tyto alba) population shows that this trait is substantially influenced by variation in genes on the Z-chromosome (sigma(2)(z) = 0.2719 and sigma(2)(a) = 0.4405). Further, a simulation study for this study system shows that the animal model accounting for both autosomal and sex-chromosome-linked inheritance is identifiable, that is, the two effects can be distinguished, and provides accurate inference on the variance components.

Optimización de la secuencia de difusión en RM 3T con modelo multifactorial IVIM en el estudio de la próstata.

La utilització de la seqüència de difusió en RM 3T amb un model multifactorial IVIM (Intravoxel Incoherent Motion) ofereix la possibilitat d'estudiar per separat la caiguda del senyal deguda a la difusió pròpiament dita, de la deguda als nuclis d'H de l'aigua lliure que es mouen en la xarxa de microcapil•lars del volum estudiat. Mostrem la nostra experiència en la implementació del model IVIM en l'estudi de la pròstata, demostrant que pot resultar útil en la comparació del teixit prostàtic respecte al teixit patològic amb diferències inicials estadísticament significatives, sent superior al càlcul de l'ADC.

Inheritance of Schistosoma mansoni infection incompatibility in Biomphalaria alexandrina snails

In this study, we looked at the inheritance of susceptibility and resistance to Schistosoma mansoni infection in the first generation of crossbred Biomphalaria alexandrina snails. Our ultimate goal is to use such information to develop a biological method of controlling schistosomiasis. We infected laboratory-bred snails with S. mansoni miracidia and examined cercarial shedding to determine susceptibility and resistance. Five parental groups were used: Group I contained 30 susceptible snails, Group II contained 30 resistant snails, Group III contained 15 susceptible and 15 resistant snails, Group IV contained 27 susceptible and three resistant snails and Group V contained three susceptible and 27 resistant snails. The percentage of resistant snails in the resulting progeny varied according to the ratio of susceptible and resistant parents per group; they are 7%, 100%, 68%, 45% and 97% from Groups I, II, III, IV and V, respectively. On increasing the percentage of resistant parent snails, the percentage of resistant progeny increased, while cercarial production in their susceptible progeny decreased.

La inseguretat al nucli antic i barri Plnas/Ca L'Escori. El Vendrell: diagnòstic multifactorial per una proposta d'intervencions més establs, responsables i duradores

El treball té com a finalitat l’estudi dels conflictes de convivència que tenen lloc amb l’ocupació i usos dels espais públics al barri dels Planas/Ca L’Escori i nucli antic del Vendrell. L’ús i l’apropiació dels espais públics és un dels aspectes fonamentals a tenir en compte en l’estudi de la vida quotidiana dels ciutadans/nes dels llocs poblats. Aquesta experiència no és igual per a totes les persones ja que segons el gènere, l’edat, així com la classe social i les identitats ètniques, es viu i percep de forma diferent, amb la qual cosa, per aproximar-se a la comprensió de l’ús diferencial del espai cal fer-ho des d’una òptica multidisciplinària. Aquest indret mostra una heterogeneïtat social i ètnica dels veïns i les veïnes que fa especialment interessant l’anàlisi dels espais públics d’aquesta zona. La riquesa poblacional (persones residents de tota la vida, persones immigrades d’altres regions d’Espanya o d’altres països, etc.) comporta una gran diversitat d’experiències quotidianes i al mateix temps, una gran varietat d’opinions sobre la percepció i la concepció dels espais públics, alhora genera un aprofitament i ús intensiu o continuat a la via pública que es tradueix en el què anomenaré "convivència intensiva". Per la qual cosa crec oportú dedicar esforços per tal d'analitzar l’ús i l’abús dels espais públics i de la convivència en aquest barri del Vendrell. Aquesta polivalència en els usos dels espais, fa que situï com a focus del meu treball, una característica que acostuma a ser, amb més o menys fonament, un agreujament de molts problemes. En concret, faig referència a l’ús i l’abús de l’espai públic i, si els conflictes que es produeixen al seu voltant respon a una fonamentació real o respon a altres factors, com poden ser causes de malestar per la immigració o la percepció social que d'aquesta es té i, que moltes vegades té un paper destacat com a causa d'estigmatització de les pràctiques de sociabilitat en públic dels immigrants, o d'una part d'ells, la qual cosa provoca una tensió estructural amb dificultats de gestió.

Comprehensive analysis of Arabidopsis expression level polymorphisms with simple inheritance.

In Arabidopsis thaliana, gene expression level polymorphisms (ELPs) between natural accessions that exhibit simple, single locus inheritance are promising quantitative trait locus (QTL) candidates to explain phenotypic variability. It is assumed that such ELPs overwhelmingly represent regulatory element polymorphisms. However, comprehensive genome-wide analyses linking expression level, regulatory sequence and gene structure variation are missing, preventing definite verification of this assumption. Here, we analyzed ELPs observed between the Eil-0 and Lc-0 accessions. Compared with non-variable controls, 5' regulatory sequence variation in the corresponding genes is indeed increased. However, approximately 42% of all the ELP genes also carry major transcription unit deletions in one parent as revealed by genome tiling arrays, representing a >4-fold enrichment over controls. Within the subset of ELPs with simple inheritance, this proportion is even higher and deletions are generally more severe. Similar results were obtained from analyses of the Bay-0 and Sha accessions, using alternative technical approaches. Collectively, our results suggest that drastic structural changes are a major cause for ELPs with simple inheritance, corroborating experimentally observed indel preponderance in cloned Arabidopsis QTL.

Multifactorial ERβ and NOTCH1 control of squamous differentiation and cancer.

Downmodulation or loss-of-function mutations of the gene encoding NOTCH1 are associated with dysfunctional squamous cell differentiation and development of squamous cell carcinoma (SCC) in skin and internal organs. While NOTCH1 receptor activation has been well characterized, little is known about how NOTCH1 gene transcription is regulated. Using bioinformatics and functional screening approaches, we identified several regulators of the NOTCH1 gene in keratinocytes, with the transcription factors DLX5 and EGR3 and estrogen receptor β (ERβ) directly controlling its expression in differentiation. DLX5 and ERG3 are required for RNA polymerase II (PolII) recruitment to the NOTCH1 locus, while ERβ controls NOTCH1 transcription through RNA PolII pause release. Expression of several identified NOTCH1 regulators, including ERβ, is frequently compromised in skin, head and neck, and lung SCCs and SCC-derived cell lines. Furthermore, a keratinocyte ERβ-dependent program of gene expression is subverted in SCCs from various body sites, and there are consistent differences in mutation and gene-expression signatures of head and neck and lung SCCs in female versus male patients. Experimentally increased ERβ expression or treatment with ERβ agonists inhibited proliferation of SCC cells and promoted NOTCH1 expression and squamous differentiation both in vitro and in mouse xenotransplants. Our data identify a link between transcriptional control of NOTCH1 expression and the estrogen response in keratinocytes, with implications for differentiation therapy of squamous cancer.

Inheritance pattern and selection criteria for resistance to soybean cyst nematode races 3 and 9

The objective of this work was to determine soybean resistance inheritance to Heterodera glycines Ichinohe (soybean cyst nematode - SCN) races 3 and 9, as well as to evaluate the efficiency of direct and indirect selection in a soybean population of 112 recombinant inbred lines (RIL) derived from the resistant cultivar Hartwig. The experiment was conducted in a completely randomized design, in Londrina, PR, Brazil. The estimated narrow-sense heritabilities for resistance to races 3 and 9 were 80.67 and 77.97%. The genetic correlation coefficient (r g = 0.17; p<0.01) shows that some genetic components of resistance to these two races are inherited together. The greatest genetic gain by indirect selection was obtained to race 9, selecting to race 3 due to simpler inheritance of resistance to race 9 and not because these two races share common resistance genes. The resistance of cultivar Hartwig to races 3 and 9 is determined by 4 and 2 genes, respectively. One of these genes confers resistance to both races, explaining a fraction of the significant genetic correlation found between resistance to these SCN races. The inheritance pattern described indicates that selection for resistance to SCN must be performed for each race individually.

Intervención multifactorial de enfermería para el tratamiento de la úlcera venosa

Siempre recordaré las clases que nos impartieron en la facultad de enfermería sobre heridas y úlceras por presión, no obstante, no fue hasta realizar las prácticas clínicas en mi tercer curso en el Hospital de Vielha, que no me percaté de lo interesante que era el tema. Pude vivir la experiencia de un caso bastante impactante, era un paciente del cual las curas se llevaban a cabo con Terapia VAC. Desde aquel momento me produjo un gran interés abarcar este género tan amplio y adquirir nuevos conocimientos sobre el tema, por lo que me decanté a realizar en mi trabajo de final de grado una intervención basada en el tratamiento de las úlceras venosas.La aparición de úlceras, sean por presión, vasculares o pie diabético son un grave problema de salud en la comunidad al que enfermería se enfrenta diariamente en cualquier ámbito de su trabajo. Este tipo de heridas tienen un gran impacto sobre la salud y la calidad de vida de los pacientes ya que el individuo se ve afectado en todas sus dimensiones, tanto físicas como psíquicas y sociales, por lo que se debe abordar su atención desde una perspectiva integral que contemple la prevención, los factores de riesgo y el tratamiento de la úlcera. Es muy importante que el profesional de enfermería conozca el proceso de desarrollo de las úlceras en general, así como los factores de riesgo, las fases de lesión, las zonas más susceptibles para su aparición, principios básicos de tratamiento, y medidas preventivas, ya que su labor es esencial no sólo en la prevención, sino también en el tratamiento integral y posterior seguimiento de las úlceras.

Inheritance of resistance to soybean cyst nematode races 3 and 14 in soybean RIL and F2 populations

The objective of this work was to evaluate the soybean inheritance of resistance to cyst nematode races 3 and 14. The following populations where evaluated: one population of recombinant inbred lines (RILs) [Hartwig (resistant) x Y23 (susceptible line)] for races 3, 14 and 9; one population of families F2:3 [M-SOY 8001 (resistant) x MB/BR 46 - Conquista (susceptible)] for race 3; and one population of families F2:3 [(S5995 (resistant) x BRSMG Renascença (susceptible)] for race 14. In RIL populations, four epistatic genes were identified which conditioned resistance to race 14, and three epistatic ones for resistance to races 3 and 9. The lack of one gene provided moderate resistance under all situations. The highest number of genes for resistance to race 14 points out that genes responsible for lower effects might be involved. In population F2:3 from M-SOY 8001 x MB/BR 46 - Conquista, one recessive gene for moderate resistance and two recessive genes complete resistance to race 3 were identified. Two recessive genes conditioning moderate resistance to race 14 were identified in population F2:3 from the crossing S5995 x BRSMG Renascença. These results will be useful in designing crossings, involving these parentals, with higher possibility to accumulating genes that provide resistance to several SCN races.

Inheritance of resistance to cotton blue disease

The objective of this work was to determine the inheritance of cotton blue disease resistance by cotton plants. Populations derived from the CD 401 and Delta Opal resistant varieties were evaluated, through a greenhouse test with artificial inoculation by viruliferous aphids. Cotton blue disease resistance is conditioned by one dominant gene, both in CD 401 and Delta Opal varieties.