51 research outputs found

    Characterization of electrical and mechanical activities of rabbit uterus associated with the presence of capacitated and non-capacitated spermatozoa

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    [EN] To investigate the effects capacitated spermatozoa may exert upon motility of the rabbit uterus, both contractility and electrical activity (frequency and intensity) were measured in 3 distinctive uterine segments of anaesthetized does: horn (UH), uterotubal junction (UTJ) and tube (UT) after 1) natural mating, 2) infusion of either seminal plasma or PBS, 3) infusion of either capacitated or non-capacitated spermatozoa. Basal values were: 17.1, 15.7, 16.4 g (contractility, P>0.05); 3.5, 3.5, 3.4 Hz (frequency, P>0.05); 0.49, 0.50, 0.57 ¿V (intensity, P>0.05) for UH, UTJ, UT, respectively. Seminal plasma caused an increase (P<0.05) in the UH contractility: 26.3 vs. 11.7 (natural mating) and 17.0 g (PBS); it also caused a decrease (P<0.05) in electrical intensity at the UTJ: 0.24 vs. 0.67 (natural mating) and 0.58 ¿V (PBS). The presence of either capacitated or non-capacitated spermatozoa caused no changes in contractility and electrical frequency in any of the uterine segments. However, there was a change in electrical intensity at UTJ (0.37 vs. 0.57 ¿V for non-capacitated and capacitated spermatozoa, respectively; P<0.05). There were also differences between segments by treatment: UTJ (0.37) vs. UT (0.59 ¿V) for non-capacitated; UH (0.46) vs. UT (0.71 ¿V) for capacitated spermatozoa (P<0.05). In conclusion, use of this experimental model showed that uterine electrical activity was slightly modified by the presence of capacitated spermatozoa.Lazcano-reyes, J.; Montiel, J.; Medrano, A. (2013). Characterization of electrical and mechanical activities of rabbit uterus associated with the presence of capacitated and non-capacitated spermatozoa. World Rabbit Science. 21(4):243-249. doi:10.4995/wrs.2013.1470.SWORD24324921

    Non-AIDS defining cancers in the D:A:D Study-time trends and predictors of survival : a cohort study

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    BACKGROUND:Non-AIDS defining cancers (NADC) are an important cause of morbidity and mortality in HIV-positive individuals. Using data from a large international cohort of HIV-positive individuals, we described the incidence of NADC from 2004-2010, and described subsequent mortality and predictors of these.METHODS:Individuals were followed from 1st January 2004/enrolment in study, until the earliest of a new NADC, 1st February 2010, death or six months after the patient's last visit. Incidence rates were estimated for each year of follow-up, overall and stratified by gender, age and mode of HIV acquisition. Cumulative risk of mortality following NADC diagnosis was summarised using Kaplan-Meier methods, with follow-up for these analyses from the date of NADC diagnosis until the patient's death, 1st February 2010 or 6 months after the patient's last visit. Factors associated with mortality following NADC diagnosis were identified using multivariable Cox proportional hazards regression.RESULTS:Over 176,775 person-years (PY), 880 (2.1%) patients developed a new NADC (incidence: 4.98/1000PY [95% confidence interval 4.65, 5.31]). Over a third of these patients (327, 37.2%) had died by 1st February 2010. Time trends for lung cancer, anal cancer and Hodgkin's lymphoma were broadly consistent. Kaplan-Meier cumulative mortality estimates at 1, 3 and 5 years after NADC diagnosis were 28.2% [95% CI 25.1-31.2], 42.0% [38.2-45.8] and 47.3% [42.4-52.2], respectively. Significant predictors of poorer survival after diagnosis of NADC were lung cancer (compared to other cancer types), male gender, non-white ethnicity, and smoking status. Later year of diagnosis and higher CD4 count at NADC diagnosis were associated with improved survival. The incidence of NADC remained stable over the period 2004-2010 in this large observational cohort.CONCLUSIONS:The prognosis after diagnosis of NADC, in particular lung cancer and disseminated cancer, is poor but has improved somewhat over time. Modifiable risk factors, such as smoking and low CD4 counts, were associated with mortality following a diagnosis of NADC

    Gene expression databases and data mining.

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    The DNA microarray technology has arguably caught the attention of the worldwide life science community and is now systematically supporting major discoveries in many fields of study. The majority of the initial technical challenges of conducting experiments are being resolved, only to be replaced with new informatics hurdles, including statistical analysis, data visualization, interpretation, and storage. Two systems of databases, one containing expression data and one containing annotation data are quickly becoming essential knowledge repositories of the research community. This present paper surveys several databases, which are considered "pillars" of research and important nodes in the network. This paper focuses on a generalized workflow scheme typical for microarray experiments using two examples related to cancer research. The workflow is used to reference appropriate databases and tools for each step in the process of array experimentation. Additionally, benefits and drawbacks of current array databases are addressed, and suggestions are made for their improvement
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