Τρίτη 17 Μαΐου 2016
Evaluation of the Effect of Aneurysmal Clipping on Electrocardiography and Echocardiographic Changes in Patients With Subarachnoid Hemorrhage: A Prospective Observational Study.
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Cognitive Functioning After Surgery in Middle-aged and Elderly Danish Twins.
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Journal Club.
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Bowel Preparation in Awake Craniotomy: An Overlooked Entity.
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Effect of Acute Exercise on Fatigue in People with ME/CFS/SEID: A Meta-analysis.
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Strategic Priorities for Physical Activity Surveillance in the United States.
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Increased Visual Utilization in Chronic Ankle Instability: A Meta-analysis.
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Contralateral Repeated Bout Effect of Eccentric Exercise of the Elbow Flexors.
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High-Intensity Interval Training on Cognitive and Mental Health in Adolescents.
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A Cluster RCT to Reduce Office Workers' Sitting Time: Impact on Activity Outcomes.
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Neutrophil Depletion Attenuates Muscle Injury following Exhaustive Exercise.
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Fitness during Breast Cancer Treatment and Recovery in an Athlete: A Case Study.
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Intensity-dependent Contribution of Neuromuscular Fatigue after Constant-Load Cycling.
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Head Impact Biomechanics in Women's College Soccer.
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Leisure-Time Physical Activity and the Risk of Suspected Bacterial Infections.
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The Relation of Arm Exercise Peak Heart Rate to Stress Test Results and Outcome.
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Ischemic Preconditioning and Repeated Sprint Swimming: A Placebo and Nocebo Study.
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A Randomized Trial on the Effect of Exercise Mode on Breast Cancer-related Lymphedema.
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The predictive roles of neural oscillations in speech motor adaptability
The human speech system exhibits a remarkable flexibility by adapting to alterations in speaking environments. While it is believed that speech motor adaptation under altered sensory feedback involves rapid reorganization of speech motor networks, the mechanisms by which different brain regions communicate and coordinate their activity to mediate adaptation remain unknown, and explanations of outcome differences in adaption remain largely elusive. In this study, under the paradigm of altered auditory feedback with continuous EEG recordings, the differential roles of oscillatory neural processes in motor speech adaptability were investigated. The predictive capacities of different EEG frequency bands were assessed, and it was found that theta-, beta-, and gamma-band activities during speech planning and production contained significant and reliable information about motor speech adaptability. It was further observed that these bands do not work independently but interact with each other suggesting an underlying brain network operating across hierarchically organized frequency bands to support motor speech adaptation. These results provide novel insights into both learning and disorders of speech using time frequency analysis of neural oscillations.
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Incorporating spike-rate adaptation into a rate code in mathematical and biological neurons
For a slowly varying stimulus, the simplest relationship between a neuron's input and output is a rate code, in which the spike rate is a unique function of the stimulus at that instant. In the case of spike-rate adaptation, there is no unique relationship between input and output, because the spike rate at any time depends both on the instantaneous stimulus and on prior spiking (the "history"). To improve the decoding of spike trains produced by neurons that show spike-rate adaptation, we developed a simple scheme that incorporates "history" into a rate code. We utilized this rate-history code successfully to decode spike trains produced by 1) mathematical models of a neuron in which the mechanism for adaptation (IAHP) is specified, and 2) the gastropyloric receptor (GPR2), a stretch-sensitive neuron in the stomatogastric nervous system of the crab Cancer borealis, that exhibits long-lasting adaptation of unknown origin. Moreover, when we modified the spike rate either mathematically in a model system or by applying neuromodulatory agents to the experimental system, we found that changes in the rate-history code could be related to the biophysical mechanisms responsible for altering the spiking.
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ON and OFF inhibition as mechanisms for forward masking in the inferior colliculus: a modeling study
Masking effects of a preceding stimulus on the detection or perception of a signal have been found in several sensory systems in mammals, including humans and rodents. In the auditory system, it has been hypothesized that a central "OFF-inhibitory" mechanism, which is generated by neurons that respond after a sound is terminated, may contribute to the observed psychophysics. The present study constructed a systems model for the inferior colliculus that includes major ascending monaural and binaural auditory pathways. The fundamental characteristics of several neuron types along the pathways were captured by Hodgkin-Huxley models with specific membrane and synaptic properties. OFF responses were reproduced with a model of the superior paraolivary nucleus containing a hyperpolarization-activated h current and a T-type calcium current. When the gap between the end of the masker and the onset of the signal was large, e.g., >5 ms, OFF inhibition generated strong suppressive effects on the signal response. For smaller gaps, an additional inhibitory source, which was modeled as ON inhibition from the contralateral dorsal nucleus of the lateral lemniscus, showed the potential of explaining the psychophysics. Meanwhile, the effect of a forward masker on the binaural sensitivity to a low-frequency signal was examined, which was consistent with previous psychophysical findings related to sound localization.
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A common control signal and a ballistic stage can explain the control of coordinated eye-hand movements
Voluntary control has been extensively studied in the context of eye and hand movements made in isolation, yet little is known about the nature of control during eye-hand coordination. We probed this with a redirect task. Here subjects had to make reaching/pointing movements accompanied by coordinated eye movements but had to change their plans when the target occasionally changed its position during some trials. Using a race model framework, we found that separate effector-specific mechanisms may be recruited to control eye and hand movements when executed in isolation but when the same effectors are coordinated a unitary mechanism to control coordinated eye-hand movements is employed. Specifically, we found that performance curves were distinct for the eye and hand when these movements were executed in isolation but were comparable when they were executed together. Second, the time to switch motor plans, called the target step reaction time, was different in the eye-alone and hand-alone conditions but was similar in the coordinated condition under assumption of a ballistic stage of ~40 ms, on average. Interestingly, the existence of this ballistic stage could predict the extent of eye-hand dissociations seen in individual subjects. Finally, when subjects were explicitly instructed to control specifically a single effector (eye or hand), redirecting one effector had a strong effect on the performance of the other effector. Taken together, these results suggest that a common control signal and a ballistic stage are recruited when coordinated eye-hand movement plans require alteration.
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Noradrenaline Reuptake Inhibition Impairs Cortical Output and Limits Endurance Time
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Diaphragm Recruitment Increases during a Bout of Targeted Inspiratory Muscle Training
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Central Regulation and Neuromuscular Fatigue during Exercise of Different Durations
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Quick Questions in Ankle Sprains: Expert Advice in Sports Medicine
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Functional and Neuromuscular Changes after Anterior Cruciate Ligament Rupture in Rats
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Correlation between Cardiorespiratory Fitness and Platelet Function in Healthy Women
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Leisure Time Physical Activity and Gestational Diabetes Mellitus in the Omega Study
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Hypoventilation Training at Supramaximal Intensity Improves Swimming Performance
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Association of Injury History and Incident Injury in Cadet Basic Military Training
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Motor Performance as Risk Factor for Lower Extremity Injuries in Children
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A recessive syndrome of intellectual disability, moderate overgrowth, and renal dysplasia predisposing to Wilms tumor is caused by a mutation in FIBP gene
Clinical classification of overgrowth syndromes represents a challenge since a wide spectrum of disorders result in marked overgrowth. Therefore, there is a continuous effort to identify the genetic basis of these disorders that will eventually facilitate their molecular classification. Here, we have identified the genetic etiology and the pathogenetic mechanism underlying a rare autosomal recessive overgrowth syndrome in three affected siblings. The overgrowth phenotype in the patients was accompanied by developmental delay, learning disabilities, and variable congenital abnormalities. To elucidate the genetic etiology of the disorder, whole-genome genotyping and whole-exome sequencing were used. The disease was mapped to 3p21.1-p14.2 and 11q13.1-q13.4, where an in-frame insertion (c.175_176insTAA) in FIBP gene was revealed. The resulting indel (p.H59LN) was predicted to change the protein conformation with likely deleterious effect on its function as one of the fibroblast growth factor signaling mediators. In vitro cellular proliferation assay and in situ hypridization in vivo were then performed to understand the pathophysiology of the disease. The patients' skin fibroblasts showed an increased proliferation capacity compared to the controls' explaining the observed overgrowth phenotype. In addition, we detected Fibp expression most notably in the brains of mice embryos suggesting a possible effect on cognitive functions early in development. To date, only one patient has been reported with a homozygous nonsense mutation in FIBP exhibiting an overgrowth syndrome with multiple congenital abnormalities. Taken all together, these findings provide convincing evidence implicating FIBP aberrations in the newly recognized overgrowth syndrome and expand the associated phenotypes to include possible Wilms tumor predisposition. © 2016 Wiley Periodicals, Inc.
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Coming of age: ten years of next-generation sequencing technologies
Nature Reviews Genetics 17, 333 (2016). doi:10.1038/nrg.2016.49
Authors: Sara Goodwin, John D. McPherson & W. Richard McCombie
Since the completion of the human genome project in 2003, extraordinary progress has been made in genome sequencing technologies, which has led to a decreased cost per megabase and an increase in the number and diversity of sequenced genomes. An astonishing complexity of genome architecture
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Genetic variation: Genomic monomorphism off the scale
Nature Reviews Genetics 17, 316 (2016). doi:10.1038/nrg.2016.61
Author: Linda Koch
The generality of the small-population paradigm in conservation genetics is called into question by a recent report in Current Biology. It has long been thought that loss of genetic variation drives the extinction of isolated populations. However, an analysis of complete genome sequence data
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Bioinformatics: Benchmarking transcript expression quantification
Nature Reviews Genetics 17, 316 (2016). doi:10.1038/nrg.2016.62
Author: Linda Koch
A new study presents a set of assessment metrics and visualization techniques for the statistical evaluation of algorithms for quantifying RNA sequencing data. The benchmarks are available as a R/Bioconductor package (http://ift.tt/23QBzZd). The new set of interpretable assessment metrics relate to the quantification
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Human genetics: Splicing: linking genetic variation and disease
Nature Reviews Genetics 17, 317 (2016). doi:10.1038/nrg.2016.64
Author: Denise Waldron
It is well known that noncoding genetic variants contribute to complex traits and diseases, but the mechanisms through which they act are not fully understood. Now, a study published in Science reports that RNA splicing is a primary link between genetic variation and complex
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Genetic sources of population epigenomic variation
Nature Reviews Genetics 17, 319 (2016). doi:10.1038/nrg.2016.45
Authors: Aaron Taudt, Maria Colomé-Tatché & Frank Johannes
The field of epigenomics has rapidly progressed from the study of individual reference epigenomes to surveying epigenomic variation in populations. Recent studies in a number of species, from yeast to humans, have begun to dissect the cis- and trans-regulatory genetic mechanisms that shape
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Genetic Engineering: A CORRECT step forward in disease modelling
Nature Reviews Genetics 17, 316 (2016). doi:10.1038/nrg.2016.60
Author: Linda Koch
A CRISPR–Cas9-based strategy enables the targeted introduction of homozygous or heterozygous sequence changes by homology-directed repair. The CORRECT (consecutive re-guide or re-Cas steps to erase CRISPR–Cas-blocked targets) method allows for the introduction of targeted modifications together with silent CRISPR–Cas-blocking mutations aimed at preventing 're-editing' due
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Genetic variation: Linking TF binding to disease risk using pooled ChIP–seq
Nature Reviews Genetics 17, 317 (2016). doi:10.1038/nrg.2016.55
Author: Bryony Jones
A pooled ChIP–seq (chromatin immunoprecipitation followed by sequencing) approach for mapping quantitative trait loci (QTLs) can identify genetic variants that affect the binding of transcription factors (TFs), according to new research published in Cell. Ultimately, this approach reveals links between binding QTLs (bQTLs), chromatin
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RNA modifications: what have we learned and where are we headed?
Nature Reviews Genetics 17, 365 (2016). doi:10.1038/nrg.2016.47
Authors: Michaela Frye, Samie R. Jaffrey, Tao Pan, Gideon Rechavi & Tsutomu Suzuki
Proper control of the transcriptome is key for diverse aspects of gene expression, cellular functions and development, and its disruption can result in disease. A rapidly accumulating wealth of studies are identifying and functionally characterizing diverse types of RNA base modifications in protein-coding and non-coding
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Genetic screens: Finding the resilient few
Nature Reviews Genetics 17, 316 (2016). doi:10.1038/nrg.2016.54
Author: Denise Waldron
Researchers of a study published in Nature Biotechnology have identified 13 healthy individuals who harbour genetic variants associated with severe Mendelian diseases that were previously thought to be completely penetrant.Studies of disease genetics are generally focused on the identification of disease-causing variants in
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Gene regulation: Finding genetic target sites
Nature Reviews Genetics 17, 314 (2016). doi:10.1038/nrg.2016.53
Author: Darren J. Burgess
There is increasing realization that genetic variation in non-coding regulatory elements, such as enhancers, has a major role in evolution, complex traits and diseases. However, a key challenge is to identify the genes regulated by these elements in order to dissect the gene regulatory networks
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The statistical properties of gene-set analysis
Nature Reviews Genetics 17, 353 (2016). doi:10.1038/nrg.2016.29
Authors: Christiaan A. de Leeuw, Benjamin M. Neale, Tom Heskes & Danielle Posthuma
The rapid increase in loci discovered in genome-wide association studies has created a need to understand the biological implications of these results. Gene-set analysis provides a means of gaining such understanding, but the statistical properties of gene-set analysis are not well understood, which compromises our
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Genetic screens: Combination screens for combination therapies
Nature Reviews Genetics 17, 313 (2016). doi:10.1038/nrg.2016.52
Author: Darren J. Burgess
Resources for genome-scale loss-of-function screens in mammalian cells have progressed rapidly, particularly with RNA interference (RNAi)-based libraries and, more recently, with CRISPR–Cas9-based libraries. A new parallel screening study leverages the complementary strengths of each system to dissect antiviral drug mechanisms and to identify potential combination
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Does Preprocedural Ultrasound Increase the First-Pass Success Rate of Epidural Catheterization Before Cesarean Delivery? A Randomized Controlled Trial.
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Continuing the Terra Firma and Establishing a New EQUATOR for Anesthesia & Analgesia.
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Advanced Uses of Pulse Oximetry for Monitoring Mechanically Ventilated Patients.
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Clostridium Difficile Infection in Children: a Review.
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