76 research outputs found
A Component of Retinal Light Adaptation Mediated by the Thyroid Hormone Cascade
Analysis with DNA-microrrays and real time PCR show that several genes involved in the thyroid hormone cascade, such as deiodinase 2 and 3 (Dio2 and Dio3) are differentially regulated by the circadian clock and by changes of the ambient light. The expression level of Dio2 in adult rats (2–3 months of age) kept continuously in darkness is modulated by the circadian clock and is up-regulated by 2 fold at midday. When the diurnal ambient light was on, the expression level of Dio2 increased by 4–8 fold and a consequent increase of the related protein was detected around the nuclei of retinal photoreceptors and of neurons in inner and outer nuclear layers. The expression level of Dio3 had a different temporal pattern and was down-regulated by diurnal light. Our results suggest that DIO2 and DIO3 have a role not only in the developing retina but also in the adult retina and are powerfully regulated by light. As the thyroid hormone is a ligand-inducible transcription factor controlling the expression of several target genes, the transcriptional activation of Dio2 could be a novel genomic component of light adaptation
A Graph Algorithmic Approach to Separate Direct from Indirect Neural Interactions
Network graphs have become a popular tool to represent complex systems
composed of many interacting subunits; especially in neuroscience, network
graphs are increasingly used to represent and analyze functional interactions
between neural sources. Interactions are often reconstructed using pairwise
bivariate analyses, overlooking their multivariate nature: it is neglected that
investigating the effect of one source on a target necessitates to take all
other sources as potential nuisance variables into account; also combinations
of sources may act jointly on a given target. Bivariate analyses produce
networks that may contain spurious interactions, which reduce the
interpretability of the network and its graph metrics. A truly multivariate
reconstruction, however, is computationally intractable due to combinatorial
explosion in the number of potential interactions. Thus, we have to resort to
approximative methods to handle the intractability of multivariate interaction
reconstruction, and thereby enable the use of networks in neuroscience. Here,
we suggest such an approximative approach in the form of an algorithm that
extends fast bivariate interaction reconstruction by identifying potentially
spurious interactions post-hoc: the algorithm flags potentially spurious edges,
which may then be pruned from the network. This produces a statistically
conservative network approximation that is guaranteed to contain non-spurious
interactions only. We describe the algorithm and present a reference
implementation to test its performance. We discuss the algorithm in relation to
other approximative multivariate methods and highlight suitable application
scenarios. Our approach is a tractable and data-efficient way of reconstructing
approximative networks of multivariate interactions. It is preferable if
available data are limited or if fully multivariate approaches are
computationally infeasible.Comment: 24 pages, 8 figures, published in PLOS On
Experimental Studies of Atomic Behavior at Crystal Surfaces
Coordinated Science Laboratory was formerly known as Control Systems LaboratoryJoint Services Electronics Program / DAAB-07-67-C-019
Low Folate and Selenium in the Mouse Maternal Diet Alters Liver Gene Expression Patterns in the Offspring after Weaning
Improving resolution of dynamic communities in human brain networks through targeted node removal
Influence of tool material properties on the wear behavior of cemented carbide tools with rounded cutting edges
Reproductive Health Issues for Adults with a Common Genomic Disorder: 22q11.2 Deletion Syndrome
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