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		<title>Nonlinear Biomedical Physics - Latest articles</title>
		<link>http://www.nonlinearbiomedphys.com</link>
		<description>The latest articles from Nonlinear Biomedical Physics (ISSN 1753-4631) published by 
				
				BioMed Central
		</description>
        <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
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				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/2/1/2"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/2/1/1"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/11"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/10"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/9"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/8"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/7"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/6"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/5"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/4"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/3"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/2"/>			    
            
				    <rdf:li rdf:resource="http://www.nonlinearbiomedphys.com/content/1/1/1"/>			    
            
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		<item rdf:about="http://www.nonlinearbiomedphys.com/content/2/1/2">
            
            <title>Global behavior of epidemic transmission on heterogeneous networks via two distinct routes</title>
			<description>In the study of epidemic spreading two natural questions are: whether the spreading of epidemics on heterogenous networks have multiple routes, and whether the spreading of an epidemic is a local or global behavior? In this paper, we answer the above two questions by studying the SIS model on heterogenous networks, and give the global conditions for the endemic state when two distinct routes with uniform rate of infection are considered. The analytical results are also verified by numerical simulations.</description>
			<link>http://www.nonlinearbiomedphys.com/content/2/1/2</link>
			
			 	<dc:creator>Haifeng Zhang, Michael Small and Xinchu Fu</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2008, 2:2</dc:source>
			<dc:date>2008-05-01</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-2-2</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>2</prism:volume>
					
			
							
					<prism:startingPage>2</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-05-01</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/2/1/1">
            
            <title>Force plate monitoring of human hemodynamics</title>
			<description>Background:
Noninvasive recording of movements caused by the heartbeat and the blood circulation is known as ballistocardiography. Several studies have shown the capability of a force plate to detect cardiac activity in the human body. The aim of this paper is to present a new method based on differential geometry of curves to handle multivariate time series obtained by ballistocardiographic force plate measurements.
Results:
We show that the recoils of the body caused by cardiac motion and blood circulation provide a noninvasive method of displaying the motions of the heart muscle and the propagation of the pulse wave along the aorta and its branches. The results are compared with the data obtained invasively during a cardiac catheterization. We show that the described noninvasive method is able to determine the moment of a particular heart movement or the time when the pulse wave reaches certain morphological structure.
Conclusions:
Monitoring of heart movements and pulse wave propagation may be used e.g. to estimate the aortic pulse wave velocity, which is widely accepted as an index of aortic stiffness with the application of predicting risk of heart disease in individuals. More extended analysis of the method is however needed to assess its possible clinical application.</description>
			<link>http://www.nonlinearbiomedphys.com/content/2/1/1</link>
			
			 	<dc:creator>Jan K&#345;&#237;&#382; and Petr &#352;eba</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2008, 2:1</dc:source>
			<dc:date>2008-02-22</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-2-1</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>2</prism:volume>
					
			
							
					<prism:startingPage>1</prism:startingPage>
					
			
							
					<prism:publicationDate>2008-02-22</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/11">
            
            <title>Developing combinatorial multi-component therapies (CMCT) of drugs that are more specific and have fewer side effects than traditional one drug therapies</title>
			<description>Drugs designed for a specific target are always found to have multiple effects. Rather than hope that one bullet can be designed to hit only one target, nonlinear interactions across genomic and proteomic networks could be used to design Combinatorial Multi-Component Therapies (CMCT) that are more targeted with fewer side effects. We show here how computational approaches can be used to predict which combinations of drugs would produce the best effects. Using a nonlinear model of how the output effect depends on multiple input drugs, we show that an artificial neural network can accurately predict the effect of all 215 = 32,768 combinations of drug inputs using only the limited data of the output effect of the drugs presented one-at-a-time and pairs-at-a-time.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/11</link>
			
			 	<dc:creator>Larry S Liebovitch, Nicholas Tsinoremas and Abhijit Pandya</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:11</dc:source>
			<dc:date>2007-08-30</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-11</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>11</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-08-30</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/10">
            
            <title>Reconstruction of cellular variability from spatiotemporal patterns of Dictyostelium discoideum</title>
			<description>Variability in cell properties can be an important driving mechanism behind spatiotemporal patterns in biological systems, as the degree of cell-to-cell differences determines the capacity of cells to locally synchronize and, consequently, form patterns on a larger spatial scale. In principle, certain features of spatial patterns emerging with time may be regulated by variability or, more specifically, by certain constellations of cell-to-cell differences. Similarly, measuring variability in a system (i.e. the spatial distribution of cell-cell differences) may help predict properties of later-stage patterns.Here we apply and compare different statistical methods of extracting such systematic cell-to-cell differences in the case of patterns generated with a simple model system of an excitable medium and of experimental data by the slime mold Dictyostelium discoideum. We demonstrate with the help of a correlation analysis that these methods produce systematic (i.e. stationary) results for cell properties. Furthermore, we discuss possible applications of our method, in particular how these cell properties may serve as predictors of certain later-stage patterns.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/10</link>
			
			 	<dc:creator>Christiane Hilgardt, Stefan C M&#252;ller and Marc-Thorsten H&#252;tt</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:10</dc:source>
			<dc:date>2007-08-30</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-10</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>10</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-08-30</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/9">
            
            <title>Methods of electroencephalographic signal analysis for detection of small hidden changes</title>
			<description>The aim of this study was to select and evaluate methods sensitive to reveal small hidden changes in the electroencephalographic (EEG) signal. Two original methods were considered.Multifractal method of scaling analysis of the EEG signal based on the length distribution of low variability periods (LDLVP) was developed and adopted for EEG analysis. The LDLVP method provides a simple route to detecting the multifractal characteristics of a time-series and yields somewhat better temporal resolution than the traditional multifractal analysis.The method of modulation with further integration of energy of the recorded signal was applied for EEG analysis. This method uses integration of differences in energy of the EEG segments with and without stressor.Microwave exposure was used as an external stressor to cause hidden changes in the EEG. Both methods were evaluated on the same EEG database. Database consists of resting EEG recordings of 15 subjects without and with low-level microwave exposure (450 MHz modulated at 40 Hz, power density 0.16 mW/cm2). The significant differences between recordings with and without exposure were detected by the LDLVP method for 4 subjects (26.7%) and energy integration method for 2 subjects (13.3%).The results show that small changes in time variability or energy of the EEG signals hidden in visual inspection can be detected by the LDLVP and integration of differences methods.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/9</link>
			
			 	<dc:creator>Hiie Hinrikus, Maie Bachmann, Jaan Kalda, Maksim Sakki, Jaanus Lass and Ruth Tomson</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:9</dc:source>
			<dc:date>2007-07-28</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-9</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>9</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-28</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/8">
            
            <title>Estimating the distribution of dynamic invariants: illustrated with an application to human photo-plethysmographic time series</title>
			<description>Dynamic invariants are often estimated from experimental time series with the aim of differentiating between different physical states in the underlying system. The most popular schemes for estimating dynamic invariants are capable of estimating confidence intervals, however, such confidence intervals do not reflect variability in the underlying dynamics. We propose a surrogate based method to estimate the expected distribution of values under the null hypothesis that the underlying deterministic dynamics are stationary. We demonstrate the application of this method by considering four recordings of human pulse waveforms in differing physiological states and show that correlation dimension and entropy are insufficient to differentiate between these states. In contrast, algorithmic complexity can clearly differentiate between all four rhythms.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/8</link>
			
			 	<dc:creator>Michael Small</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:8</dc:source>
			<dc:date>2007-07-23</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-8</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>8</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-23</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/7">
            
            <title>Bioactive peptide design using the Resonant Recognition Model</title>
			<description>With a large number of DNA and protein sequences already known, the crucial question is to find out how the biological function of these macromolecules is "written" in the sequence of nucleotides or amino acids. Biological processes in any living organism are based on selective interactions between particular bio-molecules, mostly proteins. The rules governing the coding of a protein's biological function, i.e. its ability to selectively interact with other molecules, are still not elucidated. In addition, with the rapid accumulation of databases of protein primary structures, there is an urgent need for theoretical approaches that are capable of analysing protein structure-function relationships. The Resonant Recognition Model (RRM) 12 is one attempt to identify the selectivity of protein interactions within the amino acid sequence. The RRM 12 is a physico-mathematical approach that interprets protein sequence linear information using digital signal processing methods. In the RRM the protein primary structure is represented as a numerical series by assigning to each amino acid in the sequence a physical parameter value relevant to the protein's biological activity. The RRM concept is based on the finding that there is a significant correlation between spectra of the numerical presentation of amino acids and their biological activity. Once the characteristic frequency for a particular protein function/interaction is identified, it is possible then to utilize the RRM approach to predict the amino acids in the protein sequence, which predominantly contribute to this frequency and thus, to the observed function, as well as to design de novo peptides having the desired periodicities. As was shown in our previous studies of fibroblast growth factor (FGF) peptidic antagonists 23 and human immunodeficiency virus (HIV) envelope agonists 24, such de novo designed peptides express desired biological function. This study utilises the RRM computational approach to the analysis of oncogene and proto-oncogene proteins. The results obtained have shown that the RRM is capable of identifying the differences between the oncogenic and proto-oncogenic proteins with the possibility of identifying the "cancer-causing" features within their protein primary structure. In addition, the rational design of bioactive peptide analogues displaying oncogenic or proto-oncogenic-like activity is presented here.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/7</link>
			
			 	<dc:creator>Irena Cosic and Elena Pirogova</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:7</dc:source>
			<dc:date>2007-07-19</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-7</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>7</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-19</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/6">
            
            <title>Virtual respiratory system in investigation of CPAP influence on optimal breathing frequency in obstructive lungs disease</title>
			<description>Background:
Continuous Positive Airway Pressure (CPAP) is a commonly accepted method of spontaneous breathing support in obstructive lung disease. Previous work suggested that the cause of the CPAP efficacy in the obstructive lung disease localized in bronchi of middle order (OLDMO) is not as obvious as, for example, in the obstructive sleep apnea. Since CPAP reduces obstruction and the optimal breathing frequency (BF) depends on the obstruction level, it seems to be important to analyze the dependence of the optimal BF on CPAP.AimTo analyze the support efficacy cause in OLDMO, esp. the relationship between the CPAP value and optimal BF.MethodInvestigations utilized previously built virtual respiratory system. Its most important factors: nonlinear lungs compliance and changeability of nonlinear airway resistance (Raw). Influence of BF and the CPAP value on the tidal volume and minute ventilation was analyzed for four exemplary virtual patients: healthy ("standard") and suffering from moderate, severe, and the very severe OLDMO (the other parameters, esp. respiratory muscles effort, were unchanged). Minute inspiratory work as a criterion of the BF optimization.
Results:
CPAP decreased Raw making breathing easier, however, it shifted the working point of the respiratory system towards the smaller lungs compliance making breathing harder. The final result depended on the Raw value: CPAP improved breathing of patients with the serious OLDMO while it worsened healthy person breathing. The optimal CPAP value depended on the Raw value. If a virtual patient suffering from the serious OLDMO was not supported with CPAP, he had to breathe with low frequency because minute ventilation did not rise with BF increase. The optimal BF depended on the CPAP value (the greater the value, the greater the frequency).
Conclusion:
The CPAP efficacy depends on the level of OLDMO. CPAP is efficient in the severe OLDMO because it increases the optimal BF, which makes possible less energy-consuming breathing with frequency close to the normal one (greater BF means smaller tidal volume and thus smaller work against lungs compliance).</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/6</link>
			
			 	<dc:creator>Tomasz Golczewski and Marek Darowski</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:6</dc:source>
			<dc:date>2007-07-16</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-6</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>6</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-16</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/5">
            
            <title>From conformons to human brains: an informal overview of nonlinear dynamics and its applications in biomedicine</title>
			<description>Methods of contemporary physics are increasingly important for biomedical research but, for a multitude of diverse reasons, most practitioners of biomedicine lack access to a comprehensive knowledge of these modern methodologies. This paper is an attempt to describe nonlinear dynamics and its methods in a way that could be read and understood by biomedical professionals who usually are not trained in advanced mathematics.    After an overview of basic concepts and vocabulary of nonlinear dynamics, deterministic chaos, and fractals, application of nonlinear methods of biosignal analysis is discussed.  In particular, five case studies are presented: 1. Monitoring the depth of anaesthesia and of sedation; 2. Bright Light Therapy and Seasonal Affective Disorder;  3. Analysis of posturographic signals;  4. Evoked  EEG  and photo-stimulation;  5. Influence of  electromagnetic  fields generated by cellular phones. </description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/5</link>
			
			 	<dc:creator>Wlodzimierz Klonowski</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:5</dc:source>
			<dc:date>2007-07-05</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-5</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>5</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-05</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/4">
            
            <title>Stochastic nonlinear dynamics pattern formation and growth models</title>
			<description>Stochastic evolutionary growth and pattern formation models are treated in a unified way in terms of algorithmic models of nonlinear dynamic systems with feedback built of a standard set of signal processing units. A number of concrete models is described and illustrated by numerous examples of artificially generated patterns that closely imitate wide variety of patterns found in the nature.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/4</link>
			
			 	<dc:creator>Leonid P Yaroslavsky</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:4</dc:source>
			<dc:date>2007-07-05</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-4</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>4</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-05</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/3">
            
            <title>Graph theoretical analysis of complex networks in the brain</title>
			<description>Since the discovery of small-world and scale-free networks the study of complex systems from a network perspective has taken an enormous flight. In recent years many important properties of complex networks have been delineated. In particular, significant progress has been made in understanding the relationship between the structural properties of networks and the nature of dynamics taking place on these networks. For instance, the 'synchronizability' of complex networks of coupled oscillators can be determined by graph spectral analysis. These developments in the theory of complex networks have inspired new applications in the field of neuroscience. Graph analysis has been used in the study of models of neural networks, anatomical connectivity, and functional connectivity based upon fMRI, EEG and MEG. These studies suggest that the human brain can be modelled as a complex network, and may have a small-world structure both at the level of anatomical as well as functional connectivity. This small-world structure is hypothesized to reflect an optimal situation associated with rapid synchronization and information transfer, minimal wiring costs, as well as a balance between local processing and global integration. The topological structure of functional networks is probably restrained by genetic and anatomical factors, but can be modified during tasks. There is also increasing evidence that various types of brain disease such as Alzheimer's disease, schizophrenia, brain tumours and epilepsy may be associated with deviations of the functional network topology from the optimal small-world pattern.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/3</link>
			
			 	<dc:creator>Cornelis J Stam and Jaap C Reijneveld</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:3</dc:source>
			<dc:date>2007-07-05</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-3</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>3</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-05</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/2">
            
            <title>Synchronized dynamics of cortical neurons with time-delay feedback</title>
			<description>The dynamics of three mutually coupled cortical neurons with time delays in the coupling are explored numerically and analytically. The neurons are coupled in a line, with the middle neuron sending a somewhat stronger projection to the outer neurons than the feedback it receives, to model for instance the relay of a signal from primary to higher cortical areas. For a given coupling architecture, the delays introduce correlations in the time series at the time-scale of the delay. It was found that the middle neuron leads the outer ones by the delay time, while the outer neurons are synchronized with zero lag times. Synchronization is found to be highly dependent on the synaptic time constant, with faster synapses increasing both the degree of synchronization and the firing rate. Analysis shows that pre-synaptic input during the inter-spike interval stabilizes the synchronous state, even for arbitrarily weak coupling, and independent of the initial phase. The finding may be of significance to synchronization of large groups of cells in the cortex that are spatially distanced from each other.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/2</link>
			
			 	<dc:creator>Alexandra S Landsman and Ira B Schwartz</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:2</dc:source>
			<dc:date>2007-07-05</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-2</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>2</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-05</prism:publicationDate>
					

            <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/>
        </item>
	
		<item rdf:about="http://www.nonlinearbiomedphys.com/content/1/1/1">
            
            <title>Why Nonlinear Biomedical Physics?</title>
			<description>The two goals of Nonlinear Biomedical Physics are: firstly to show how nonlinear methods can shed new light on biological phenomena and medical applications and secondly to bridge the technical, mathematical, and cultural divides between the physical disciplines where these methods are being developed and the audience for their use in the biological and medical sciences.</description>
			<link>http://www.nonlinearbiomedphys.com/content/1/1/1</link>
			
			 	<dc:creator>Zbigniew Czernicki, Wlodzimierz Klonowski and Larry Liebovitch</dc:creator>
			
			<dc:source>Nonlinear Biomedical Physics 2007, 1:1</dc:source>
			<dc:date>2007-07-05</dc:date>
			<dc:identifier>doi:10.1186/1753-4631-1-1</dc:identifier>
			
			
							
					<prism:publicationName>Nonlinear Biomedical Physics</prism:publicationName>
					
			
							
					<prism:issn>1753-4631</prism:issn>
					
			
							
					<prism:volume>1</prism:volume>
					
			
							
					<prism:startingPage>1</prism:startingPage>
					
			
							
					<prism:publicationDate>2007-07-05</prism:publicationDate>
					

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