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        <title>Immunome Research via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Immunome Research' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Immunome+Research&t=Immunome+Research&s=Search&f=source]]></link>
        <lastBuildDate>Fri, 04 Feb 2011 15:00:01 +0100</lastBuildDate>
        <item>
            <title>Factors important in evolutionary shaping of immunoglobulin gene loci</title>
            <link>http://www.immunome-research.com/content/6/1/13</link>
            <description>Conclusions:
We conclude that contemporary species' Ig libraries have been optimized by evolution in terms of Ig sequence lengths, the number and diversity of Ig genes, and antibody-antigen affinities. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4230590</comments>
            <pubDate>Mon, 06 Dec 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4230590</guid>        </item>
        <item>
            <title>DC-ATLAS, a Systems Biology Resource to Dissect Receptor Specific Signal Transduction in Dendritic Cells.</title>
            <link>http://www.immunome-research.com/content/6/1/10</link>
            <description>Conclusions:
The initiative significantly improves our understanding of DC biology and regulatory networks. Developing a systems biology approach for immune system holds the promise of translating knowledge on the immune system into more successful immunotherapy strategies. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4183755</comments>
            <pubDate>Fri, 19 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4183755</guid>        </item>
        <item>
            <title>Automated processing of label-free Raman microscope images of macrophage cells with standardized regression for high-throughput analysis</title>
            <link>http://www.immunome-research.com/content/6/1/11</link>
            <description>Conclusions:
The computational efficiency of Z-LSR enables automated resolution of sub-cellular features in large Raman microscopy data sets without compromise in image quality or information loss in associated spectra. These results motivate further use of label free microscopy techniques in real-time imaging of live immune cells. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4183754</comments>
            <pubDate>Fri, 19 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4183754</guid>        </item>
        <item>
            <title>NetMHCIIpan-2.0 - Improved pan-specific HLA-DR predictions using a novel concurrent alignment and weight optimization training procedure</title>
            <link>http://www.immunome-research.com/content/6/1/9</link>
            <description>Conclusions:
The method thus shows great potential for efficient boosting the accuracy of MHC-II binding prediction, as accurate predictions can be obtained for novel alleles at highly reduced experimental costs. Pan-specific binding predictions can be obtained for all alleles with know protein sequence and the method can benefit by including data in the training from alleles even where only few binders are known. The method and benchmark data are available at www.cbs.dtu.dk/services/NetMHCIIpan-2.0 (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4163183</comments>
            <pubDate>Sat, 13 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4163183</guid>        </item>
        <item>
            <title>An integrated approach to epitope analysis I: Dimensional reduction, visualization and prediction of MHC binding using amino acid principal components and regression approaches</title>
            <link>http://www.immunome-research.com/content/6/1/7</link>
            <description>Conclusions:
As opposed to the highly constrained user-interaction paradigms of web-server approaches, local computational approaches enable interactive analysis and visualization of complex multidimensional data using robust mathematical tools. Our work shows that prediction tools such as these can be constructed on the widely available JMP platform, can operate in a spreadsheet environment on a desktop computer, and are capable of handling proteome-scale analysis with high throughput. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4126346</comments>
            <pubDate>Tue, 02 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4126346</guid>        </item>
        <item>
            <title>An integrated approach to epitope analysis II: A system for proteomic-scale prediction of immunological characteristics</title>
            <link>http://www.immunome-research.com/content/6/1/8</link>
            <description>Conclusions:
A desktop application with interactive graphic capability is shown to be a useful platform for development of prediction and visualization tools for epitope mapping at scales ranging from individual proteins to proteomes from multiple strains of an organism. The possible functional implications of the patterns of peptide epitopes observed are discussed, including their implications for B-cell and T-cell cooperation and cross presentation. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4126345</comments>
            <pubDate>Tue, 02 Nov 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4126345</guid>        </item>
        <item>
            <title>Identification of conformational B-cell Epitopes in an antigen from its primary sequence</title>
            <link>http://www.immunome-research.com/content/6/1/6</link>
            <description>Conclusion:
This study demonstrates that prediction of conformational B-cell epitope in an antigen is possible from is primary sequence. This study will be very useful in predicting conformational B-cell epitopes in antigens whose tertiary structures are not available. A web server CBTOPE has been developed for predicting B-cell epitope (http://www.imtech.res.in/raghava/cbtope/). (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4088986</comments>
            <pubDate>Tue, 19 Oct 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">4088986</guid>        </item>
        <item>
            <title>Motif prediction to distinguish LPS-stimulated pro-inflammatory vs. antibacterial macrophage genes</title>
            <link>http://www.immunome-research.com/content/6/1/5</link>
            <description>Conclusions:
Our analysis distinguished pro-inflammatory vs. antibacterial transcriptomic signatures that classified their respective gene expression patterns and the corresponding TF-TFBS interactions in LPS-stimulated macrophages. By doing so, this study has attempted to characterize the temporal differences in gene expression associated with LPS tolerance, a major immune phenomenon implicated in various pathological disorders. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3988784</comments>
            <pubDate>Mon, 20 Sep 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3988784</guid>        </item>
        <item>
            <title>Polyfunctional CD4+ T cell responses to a set of pathogenic arenaviruses provide broad population coverage</title>
            <link>http://www.immunome-research.com/content/6/1/4</link>
            <description>Conclusions:
The identification of CD4+ T cell epitopes, with promiscuous binding properties, derived from 7 different arenavirus species will aid in the development of a T cell-based vaccine strategy with the potential to target a broad range of ethnicities within the general population and to protect against both Old and New World arenavirus infection. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3570567</comments>
            <pubDate>Sun, 16 May 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3570567</guid>        </item>
        <item>
            <title>Evolution of a cluster of innate immune genes (beta-defensins) along the ancestral lines of chicken and zebra finch</title>
            <link>http://www.immunome-research.com/content/6/1/3</link>
            <description>Conclusion:
The genomic comparisons of the beta-defensins gene clusters of the chicken and zebra finch illuminate the evolutionary history of this gene complex. Along their ancestral lines, several gene duplication events have occurred in the passerine line after the galliformes-passeriformes split giving rise to 12 novel genes compared to a single duplication event in the galliformes line. After the duplication events, the duplicated genes have been subject to a relaxed selection pressure compared to the non-duplicated genes, thus supporting models of evolution by gene duplication. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3425969</comments>
            <pubDate>Wed, 31 Mar 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3425969</guid>        </item>
        <item>
            <title>Coregulation mapping based on individual phenotypic variation in response to virus infection</title>
            <link>http://www.immunome-research.com/content/6/1/2</link>
            <description>Conclusions:
MDS mapping based on correlation in conjunction with TF enrichment analysis represents a useful computational method to generate predictions underlying gene coregulation across a population. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3379862</comments>
            <pubDate>Thu, 18 Mar 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3379862</guid>        </item>
        <item>
            <title>A novel paradigm for cell and molecule interaction ontology:
from the CMM model to IMGT-ONTOLOGY</title>
            <link>http://www.immunome-research.com/content/6/1/1</link>
            <description>Conclusions:
This effort represents the first attempt at linking molecule ontology with cell ontology, in IMGT-ONTOLOGY, the well established ontology in immunogenetics and immunoinformatics, and a paradigm for life science biology. With the increasing use of models in biology and medicine, the need to link different levels, from molecules to cells to tissues and organs, is increasingly important. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3284908</comments>
            <pubDate>Thu, 18 Feb 2010 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3284908</guid>        </item>
        <item>
            <title>Ribosomal protein mRNAs are translationally-regulated 
during human dendritic cells activation by LPS</title>
            <link>http://www.immunome-research.com/content/5/1/5</link>
            <description>Conclusion:
Our observations highlight the importance of translation regulation during the immune response, and may favor the identification of novel protein networks relevant for immunity. Our study also provides information on the potential absence of correlation between gene expression and protein production for specific mRNA molecules present in DCs. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3034771</comments>
            <pubDate>Fri, 27 Nov 2009 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">3034771</guid>        </item>
        <item>
            <title>Critical role of glycosylation in determining the length and structure of T cell epitopes
- As suggested by a combined in silico systems biology approach</title>
            <link>http://www.immunome-research.com/content/5/1/4</link>
            <description>Conclusions The findings of this bioinformatical approach shed light on fundamental factors that might have shaped adaptive immunity during evolution. Our data suggest that amino acid sequence-based hypo/non-glycosylation of certain segments of proteins might be substantial for determining T cell immunity/autoimmunity. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2825572</comments>
            <pubDate>Wed, 23 Sep 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2825572</guid>        </item>
        <item>
            <title>Of mice and humans: how good are HLA transgenic mice as a model of human immune responses?</title>
            <link>http://www.immunome-research.com/content/5/1/3</link>
            <description>Conclusions:
These data suggest that differences in immunodominance patterns might explain the incomplete response overlap, and that with limitations, HLA Tg mice represent a relevant and suitable model system to study immune responses against complex pathogens. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2485573</comments>
            <pubDate>Tue, 16 Jun 2009 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">2485573</guid>        </item>
        <item>
            <title>Functional recombinant MHC class II molecules and high-throughput peptide-binding assays</title>
            <link>http://www.immunome-research.com/content/5/1/2</link>
            <description>Conclusions:
We have successfully developed versatile MHC-II resources, which may assist in the generation of MHC class II -wide reagents, data, and tools. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2390590</comments>
            <pubDate>Tue, 05 May 2009 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">2390590</guid>        </item>
        <item>
            <title>Genetic correlates of autoreactivity and autoreactive potential in human Ig heavy chains</title>
            <link>http://www.immunome-research.com/content/5/1/1</link>
            <description>Conclusions:
We hypothesize that peripheral autoreactivity results primarily from somatic mutation, and that the genetic correlates of autoreactivity in mature B-cells are not the same as those for autoreactivity in immature B cells. What is seen in mature autoreactive B cells are the correlates of {\it autoreactive potential}, not of autoreactivity per se. The autoreactive potential is higher for V(D)J rearrangements encoded to a large extent by N-nucleotides rather than by the gene segments that, we posit, have been selected in germline evolution for their suppression of autoreactive potential. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2220029</comments>
            <pubDate>Fri, 27 Feb 2009 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2220029</guid>        </item>
        <item>
            <title>Data mining of cancer vaccine trials: a bird's-eye view</title>
            <link>http://www.immunome-research.com/content/4/1/7</link>
            <description>Conclusion:
We have developed a data mining approach that enables rapid extraction of complex data from the major clinical trial repository. Summarization and visualization of these data represents a cost-effective means of making informed decisions about the future cancer vaccine clinical trials. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2031080</comments>
            <pubDate>Fri, 12 Dec 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">2031080</guid>        </item>
        <item>
            <title>Peptide length significantly influences in vitro affinity for MHC class II molecules</title>
            <link>http://www.immunome-research.com/content/4/1/6</link>
            <description>Conclusions:
The observed relationship between peptide length and MHC class II affinity is likely to have clear implications for vaccine design and the study of immunological disease. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1987819</comments>
            <pubDate>Wed, 26 Nov 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">1987819</guid>        </item>
        <item>
            <title>Expression Analysis of G Protein-Coupled Receptors in Mouse Macrophages</title>
            <link>http://www.immunome-research.com/content/4/1/5</link>
            <description>Conclusion:
The constitutive or regulated expression in macrophages of several GPCRs identified in this study has not previously been described. Future studies on such GPCRs and their agonists are likely to provide important insights into macrophage biology, as well as novel inflammatory pathways that could be future targets for drug discovery. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1404680</comments>
            <pubDate>Tue, 29 Apr 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1404680</guid>        </item>
        <item>
            <title>Efficiency of the immunome protein interaction network increases during evolution</title>
            <link>http://www.immunome-research.com/content/4/1/4</link>
            <description>Conclusions:
Our results shed light on selective forces acting on the emergence of biological networks. It is likely that the high efficiency and low vulnerability are intrinsic properties of many biological networks, which arise from the effects of evolutionary processes yet to be uncovered. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1389934</comments>
            <pubDate>Tue, 22 Apr 2008 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">1389934</guid>        </item>
        <item>
            <title>Large-scale analysis of human heavy chain V(D)J recombination patterns</title>
            <link>http://www.immunome-research.com/content/4/1/3</link>
            <description>Conclusions:
We present here the most precise estimates of gene segment usage frequencies currently available along with analyses regarding n-nucleotide distributions and D-J segment pair preferences. Additionally, we provide the first statistical evidence that sequential D-J recombinations occur at the human heavy chain locus during B-cell ontogeny with an approximate frequency of 20%. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1260604</comments>
            <pubDate>Wed, 27 Feb 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">1260604</guid>        </item>
        <item>
            <title>Quantitative peptide binding motifs for 19 human and mouse MHC class I molecules derived using positional scanning combinatorial peptide libraries</title>
            <link>http://www.immunome-research.com/content/4/1/2</link>
            <description>Conclusions:
These data confirm, on a large scale, including 15 human and 4 mouse class I alleles, the efficacy of the positional scanning combinatorial library approach for describing MHC class I binding specificity and identifying high affinity binding peptides. These libraries were shown to be useful for identifying specific primary and secondary anchor positions, and thereby simpler motifs, analogous to those described by other approaches. The present study also provides matrices useful for predicting high affinity binders for several alleles for which detailed quantitative descriptions of binding specificity were previously unavailable, including A*3001, A*3201, B*0801, B*1501 and B*1503. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1176690</comments>
            <pubDate>Fri, 25 Jan 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">1176690</guid>        </item>
        <item>
            <title>Analysis and prediction of protective continuous B-cell epitopes on pathogen proteins</title>
            <link>http://www.immunome-research.com/content/4/1/1</link>
            <description>Background:
The application of peptide based diagnostics and therapeutics mimicking part of protein antigen is experiencing renewed interest. So far selection and design rationale for such peptides is usually driven by T-cell epitope prediction, available experimental and modelled 3D structure, B-cell epitope predictions such as hydrophilicity plots or experience. If no structure is available the rational selection of peptides for the production of functionally altering or neutralizing antibodies is practically impossible. Specifically if many alternative antigen are available the reduction of required synthesized peptides until one successful candidate is found is of central technical interest. We have investigated the integration of B-cell epitope prediction with the variability of antig...</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1133171</comments>
            <pubDate>Mon, 07 Jan 2008 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">1133171</guid>        </item>
        <item>
            <title>An analysis of the epitope knowledge related to Mycobacteria</title>
            <link>http://www.immunome-research.com/content/3/1/10</link>
            <description>Conclusions: All current TB-related epitope data was cataloged for the first time from the published literature. The resulting inventory of more than a thousand different epitopes should prove a useful tool for the broad scientific community. Knowledge gaps specific to TB epitope data were also identified. In summary, few non-peptidic or post-translationally modified epitopes have been defined. Most importantly epitopes have apparently been defined from only 7% of all ORFs, and the top 30 most frequently studied protein antigens contain 65% of the epitopes, leaving the majority of M. tuberculosis genome unexplored. A lack of information related to the specific strains from which epitopes are derived is also evident. Finally, the generation of reference lists of mycobacterial epitopes shoul...</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=1094906</comments>
            <pubDate>Fri, 14 Dec 2007 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">1094906</guid>        </item>
        <item>
            <title>Amino acid biophysical properties in the statistical prediction of peptide-MHC class I binding</title>
            <link>http://www.immunome-research.com/content/3/1/9</link>
            <description>Conclusion:
Representation of amino acids using a few important bio-physio-chemical property provide a natural basis for representing peptides and greatly improves peptide-MHC class I binding prediction. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=986448</comments>
            <pubDate>Mon, 29 Oct 2007 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">986448</guid>        </item>
        <item>
            <title>Using the natural evolution of a rotavirus-specific human monoclonal antibody to predict the complex topography of a viral antigenic site</title>
            <link>http://www.immunome-research.com/content/3/1/8</link>
            <description>Conclusions:
The use of mutagenesis constraints in docking calculations allows for the identification of a small number of alternative arrangements of the antigen-antibody interface. The mutagenesis information from the natural evolution of a neutralizing antibody can be used to discriminate between residue-scale models and create distance constraints for atomic-resolution docking. The integration of binding affinity data or other information with computation may be an advantageous approach to assist peptide engineering or therapeutic antibody design. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=880955</comments>
            <pubDate>Tue, 18 Sep 2007 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">880955</guid>        </item>
        <item>
            <title>In silico characterization of immunogenic epitopes presented by HLA-Cw*0401</title>
            <link>http://www.immunome-research.com/content/3/1/7</link>
            <description>Conclusions:
The analysis of predicted Cw*0401-binding peptides showed that anchor residues may not be restrictive and the Cw*0401 binding pockets may possibly accommodate a wide variety of peptides with common physico-chemical properties. The potential Cw*0401-specific T-cell epitope repertoires for HIV-1 p24gag and gp160gag glycoproteins are well distributed throughout both glycoproteins, with thirteen and nine immunological hot spots for HIV-1 p24gag and gp160gag glycoproteins respectively. These findings provide new insights into HLA-C peptide selectivity, indicating that pre-selection of candidate HLA-C peptides may occur at the TAP level, prior to peptide loading in the endoplasmic reticulum. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=809185</comments>
            <pubDate>Mon, 20 Aug 2007 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">809185</guid>        </item>
        <item>
            <title>IDR knowledge base for primary immunodeficiencies</title>
            <link>http://www.immunome-research.com/content/3/1/6</link>
            <description>Conclusions:
The IDR is the first knowledge base specifically designed to capture in a systematic and validated way both clinical and molecular information for primary immunodeficiency. The service is freely available at http://bioinf.uta.fi/idr and is regularly updated. The IDR facilitates primary immunodeficiency informatics and helps to parameterise in silico modelling of these diseases. The IDR is useful also as an advanced education tool for medical students, and physicians. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=519347</comments>
            <pubDate>Thu, 29 Mar 2007 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">519347</guid>        </item>
        <item>
            <title>Strength in numbers: achieving greater accuracy in MHC-I binding prediction by combining the results from multiple prediction tools</title>
            <link>http://www.immunome-research.com/content/3/1/5</link>
            <description>Conclusions:
A heuristic-based method of combining the results of the individual tools better facilitates the scanning of large proteomes for potential epitopes, yielding more actual high-affinity binders while reporting very few false positives. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=507159</comments>
            <pubDate>Sat, 24 Mar 2007 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">507159</guid>        </item>
        <item>
            <title>ImmTree: Database of evolutionary relationships of genes and proteins in the human immune system</title>
            <link>http://www.immunome-research.com/content/3/1/4</link>
            <description>Conclusions:
ImmTree provides a unique data set of genes and proteins from the human immune system, their phylogenetics, and information for comparisons of human-mouse ortholog pairs, synonymous and non-synonymous mutation rates, as well as other statistical information. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=490088</comments>
            <pubDate>Wed, 21 Mar 2007 04:00:00 +0100</pubDate>
            <guid isPermaLink="false">490088</guid>        </item>
        <item>
            <title>EpitopeViewer: a Java application for the visualization and analysis of immune epitopes in the Immune Epitope Database and Analysis Resource (IEDB)</title>
            <link>http://www.immunome-research.com/content/3/1/3</link>
            <description>Conclusion:
The EpitopeViewer is designed and been tested for use by immunologists with little or no training in molecular graphics. The EpitopeViewer can be launched from most popular Web browsers without user intervention. A Java Runtime Environment (RJE) 1.4.2 or higher is required. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=431867</comments>
            <pubDate>Wed, 21 Feb 2007 07:00:00 +0100</pubDate>
            <guid isPermaLink="false">431867</guid>        </item>
        <item>
            <title>A novel strategy for the identification of antigens that are recognised by bovine MHC class I restricted cytotoxic T cells in a protozoan infection using reverse vaccinology</title>
            <link>http://www.immunome-research.com/content/3/1/2</link>
            <description>Conclusions:
The identification of an antigen containing multiple CTL epitopes and its apparent immunodominance during a protective anti-parasite response makes Tp2 an attractive candidate for evaluation of its vaccine potential. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=407896</comments>
            <pubDate>Fri, 09 Feb 2007 07:00:00 +0100</pubDate>
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        <item>
            <title>Protein sequence database for pathogenic arenaviruses</title>
            <link>http://www.immunome-research.com/content/3/1/1</link>
            <description>Conclusions:
The database is available at http://epitope.liai.org:8080/projects/arena and can be used to aid in studies that require proteomic information from pathogenic arenaviruses. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=407897</comments>
            <pubDate>Thu, 08 Feb 2007 07:00:00 +0100</pubDate>
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        <item>
            <title>In silicoidentification of opossum cytokine genes suggests the complexity of the marsupial immune system rivals that of eutherian mammals</title>
            <link>http://www.immunome-research.com/content/2/1/4</link>
            <description>Conclusions:
The power of this approach was demonstrated by the identification of orthologous cytokines between marsupials and eutherians that share only 30% identity at the amino acid level. Furthermore, the presence of key immunological genes suggests that marsupials do indeed possess a sophisticated immune system, whose function may parallel that of eutherian mammals. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=277545</comments>
            <pubDate>Fri, 10 Nov 2006 07:00:00 +0100</pubDate>
            <guid isPermaLink="false">277545</guid>        </item>
        <item>
            <title>PREDTAP: a system for prediction of peptide binding to the human transporter associated with antigen processing</title>
            <link>http://www.immunome-research.com/content/2/1/3</link>
            <description>Conclusion:
PREDTAP can be integrated with prediction systems for MHC class I binding peptides for improved performance of in silico prediction of T-cell epitopes. PREDTAP is available at http://antigen.i2r.a-star.edu.sg/predTAP. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=32660</comments>
            <pubDate>Tue, 23 May 2006 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">32660</guid>        </item>
        <item>
            <title>Improved method for predicting linear B-cell epitopes</title>
            <link>http://www.immunome-research.com/content/2/1/2</link>
            <description>Conclusions:
The best single method for predicting linear B-cell epitopes is the hidden Markov model. Combining the hidden Markov model with one of the best propensity scale methods, we obtained the BepiPred method. When tested on the validation data set this method performs significantly better than any of the other methods tested. The server and data sets are publicly available at www.cbs.dtu.dk/services/BepiPred. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=189</comments>
            <pubDate>Mon, 24 Apr 2006 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">189</guid>        </item>
        <item>
            <title>Modeling the bound conformation of Pemphigus Vulgaris-associated peptides to MHC Class II DR and DQ Alleles</title>
            <link>http://www.immunome-research.com/content/2/1/1</link>
            <description>Conclusion:
Our docking simulations are entirely consistent with functional data obtained from in vitro competitive binding assays and T cell proliferation studies in DR4 and DR6 PV patients. Our findings ascertain that DRB1*0402 plays a crucial role in the selection of specific self-peptides in DR4 PV. DRB1*0402 and DQB1*0503 do not necessarily share the same core residues, indicating that both alleles may have different binding specificities. In addition, our results lend credence to the hypothesis that the alleles DQB1*0201 and *0202 play a protective role by binding Dsg3 peptides with greater affinity than the susceptible alleles, allowing for efficient deletion of autoreactive T cells. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=190</comments>
            <pubDate>Sat, 21 Jan 2006 07:00:00 +0100</pubDate>
            <guid isPermaLink="false">190</guid>        </item>
        <item>
            <title>Prediction of MHC class II binding peptides based on an iterative learning model</title>
            <link>http://www.immunome-research.com/content/1/1/6</link>
            <description>Conclusion:
The iterative learning procedure appears to be effective in prediction of MHC class II binders. It offers an alternative approach to this important predictionproblem. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=191</comments>
            <pubDate>Tue, 13 Dec 2005 07:00:00 +0100</pubDate>
            <guid isPermaLink="false">191</guid>        </item>
        <item>
            <title>Modelling  vaccination schedules for a cancer immunoprevention vaccine</title>
            <link>http://www.immunome-research.com/content/1/1/5</link>
            <description>We present a systematic approach to search for an effective vaccination schedule using mathematical computerized models. Our study is based on our previous model that simulates the cancer vs immune system competition activated by tumor vaccine. This model accurately reproduces in-vivo experiments results on HER-2/neu mice treated with the immuno-prevention cancer vaccine (Triplex) for mammary carcinoma. In vivo experiments have shown the effectiveness of Triplex vaccine in protection of mice from mammary carcinoma. The full protection was conferred using chronic (prophylactic) vaccination protocol while therapeutic vaccination was less effcient.In the present paper we use the computer simulations to systematically search for a vaccination schedule which prevents solid tumor formation. The ...</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=192</comments>
            <pubDate>Fri, 07 Oct 2005 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">192</guid>        </item>
        <item>
            <title>AntiJen: a quantitative immunology database integrating functional, thermodynamic, kinetic, biophysical, and cellular data</title>
            <link>http://www.immunome-research.com/content/1/1/4</link>
            <description>AntiJen is a database system focused on the integration of kinetic, thermodynamic, functional, and cellular data within the context of immunology and vaccinology. Compared to its progenitor JenPep, the interface has been completely rewritten and redesigned and now offers a wider variety of search methods, including a nucleotide and a peptide BLAST search. In terms of data archived, AntiJen has a richer and more complete breadth, depth, and scope, and this has seen the database increase to over 31,000 entries. AntiJen provides the most complete and up-to-date dataset of its kind. While AntiJen v2.0 retains a focus on both T cell and B cell epitopes, its greatest novelty is the archiving of continuous quantitative data on a variety of immunological molecular interactions. This includes therm...</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=193</comments>
            <pubDate>Thu, 06 Oct 2005 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">193</guid>        </item>
        <item>
            <title>Immunome Research</title>
            <link>http://www.immunome-research.com/content/1/1/1</link>
            <description>Immunology research has been transformed in the post-genomics era, with high throughput molecular biology and information technologies taking an increasingly central role. This has led to the development of a new area of science termed &quot;Immunomics&quot;, that encompasses genomic, high throughput and bioinformatic approaches to immunology. In recognition of the increasing importance of this field, Immunome Research is a new Open Access, online journal, that will publish cutting edge research across the field of Immunomics. Immunome Research will publish a wide range of article types including specialty immunology databases, immunology database tools, immunome epitope research, epitope analysis tools, high-throughput technologies (gene sequencing, microarrays, proteomics), white papers, mathemati...</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=196</comments>
            <pubDate>Tue, 20 Sep 2005 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">196</guid>        </item>
        <item>
            <title>An ontology for immune epitopes: application to the design of a broad scope database of immune reactivities</title>
            <link>http://www.immunome-research.com/content/1/1/2</link>
            <description>Conclusion:
The IEDB's ontology is the first ontology specifically designed to capture both intrinsic chemical and biochemical information relating to immune epitopes with information relating to the interaction of these structures with molecules derived from the host immune system. We anticipate that the development of this type of ontology and associated databases will facilitate rigorous description of data related to immune epitopes, and might ultimately lead to completely new methods for describing and modeling immune responses. (Source: Immunome Research)</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=195</comments>
            <pubDate>Tue, 20 Sep 2005 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">195</guid>        </item>
        <item>
            <title>IMGT, the international ImMunoGeneTics information system®: a standardized approach for immunogenetics and immunoinformatics</title>
            <link>http://www.immunome-research.com/content/1/1/3</link>
            <description>IMGT, the international ImMunoGeneTics information system®http://imgt.cines.fr, was created in 1989 by the Laboratoire d'ImmunoGénétique Moléculaire (LIGM) (Université Montpellier II and CNRS) at Montpellier, France. IMGT is a high quality integrated knowledge resource specialized in immunoglobulins (IG), T cell receptors (TR), major histocompatibility complex (MHC) of human and other vertebrates, and related proteins of the immune system (RPI) of any species which belong to the immunoglobulin superfamily (IgSF) and to the MHC superfamily (MhcSF). IMGT consists of five databases, ten on-line tools and more than 8,000 HTML pages of Web resources. IMGT provides a common access to standardized data from genome, genetics, proteome and three-dimensional structures. The accuracy and the con...</description>
            <author>Immunome Research</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=194</comments>
            <pubDate>Tue, 20 Sep 2005 06:00:00 +0100</pubDate>
            <guid isPermaLink="false">194</guid>        </item>
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