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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Network analysis of genes and their association with diseases

Thumbnail
Συγγραφέας
Kontou P.I., Pavlopoulou A., Dimou N.L., Pavlopoulos G.A., Bagos P.G.
Ημερομηνία
2016
Γλώσσα
en
DOI
10.1016/j.gene.2016.05.044
Λέξη-κλειδί
Article
disease association
gene cluster
gene regulatory network
genetic analysis
genetic association
human
monogenic disorder
phenotype
priority journal
protein tertiary structure
gene expression regulation
genetic disorder
genetics
genotype
pathology
procedures
protein analysis
signal transduction
software
statistics and numerical data
systems biology
Gene Expression Regulation
Gene Regulatory Networks
Genetic Diseases, Inborn
Genotype
Humans
Phenotype
Protein Interaction Mapping
Signal Transduction
Software
Systems Biology
Elsevier B.V.
Εμφάνιση Μεταδεδομένων
Επιτομή
A plethora of network-based approaches within the Systems Biology universe have been applied, to date, to investigate the underlying molecular mechanisms of various human diseases. In the present study, we perform a bipartite, topological and clustering graph analysis in order to gain a better understanding of the relationships between human genetic diseases and the relationships between the genes that are implicated in them. For this purpose, disease-disease and gene-gene networks were constructed from combined gene-disease association networks. The latter, were created by collecting and integrating data from three diverse resources, each one with different content covering from rare monogenic disorders to common complex diseases. This data pluralism enabled us to uncover important associations between diseases with unrelated phenotypic manifestations but with common genetic origin. For our analysis, the topological attributes and the functional implications of the individual networks were taken into account and are shortly discussed. We believe that some observations of this study could advance our understanding regarding the etiology of a disease with distinct pathological manifestations, and simultaneously provide the springboard for the development of preventive and therapeutic strategies and its underlying genetic mechanisms. © 2016 Elsevier B.V.
URI
http://hdl.handle.net/11615/75105
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19743]

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