<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2</volume><submitter>Shih CT</submitter><pubmed_abstract>Electronic properties of DNA are believed to play a crucial role in many phenomena in living organisms, for example the location of DNA lesions by base excision repair (BER) glycosylases and the regulation of tumor-suppressor genes such as p53 by detection of oxidative damage. However, the reproducible measurement and modelling of charge migration through DNA molecules at the nanometer scale remains a challenging and controversial subject even after more than a decade of intense efforts. Here we show, by analysing 162 disease-related genes from a variety of medical databases with a total of almost 20,000 observed pathogenic mutations, a significant difference in the electronic properties of the population of observed mutations compared to the set of all possible mutations. Our results have</pubmed_abstract><journal>Scientific reports</journal><pagination>272</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3280594</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The interplay of mutations and electronic properties in disease-related genes.</pubmed_title><pmcid>PMC3280594</pmcid><pubmed_authors>Wells SA</pubmed_authors><pubmed_authors>Romer RA</pubmed_authors><pubmed_authors>Hsu CL</pubmed_authors><pubmed_authors>Shih CT</pubmed_authors><pubmed_authors>Cheng YY</pubmed_authors></additional><is_claimable>false</is_claimable><name>The interplay of mutations and electronic properties in disease-related genes.</name><description>Electronic properties of DNA are believed to play a crucial role in many phenomena in living organisms, for example the location of DNA lesions by base excision repair (BER) glycosylases and the regulation of tumor-suppressor genes such as p53 by detection of oxidative damage. However, the reproducible measurement and modelling of charge migration through DNA molecules at the nanometer scale remains a challenging and controversial subject even after more than a decade of intense efforts. Here we show, by analysing 162 disease-related genes from a variety of medical databases with a total of almost 20,000 observed pathogenic mutations, a significant difference in the electronic properties of the population of observed mutations compared to the set of all possible mutations. Our results have</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2025-04-18T14:00:15.922Z</modification><creation>2019-03-27T00:49:12Z</creation></dates><accession>S-EPMC3280594</accession><cross_references><pubmed>22355784</pubmed><doi>10.1038/srep00272</doi></cross_references></HashMap>