<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nkuipou-Kenfack E</submitter><funding>Mathilde-Wagner-Habilitationspreis</funding><funding>BMBF Gerontosys II prpject</funding><funding>Excellence Initiative of the German Federal and State Governments</funding><funding>European Research Council</funding><funding>BMBF-STOP-FSGS</funding><funding>Margarete von Wrangell Habilitationsprogramm</funding><funding>EU FP7</funding><funding>Heisenberg program</funding><funding>German Research Foundation (DFG)</funding><pagination>e0166875</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5310860</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(2)</volume><pubmed_abstract>Ageing is a complex process characterised by a systemic and progressive deterioration of biological functions. As ageing is associated with an increased prevalence of age-related chronic disorders, understanding its underlying molecular mechanisms can pave the way for therapeutic interventions and managing complications. Animal models such as mice are commonly used in ageing research as they have a shorter lifespan in comparison to humans and are also genetically close to humans. To assess the translatability of mouse ageing to human ageing, the urinary proteome in 89 wild-type (C57BL/6) mice aged between 8-96 weeks was investigated using capillary electrophoresis coupled to mass spectrometry (CE-MS). Using age as a continuous variable, 295 peptides significantly correlated with age in mic</pubmed_abstract><journal>PloS one</journal><pubmed_title>The use of urinary proteomics in the assessment of suitability of mouse models for ageing.</pubmed_title><pmcid>PMC5310860</pmcid><funding_grant_id>Mathilde-Wagner-Habilitationspreis</funding_grant_id><funding_grant_id>CIG-293568</funding_grant_id><funding_grant_id>616891</funding_grant_id><funding_grant_id>CodeAge-31354</funding_grant_id><funding_grant_id>Heisenberg program</funding_grant_id><funding_grant_id>01GM1518C</funding_grant_id><funding_grant_id>EXC294</funding_grant_id><funding_grant_id>NephAge-031 5896A</funding_grant_id><funding_grant_id>Ministerium für Wissenschaft Baden-Württemberg</funding_grant_id><funding_grant_id>CRC-992</funding_grant_id><pubmed_authors>Huber TB</pubmed_authors><pubmed_authors>Bajwa S</pubmed_authors><pubmed_authors>Koeck T</pubmed_authors><pubmed_authors>Pich A</pubmed_authors><pubmed_authors>Pejchinovski M</pubmed_authors><pubmed_authors>Vinel C</pubmed_authors><pubmed_authors>Busch H</pubmed_authors><pubmed_authors>Rudolph KL</pubmed_authors><pubmed_authors>Nkuipou-Kenfack E</pubmed_authors><pubmed_authors>Schanstra JP</pubmed_authors><pubmed_authors>Bechtel-Walz W</pubmed_authors><pubmed_authors>Dray C</pubmed_authors><pubmed_authors>Bascands JL</pubmed_authors><pubmed_authors>Zurbig P</pubmed_authors><pubmed_authors>Borries M</pubmed_authors><pubmed_authors>Mischak H</pubmed_authors><pubmed_authors>Vlahou A</pubmed_authors><pubmed_authors>Valet P</pubmed_authors></additional><is_claimable>false</is_claimable><name>The use of urinary proteomics in the assessment of suitability of mouse models for ageing.</name><description>Ageing is a complex process characterised by a systemic and progressive deterioration of biological functions. As ageing is associated with an increased prevalence of age-related chronic disorders, understanding its underlying molecular mechanisms can pave the way for therapeutic interventions and managing complications. Animal models such as mice are commonly used in ageing research as they have a shorter lifespan in comparison to humans and are also genetically close to humans. To assess the translatability of mouse ageing to human ageing, the urinary proteome in 89 wild-type (C57BL/6) mice aged between 8-96 weeks was investigated using capillary electrophoresis coupled to mass spectrometry (CE-MS). Using age as a continuous variable, 295 peptides significantly correlated with age in mic</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2026-04-07T14:43:40.051Z</modification><creation>2019-03-26T22:52:54Z</creation></dates><accession>S-EPMC5310860</accession><cross_references><pubmed>28199320</pubmed><doi>10.1371/journal.pone.0166875</doi></cross_references></HashMap>