/manager/Index ${session.getAttribute("locale")} 5 Pathological relationships involving iron and myelin may constitute a shared mechanism linking various rare and common brain diseases /manager/Repository/uon:30189 Hfe−/−xTfr2mut mouse model. This was accompanied by altered expression of a group of myelin-related genes, including a suite of genes causatively linked to the rare disease family ‘neurodegeneration with brain iron accumulation’ (NBIA). Expanded data mining and ontological analyses have now identified additional myelin-related transcriptome changes in response to brain iron loading. Concordance between the mouse transcriptome changes and human myelin-related gene expression networks in normal and NBIA basal ganglia testifies to potential clinical relevance. These analyses implicate, among others, genes linked to various rare central hypomyelinating leukodystrophies and peripheral neuropathies including Pelizaeus-Merzbacher-like disease and Charcot-Marie-Tooth disease as well as genes linked to other rare neurological diseases such as Niemann-Pick disease. The findings may help understand interrelationships of iron and myelin in more common conditions such as hemochromatosis, multiple sclerosis and various psychiatric disorders.]]> Wed 11 Apr 2018 16:58:00 AEST ]]> Cellular and molecular changes in the brain of the Hfe-/-xTfr2mut mouse, a model of human iron loading /manager/Repository/uon:22505 Wed 11 Apr 2018 16:25:30 AEST ]]> Advantages of array-based technologies for pre-emptive pharmacogenomics testing /manager/Repository/uon:29574 Wed 11 Apr 2018 14:11:09 AEST ]]> Evaluation of different normalization and analysis procedures for Illumina gene expression microarray data involving small changes /manager/Repository/uon:28613 Wed 11 Apr 2018 09:21:51 AEST ]]> Gene co-expression networks shed light into diseases of brain iron accumulation /manager/Repository/uon:24321 Sat 24 Mar 2018 07:14:41 AEDT ]]>