| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1000311963 |
| P356 | DOI | 10.1038/MP.2015.192 |
| P932 | PMC publication ID | 5078858 |
| P698 | PubMed publication ID | 26728570 |
| P5875 | ResearchGate publication ID | 289489724 |
| P50 | author | Joanna Collingwood | Q52566372 |
| Conceicao Bettencourt | Q55168655 | ||
| John K. Olynyk | Q37830523 | ||
| P2093 | author name string | R M Graham | |
| H Houlden | |||
| A C G Chua | |||
| B Bassett | |||
| D M Johnstone | |||
| D Trinder | |||
| E A Milward | |||
| M Heidari | |||
| M J House | |||
| M Ryten | |||
| P2860 | cites work | Targeted mutagenesis of the murine transferrin receptor-2 gene produces hemochromatosis | Q24533580 |
| Cellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disorders | Q27003886 | ||
| Molecular regulators of nerve conduction - Lessons from inherited neuropathies and rodent genetic models | Q28084798 | ||
| Neurodegeneration with brain iron accumulation: diagnosis and management | Q28085510 | ||
| HFE gene knockout produces mouse model of hereditary hemochromatosis | Q28263309 | ||
| Pantothenate kinase-associated neurodegeneration: altered mitochondria membrane potential and defective respiration in Pank2 knock-out mouse model | Q28505781 | ||
| Absence of 2-hydroxylated sphingolipids is compatible with normal neural development but causes late-onset axon and myelin sheath degeneration | Q28507237 | ||
| A mammalian fatty acid hydroxylase responsible for the formation of alpha-hydroxylated galactosylceramide in myelin | Q28590827 | ||
| The ferritins: molecular properties, iron storage function and cellular regulation | Q28609366 | ||
| Myelin staining of deep white matter in the dorsolateral prefrontal cortex in schizophrenia, bipolar disorder, and unipolar major depression | Q39793664 | ||
| Iron overload among a psychiatric outpatient population | Q41376649 | ||
| Disruption of hemochromatosis protein and transferrin receptor 2 causes iron-induced liver injury in mice. | Q42720829 | ||
| Glycosylphosphatidylinositol-anchored ceruloplasmin is required for iron efflux from cells in the central nervous system | Q44438522 | ||
| Movement disorders in the Hfe knockout mouse | Q44452286 | ||
| A comparison of learning and memory characteristics of young and middle-aged wild-type mice in the IntelliCage | Q44579304 | ||
| Severity of neurodegeneration correlates with compromise of iron metabolism in mice with iron regulatory protein deficiencies | Q44856752 | ||
| MRI measures of corpus callosum iron and myelin in early Huntington's disease. | Q45299568 | ||
| Adult neural precursor cells from the subventricular zone contribute significantly to oligodendrocyte regeneration and remyelination. | Q46822486 | ||
| Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights | Q47813038 | ||
| A mutation in the HFE gene is associated with altered brain iron profiles and increased oxidative stress in mice | Q48154144 | ||
| Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiation. | Q48202596 | ||
| The Parkinson-associated human P5B-ATPase ATP13A2 protects against the iron-induced cytotoxicity | Q48209774 | ||
| Genome-wide microarray analysis of brain gene expression in mice on a short-term high iron diet | Q48255631 | ||
| Transferrin is an essential factor for myelination | Q48286551 | ||
| Non-protein-bound iron and 4-hydroxynonenal protein adducts in classic autism | Q48548948 | ||
| Arachidonic acid inhibits myelin basic protein phosphorylation in cultured oligodendrocytes | Q48578238 | ||
| Brain transcriptome perturbations in the Hfe(-/-) mouse model of genetic iron loading. | Q48638376 | ||
| Novel mutation of the WDR45 gene causing beta-propeller protein-associated neurodegeneration. | Q50681545 | ||
| Brain iron takes off: a new propeller protein links neurodegeneration with autophagy. | Q50993710 | ||
| The effect of age on the non-haemin iron in the human brain. | Q51318963 | ||
| Defective FA2H leads to a novel form of neurodegeneration with brain iron accumulation (NBIA). | Q51899563 | ||
| Effects of development and iron status on ceruloplasmin expression in rat brain. | Q52056095 | ||
| Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis. | Q54296830 | ||
| Mutations in HFE and TFR2 genes in a Spanish patient with hemochromatosis. | Q54358723 | ||
| Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes | Q61638656 | ||
| Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 gene | Q64041013 | ||
| The Effect of Injections of Lysophosphatidyl Choline into White Matter of the Adult Mouse Spinal Cord | Q70350200 | ||
| Investigations on Pantothenic Acid and Its Related Compounds: IX. Biochemical Studies (4).* Separation and Substrate Specificity of Pantothenate Kinase and Phosphopantothenoylcysteine Synthetase** | Q72295323 | ||
| Early manifestations of BPAN in a pediatric patient | Q85644893 | ||
| Proceedings of the third joint symposium on neuroacanthocytosis and neurodegeneration with brain iron accumulation: from benchside to bedside | Q86598920 | ||
| Repeated mild traumatic brain injury results in long-term white-matter disruption. | Q30575806 | ||
| The role of iron in brain ageing and neurodegenerative disorders. | Q30852753 | ||
| Evaluation of Different Normalization and Analysis Procedures for Illumina Gene Expression Microarray Data Involving Small Changes. | Q31127418 | ||
| LPA-mediated demyelination in ex vivo culture of dorsal root | Q33261102 | ||
| Fatty acid 2-Hydroxylation in mammalian sphingolipid biology | Q33678737 | ||
| Role of myelin plasticity in oscillations and synchrony of neuronal activity | Q33680654 | ||
| Catalytic Function of PLA2G6 Is Impaired by Mutations Associated with Infantile Neuroaxonal Dystrophy but Not Dystonia-Parkinsonism | Q33707768 | ||
| PLA2G6-associated neurodegeneration (PLAN): further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease | Q33722781 | ||
| Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia | Q33941953 | ||
| C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients. | Q34117723 | ||
| Ceruloplasmin metabolism and function | Q34132626 | ||
| Adjusting for multiple testing--when and how? | Q34215794 | ||
| Mouse strain differences determine severity of iron accumulation in Hfe knockout model of hereditary hemochromatosis | Q34486746 | ||
| PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron | Q34568479 | ||
| Characterization of PLA2G6 as a locus for dystonia-parkinsonism | Q34593410 | ||
| In silico QTL mapping of basal liver iron levels in inbred mouse strains | Q34661915 | ||
| Non-classical hereditary hemochromatosis in Portugal: novel mutations identified in iron metabolism-related genes | Q34819066 | ||
| Novel histopathologic findings in molecularly-confirmed pantothenate kinase-associated neurodegeneration | Q35018106 | ||
| Glial cell ceruloplasmin and hepcidin differentially regulate iron efflux from brain microvascular endothelial cells | Q35095623 | ||
| Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation | Q35286584 | ||
| Iron status in children with autism spectrum disorder | Q35953702 | ||
| Disrupted membrane homeostasis and accumulation of ubiquitinated proteins in a mouse model of infantile neuroaxonal dystrophy caused by PLA2G6 mutations | Q36559669 | ||
| Nonheme-iron histochemistry for light and electron microscopy: a historical, theoretical and technical review | Q36844546 | ||
| Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations | Q36854793 | ||
| FA2H is responsible for the formation of 2-hydroxy galactolipids in peripheral nervous system myelin | Q37142657 | ||
| Oligodendrocytes and myelination: the role of iron | Q37287582 | ||
| AQP4 gene deletion in mice does not alter blood-brain barrier integrity or brain morphology. | Q37433008 | ||
| Molecular genetic approaches to understanding the roles and regulation of iron in brain health and disease | Q37719690 | ||
| Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations | Q37776461 | ||
| Hemochromatosis-induced bipolar disorder: a case report | Q37900387 | ||
| Neuroimaging features of neurodegeneration with brain iron accumulation. | Q37932848 | ||
| Iron sensing and signalling | Q37948025 | ||
| Iron dysregulation in movement disorders | Q37977795 | ||
| Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological Mechanisms | Q38479278 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | neurogenesis | Q1456827 |
| P304 | page(s) | 1599-1607 | |
| P577 | publication date | 2016-01-05 | |
| P1433 | published in | Molecular Psychiatry | Q6895973 |
| P1476 | title | Brain iron accumulation affects myelin-related molecular systems implicated in a rare neurogenetic disease family with neuropsychiatric features | |
| P478 | volume | 21 |
| Q57046102 | Brain iron loading impairs DNA methylation and alters GABAergic function in mice |
| Q37307471 | Coenzyme A corrects pathological defects in human neurons of PANK2-associated neurodegeneration |
| Q90639131 | Combined Diffusion Tensor Imaging and Quantitative Susceptibility Mapping Discern Discrete Facets of White Matter Pathology Post-injury in the Rodent Brain |
| Q64228674 | Deciphering the Iron Side of Stroke: Neurodegeneration at the Crossroads Between Iron Dyshomeostasis, Excitotoxicity, and Ferroptosis |
| Q47371821 | Dietary lipophilic iron accelerates regional brain iron-load in C57BL6 mice. |
| Q91638221 | Iron Deposition Leads to Hyperphosphorylation of Tau and Disruption of Insulin Signaling |
| Q33841090 | Pathogenic implications of distinct patterns of iron and zinc in chronic MS lesions |
| Q37127064 | Pathological relationships involving iron and myelin may constitute a shared mechanism linking various rare and common brain diseases |
| Q47093884 | Quantitative Susceptibility Mapping Reveals an Association between Brain Iron Load and Depression Severity |
| Q91744562 | Quantitative magnetic susceptibility assessed by 7T magnetic resonance imaging in Alzheimer's disease caused by streptozotocin administration |
| Q64928017 | Relationship of Iron Metabolism and Short-Term Cuprizone Treatment of C57BL/6 Mice. |
| Q57666825 | Striking while the iron is hot: Iron metabolism and ferroptosis in neurodegeneration |
| Q47607700 | Transcranial sonography in psychiatry as a potential tool in diagnosis and research |
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