Pathology of inherited manganese transporter deficiency. - Wikidata - wikimedia - TriplyDB

Pathology of inherited manganese transporter deficiency.

Pathology of inherited manganese transporter deficiency.

http://www.wikidata.org/entity/Q46134590

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Manganese-Induced Parkinsonism Is Not Idiopathic Parkinson's Disease: Environmental and Genetic Evidence Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia Manganese homeostasis in the nervous system Manganese-Induced Parkinsonism and Parkinson's Disease: Shared and Distinguishable Features Manganese-induced Neurotoxicity: From C. elegans to Humans SLC30A10 is a cell surface-localized manganese efflux transporter, and parkinsonism-causing mutations block its intracellular trafficking and efflux activity Dysregulation of FMRP/mTOR Signaling Cascade in Hypoxic-Ischemic Injury of Premature Human Brain.Cellular manganese content is developmentally regulated in human dopaminergic neurons.Role of neurotoxicants and traumatic brain injury in α-synuclein protein misfolding and aggregation.Influence of iron metabolism on manganese transport and toxicity.Zebrafish slc30a10 deficiency revealed a novel compensatory mechanism of Atp2c1 in maintaining manganese homeostasis.Recent Updates on Acquired Hepatocerebral Degeneration.Structural Elements in the Transmembrane and Cytoplasmic Domains of the Metal Transporter SLC30A10 Are Required for Its Manganese Efflux Activity.Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous system.Hypothyroidism induced by loss of the manganese efflux transporter SLC30A10 may be explained by reduced thyroxine production.Inherited Disorders of Manganese Metabolism.Familial manganese-induced neurotoxicity due to mutations in SLC30A10 or SLC39A14.Manganese transport disorder: novel SLC30A10 mutations and early phenotypes.Deficiency in the manganese efflux transporter SLC30A10 induces severe hypothyroidism in mice.Microscopy with ultraviolet surface excitation for rapid slide-free histology

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Pathology of inherited manganese transporter deficiency.

http://www.wikidata.org/entity/Q46134590

description

2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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name

Pathology of inherited manganese transporter deficiency.

@en

Pathology of inherited manganese transporter deficiency.

@nl

type

label

Pathology of inherited manganese transporter deficiency.

@en

Pathology of inherited manganese transporter deficiency.

@nl

prefLabel

Pathology of inherited manganese transporter deficiency.

@en

Pathology of inherited manganese transporter deficiency.

@nl

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Annals of Neurology

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Pathology of inherited manganese transporter deficiency.

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Lee-Way Jin

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Michael S Clegg

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Mirna Lechpammer

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Philip A Huebner

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Sidney M Gospe

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Zukhrofi Muzar

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P2860

Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man

Dystonia with brain manganese accumulation resulting from SLC30A10 mutations: a new treatable disorder.

Intermediate filaments and their associates: multi-talented structural elements specifying cytoarchitecture and cytodynamics.

The parkin mutant phenotype in the fly is largely rescued by metal-responsive transcription factor (MTF-1)

Metallothionein (MT) -I and MT-II expression are induced and cause zinc sequestration in the liver after brain injury.

A method for the combined staining of cells and fibers in the nervous system.

Role of astrocytes in manganese mediated neurotoxicity.

Manganese induces oxidative stress, redox state unbalance and disrupts membrane bound ATPases on murine neuroblastoma cells in vitro: protective role of silymarin.

Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease.

Estrogen attenuates manganese-induced glutamate transporter impairment in rat primary astrocytes

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608-612

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10.1002/ANA.24131

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4

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75

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260604758

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24599576

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