Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
about
Dopamine beta-hydroxylase deficiencyMolecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypesMenkes disease: what a multidisciplinary approach can doMottled Mice and Non-Mammalian Models of Menkes DiseaseATP7A-related copper transport diseases-emerging concepts and future trendsA novel frameshift mutation in exon 23 of ATP7A (MNK) results in occipital horn syndrome and not in Menkes diseaseRole of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicityThe soluble metal-binding domain of the copper transporter ATP7B binds and detoxifies cisplatin.Decreased erythrocyte CCS content is a biomarker of copper overload in rats.Inborn errors of copper metabolism.Copper and human health: biochemistry, genetics, and strategies for modeling dose-response relationships.Impairment of interrelated iron- and copper homeostatic mechanisms in brain contributes to the pathogenesis of neurodegenerative disorders.In vivo correction of a Menkes disease model using antisense oligonucleotides.Increased apoptosis and hypomyelination in cerebral white matter of macular mutant mouse brain.Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathyRole of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis.Copper transport into the secretory pathway is regulated by oxygen in macrophages.Advances in the understanding of mammalian copper transporters.Targeting copper in cancer therapy: 'Copper That Cancer'.Copper transporters and chaperones: Their function on angiogenesis and cellular signalling.Interaction between periostin and BMP-1 promotes proteolytic activation of lysyl oxidase.Localization of the Wilson disease protein in murine intestine.Epilepsy in Menkes disease: analysis of clinical stages.Impact of copper oxide nanomaterials on differentiated and undifferentiated Caco-2 intestinal epithelial cells; assessment of cytotoxicity, barrier integrity, cytokine production and nanomaterial penetrationCharacterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX).Impaired osteogenesis in Menkes disease-derived induced pluripotent stem cells.Occipital horn syndrome in a woman: skeletal radiological findings.The use of categorical regression in modeling copper exposure-response relationships.Activation of ADP-ribosylation factor regulates biogenesis of the ATP7A-containing trans-Golgi network compartment and its Cu-induced trafficking
P2860
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P2860
Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
@ast
Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
@en
type
label
Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
@ast
Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
@en
prefLabel
Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
@ast
Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
@en
P356
P1476
Metabolic and molecular bases of Menkes disease and occipital horn syndrome.
@en
P2093
P2888
P356
10.1007/S100249900011
P577
1998-01-01T00:00:00Z
P6179
1000005717