Modifying factors and phenotypic diversity in Wilson's disease

Modifying factors and phenotypic diversity in Wilson's disease

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http://www.wikidata.org/entity/Q33851780
Mechanism of Copper Uptake from Blood Plasma Ceruloplasmin by Mammalian Cells.Genome-wide association between single nucleotide polymorphisms with beef fatty acid profile in Nellore cattle using the single step procedure.Targeting copper in cancer therapy: 'Copper That Cancer'.Age-dependent changes of cerebral copper metabolism in Atp7b -/- knockout mouse model of Wilson's disease by [64Cu]CuCl2-PET/CT.Cellular copper homeostasis: current concepts on its interplay with glutathione homeostasis and its implication in physiology and human diseases.Wilson Disease: Epigenetic effects of choline supplementation on phenotype and clinical course in a mouse model.The genetics of Wilson disease.Copper Signaling in the Brain and Beyond.Non-ceruloplasmin bound copper and ATP7B gene variants in Alzheimer's disease.Multimodal LA-ICP-MS and nanoSIMS imaging enables copper mapping within photoreceptor megamitochondria in a zebrafish model of Menkes disease.Curcumin Effect on Copper Transport in HepG2 Cells
P2860

Modifying factors and phenotypic diversity in Wilson's disease

Item
http://www.wikidata.org/entity/Q33851780
description
2014 nî lūn-bûn
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2014 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Modifying factors and phenotypic diversity in Wilson's disease
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Modifying factors and phenotypic diversity in Wilson's disease
@en
type
label
Modifying factors and phenotypic diversity in Wilson's disease
@ast
Modifying factors and phenotypic diversity in Wilson's disease
@en
prefLabel
Modifying factors and phenotypic diversity in Wilson's disease
@ast
Modifying factors and phenotypic diversity in Wilson's disease
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P478
P577
P698
P932
P356
P1433
P1476
Modifying factors and phenotypic diversity in Wilson's disease
@en
P2093
P2860
P304
P31
P356
P407
P478
P577
P698
P932