Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
about
Outward- and inward-facing structures of a putative bacterial transition-metal transporter with homology to ferroportin.Ceruloplasmin-ferroportin system of iron traffic in vertebrates.Pathophysiological consequences and benefits of HFE mutations: 20 years of research.Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3.A bacterial homologue of the human iron exporter ferroportin.A novel mutation in the SLC40A1 gene associated with reduced iron export in vitro.Structure-function analysis of ferroportin defines the binding site and an alternative mechanism of action of hepcidin.A composite mouse model of aplastic anemia complicated with iron overload.A structural model of human ferroportin and of its iron binding site.Comparison of the effects of deferasirox, deferoxamine, and combination of deferasirox and deferoxamine on an aplastic anemia mouse model complicated with iron overload.
P2860
Q27321351-0EB8B4F6-C23D-42B8-9E65-C7CEE4876F2DQ33728846-0424DFCC-1A7C-41D3-B40F-AAD9C94B5A05Q33815961-B88F0BB1-FBE3-4374-A4CB-D97F4D0F0A79Q35648084-42EB716E-27CC-4637-AE9C-F561E7DB2BC8Q40274225-5A03B89D-5687-43C4-AC65-6769FF053D8CQ45905043-90B57016-4B5D-4B3F-B83F-AFC05A0751C0Q46152147-2DD7BC22-8B52-45FC-83DA-5102363F4AA8Q50054152-852E43FB-20F1-4B1B-9B93-6433964C11DEQ54290351-0E1E9C47-4E04-4037-84AA-D5A70CC97F39Q55365418-96EE729B-49D6-490F-B8C3-45B5CE57853C
P2860
Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
@en
Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
@nl
type
label
Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
@en
Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
@nl
prefLabel
Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
@en
Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
@nl
P2093
P2860
P356
P1433
P1476
Ferroportin diseases: functional studies, a link between genetic and clinical phenotype.
@en
P2093
Anne-Marie Jouanolle
Annick Mosser
Caroline Le Lan
Lénaïck Détivaud
Marie-Laure Island
Martine Ropert
Olivier Loréal
Patricia Leroyer
Pierre Brissot
Véronique David
P2860
P304
P356
10.1002/HUMU.22396
P577
2013-09-11T00:00:00Z