Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.
about
Pathophysiology of hereditary hemochromatosisRecent advances in understanding haemochromatosis: a transition stateThe unusual distribution of the neuronal/lymphoid cell surface CD200 (OX2) glycoprotein is conserved in humansHaemochromatosisExperimental hemochromatosis due to MHC class I HFE deficiency: immune status and iron metabolismDifferential HFE gene expression is regulated by alternative splicing in human tissuesContribution of Hfe expression in macrophages to the regulation of hepatic hepcidin levels and iron loadingThe haemochromatosis gene: a global perspective and implications for the Asia-Pacific region.HIV-1 Nef down-regulates the hemochromatosis protein HFE, manipulating cellular iron homeostasisThe hemochromatosis protein HFE inhibits iron export from macrophages.Physiology of iron transport and the hemochromatosis gene.Molecular pathogenesis of iron overload.Liver iron transportLevodopa Responsive Parkinsonism in Patients with Hemochromatosis: Case Presentation and Literature Review.Iron Imports. VI. HFE and regulation of intestinal iron absorption.The regulation of cellular iron metabolism.Iron uptake and transport across physiological barriers.A general map of iron metabolism and tissue-specific subnetworks.HFE gene variants affect iron in the brain.The liver in regulation of iron homeostasis.Nigral iron elevation is an invariable feature of Parkinson's disease and is a sufficient cause of neurodegeneration.Localisation of proteins of iron metabolism in the human placenta and liver.Type 3 hemochromatosis and beta-thalassemia trait.Overexpression of the hereditary hemochromatosis protein, HFE, in HeLa cells induces an iron-deficient phenotype
P2860
Q24654441-441D325E-6434-4C24-B598-687F3B255B3FQ24676226-CF51CFE5-723A-4E14-919E-1D42893F8EE3Q24682507-1206F2E9-DCE5-495E-A9EE-438C16B0B01FQ24685891-D1C4B185-AC22-44FD-86D8-02B5D441A466Q28137777-02129F8A-AEC8-4719-8EB0-7484707786D9Q28307418-AF695550-D740-44FA-BFD7-3054AD1D6CF4Q28512327-5AE73794-24D4-48B3-9BDA-80B74704B41FQ33760038-3F992D44-D0F0-4FB2-8926-79C8C0889CB7Q33905716-1AE30D61-EDA8-4829-A1BD-49D1B1F6CFAEQ34388109-F1E6450D-5D55-4287-9A98-1D3EACAD405FQ34528167-98CD8EA5-A273-4F94-9CAC-08D50FF9214BQ34739178-0C26F300-4D40-4D66-907B-D75C929AF947Q36177913-E4D03A24-5D75-4AC8-8FAF-B9F5F6D65A11Q36351447-4C7826BC-D4EA-4AAF-8776-BFEFA075DA18Q36421527-2B1261F3-FCA6-483A-A19F-0682475C4234Q36974377-C891EE9B-B78A-4B2F-9DA5-D5FD782E4444Q37150438-E52F9B77-BC29-4668-880E-EB47FA8BA21EQ37187218-2A73AF39-C473-4B82-8C32-4EA8C9B33201Q37846398-88E32053-7F1A-4F76-990B-A41892DFBF8DQ39360612-D627115C-62C1-4A77-9DD4-9AFC554F999BQ41825693-5E5F8BA3-F618-42BF-AFA4-ABD382A42E37Q42498536-E2726CEE-49A1-42E4-BA65-6AA35B3A953FQ44826224-AC2CFD2C-60C9-4539-AE95-362D8351E07DQ57951015-92D7FB43-789D-4309-BE57-FBCBA4E96BCF
P2860
Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.
description
1998 nî lūn-bûn
@nan
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
1998年论文
@zh
1998年论文
@zh-cn
name
Kupffer cell staining by an HF ...... r hereditary haemochromatosis.
@en
type
label
Kupffer cell staining by an HF ...... r hereditary haemochromatosis.
@en
prefLabel
Kupffer cell staining by an HF ...... r hereditary haemochromatosis.
@en
P2093
P2860
P1476
Kupffer cell staining by an HF ...... or hereditary haemochromatosis
@en
P2093
C A O'Callaghan
J M Bastin
L Schimanski
P2860
P304
P356
10.1046/J.1365-2141.1998.01102.X
P407
P577
1998-12-01T00:00:00Z