Intracellular transport blockade caused by disruption of the disulfide bridge in the third external domain of major histocompatibility complex class I antigen.
about
The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expressionCalnexin influences folding of human class I histocompatibility proteins but not their assembly with beta 2-microglobulinThe E3/19K protein of adenovirus type 2 binds to the domains of histocompatibility antigens required for CTL recognitionRegulation of transferrin-mediated iron uptake by HFE, the protein defective in hereditary hemochromatosis.Pumping iron: the strange partnership of the hemochromatosis protein, a class I MHC homolog, with the transferrin receptor.Site-directed mutagenesis of an HLA-A3 gene identifies amino acid 152 as crucial for major-histocompatibility-complex-restricted and alloreactive cytotoxic-T-lymphocyte recognition.Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract.Differential expression of MHC class I antigens on the placenta of the rat. A mechanism for the survival of the fetal allograftStructural mutation affecting intracellular transport and cell surface expression of murine class II moleculesFine mapping of epitopes by intradomain Kd/Dd recombinantsHereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells.Expression of bovine herpesvirus 1 glycoproteins gI and gIII in transfected murine cells.HFE gene variants affect iron in the brain.Functions of ERp57 in the folding and assembly of major histocompatibility complex class I molecules.Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiency.Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis.Efficiency of acetylcholine receptor subunit assembly and its regulation by cAMP.A murine hybridoma with large cytoplasmic inclusions of kappa light chains.
P2860
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P2860
Intracellular transport blockade caused by disruption of the disulfide bridge in the third external domain of major histocompatibility complex class I antigen.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
1986年论文
@zh
1986年论文
@zh-cn
name
Intracellular transport blocka ...... ility complex class I antigen.
@ast
Intracellular transport blocka ...... ility complex class I antigen.
@en
type
label
Intracellular transport blocka ...... ility complex class I antigen.
@ast
Intracellular transport blocka ...... ility complex class I antigen.
@en
prefLabel
Intracellular transport blocka ...... ility complex class I antigen.
@ast
Intracellular transport blocka ...... ility complex class I antigen.
@en
P2093
P2860
P356
P1476
Intracellular transport blocka ...... ility complex class I antigen.
@en
P2093
P2860
P304
P356
10.1073/PNAS.83.3.757
P407
P577
1986-02-01T00:00:00Z