Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis. (Q40981523)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9886303%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

Kupffer cell staining by an HFE-specific monoclonal antibody: implications for hereditary haemochromatosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9886303%20AND%20SRC:MED&resulttype=core&format=json

Alain Robert Michael Townsend

8 December 2019

author

6

1 reference

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8 December 2019

author name string

J M Bastin

1

1 reference

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8 December 2019

M Jones

2

1 reference

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8 December 2019

C A O'Callaghan

3

1 reference

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8 December 2019

L Schimanski

4

1 reference

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8 December 2019

D Y Mason

5

1 reference

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8 December 2019

language of work or name

English

0 references

publication date

1 December 1998

1 reference

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British Journal of Haematology

8 December 2019

published in

1 reference

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8 December 2019

volume

103

1 reference

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8 December 2019

page(s)

931-941

1 reference

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8 December 2019

issue

4

1 reference

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Mapping the gene for sex-linked anemia: an inherited defect of intestinal iron absorption in the mouse.

8 December 2019

cites work

1 reference

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Hemochromatosis: the genetic disorder of the twenty-first century

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Monoclonal antibodies for analysis of the HLA system

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Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous for the C282Y mutation.

21 January 2018

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Screening for hemochromatosis

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Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-Sepharose

21 January 2018

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A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

21 January 2018

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The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

21 January 2018

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The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression

21 January 2018

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Hereditary haemochromatosis as an immunological disease

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Identification of a mouse homolog for the human hereditary haemochromatosis candidate gene.

21 January 2018

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Transferrin receptor on endothelium of brain capillaries

21 January 2018

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Continuous cultures of fused cells secreting antibody of predefined specificity

21 January 2018

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Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor

21 January 2018

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Differential expression of transferrin receptor in duodenal mucosa in iron overload. Evidence for a site-specific defect in genetic hemochromatosis

21 January 2018

1 reference

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High level transient expression of a chloramphenicol acetyl transferase gene by DEAE-dextran mediated DNA transfection coupled with a dimethyl sulfoxide or glycerol shock treatment.

21 January 2018

1 reference

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High efficiency polyoma DNA transfection of chloroquine treated cells

21 January 2018

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Global prevalence of putative haemochromatosis mutations

21 January 2018

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A human macrophage-associated antigen (CD68) detected by six different monoclonal antibodies

21 January 2018

1 reference

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Intracellular transport blockade caused by disruption of the disulfide bridge in the third external domain of major histocompatibility complex class I antigen

21 January 2018

1 reference

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Production, crystallization, and preliminary X-ray analysis of the human MHC class Ib molecule HLA-E.

21 January 2018

1 reference

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Restoration of H-2b expression and processing of endogenous antigens in the MHC class I pathway by fusion of a lymphoma mutant to L cells of the H-2k haplotype

21 January 2018

1 reference

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Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis

21 January 2018

1 reference

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Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastrointestinal tract

21 January 2018

1 reference

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Defective iron homeostasis in beta 2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man.

21 January 2018

1 reference

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Establishment and characterization of a human histiocytic lymphoma cell line (U-937)

21 January 2018

1 reference

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Hereditary 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

21 January 2018

1 reference

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HFE gene knockout produces mouse model of hereditary hemochromatosis

21 January 2018

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Association of class I major histocompatibility heavy and light chains induced by viral peptides

21 January 2018

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