(Q36809964)

English

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

scientific article published on November 1997

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

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 (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

author name string

A Waheed

1

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

S Parkkila

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

X Y Zhou

3

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

S Tomatsu

4

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Z Tsuchihashi

5

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

J N Feder

6

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

R C Schatzman

7

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

R S Britton

8

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

B R Bacon

9

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

W S Sly

10

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

language of work or name

0 references

publication date

1 November 1997

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

94

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

23

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

12384-12389

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Regulation of intestinal non-haem iron absorption

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Mutation analysis of the HLA-H gene in Italian hemochromatosis patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Misfolded major histocompatibility complex class I heavy chains are translocated into the cytoplasm and degraded by the proteasome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

beta2 knockout mice develop parenchymal iron overload: A putative role for class I genes of the major histocompatibility complex in iron metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Hemochromatosis: the genetic disorder of the twenty-first century

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Misfolded major histocompatibility complex class I molecules accumulate in an expanded ER-Golgi intermediate compartment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Quality control in the secretory pathway: retention of a misfolded viral membrane glycoprotein involves cycling between the ER, intermediate compartment, and Golgi apparatus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Carbonic anhydrase IV: role of removal of C-terminal domain in glycosylphosphatidylinositol anchoring and realization of enzyme activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Primary structural: analysis of the transplantation antigens of the murine H-2 major histocompatibility complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

High efficiency polyoma DNA transfection of chloroquine treated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Assembly of asparagine-linked oligosaccharides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Structure, function, and diversity of class I major histocompatibility complex molecules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Comparison of amino acid sequences of two human histocompatibility antigens, HLA-A2 and HLA-B7: location of putative alloantigenic sites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

29 September 2017

Mutation analysis in hereditary hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

27 June 2018

Haemochromatosis and HLA-H.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

27 June 2018

Role of .beta.2-microglobulin in the intracellular processing of HLA antigens

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

27 June 2018

Site-directed mutagenesis of virtually any plasmid by eliminating a unique site

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

27 June 2018

Hereditary hemochromatosis. Phenotypic expression of the disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

27 June 2018

Putting a hold on "HLA-H'. The WHO Nomenclature Committee for Factors of the HLA System

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

5 September 2018

Biosynthesis of HLA-A and HLA-B antigens in vivo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=24956

5 September 2018

Haemochromatosis and HLA-H

1 reference

https://pubmed.ncbi.nlm.nih.gov/9356458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/9356458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Demonstration of an extensive trans-tubular network continuous with the Golgi apparatus stack that may function in glycosylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9356458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

1 reference

https://pubmed.ncbi.nlm.nih.gov/9356458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9356458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.94.23.12384

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

1997PNAS...9412384W

0 references

release_3xer2zr2y5gxtllvgbueqf4lhy

1 reference

https://api.fatcat.wiki/v0/release/3xer2zr2y5gxtllvgbueqf4lhy

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

0 references

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