(Q35055043)

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Effects of highly conserved major histocompatibility complex (MHC) extended haplotypes on iron and low CD8+ T lymphocyte phenotypes in HFE C282Y homozygous hemochromatosis patients from three geographically distant areas

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Europe PubMed Central

PubMed publication ID

6 August 2017

Effects of highly conserved major histocompatibility complex (MHC) extended haplotypes on iron and low CD8+ T lymphocyte phenotypes in HFE C282Y homozygous hemochromatosis patients from three geographically distant areas (English)

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Europe PubMed Central

PubMed publication ID

6 August 2017

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Jorge Vieira

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Cristina P Vieira

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Graça Porto

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Berta Martins Silva

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Berta M da Silva

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Mónica Costa

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Europe PubMed Central

PubMed publication ID

6 August 2017

Eugénia Cruz

2

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Europe PubMed Central

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6 August 2017

James C Barton

3

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Europe PubMed Central

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6 August 2017

Ketil Thorstensen

4

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Europe PubMed Central

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6 August 2017

Sandra Morais

5

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Europe PubMed Central

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6 August 2017

Jorge P Pinto

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6 August 2017

Ronald T Acton

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6 August 2017

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25 November 2013

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Europe PubMed Central

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6 August 2017

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Europe PubMed Central

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6 August 2017

8

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Europe PubMed Central

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6 August 2017

11

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Europe PubMed Central

PubMed publication ID

6 August 2017

e79990

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Europe PubMed Central

PubMed publication ID

6 August 2017

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Creative Commons Attribution 3.0 Unported

25 November 2013

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April 2022 Public Data File from Crossref

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0 references

Allele frequency net: a database and online repository for immune gene frequencies in worldwide populations

1 reference

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Norwegian Sami differs significantly from other Norwegians according to their HLA profile.

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8 July 2018

Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control

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The human Major Histocompatibility Complex as a paradigm in genomics research

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Defining multiple common "completely" conserved major histocompatibility complex SNP haplotypes

1 reference

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A new 500 kb haplotype associated with high CD8+ T-lymphocyte numbers predicts a less severe expression of hereditary hemochromatosis.

1 reference

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8 July 2018

The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects

1 reference

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Effect of Native American ancestry on iron-related phenotypes of Alabama hemochromatosis probands with HFE C282Y homozygosity

1 reference

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A study of 82 extended HLA haplotypes in HFE-C282Y homozygous hemochromatosis subjects: relationship to the genetic control of CD8+ T-lymphocyte numbers and severity of iron overload

1 reference

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8 July 2018

Total blood lymphocyte counts in hemochromatosis probands with HFE C282Y homozygosity: relationship to severity of iron overload and HLA-A and -B alleles and haplotypes

1 reference

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8 July 2018

HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload

1 reference

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8 July 2018

HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama.

1 reference

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8 July 2018

Recombinations defining centromeric and telomeric borders for the hereditary haemochromatosis locus

1 reference

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8 July 2018

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

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8 July 2018

Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839968

8 July 2018

Measuring the strength of associations between HLA antigens and diseases

1 reference

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A review of theoretical aspects of HLA and disease associations

1 reference

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8 July 2018

Statistical aspects of measuring the strength of associations between HLA antigens and diseases.

1 reference

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8 July 2018

A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA as

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3839968

8 July 2018

Hemochromatosis: association of severity of iron overload with genetic markers

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0079990

21 January 2018

The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype?

1 reference

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Relative impact of HLA phenotype and CD4-CD8 ratios on the clinical expression of hemochromatosis

1 reference

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Involvement of the major histocompatibility complex region in the genetic regulation of circulating CD8 T-cell numbers in humans.

1 reference

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21 January 2018

Persons with screening-detected haemochromatosis: as healthy as the general population?

1 reference

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HLA gene haplotype frequencies in bone marrow donors worldwide registries

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0079990

21 January 2018

Was the C282Y mutation an Irish Gaelic mutation that the Vikings helped disseminate? HLA haplotype observations of hemochromatosis from the west coast of Sweden.

1 reference

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21 January 2018

Screening for C282Y homozygosity in a Norwegian population (HUNT2): The sensitivity and specificity of transferrin saturation

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Countries of ancestry reported by hemochromatosis probands and control subjects in central Alabama

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Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis

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Linkage disequilibrium analysis in Australian haemochromatosis patients indicates bipartite association with clinical expression

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The origin and spread of the HFE-C282Y haemochromatosis mutation

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HLA-A3-B14 and the origin of the haemochromatosis C282Y mutation: founder effects and recombination events during 12 generations in a Scandinavian family with major iron overload

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Stability of CD4/CD8 ratios in man: new correlation between CD4/CD8 profiles and iron overload in idiopathic haemochromatosis patients

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The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients

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Heterogeneity of hemochromatosis in Italy

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T-Cell receptor repertoire in hereditary hemochromatosis: a study of 32 hemochromatosis patients and 274 healthy subjects

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Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC region

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Screening for hemochromatosis: high prevalence and low morbidity in an unselected population of 65,238 persons

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10.1371/JOURNAL.PONE.0079990

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

2013PLoSO...879990C

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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