(Q24810582)

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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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

James C Barton

1

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Howard W Wiener

2

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Ronald T Acton

3

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Rodney C P Go

4

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

language of work or name

0 references

publication date

25 July 2005

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

BMC Blood Disorders

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

1

0 references

5

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

HLA-A and -B alleles and haplotypes in 240 index patients with common variable immunodeficiency and selective IgG subclass deficiency in central Alabama

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 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=1198220

7 April 2017

Resistance to hepcidin is conferred by hemochromatosis-associated mutations of ferroportin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 2017

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 2017

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 2017

Hemochromatosis and Iron Overload Screening (HEIRS) study design for an evaluation of 100,000 primary care-based adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 2017

Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 2017

Iron overload in Africa. Interaction between a gene and dietary iron content

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 2017

Performing the exact test of Hardy-Weinberg proportion for multiple alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

7 April 2017

Pathogenesis of autoimmune diseases associated with 8.1 ancestral haplotype: effect of multiple gene interactions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

28 September 2017

Quantitative trait loci on chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 control variation in levels of T and B lymphocyte subpopulations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

28 September 2017

Ethnic and sex differences in the total and differential white cell count and platelet count

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

28 September 2017

Practice guideline development task force of the College of American Pathologists. Hereditary hemochromatosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

28 September 2017

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=1198220

28 September 2017

Contributions of beta2-microglobulin-dependent molecules and lymphocytes to iron regulation: insights from HfeRag1(-/-) and beta2mRag1(-/-) double knock-out mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1198220

28 September 2017

Inheritance of two HFE mutations in African Americans: cases with hemochromatosis phenotypes and estimates of hemochromatosis phenotype frequency.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

Hemochromatosis: association of severity of iron overload with genetic markers.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

Hepcidin is decreased in TFR2 hemochromatosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

Tumor necrosis factor alpha promoter polymorphisms influence the phenotypic expression of hereditary hemochromatosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

Association of HLA types A1-B8-DR3 and B27 with rapid and slow progression of HIV disease

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

Genetic influence on peripheral blood T lymphocyte levels

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

Common variable immunodeficiency: clinical and immunological features of 248 patients.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

Absence of memory B cells in patients with common variable immunodeficiency

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

Management of Hemochromatosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Consensus of a group of professional societies and diagnostic companies on guidelines for interim reference ranges for 14 proteins in serum based on the standardization against the IFCC/BCR/CAP Reference Material (CRM 470). International Federation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of hemochromatosis probands in a community hospital

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype and frequency of cells secreting IL-2, IL-4, IL-6, IL-10, IFN and TNF-alpha in human peripheral blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth hormone (GH)-induced reconstitution of CD8+ CD28+ T lymphocytes in a rare case of severe lymphopenia associated with Juvenile Haemochromatosis and Turner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA-B8,DR3 haplotype affects lymphocyte blood levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population genetic analyses of insulin dependent diabetes mellitus using HLA allele frequencies

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variable immunodeficiency and IgG subclass deficiency in central Alabama hemochromatosis probands homozygous for HFE C282Y

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic determinism in the relationship between human CD4 + and CD8 + T lymphocyte populations?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor necrosis factor alpha promoter polymorphisms and liver abnormalities of homozygotes for the 845G>A(C282Y) hereditary hemochromatosis mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential inhibition of the MLR by iron: Association with HLA phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and genetic heterogeneity in hereditary haemochromatosis: association between lymphocyte counts and expression of iron overload

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secretion of IL-2, IL-3, IL-4, IL-6 and GM-CSF by CD4+ and CD8+ TCR alpha beta+ T-cell clones derived early after allogeneic bone marrow transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lymphocyte subsets in experimental hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of transfusional iron overload on immune response

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary immunodeficiency diseases. Report of a WHO scientific group

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haemochromatosis as a window into the study of the immunological system: A novel correlation between CD8+ lymphocytes and iron overload

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhanced apoptosis of T cells in common variable immunodeficiency (CVID): role of defective CD28 co-stimulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disproportionate lymphoid cell subsets in thalassaemia major: the relative contributions of transfusion and splenectomy

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anomalies of the CD8+ T cell pool in haemochromatosis: HLA-A3-linked expansions of CD8+CD28- T cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[T-helper (CD4+) cytopenia and HLA-A1, -B8, -C27, -DR3]

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Co-selection of the H63D mutation and the HLA-A29 allele: a new paradigm of linkage disequilibrium?

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16042809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An Analysis of Transformations

1 reference

https://api.crossref.org/works/10.1186%2F1471-2326-5-5

7 January 2021

based on heuristic

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Identifiers

10.1186/1471-2326-5-5

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 July 2017

ResearchGate publication ID

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