(Q24799115)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

0 references

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

author name string

Ronald T Acton

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

language of work or name

English

0 references

publication date

7 October 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

volume

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

issue

1

0 references

page(s)

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1186/1471-2350-3-9

13 December 2019

exact match

0 references

cites work

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=137582

On estimating the relation between blood group and disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Hereditary haemochromatosis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Idiopathic haemochromatosis and HLA antigens in Italy: is A3 Bw35 HLA haplotype a marker for idiopathic haemochromatosis gene in north east regions?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Genetics of hemochromatosis: HLA association and mode of inheritance

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

HLA determinants in an Australian population of hemochromatosis patients and their families

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Histocompatibility antigens as markers of abnormal iron metabolism in idiopathic hemochromatosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Homogeneous multiplex genotyping of hemochromatosis mutations with fluorescent hybridization probes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Heterogeneity in rates of recombination in the 6-Mb region telomeric to the human major histocompatibility complex.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Haemochromatosis and HLA-H.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Hemochromatosis: genetic or alcohol-induced?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

HLA determinants in 70 Danish patients with idiopathic haemochromatosis.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

Idiopathic haemochromatosis in north Portugal: association with haplotype A3B7.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137582

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

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

Gluconate metabolism of Pasteurellapestis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

Prevalence of the C282Y and H63D mutations in the HFE gene in patients with hereditary haemochromatosis and in control subjects from Northern Germany.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

High incidence of the Cys 282 Tyr mutation in the HFE gene in the Irish population--implications for haemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

Is all genetic (hereditary) hemochromatosis HLA-associated

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

HLA as a marker of the hemochromatosis gene in Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

The major histocompatability complex (MHC) contains conserved polymorphic genomic sequences that are shuffled by recombination to form ethnic-specific haplotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

HLA class I gene polymorphism in genetic hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

HFEmutations in patients with hereditary haemochromatosis in Sweden

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

HFE codon 63/282 (H63D/C282Y) dimorphism in German patients with genetic hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

Major histocompatibility complex class I associations in iron overload: evidence for a new link between the HFE H63D mutation, HLA-A29, and non-classical forms of hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

Transferrin saturation phenotype and HFE genotype screening for hemochromatosis and primary iron overload: predictions from a model based on national, racial, and ethnic group composition in central Alabama

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

HFE genotype frequencies in consecutive reference laboratory specimens: comparisons among referral sources and association with initial diagnosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

Two novel missense mutations of the HFE gene (I105T and G93R) and identification of the S65C mutation in Alabama hemochromatosis probands

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-9

Idiopathic hemochromatosis: association with antigens of the HLA system

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12370085

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hepatic pathology in relatives of patients with hæmochromatosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12370085

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A genotypic study of 217 unrelated probands diagnosed as "genetic hemochromatosis" on "classical" phenotypic criteria

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12370085

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-3-9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

13 December 2019

1030195795

0 references

OpenCitations bibliographic resource ID

690438

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12370085%20AND%20SRC:MED&resulttype=core&format=json

13 December 2019

1 reference