Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis (Q47967208)

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scientific article published on 11 March 2004

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English	Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis	scientific article published on 11 March 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Helmut Butzkueven

6

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

15

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Trevor Kilpatrick

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

14

object named as

Terence P Speed

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

author name string

Justin P Rubio

1

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Melanie Bahlo

2

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Niall Tubridy

3

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Jim Stankovich

4

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Rachel Burfoot

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Caron Chapman

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Laura Johnson

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Mark Marriott

9

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Grant Mraz

10

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Brian Tait

11

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Chris Wilkinson

12

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Bruce Taylor

13

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

publication date

11 March 2004

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

114

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

6

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

573-580

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Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

Genomics of the major histocompatibility complex: haplotypes, duplication, retroviruses and disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gray matter T2 hypointensity is related to plaques and atrophy in the brains of multiple sclerosis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further characterization of MHC haplotypes demonstrates conservation telomeric of HLA-A: update of the 4AOH and 10IHW cell panels

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Global prevalence of putative haemochromatosis mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: implications for cellular iron homeostasis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GOLD--graphical overview of linkage disequilibrium

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structure of haplotype blocks in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterogeneity in Rates of Recombination in the 6-Mb Region Telomeric to the Human Major Histocompatibility Complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of HLA-A3 and HLA-B14 antigens with idiopathic haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Celtic origin of the C282Y mutation of hemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple sclerosis: a modifying influence of HLA class I genes in an HLA class II associated autoimmune disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities in iron metabolism in multiple sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ancestral haplotypes: conserved population MHC haplotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene region

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multicentric origin of hemochromatosis gene (HFE) mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conservation of ancestral haplotypes telomeric of HLA-A

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

T2 hypointensity in the deep gray matter of patients with multiple sclerosis: a quantitative magnetic resonance imaging study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

the screening, diagnosis and optimal management of haemochromatosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HL-A antigens and multiple sclerosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course

1 reference

https://pubmed.ncbi.nlm.nih.gov/15014978

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-004-1095-9

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/15014978

ResearchGate publication ID

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