Human MHC architecture and evolution: implications for disease association studies (Q37132341)

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scientific article published on 08 April 2008

Language	Label	Description	Also known as
English	Human MHC architecture and evolution: implications for disease association studies	scientific article published on 08 April 2008

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

4 references

Europe PubMed Central

23 July 2020

4 August 2020

10 September 2020

Human MHC architecture and evolution: implications for disease association studies (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

genetic predisposition to disease

2 references

23 July 2020

10 September 2020

major histocompatibility complex

1 reference

4 August 2020

author name string

J A Traherne

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

publication date

8 April 2008

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

1 June 2008

2 references

23 July 2020

4 August 2020

International Journal of Immunogenetics

3 references

Europe PubMed Central

PMC publication ID

18 August 2017

23 July 2020

4 August 2020

35

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

179-192

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

1 reference

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Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

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Genome-wide detection and characterization of positive selection in human populations

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Paired-end mapping reveals extensive structural variation in the human genome

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Genetic basis for MHC-dependent mate choice

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Transgenerational epigenetic imprints on mate preference

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Recurrent DNA inversion rearrangements in the human genome

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The mammalian epigenome

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Common genetic variants account for differences in gene expression among ethnic groups

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Global variation in copy number in the human genome

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3 September 2018

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Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis

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Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation.

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3 September 2018

Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2408657

3 September 2018

Pathogen-Driven Selection and Worldwide HLA Class I Diversity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2408657

4 December 2018

Transferability of tag SNPs in genetic association studies in multiple populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transcriptional regulation of MICA and MICB: A novel polymorphism in MICB promoter alters transcriptional regulation by Sp1

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional characterization of NF- B inhibitor-like protein 1 (NF BIL1), a candidate susceptibility gene for rheumatoid arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An integrated epigenetic and genetic approach to common human disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of base pair mismatches on recombination via the RecBCD pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WHO warns of microbial threat

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The origin and spread of the HFE-C282Y haemochromatosis mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Branch site haplotypes that control alternative splicing

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of in vivo recombination activities in the mouse embryo

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A high-resolution survey of deletion polymorphism in the human genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18397301

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/J.1744-313X.2008.00765.X

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

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Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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