(Q36017054)

English

Evolutionary history of copy-number-variable locus for the low-affinity Fcγ receptor: mutation rate, autoimmune disease, and the legacy of helminth infection

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Evolutionary history of copy-number-variable locus for the low-affinity Fcγ receptor: mutation rate, autoimmune disease, and the legacy of helminth infection (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

autoimmune disease

1 reference

based on heuristic

inferred from title

object named as

Lee R Machado

1

0 references

Edward J Hollox

object named as

Edward J Hollox

7

0 references

object named as

Manuela Sironi

6

0 references

Jennifer Bowdrey

3

object named as

Jennifer Bowdrey

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Robert M Hardwick

2

object named as

Robert J Hardwick

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

author name string

Helen Bogle

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Timothy J Knowles

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

language of work or name

0 references

publication date

17 May 2012

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

90

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

973-985

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3370267

2 October 2017

Diversity and dialogue in immunity to helminths.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3370267

2 October 2017

Genetic variation, Fcγ receptors, KIRs and infection: the evolution of autoimmunity.

1 reference

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2 October 2017

Diversity of human copy number variation and multicopy genes

1 reference

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2 October 2017

Identification of copy number variation hotspots in human populations

1 reference

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2 October 2017

The landscape of human genes involved in the immune response to parasitic worms

1 reference

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2 October 2017

Copy number, linkage disequilibrium and disease association in the FCGR locus

1 reference

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2 October 2017

Association of variation in Fcgamma receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples

1 reference

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2 October 2017

A defunctioning polymorphism in FCGR2B is associated with protection against malaria but susceptibility to systemic lupus erythematosus

1 reference

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2 October 2017

The hygiene hypothesis: an evolutionary perspective

1 reference

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2 October 2017

FcgammaRIIB, FcgammaRIIIB, and systemic lupus erythematosus.

1 reference

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An expectation-maximization program for determining allelic spectrum from CNV data (CoNVEM): insights into population allelic architecture and its mutational history

1 reference

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2 October 2017

From evolutionary genetics to human immunology: how selection shapes host defence genes

1 reference

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Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions

1 reference

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2 October 2017

Copy number variation at the FCGR locus includes FCGR3A, FCGR2C and FCGR3B but not FCGR2A and FCGR2B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3370267

2 October 2017

Copy number variation of Fc gamma receptor genes and disease predisposition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3370267

2 October 2017

Allelic recombination between distinct genomic locations generates copy number diversity in human beta-defensins.

1 reference

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2 October 2017

Review series on helminths, immune modulation and the hygiene hypothesis: immunity against helminths and immunological phenomena in modern human populations: coevolutionary legacies?

1 reference

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2 October 2017

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1 reference

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2 October 2017

Worldwide human relationships inferred from genome-wide patterns of variation

1 reference

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2 October 2017

Human neutrophil alloantigens

1 reference

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2 October 2017

Fcgamma receptors as regulators of immune responses

1 reference

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2 October 2017

Copy number variation of the activating FCGR2C gene predisposes to idiopathic thrombocytopenic purpura

1 reference

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2 October 2017

Going the distance: human population genetics in a clinal world.

1 reference

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2 October 2017

PAML 4: phylogenetic analysis by maximum likelihood

1 reference

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2 October 2017

Recent human effective population size estimated from linkage disequilibrium

1 reference

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2 October 2017

Standardized subsets of the HGDP-CEPH Human Genome Diversity Cell Line Panel, accounting for atypical and duplicated samples and pairs of close relatives.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3370267

2 October 2017

A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3370267

2 October 2017

Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans

1 reference

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2 October 2017

A human genome diversity cell line panel

1 reference

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2 October 2017

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

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2 October 2017

Expression of functional CD32 molecules on human NK cells is determined by an allelic polymorphism of the FcgammaRIIC gene.

1 reference

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2 October 2017

Characterization of a new alloantigen (SH) on the human neutrophil Fc gamma receptor IIIb.

1 reference

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2 October 2017

Statistical properties of the number of recombination events in the history of a sample of DNA sequences

1 reference

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2 October 2017

Antibacterial activity of human natural killer cells

1 reference

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2 October 2017

Alternative membrane forms of Fc gamma RIII(CD16) on human natural killer cells and neutrophils. Cell type-specific expression of two genes that differ in single nucleotide substitutions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3370267

2 October 2017

Organization of the human and mouse low-affinity Fc gamma R genes: duplication and recombination

1 reference

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2 October 2017

Confirmation of association of FCGR3B but not FCGR3A copy number with susceptibility to autoantibody positive rheumatoid arthritis.

1 reference

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23 September 2018

Evidence for both copy number and allelic (NA1/NA2) risk at the FCGR3B locus in systemic lupus erythematosus

1 reference

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23 September 2018

The role of protozoa-driven selection in shaping human genetic variability

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23 September 2018

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1 reference

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23 September 2018

Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats.

1 reference

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23 September 2018

A worm's eye view of the immune system: consequences for evolution of human autoimmune disease.

1 reference

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23 September 2018

Variation in human FCGR2C gene copy number

1 reference

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23 September 2018

Functional role of human IgG subclasses in eosinophil-mediated killing of schistosomula of Schistosoma mansoni

1 reference

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21 October 2018

Meta-analysis confirms a role for deletion in FCGR3B in autoimmune phenotypes

1 reference

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5 December 2018

Loss of function of a lupus-associated FcγRIIb polymorphism through exclusion from lipid rafts

1 reference

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5 December 2018

FcγR expression on NK cells influences disease severity in rheumatoid arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22608500

12 December 2020

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Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22608500

12 December 2020

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Inhibition of IgG-triggered human eosinophil function by IL-4

1 reference

https://pubmed.ncbi.nlm.nih.gov/22608500

12 December 2020

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1 reference

https://pubmed.ncbi.nlm.nih.gov/22608500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJHG.2012.04.018

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

ResearchGate publication ID

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