(Q36148396)

12 August 2017

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title

Paths to understanding the genetic basis of autoimmune disease (English)

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12 August 2017

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John D Rioux

1

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Abul K. Abbas

series ordinal

2

object named as

Abul K Abbas

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PubMed ID

15931210

12 August 2017

language of work or name

English

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publication date

1 June 2005

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12 August 2017

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12 August 2017

435

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12 August 2017

584-589

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12 August 2017

7042

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https://scigraph.springernature.com/pub.10.1038/nature03723

12 August 2017

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cites work

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Gene defect behind APECED: a new clue to autoimmunity

21 January 2018

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Projection of an immunological self shadow within the thymus by the aire protein

21 January 2018

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Aire regulates negative selection of organ-specific T cells

21 January 2018

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Back to central tolerance

21 January 2018

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Complexities of CD28/B7: CTLA-4 costimulatory pathways in autoimmunity and transplantation

21 January 2018

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Inhibition of CTLA-4 function by the regulatory subunit of serine/threonine phosphatase 2A

21 January 2018

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Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

21 January 2018

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Naturally arising CD4+ regulatory t cells for immunologic self-tolerance and negative control of immune responses

21 January 2018

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Control of regulatory T cell development by the transcription factor Foxp3

21 January 2018

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Foxp3 programs the development and function of CD4+CD25+ regulatory T cells

21 January 2018

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An essential role for Scurfin in CD4+CD25+ T regulatory cells

21 January 2018

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Fas and Fas ligand: lpr and gld mutations

21 January 2018

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Mature T lymphocyte apoptosis--immune regulation in a dynamic and unpredictable antigenic environment

21 January 2018

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

21 January 2018

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Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

21 January 2018

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Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

21 January 2018

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High-resolution haplotype structure in the human genome

21 January 2018

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Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

21 January 2018

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The structure of haplotype blocks in the human genome

21 January 2018

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Human genome sequence variation and the influence of gene history, mutation and recombination

21 January 2018

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The fine-scale structure of recombination rate variation in the human genome

21 January 2018

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Genome-wide association studies for common diseases and complex traits

21 January 2018

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Genome-wide association studies: theoretical and practical concerns

21 January 2018

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

21 January 2018

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Functional variants of OCTN cation transporter genes are associated with Crohn disease

21 January 2018

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Characterization of a common susceptibility locus for asthma-related traits

21 January 2018

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

21 January 2018

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A functional polymorphism (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families

21 January 2018

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Replication of an association between the lymphoid tyrosine phosphatase locus (LYP/PTPN22) with type 1 diabetes, and evidence for its role as a general autoimmunity locus

21 January 2018

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Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE.

21 January 2018

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A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis

21 January 2018

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Association of a programmed death 1 gene polymorphism with the development of rheumatoid arthritis, but not systemic lupus erythematosus

21 January 2018

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A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans

21 January 2018

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An autoimmune disease-associated CTLA-4 splice variant lacking the B7 binding domain signals negatively in T cells

21 January 2018

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A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes

21 January 2018

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Absence of Programmed Death Receptor 1 Alters Thymic Development and Enhances Generation of CD4/CD8 Double-Negative TCR-Transgenic T Cells

21 January 2018

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NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses

21 January 2018

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Nod2 is a general sensor of peptidoglycan through muramyl dipeptide (MDP) detection

21 January 2018

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Role of Nod2 in the Response of Macrophages to Toll-Like Receptor Agonists

21 January 2018

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Nod2-dependent regulation of innate and adaptive immunity in the intestinal tract

21 January 2018

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Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE03723

Replication validity of genetic association studies

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE03723

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

21 January 2018

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A comprehensive review of genetic association studies

21 January 2018

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Genetic associations in large versus small studies: an empirical assessment

21 January 2018

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New approaches to gene hunting in IBD.

21 January 2018

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21 January 2018

Genetic origin of IBD.

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Gene map of the extended human MHC.

21 January 2018

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An integrated haplotype map of the human major histocompatibility complex

21 January 2018

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A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms

21 January 2018

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Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE03723

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

21 January 2018

1 reference

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Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

Patterns of linkage disequilibrium in the MHC region on human chromosome 6p

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

Reply to 'Haplotype block structure of the cytochrome P450 CYP2C gene cluster on chromosome 10'

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

Insulin autoimmunity: immunogenetics/immunopathogenesis of type 1A diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

7 January 2021

Finishing the euchromatic sequence of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

7 January 2021

The International HapMap Project

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

7 January 2021

Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

7 January 2021

PD-1: an inhibitory immunoreceptor involved in peripheral tolerance

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

7 January 2021

A single-nucleotide polymorphism tagging set for human drug metabolism and transport

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

7 January 2021

Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNATURE03723

7 January 2021

Identifiers

DOI

10.1038/NATURE03723

1 reference

PubMed ID

15931210

Dimensions Publication ID

12 August 2017

0 references

1 reference

PubMed ID

15931210