Results 181 to 190 of about 6,026 (227)
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ERAP1 as an emerging therapeutic target for medulloblastoma
Trends in Cancer, 2022Endoplasmic reticulum aminopeptidase 1 (ERAP1) is a multifunctional enzyme that shapes the peptide repertoire presented by major histocompatibility complex class I (MHC-I) molecules, thereby affecting tumor immunogenicity. ERAP1 is altered in many tumors, including medulloblastoma (MB).
Bufalieri F. +2 more
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ERAP1 and the return of the UPR in ankylosing spondylitis
Nature Reviews Rheumatology, 2023N. Haroon, R. Inman
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Annals of the Rheumatic Diseases, 2016
Background Single nucleotide polymorphisms (SNPs) in ERAP1 are strongly associated with ankylosing spondylitis (AS) (1,2). ERAP1 is an aminopeptidase involved in the generation of optimal peptide epitopes for presentation by T-cells in the context of major histocompatibility complex (MHC) class I molecules such as HLA-B27.
Appleton, LH +3 more
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Background Single nucleotide polymorphisms (SNPs) in ERAP1 are strongly associated with ankylosing spondylitis (AS) (1,2). ERAP1 is an aminopeptidase involved in the generation of optimal peptide epitopes for presentation by T-cells in the context of major histocompatibility complex (MHC) class I molecules such as HLA-B27.
Appleton, LH +3 more
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ERAP1 in the pathogenesis of ankylosing spondylitis
Immunologic Research, 2014The endoplasmic reticulum aminopeptidase 1 (ERAP1) performs a major role in antigen processing, trimming N-terminally extended peptides to the final epitope for presentation by major histocompatibility complex class I molecules. Recent genome-wide association studies have identified single nucleotide polymorphisms (SNPs) within ERAP1 as being ...
Reeves, Emma +3 more
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Polymorphisms in ERAP1 gene are associated with psoriasis
Meta Gene, 2022Abstract Background Several polymorphisms in ERAP1 gene has been reported to be associated with psoriasis in several different populations. Objective To better understand the association between ERAP1 and psoriasis in Chinese Han population. Methods Seven SNPs (rs27044, rs27043, rs26510, rs469758, rs30378, rs30186 and rs2303208) in ERAP1 ...
Weiwei Chen +13 more
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The role of ERAP1 in autoinflammation and autoimmunity
Human Immunology, 2019Autoimmune and autoinflammatory diseases affect millions worldwide. These classes of disease involve abnormal immune activation of both the innate and adaptive immune systems. While both classes of disease represent a spectrum of aberrant immune activation, excessive activation of the innate immune system has been considered causal for the inflammation
Yuliya Pepelyayeva, Andrea Amalfitano
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Investigating the genetic association between ERAP1 and spondyloarthritis
Annals of the Rheumatic Diseases, 2013A robust association between polymorphisms in the non-major histocompatibility complex gene ERAP1 and ankylosing spondylitis (AS) in several populations was recently identified. The aim of the current study was to determine the level of association of ERAP1 polymorphisms with spondyloarthritis (SpA) in French/Belgian populations with particular ...
Amir, Kadi +8 more
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ERAP1-dependent extreme antigen processing efficacy can govern MHC class I expression hierarchy.
Journal of ImmunologyPeptide presentation by major histocompatibility complex (MHC) class I molecules enables CD8+ T lymphocytes to monitor the intracellular proteome of tissue cells.
Jacqueline Leib +8 more
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Human Immunology
Single nucleotide polymorphisms (SNPs) in the endoplasmic reticulum aminopeptidase 1 (ERAP1) and ERAP2 genes have been associated with susceptibility to various immune-mediated inflammatory diseases (IMIDs).
Sofie Jørgensen +8 more
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Single nucleotide polymorphisms (SNPs) in the endoplasmic reticulum aminopeptidase 1 (ERAP1) and ERAP2 genes have been associated with susceptibility to various immune-mediated inflammatory diseases (IMIDs).
Sofie Jørgensen +8 more
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ERAP1 shapes just part of the immunopeptidome
Human Immunology, 2019ERAP1 is an aminopeptidase involved in trimming long peptides to the lengths required for presentation by MHC class I. ERAP1 substrate preference is for peptides with hydrophobic or aliphatic N-terminal amino acids, with lower efficacy with charged and small hydrophilic amino acids and almost complete inefficiency with proline.
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