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Index HLA-B51

HLA-B51 (B51) is an HLA-B serotype. [1]

15 relations: Behçet's disease, European Bioinformatics Institute, HLA-B, HLA-B27, HLA-B5, HLA-B52, Human leukocyte antigen, Kawasaki disease, MHC class I polypeptide-related sequence A, Rubella, Rubella virus, Serotype, Sister chromatid exchange, SUMO4, Vasculitis.

Behçet's disease

Behçet's disease (BD) is a type of inflammatory disorder which affects multiple parts of the body.

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European Bioinformatics Institute

The European Bioinformatics Institute (EMBL-EBI) is a centre for research and services in bioinformatics, and is part of European Molecular Biology Laboratory (EMBL).

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HLA-B (major histocompatibility complex, class I, B) is a human gene that provides instructions for making a protein that plays a critical role in the immune system.

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Human leukocyte antigen (HLA) B27 (subtypes B*2701-2759) is a class I surface antigen encoded by the B locus in the major histocompatibility complex (MHC) on chromosome 6 and presents antigenic peptides (derived from self and non-self antigens) to T cells.

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HLA-B5 (B5) is an HLA-B serotype.

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HLA-B52 (B52) is an HLA-B serotype.

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Human leukocyte antigen

The human leukocyte antigen (HLA) system or complex is a gene complex encoding the major histocompatibility complex (MHC) proteins in humans.

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Kawasaki disease

Kawasaki disease, also known as mucocutaneous lymph node syndrome, is a disease in which blood vessels throughout the body become inflamed.

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MHC class I polypeptide-related sequence A

MHC class I polypeptide-related sequence A (MICA) is a cell surface glycoprotein encoded by the MICA gene located within MHC locus.

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Rubella, also known as German measles or three-day measles, is an infection caused by the rubella virus.

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Rubella virus

Rubella virus (RuV) is the pathogenic agent of the disease rubella, and is the cause of congenital rubella syndrome when infection occurs during the first weeks of pregnancy.

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A serotype or serovar is a distinct variation within a species of bacteria or virus or among immune cells of different individuals.

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Sister chromatid exchange

Sister chromatid exchange (SCE) is the exchange of genetic material between two identical sister chromatids.

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Small ubiquitin-related modifier 4 is a protein that in humans is encoded by the SUMO4 gene.

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Vasculitis is a group of disorders that destroy blood vessels by inflammation.

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[1] https://en.wikipedia.org/wiki/HLA-B51

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