Receptors, Antigen, B-Cell
"Receptors, Antigen, B-Cell" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
IMMUNOGLOBULINS on the surface of B-LYMPHOCYTES. Their MESSENGER RNA contains an EXON with a membrane spanning sequence, producing immunoglobulins in the form of type I transmembrane proteins as opposed to secreted immunoglobulins (ANTIBODIES) which do not contain the membrane spanning segment.
| Descriptor ID |
D011947
|
| MeSH Number(s) |
D12.776.124.790.651.950 D12.776.377.715.548.950 D12.776.543.750.705.816.821
|
| Concept/Terms |
Receptors, Antigen, B-Cell- Receptors, Antigen, B-Cell
- Membrane Bound Immunoglobulin
- Bound Immunoglobulin, Membrane
- Immunoglobulin, Membrane Bound
- Membrane-Bound Immunoglobulins
- Membrane Bound Immunoglobulins
- B-Cell Antigen Receptors
- B Cell Antigen Receptors
- Immunoglobulins, Surface
- Receptors, Antigen, B Cell
- Antigen Receptors, B-Cell
- Antigen Receptors, B Cell
- Receptors, B-Cell Antigen
- Immunoglobulins, Membrane-Bound
- Immunoglobulins, Membrane Bound
- Surface Immunoglobulins
|
Below are MeSH descriptors whose meaning is more general than "Receptors, Antigen, B-Cell".
- Chemicals and Drugs [D]
- Amino Acids, Peptides, and Proteins [D12]
- Proteins [D12.776]
- Blood Proteins [D12.776.124]
- Serum Globulins [D12.776.124.790]
- Immunoglobulins [D12.776.124.790.651]
- Receptors, Antigen, B-Cell [D12.776.124.790.651.950]
- Globulins [D12.776.377]
- Serum Globulins [D12.776.377.715]
- Immunoglobulins [D12.776.377.715.548]
- Receptors, Antigen, B-Cell [D12.776.377.715.548.950]
- Membrane Proteins [D12.776.543]
- Receptors, Cell Surface [D12.776.543.750]
- Receptors, Immunologic [D12.776.543.750.705]
- Receptors, Antigen [D12.776.543.750.705.816]
- Receptors, Antigen, B-Cell [D12.776.543.750.705.816.821]
Below are MeSH descriptors whose meaning is more specific than "Receptors, Antigen, B-Cell".
This graph shows the total number of publications written about "Receptors, Antigen, B-Cell" by people in this website by year, and whether "Receptors, Antigen, B-Cell" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 1 | 2 |
| 1997 | 1 | 1 | 2 |
| 1998 | 1 | 0 | 1 |
| 1999 | 0 | 2 | 2 |
| 2002 | 1 | 2 | 3 |
| 2005 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
| 2008 | 1 | 0 | 1 |
| 2009 | 3 | 0 | 3 |
| 2012 | 0 | 1 | 1 |
| 2013 | 1 | 1 | 2 |
| 2018 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Receptors, Antigen, B-Cell" by people in Profiles.
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Accumulation of Antigen-Driven Lymphoproliferations in Complement Receptor 2/CD21-/low B Cells From Patients With Sjögren's Syndrome. Arthritis Rheumatol. 2018 02; 70(2):298-307.
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Critical signal transduction pathways in CLL. Adv Exp Med Biol. 2013; 792:215-39.
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Integrin CD11b negatively regulates BCR signalling to maintain autoreactive B cell tolerance. Nat Commun. 2013; 4:2813.
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Global analysis of B cell selection using an immunoglobulin light chain-mediated model of autoreactivity. J Exp Med. 2013 Jan 14; 210(1):125-42.
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Vav and Rac activation in B cell antigen receptor endocytosis involves Vav recruitment to the adapter protein LAB. J Biol Chem. 2009 Dec 25; 284(52):36202-36212.
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B cell antigen receptor endocytosis and antigen presentation to T cells require Vav and dynamin. J Biol Chem. 2009 Sep 04; 284(36):24088-97.
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Signalling of the BCR is regulated by a lipid rafts-localised transcription factor, Bright. EMBO J. 2009 Mar 18; 28(6):711-24.
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Functional anergy in a subpopulation of naive B cells from healthy humans that express autoreactive immunoglobulin receptors. J Exp Med. 2009 Jan 16; 206(1):139-51.
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Cutting edge: Transitional T3 B cells do not give rise to mature B cells, have undergone selection, and are reduced in murine lupus. J Immunol. 2007 Jun 15; 178(12):7511-5.
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BCR targeting of biotin-{alpha}-galactosylceramide leads to enhanced presentation on CD1d and requires transport of BCR to CD1d-containing endocytic compartments. Int Immunol. 2005 Jul; 17(7):899-908.