Promoter choice and translational repression determine cell type-specific cell surface density of the inhibitory receptor CD85j expressed on different hematopoietic lineages (Q33806012)

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English	Promoter choice and translational repression determine cell type-specific cell surface density of the inhibitory receptor CD85j expressed on different hematopoietic lineages	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 July 2017

Promoter choice and translational repression determine cell type-specific cell surface density of the inhibitory receptor CD85j expressed on different hematopoietic lineages (English)

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Europe PubMed Central

PubMed publication ID

29 July 2017

Cornelia Weyand

2

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Cornelia M Weyand

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Europe PubMed Central

PubMed publication ID

29 July 2017

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David L Lamar

1

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Europe PubMed Central

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29 July 2017

Jörg J Goronzy

3

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Europe PubMed Central

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29 July 2017

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publication date

1 March 2010

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Europe PubMed Central

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29 July 2017

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Europe PubMed Central

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29 July 2017

115

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Europe PubMed Central

PubMed publication ID

29 July 2017

16

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Europe PubMed Central

PubMed publication ID

29 July 2017

3278-3286

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Europe PubMed Central

PubMed publication ID

29 July 2017

Novel human transitional B cell populations revealed by B cell depletion therapy

1 reference

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Tyrosine kinases and their substrates in B lymphocytes

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Homeostatic control of B lymphocyte subsets

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The functional consequences of alternative promoter use in mammalian genomes

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Inhibitory receptors CD85j, LAIR-1, and CD152 down-regulate immunoglobulin and cytokine production by human B lymphocytes.

1 reference

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CD85j (leukocyte Ig-like receptor-1/Ig-like transcript 2) inhibits human osteoclast-associated receptor-mediated activation of human dendritic cells

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Human inhibitory receptors Ig-like transcript 2 (ILT2) and ILT4 compete with CD8 for MHC class I binding and bind preferentially to HLA-G

1 reference

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Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

https://pubmed.ncbi.nlm.nih.gov/20194892

12 December 2020

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10.1182/BLOOD-2009-09-243493

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Europe PubMed Central

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29 July 2017

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29 July 2017

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29 July 2017

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