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TNFRSF17 — TNFSF13B
Pathways - manually collected, often from reviews:
Protein-Protein interactions - manually collected from original source literature:
Studies that report less than 10 interactions are marked with *
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IRef Biogrid Interaction:
TNFSF13B
—
TNFRSF17
(physical association, affinity chromatography technology)
Shu et al., Proc Natl Acad Sci U S A 2000*
-
IRef Biogrid Interaction:
TNFSF13B
—
TNFRSF17
(association, x-ray crystallography)
Liu et al., Nature 2003*
-
IRef Hprd Interaction:
TNFSF13B
—
TNFRSF17
(in vitro)
Gross et al., Nature 2000*, Shu et al., Proc Natl Acad Sci U S A 2000*, Yu et al., Nat Immunol 2000*
-
IRef Hprd Interaction:
TNFSF13B
—
TNFRSF17
(in vivo)
Gross et al., Nature 2000*, Shu et al., Proc Natl Acad Sci U S A 2000*, Yu et al., Nat Immunol 2000*
-
IRef Intact Interaction:
TNFSF13B
—
TNFRSF17
(physical association, saturation binding)
Gross et al., Nature 2000*
-
IRef Ophid Interaction:
TNFSF13B
—
TNFRSF17
(aggregation, confirmational text mining)
Yu et al., Nat Immunol 2000*
-
IRef Ophid Interaction:
TNFSF13B
—
TNFRSF17
(aggregation, interologs mapping)
Brown et al., Bioinformatics 2005
Text-mined interactions from Literome
Chiu et al., Blood 2007
(Hodgkin Disease) :
Hodgkin lymphoma cells express TACI and
BCMA receptors and generate survival and proliferation signals in
response to
BAFF and APRIL
Koarada et al., Rheumatology (Oxford) 2010
(Lupus Erythematosus, Systemic) :
RP105 ( - ) B cells from SLE patients showed more preferential expression of
BCMA compared with BAFF-R than normal subjects, and were possibly
regulated by
BAFF/APRIL
Kim et al., J Leukoc Biol 2011
:
Subsequent analysis of BAFF signaling suggested that
BAFF induces AID through
BCMA , a BAFF-receptor, and p38MAPK and CREB act as intermediates in AID expression