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A novel gene coding for a Fas apoptosis inhibitory molecule (FAIM) isolated from inducibly Fas-resistant B lymphocytes
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
title
A novel gene coding for a Fas apoptosis inhibitory molecule (FAIM) isolated from inducibly Fas-resistant B lymphocytes
(English)
1 reference
stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
main subject
apoptotic process
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lymphocyte
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Fas apoptotic inhibitory molecule
1 reference
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GOA release 2020-03-11
author name string
T. J. Schneider
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
G. M. Fischer
series ordinal
2
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stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
T. J. Donohoe
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3
1 reference
stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
T. P. Colarusso
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4
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stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
T. L. Rothstein
series ordinal
5
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PubMed
PubMed ID
10075978
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31 January 2017
language of work or name
English
0 references
publication date
15 March 1999
1 reference
stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
published in
Journal of Experimental Medicine
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stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
volume
189
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stated in
PubMed
PubMed ID
10075978
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31 January 2017
page(s)
949–956
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PubMed
PubMed ID
10075978
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31 January 2017
issue
6
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PubMed
PubMed ID
10075978
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31 January 2017
cites work
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ARC, an inhibitor of apoptosis expressed in skeletal muscle and heart that interacts selectively with caspases
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A single BIR domain of XIAP sufficient for inhibiting caspases
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Cytochrome c and dATP-dependent formation of Apaf-1/caspase-9 complex initiates an apoptotic protease cascade
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17 March 2017
The c-IAP-1 and c-IAP-2 proteins are direct inhibitors of specific caspases
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Apaf-1, a human protein homologous to C. elegans CED-4, participates in cytochrome c-dependent activation of caspase-3
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Prevention of apoptosis by Bcl-2: release of cytochrome c from mitochondria blocked
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Molecular ordering of the Fas-apoptotic pathway: the Fas/APO-1 protease Mch5 is a CrmA-inhibitable protease that activates multiple Ced-3/ICE-like cysteine proteases
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Protection against Fas/APO-1- and tumor necrosis factor-mediated cell death by a novel protein, sentrin
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Induction of apoptotic program in cell-free extracts: requirement for dATP and cytochrome c
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FLICE, a novel FADD-homologous ICE/CED-3-like protease, is recruited to the CD95 (Fas/APO-1) death--inducing signaling complex
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Involvement of MACH, a novel MORT1/FADD-interacting protease, in Fas/APO-1- and TNF receptor-induced cell death
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17 March 2017
The C. elegans cell death gene ced-3 encodes a protein similar to mammalian interleukin-1 beta-converting enzyme
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17 March 2017
Yama/CPP32 beta, a mammalian homolog of CED-3, is a CrmA-inhibitable protease that cleaves the death substrate poly(ADP-ribose) polymerase
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17 March 2017
FADD, a novel death domain-containing protein, interacts with the death domain of Fas and initiates apoptosis
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A simple method for displaying the hydropathic character of a protein
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17 March 2017
Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction
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The release of cytochrome c from mitochondria: a primary site for Bcl-2 regulation of apoptosis
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PubMed Central
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Two CD95 (APO-1/Fas) signaling pathways
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7 April 2017
The Fas death factor
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Tolerant B lymphocytes acquire resistance to Fas-mediated apoptosis after treatment with interleukin 4 but not after treatment with specific antigen unless a surface immunoglobulin threshold is exceeded
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Concurrent engagement of CD40 and the antigen receptor protects naive and memory human B cells from APO-1/Fas-mediated apoptosis
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Soluble CD40 ligand can replace the normal T cell-derived CD40 ligand signal to B cells in T cell-dependent activation
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Induction of the transcription factors NF-kappa B, AP-1 and NF-AT during B cell stimulation through the CD40 receptor
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Electroporation for the efficient transfection of mammalian cells with DNA.
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Expansion or elimination of B cells in vivo: dual roles for CD40- and Fas (CD95)-ligands modulated by the B cell antigen receptor.
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Bcl-x and Bcl-2 inhibit TNF and Fas-induced apoptosis and activation of phospholipase A2 in breast carcinoma cells.
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3 June 2018
Protection against Fas-dependent Th1-mediated apoptosis by antigen receptor engagement in B cells.
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3 June 2018
Protein kinase C activation blocks anti-IgM-mediated signaling BAL17 B lymphoma cells
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3 June 2018
Egr-1 expression in surface Ig-mediated B cell activation. Kinetics and association with protein kinase C activation
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3 June 2018
Identification of an AUUUA-specific messenger RNA binding protein
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Cross-linking of surface Ig receptors on murine B lymphocytes stimulates the expression of nuclear tetradecanoyl phorbol acetate-response element-binding proteins
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PubMed
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https://pubmed.ncbi.nlm.nih.gov/10075978
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Rapid, small-scale RNA isolation from tissue culture cells
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PubMed
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https://pubmed.ncbi.nlm.nih.gov/10075978
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Intracellular signaling for inducible antigen receptor-mediated Fas resistance in B cells
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10075978
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
IL-4 induces Fas resistance in B cells
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10075978
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Dissociation of apoptosis and activation of IL-1beta-converting enzyme/Ced-3 proteases by ALG-2 and the truncated Alzheimer's gene ALG-3
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10075978
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Bcl-x protects primary B cells against Fas-mediated apoptosis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10075978
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Antigen-receptor engagement in B cells induces nuclear expression of STAT5 and STAT6 proteins that bind and transactivate an IFN-gamma activation site
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10075978
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1084/JEM.189.6.949
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PMCID
2193037
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PubMed ID
10075978
1 reference
stated in
PubMed
PubMed ID
10075978
retrieved
31 January 2017
ResearchGate publication ID
13214906
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