(Q24309135)

positive regulation of type I interferon-mediated signaling pathway

GOA release 2020-03-11

1 reference

FADD-related immunodeficiency

GOA release 2020-03-11

1 reference

inferred from title

author

Jean-Laurent Casanova

17

0 references

Anne Puel

7

Anne Puel

0 references

Frédéric Rieux-Laucat

9

Frédéric Rieux-Laucat

0 references

Neil V Morgan

Neil V Morgan

4

0 references

Laurent Abel

Laurent Abel

12

0 references

Eamonn R Maher

Eamonn R Maher

14

0 references

Minji Byun

Minji Byun

2

0 references

Avinash Abhyankar

5

Avinash Abhyankar

0 references

author name string

Alexandre Bolze

1

0 references

David McDonald

3

0 references

Lakshmanane Premkumar

6

0 references

Chris M Bacon

8

0 references

Ki Pang

10

0 references

Alison Britland

11

0 references

Andrew Cant

13

0 references

Stefan J Riedl

15

0 references

Sophie Hambleton

American Journal of Human Genetics

16

0 references

language of work or name

English

0 references

publication date

10 December 2010

0 references

published in

0 references

volume

87

0 references

issue

6

0 references

page(s)

873-81

0 references

cites work

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19 March 2017

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The Fas-FADD death domain complex structure unravels signalling by receptor clustering

19 March 2017

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Inherited human Caspase 10 mutations underlie defective lymphocyte and dendritic cell apoptosis in autoimmune lymphoproliferative syndrome type II

19 March 2017

1 reference

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FADD, a novel death domain-containing protein, interacts with the death domain of Fas and initiates apoptosis

19 March 2017

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

19 March 2017

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The Sequence Alignment/Map format and SAMtools

19 March 2017

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FADD: a regulator of life and death

19 March 2017

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FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

19 March 2017

1 reference

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Fas-associated death domain-containing protein-mediated antiviral innate immune signaling involves the regulation of Irf7

19 March 2017

1 reference

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Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency

19 March 2017

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Detection, education and management of the asplenic or hyposplenic patient

19 March 2017

1 reference

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FADD: essential for embryo development and signaling from some, but not all, inducers of apoptosis

19 March 2017

1 reference

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Apoptosis: controlled demolition at the cellular level

19 March 2017

1 reference

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Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma

7 April 2017

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Isolated congenital asplenia: a French nationwide retrospective survey of 20 cases

27 September 2017

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Fas-associated death domain (FADD) is a negative regulator of T-cell receptor-mediated necroptosis

27 September 2017

1 reference

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Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.

27 September 2017

1 reference

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T cell intrinsic roles of autophagy in promoting adaptive immunity

27 September 2017

1 reference

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A partial form of recessive STAT1 deficiency in humans

27 September 2017

1 reference

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Death receptor signal transducers: nodes of coordination in immune signaling networks

27 September 2017

1 reference

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Genetic defects of apoptosis and primary immunodeficiency

27 September 2017

1 reference

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Primary immunodeficiencies: a field in its infancy

27 September 2017

1 reference

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A homozygous Fas ligand gene mutation in a patient causes a new type of autoimmune lymphoproliferative syndrome.

27 September 2017

1 reference

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Human complete Stat-1 deficiency is associated with defective type I and II IFN responses in vitro but immunity to some low virulence viruses in vivo

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2997374

A FADD-dependent innate immune mechanism in mammalian cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2997374

Primary immunodeficiencies associated with pneumococcal disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2997374

The CD95(APO-1/Fas) DISC and beyond

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2997374

Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2997374

Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2997374

Familial asplenia, other malformations, and sudden death

28 July 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21109225

12 December 2020

inferred from PubMed ID database lookup

Functional hyposplenism

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21109225

12 December 2020

inferred from PubMed ID database lookup

Immunophenotypic profiles in families with autoimmune lymphoproliferative syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21109225

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1016/J.AJHG.2010.10.028

1 reference

release_mcjtzgelorbkbk7za4tfmqvk2q

3000586

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/mcjtzgelorbkbk7za4tfmqvk2q

24 November 2022

mapped directly with Wikidata item

3000586

1 reference

1 reference

1 reference