(Q33289658)

English

Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type Ib

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type Ib (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

autoimmune lymphoproliferative syndrome

0 references

1 reference

based on heuristic

inferred from title

Vishnu V B Reddy

object named as

Vishnu Reddy

7

0 references

Jennifer M Puck

10

object named as

Jennifer M Puck

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

author name string

Lilia L Bi

1

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

George Pan

2

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

T Prescott Atkinson

3

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Lixin Zheng

4

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Janet K Dale

5

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Christopher Makris

6

1 reference

Europe PubMed Central

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25 July 2017

Jay M McDonald

8

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Richard M Siegel

9

1 reference

Europe PubMed Central

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25 July 2017

Michael J Lenardo

11

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Europe PubMed Central

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25 July 2017

Stephen E Straus

12

1 reference

Europe PubMed Central

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25 July 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

2 July 2007

1 reference

Europe PubMed Central

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25 July 2017

BMC Medical Genetics

1 reference

Europe PubMed Central

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25 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

41

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

NRAS mutation causes a human autoimmune lymphoproliferative syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

HLA B44 is associated with decreased severity of autoimmune lymphoproliferative syndrome in patients with CD95 defects (ALPS type Ia).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

The -844C/T polymorphism in the Fas ligand promoter associates with Taiwanese SLE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

FAS gene mutation in a case of autoimmune lymphoproliferative syndrome type IA with accumulation of gammadelta+ T cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Fas preassociation required for apoptosis signaling and dominant inhibition by pathogenic mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Antigen presenting cells expressing Fas ligand down-modulate chronic inflammatory disease in Fas ligand-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

The dual functions of fas ligand in the regulation of peripheral CD8+ and CD4+ T cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

An inherited disorder of lymphocyte apoptosis: the autoimmune lymphoproliferative syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Autoimmune lymphoproliferative syndrome with defective Fas: genotype influences penetrance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

The molecular basis for apoptotic defects in patients with CD95 (Fas/Apo-1) mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Maximal proliferation of cytotoxic T lymphocytes requires reverse signaling through Fas ligand

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Separate domains of the human fas ligand dictate self-association and receptor binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Characterization of Fas (Apo-1, CD95)-Fas ligand interaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Fas ligand mutation in a patient with systemic lupus erythematosus and lymphoproliferative disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Human Fas ligand: gene structure, chromosomal location and species specificity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Mutations in the Fas antigen gene in lpr mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Generalized lymphoproliferative disease in mice, caused by a point mutation in the Fas ligand

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

Fas transduces activation signals in normal human T lymphocytes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

28 July 2018

Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-41

21 January 2018

Association of a common variant of the CASP8 gene with reduced risk of breast cancer

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-41

21 January 2018

Association of apoptosis-related microsatellite polymorphisms on chromosome 1q in Taiwanese systemic lupus erythematosus patients.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-41

21 January 2018

Comparative molecular modelling of the Fas-ligand and other members of the TNF family

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-41

21 January 2018

The V410I (G1228A) variant of the caspase-10 gene is a common polymorphism of the Danish population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1931585

31 October 2018

Complete mutation scan of the human Fas ligand gene: Linkage studies in Type I diabetes mellitus families

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-41

21 January 2018

Analysis of fas ligand gene mutation in patients with systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17605793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fas and Fas ligand gene polymorphisms in primary Sjögren's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17605793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increases in circulating and lymphoid tissue interleukin-10 in autoimmune lymphoproliferative syndrome are associated with disease expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/17605793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunophenotypic profiles in families with autoimmune lymphoproliferative syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17605793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complete mutation scan of the human Fas ligand gene: linkage studies in Type I diabetes mellitus families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17605793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fas ligand gene polymorphisms are not associated with Hashimoto's thyroiditis and Graves' disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17605793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Murine models of systemic lupus erythematosus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17605793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characteristic T helper 2 T cell cytokine abnormalities in autoimmune lymphoproliferative syndrome, a syndrome marked by defective apoptosis and humoral autoimmunity

1 reference

https://pubmed.ncbi.nlm.nih.gov/17605793

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2350-8-41

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

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0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

ResearchGate publication ID

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