(Q38414568)

2 September 2017

1 reference

title

Update on genetics and pathogenesis of autoinflammatory diseases: the last 2 years (English)

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2 September 2017

1

Ivona Aksentijevich

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2 September 2017

publication date

10 April 2015

1 reference

Seminars in Immunopathology

2 September 2017

published in

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2 September 2017

volume

37

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2 September 2017

issue

4

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2 September 2017

page(s)

395-401

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https://scigraph.springernature.com/pub.10.1007/s00281-015-0478-4

2 September 2017

exact match

0 references

cites work

Genetics, genomics, and their relevance to pathology and therapy

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Early-onset stroke and vasculopathy associated with mutations in ADA2

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Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy.

21 January 2018

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Mutant ADA2 in vasculopathies

21 January 2018

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Structural basis for the growth factor activity of human adenosine deaminase ADA2

21 January 2018

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The extracellular adenosine deaminase growth factor, ADGF/CECR1, plays a role in Xenopus embryogenesis via the adenosine/P1 receptor

21 January 2018

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A role for adenosine deaminase in Drosophila larval development

21 January 2018

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Human adenosine deaminase 2 induces differentiation of monocytes into macrophages and stimulates proliferation of T helper cells and macrophages.

21 January 2018

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Mutations in CECR1 associated with a neutrophil signature in peripheral blood

21 January 2018

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Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency.

21 January 2018

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Activated STING in a vascular and pulmonary syndrome

21 January 2018

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Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations

21 January 2018

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STING is a direct innate immune sensor of cyclic di-GMP

21 January 2018

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STING-dependent cytosolic DNA sensing pathways

21 January 2018

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STING and the innate immune response to nucleic acids in the cytosol

21 January 2018

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STING is an endoplasmic reticulum adaptor that facilitates innate immune signalling

21 January 2018

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NLRC3, a member of the NLR family of proteins, is a negative regulator of innate immune signaling induced by the DNA sensor STING

21 January 2018

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Biology of the RANKL-RANK-OPG System in Immunity, Bone, and Beyond

21 January 2018

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Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling

21 January 2018

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Central control of fever and female body temperature by RANKL/RANK

21 January 2018

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Brief Report: Involvement of TNFRSF11A molecular defects in autoinflammatory disorders

21 January 2018

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A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function

21 January 2018

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RANK is essential for osteoclast and lymph node development

21 January 2018

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An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome

21 January 2018

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Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

21 January 2018

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An inherited mutation in NLRC4 causes autoinflammation in human and mice

21 January 2018

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Cytosolic flagellin requires Ipaf for activation of caspase-1 and interleukin 1beta in salmonella-infected macrophages

21 January 2018

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The NAIP/NLRC4 inflammasomes

21 January 2018

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Epithelium-intrinsic NAIP/NLRC4 inflammasome drives infected enterocyte expulsion to restrict Salmonella replication in the intestinal mucosa

21 January 2018

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The NLRC4 inflammasome receptors for bacterial flagellin and type III secretion apparatus.

21 January 2018

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A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD).

21 January 2018

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Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

21 January 2018

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A story with a good ending: tRNA 3'-end maturation by CCA-adding enzymes

21 January 2018

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How the study of children with rheumatic diseases identified interferon-alpha and interleukin-1 as novel therapeutic targets

21 January 2018

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Role of interleukin-1 (IL-1) in the pathogenesis of systemic onset juvenile idiopathic arthritis and clinical response to IL-1 blockade

21 January 2018

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Genomewide association study of leprosy

21 January 2018

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Genomewide association study of leprosy

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00281-015-0478-4

NOD2 and CCDC122-LACC1 genes are associated with leprosy susceptibility in Brazilians.

21 January 2018

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https://api.crossref.org/works/10.1007%2FS00281-015-0478-4

The 3' addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1.

21 January 2018

1 reference

12 December 2020

Novel adenosine deaminase 2 mutations in a child with a fatal vasculopathy

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12 December 2020

Osteoclast formation and differentiation: an overview

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12 December 2020

NLRC4 expression in intestinal epithelial cells mediates protection against an enteric pathogen.

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12 December 2020

The RANKL/RANK/OPG pathway

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12 December 2020

Association of a mutation in LACC1 with a monogenic form of systemic juvenile idiopathic arthritis

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12 December 2020

Systemic-onset juvenile idiopathic arthritis: the changing life of a rare disease

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12 December 2020

10.1007/S00281-015-0478-4

Identifiers

DOI

1 reference

Dimensions Publication ID

2 September 2017

1022126760

0 references

1 reference