(Q38375236)

2 September 2017

3 references

11 December 2019

19 December 2019

22 December 2019

Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling (English)

1 reference

primary immunodeficiency disease

2 September 2017

0 references

1 reference

11 December 2019

3 references

11 December 2019

19 December 2019

22 December 2019

1 reference

19 December 2019

1 reference

22 December 2019

Mariarosaria Incoronato

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

author name string

M Paciolla

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

A Pescatore

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

M I Conte

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

E Esposito

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

M B Lioi

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

F Fusco

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

M V Ursini

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

publication date

12 March 2015

1 reference

2 September 2017

1 June 2015

3 references

11 December 2019

19 December 2019

22 December 2019

4 references

11 December 2019

19 December 2019

22 December 2019

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

page(s)

239-246

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/gene.2015.3

5 June 2020

exact match

0 references

cites work

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1 reference

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Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency

6 September 2017

1 reference

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Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation

6 September 2017

1 reference

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Experimental and natural infections in MyD88- and IRAK-4-deficient mice and humans

6 September 2017

1 reference

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Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency

6 September 2017

1 reference

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Clinical Utility Gene Card for: incontinentia pigmenti

6 September 2017

1 reference

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Diagnosis and treatment in anhidrotic ectodermal dysplasia with immunodeficiency

6 September 2017

1 reference

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The noncanonical NF-κB pathway

6 September 2017

1 reference

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It takes two to tango: IκBs, the multifunctional partners of NF-κB.

6 September 2017

1 reference

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Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

6 September 2017

1 reference

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Infectious diseases in patients with IRAK-4, MyD88, NEMO, or IκBα deficiency

6 September 2017

1 reference

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New mechanism of X-linked anhidrotic ectodermal dysplasia with immunodeficiency: impairment of ubiquitin binding despite normal folding of NEMO protein

6 September 2017

1 reference

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6 September 2017

NF-κB in immunobiology.

1 reference

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Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis

6 September 2017

1 reference

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Posttranslational modifications of NF-kappaB: another layer of regulation for NF-kappaB signaling pathway

6 September 2017

1 reference

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Regulation of NF-kappaB activity through lysine monomethylation of p65.

6 September 2017

1 reference

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Key role of Ubc5 and lysine-63 polyubiquitination in viral activation of IRF3

6 September 2017

1 reference

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NEMO specifically recognizes K63-linked poly-ubiquitin chains through a new bipartite ubiquitin-binding domain

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Specific recognition of linear ubiquitin chains by NEMO is important for NF-kappaB activation

6 September 2017

1 reference

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Regulation and function of NF-kappaB transcription factors in the immune system

6 September 2017

1 reference

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Nonproteolytic functions of ubiquitin in cell signaling

6 September 2017

1 reference

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Structural Basis for Recognition of Diubiquitins by NEMO

6 September 2017

1 reference

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Involvement of linear polyubiquitylation of NEMO in NF-kappaB activation

6 September 2017

1 reference

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Hypomorphic nuclear factor-kappaB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity

6 September 2017

1 reference

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Pyogenic bacterial infections in humans with MyD88 deficiency

6 September 2017

1 reference

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A novel mutation in NFKBIA/IKBA results in a degradation-resistant N-truncated protein and is associated with ectodermal dysplasia with immunodeficiency

6 September 2017

1 reference

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Solution structure of NEMO zinc finger and impact of an anhidrotic ectodermal dysplasia with immunodeficiency-related point mutation

6 September 2017

1 reference

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Novel primary immunodeficiencies revealed by the investigation of paediatric infectious diseases

6 September 2017

1 reference

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6 September 2017

1 reference

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Selective predisposition to bacterial infections in IRAK-4-deficient children: IRAK-4-dependent TLRs are otherwise redundant in protective immunity

6 September 2017

1 reference

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TLR9 activation induces normal neutrophil responses in a child with IRAK-4 deficiency: involvement of the direct PI3K pathway

6 September 2017

1 reference

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Promiscuous mutations activate the noncanonical NF-kappaB pathway in multiple myeloma.

6 September 2017

1 reference

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Frequent engagement of the classical and alternative NF-kappaB pathways by diverse genetic abnormalities in multiple myeloma

6 September 2017

1 reference

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Essential role of IRAK-4 protein and its kinase activity in Toll-like receptor-mediated immune responses but not in TCR signaling

6 September 2017

1 reference

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Mutations in the NF-kappaB signaling pathway: implications for human disease

6 September 2017

1 reference

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IRAK-4--a shared NF-kappaB activator in innate and acquired immunity

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Impaired dendritic-cell function in ectodermal dysplasia with immune deficiency is linked to defective NEMO ubiquitination

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Molecular defects in T- and B-cell primary immunodeficiency diseases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Heritable defects of the human TLR signalling pathways

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Inherited disorders of NF-kappaB-mediated immunity in man.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Primary immunodeficiencies associated with pneumococcal disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Distinct mutations in IRAK-4 confer hyporesponsiveness to lipopolysaccharide and interleukin-1 in a patient with recurrent bacterial infections

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Pyogenic bacterial infections in humans with IRAK-4 deficiency

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

IRAK-4: a novel member of the IRAK family with the properties of an IRAK-kinase

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

The zinc finger of NEMO is a functional ubiquitin-binding domain

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

A point mutation in NEMO associated with anhidrotic ectodermal dysplasia with immunodeficiency pathology results in destabilization of the oligomer and reduces lipopolysaccharide- and tumor necrosis factor-mediated NF-kappa B activation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Deficiency of innate and acquired immunity caused by an IKBKB mutation.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Novel NFKB2 mutation in early-onset CVID.

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Celebrating 25 years of NF-κB research

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

X-linked ectodermal dysplasia with immunodeficiency caused by NEMO mutation: early recognition and diagnosis

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Heterozygous N-terminal deletion of IkappaBalpha results in functional nuclear factor kappaB haploinsufficiency, ectodermal dysplasia, and immune deficiency.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Clinical diagnosis of incontinentia pigmenti in a cohort of male patients.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Endotoxin and IL-1 hyporesponsiveness in a patient with recurrent bacterial infections.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4457537

Successful Allogeneic Hemopoietic Stem Cell Transplantation in a Child Who Had Anhidrotic Ectodermal Dysplasia With Immunodeficiency

31 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGENE.2015.3

Autosomal recessive Interleukin-1 receptor-associated kinase 4 deficiency in fourth-degree relatives

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FGENE.2015.3

Two siblings with lethal pneumococcal meningitis in a family with a mutation in Interleukin-1 receptor-associated kinase 4

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25764117

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25764117

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Delayed separation of the umbilical cord in two siblings with Interleukin-1 receptor-associated kinase 4 deficiency: rapid screening by flow cytometer

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25764117

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/GENE.2015.3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

5 June 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json

5 June 2020

PubMed publication ID

25764117

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25764117%20AND%20SRC:MED&resulttype=core&format=json