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NEMO/IKK gamma: linking NF-kappa B to human disease.
scientific article published in October 2001
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
title
NEMO/IKK gamma: linking NF-kappa B to human disease.
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
main subject
NF-κB
1 reference
based on heuristic
inferred from title
author
Asma Smahi
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
author name string
G Courtois
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
A Israël
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
publication date
1 October 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
published in
Trends in Molecular Medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
volume
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
issue
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
page(s)
427-430
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
cites work
Phosphorylation meets ubiquitination: the control of NF-[kappa]B activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The IKK complex: an integrator of all signals that activate NF-kappaB?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
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inferred from DOI database lookup
Complementation cloning of NEMO, a component of the IkappaB kinase complex essential for NF-kappaB activation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
IKK-gamma is an essential regulatory subunit of the IkappaB kinase complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
IkappaB kinase (IKK)-associated protein 1, a common component of the heterogeneous IKK complex
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Incontinentia pigmenti (Bloch-Sulzberger syndrome).
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
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inferred from DOI database lookup
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Female mice heterozygous for IKK gamma/NEMO deficiencies develop a dermatopathy similar to the human X-linked disorder incontinentia pigmenti
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
NEMO/IKK gamma-deficient mice model incontinentia pigmenti.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic approaches in mice to understand Rel/NF-kappaB and IkappaB function: transgenics and knockouts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Absence of tumor necrosis factor rescues RelA-deficient mice from embryonic lethality
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe liver degeneration in mice lacking the IkappaB kinase 2 gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ectodermal dysplasias: a clinical classification and a causal review
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Involvement of a novel Tnf receptor homologue in hair follicle induction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The ectodermal dysplasia receptor activates the nuclear factor-kappaB, JNK, and cell death pathways and binds to ectodysplasin A
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
TNF signaling via the ligand-receptor pair ectodysplasin and edar controls the function of epithelial signaling centers and is regulated by Wnt and activin during tooth organogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Incontinentia pigmenti in a newborn male infant with DNA confirmation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Requirement for NF-kappaB in osteoclast and B-cell development
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tumor necrosis factor receptor family member RANK mediates osteoclast differentiation and activation induced by osteoprotegerin ligand
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1471-4914(01)02154-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
PubMed publication ID
11597506
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11597506
retrieved
2 July 2019
reference URL
http://europepmc.org/abstract/MED/11597506
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