(Q62806043)

2 July 2019

title

NEMO/IKK gamma: linking NF-kappa B to human disease. (English)

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2 July 2019

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2

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2 July 2019

author name string

G Courtois

series ordinal

1

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2 July 2019

A Israël

series ordinal

3

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2 July 2019

publication date

1 October 2001

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2 July 2019

Trends in Molecular Medicine

published in

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2 July 2019

volume

7

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2 July 2019

issue

10

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2 July 2019

page(s)

427-430

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2 July 2019

Phosphorylation meets ubiquitination: the control of NF-[kappa]B activity

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7 January 2021

The IKK complex: an integrator of all signals that activate NF-kappaB?

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7 January 2021

Complementation cloning of NEMO, a component of the IkappaB kinase complex essential for NF-kappaB activation

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7 January 2021

IKK-gamma is an essential regulatory subunit of the IkappaB kinase complex

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7 January 2021

IkappaB kinase (IKK)-associated protein 1, a common component of the heterogeneous IKK complex

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Incontinentia pigmenti (Bloch-Sulzberger syndrome).

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7 January 2021

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium

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7 January 2021

Female mice heterozygous for IKK gamma/NEMO deficiencies develop a dermatopathy similar to the human X-linked disorder incontinentia pigmenti

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7 January 2021

NEMO/IKK gamma-deficient mice model incontinentia pigmenti.

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7 January 2021

Genetic approaches in mice to understand Rel/NF-kappaB and IkappaB function: transgenics and knockouts

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7 January 2021

Absence of tumor necrosis factor rescues RelA-deficient mice from embryonic lethality

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7 January 2021

Severe liver degeneration in mice lacking the IkappaB kinase 2 gene

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7 January 2021

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)

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7 January 2021

Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma)

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7 January 2021

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

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7 January 2021

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

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7 January 2021

Ectodermal dysplasias: a clinical classification and a causal review

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7 January 2021

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

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7 January 2021

The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and bone

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7 January 2021

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

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7 January 2021

Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion

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7 January 2021

Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A.

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7 January 2021

Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein

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7 January 2021

Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia

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7 January 2021

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

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7 January 2021

Involvement of a novel Tnf receptor homologue in hair follicle induction

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7 January 2021

The ectodermal dysplasia receptor activates the nuclear factor-kappaB, JNK, and cell death pathways and binds to ectodysplasin A

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7 January 2021

Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors

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7 January 2021

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

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7 January 2021

Incontinentia pigmenti in a newborn male infant with DNA confirmation.

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2

7 January 2021

Incontinentia pigmenti in a surviving male is accompanied by hypohidrotic ectodermal dysplasia and recurrent infection

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2

7 January 2021

Requirement for NF-kappaB in osteoclast and B-cell development

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2

7 January 2021

Osteopetrosis in mice lacking NF-kappaB1 and NF-kappaB2.

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2

7 January 2021

Tumor necrosis factor receptor family member RANK mediates osteoclast differentiation and activation induced by osteoprotegerin ligand

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https://api.crossref.org/works/10.1016%2FS1471-4914%2801%2902154-2

7 January 2021

Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema

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7 January 2021

10.1016/S1471-4914(01)02154-2

Identifiers

DOI

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2 July 2019

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2 July 2019