(Q28592979)

GOA release 2020-03-11

6

Michael Karin

1 reference

31 January 2017

Atsushi Ohazama

1

1 reference

31 January 2017

Yinling Hu

2

1 reference

31 January 2017

Ruth Schmidt-Ullrich

3

1 reference

31 January 2017

Yixue Cao

4

1 reference

31 January 2017

Claus Scheidereit

5

1 reference

31 January 2017

Paul T. Sharpe

IKKalpha provides an essential link between RANK signaling and cyclin D1 expression during mammary gland development

7

1 reference

31 January 2017

language of work or name

English

0 references

publication date

1 February 2004

1 reference

31 January 2017

1 reference

31 January 2017

6

1 reference

31 January 2017

219–227

1 reference

31 January 2017

2

1 reference

31 January 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Tooth and jaw: molecular mechanisms of patterning in the first branchial arch

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Positive and negative regulation of IkappaB kinase activity through IKKbeta subunit phosphorylation

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain.

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

The world according to hedgehog

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Gene defect in ectodermal dysplasia implicates a death domain adapter in development

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

The IkappaB-NF-kappaB signaling module: temporal control and selective gene activation

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

IKKalpha controls formation of the epidermis independently of NF-kappaB.

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

The I kappa B kinase (IKK) and NF-kappa B: key elements of proinflammatory signalling

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Different mechanisms control signal-induced degradation and basal turnover of the NF-kappaB inhibitor IkappaB alpha in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

IKK1-deficient mice exhibit abnormal development of skin and skeleton

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

IKK-1 and IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB activation

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Correlation of asymmetric Notch2 expression and mouse incisor rotation.

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Cusp patterning defect in Tabby mouse teeth and its partial rescue by FGF.

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Dynamic Lunatic fringe expression is correlated with boundaries formation in developing mouse teeth.

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Wnt/Shh interactions regulate ectodermal boundary formation during mammalian tooth development

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

NEMO/IKK gamma-deficient mice model incontinentia pigmenti.

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Limb and skin abnormalities in mice lacking IKKalpha

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Signalling networks regulating dental development

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Transformation of tooth type induced by inhibition of BMP signaling

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

Interactions between Bmp-4 and Msx-1 act to restrict gene expression to odontogenic mesenchyme

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

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)

1 reference

https://api.crossref.org/works/10.1016%2FS1534-5807%2804%2900024-3

7 January 2021