(Q35145617)

6 August 2017

1 reference

title

Ectodysplasin signaling in development (English)

1 reference

6 August 2017

2

Irma Thesleff

1 reference

6 August 2017

Marja L Mikkola

1

1 reference

6 August 2017

1 June 2003

1 reference

Cytokine and Growth Factor Reviews

6 August 2017

1 reference

6 August 2017

14

1 reference

6 August 2017

211-224

1 reference

6 August 2017

3-4

1 reference

Death receptor signaling giving life to ectodermal organs

6 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

7 January 2021

Ectodermal dysplasias: a clinical classification and a causal review

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Clinical aspects of X-linked hypohidrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

A totally sex-linked gene in the house mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The Mouse Genome Database (MGD): the model organism database for the laboratory mouse

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

7 January 2021

Involvement of a novel Tnf receptor homologue in hair follicle induction.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Identification of a novel death domain-containing adaptor molecule for ectodysplasin-A receptor that is mutated in crinkled mice

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

7 January 2021

Pleiotropic effect of Tabby gene on epidermal growth factor-containing cells of mouse submandibular gland

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

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

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The gene for X-linked anhidrotic ectodermal dysplasia encodes a TNF-like domain

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

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.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Modular organization of proteins containing C1q-like globular domain

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The crystal structure of a complement-1q family protein suggests an evolutionary link to tumor necrosis factor

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

A novel missense mutation (402C-->T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T > G (Leu55Arg)

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

A novel point mutation of the EDA gene in a Japanese family with anhidrotic ectodermal dysplasia.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

A novel arginine-->Serine mutation in EDA1 in a Japanese family with X-linked anhidrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Mutations in the EDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

7 January 2021

Characterization of TNFRSF19, a novel member of the tumor necrosis factor receptor superfamily

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

TAJ, a novel member of the tumor necrosis factor receptor family, activates the c-Jun N-terminal kinase pathway and mediates caspase-independent cell death

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

TROY, a newly identified member of the tumor necrosis factor receptor superfamily, exhibits a homology with Edar and is expressed in embryonic skin and hair follicles

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Role of TRAF3 and -6 in the activation of the NF-kappa B and JNK pathways by X-linked ectodermal dysplasia receptor

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Signaling and subcellular localization of the TNF receptor Edar

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

EDA targets revealed by skin gene expression profiles of wild-type, Tabby and Tabby EDA-A1 transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

TRAF6-deficient mice display hypohidrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Missing pieces in the NF-kappaB puzzle

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

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%2FS1359-6101%2803%2900020-0

7 January 2021

A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The NF-kappaB signalling pathway in human diseases: from incontinentia pigmenti to ectodermal dysplasias and immune-deficiency syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

TRANCE, a TNF family member, activates Akt/PKB through a signaling complex involving TRAF6 and c-Src

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

TRAF6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Severe osteopetrosis, defective interleukin-1 signalling and lymph node organogenesis in TRAF6-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Noggin is a mesenchymally derived stimulator of hair-follicle induction

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Patterns of proliferation and apoptosis during murine hair follicle morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The role of growth factors in tooth development

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Molecular mechanisms regulating hair follicle development

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Controls of hair follicle cycling

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Reiterative signaling and patterning during mammalian tooth morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Expression of the anhidrotic ectodermal dysplasia gene is reduced in skin cancer coinciding with reduced E-cadherin

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The angora locus (go) in the mouse: hair morphology, duration of growth cycle and site of action

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The EDA gene is a target of, but does not regulate Wnt signaling

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

De Novo hair follicle morphogenesis and hair tumors in mice expressing a truncated beta-catenin in skin

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Dorsal dermis development depends on a signal from the dorsal neural tube, which can be substituted by Wnt-1.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Functional analysis of activins during mammalian development.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Splitting hairs: dissecting roles of signaling systems in epidermal development

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

beta-Catenin controls hair follicle morphogenesis and stem cell differentiation in the skin

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Mucosal addressin cell adhesion molecule 1 plays an unexpected role in the development of mouse guard hair

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Induction of the gene encoding mucosal vascular addressin cell adhesion molecule 1 by tumor necrosis factor alpha is mediated by NF-kappa B proteins

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Stimulation of ectodermal organ development by Ectodysplasin-A1.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Signaling pathways in mammary gland development.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

WNT signals are required for the initiation of hair follicle development

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

Permanent correction of an inherited ectodermal dysplasia with recombinant EDA.

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

The medaka rs-3 locus required for scale development encodes ectodysplasin-A receptor

1 reference

https://api.crossref.org/works/10.1016%2FS1359-6101%2803%2900020-0

7 January 2021

10.1016/S1359-6101(03)00020-0

Identifiers

DOI

1 reference

6 August 2017

1 reference

PubMed ID

12787560