| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S1471-4914(02)02342-0 |
| P698 | PubMed publication ID | 12067623 |
| P50 | author | Juha Kere | Q11867366 |
| P2093 | author name string | Outi Elomaa | |
| P2860 | cites work | 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 | Q22010370 |
| Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia | Q22010459 | ||
| Two-amino acid molecular switch in an epithelial morphogen that regulates binding to two distinct receptors | Q24290424 | ||
| Gene defect in ectodermal dysplasia implicates a death domain adapter in development | Q24292109 | ||
| X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein | Q24310290 | ||
| 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) | Q24538937 | ||
| Mutations within a furin consensus sequence block proteolytic release of ectodysplasin-A and cause X-linked hypohidrotic ectodermal dysplasia | Q24631099 | ||
| The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats | Q28117141 | ||
| Mutations in GJB6 cause hidrotic ectodermal dysplasia | Q28140272 | ||
| The ectodermal dysplasia receptor activates the nuclear factor-kappaB, JNK, and cell death pathways and binds to ectodysplasin A | Q28141467 | ||
| Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium | Q28145744 | ||
| beta-Catenin controls hair follicle morphogenesis and stem cell differentiation in the skin | Q28190343 | ||
| The TNF and TNF receptor superfamilies: integrating mammalian biology | Q28203717 | ||
| X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling | Q28204249 | ||
| Ectodysplasin is released by proteolytic shedding and binds to the EDAR protein | Q28213298 | ||
| Ectodysplasin, a protein required for epithelial morphogenesis, is a novel TNF homologue and promotes cell-matrix adhesion | Q28508061 | ||
| Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice | Q29618462 | ||
| 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 | Q32003547 | ||
| The IKK complex: an integrator of all signals that activate NF-kappaB? | Q33877083 | ||
| Signaling and subcellular localization of the TNF receptor Edar | Q34092422 | ||
| 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 | Q36717195 | ||
| Cloning of Tabby, the murine homolog of the human EDA gene: evidence for a membrane-associated protein with a short collagenous domain. | Q36880933 | ||
| Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A. | Q40816214 | ||
| Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice | Q43829636 | ||
| Involvement of a novel Tnf receptor homologue in hair follicle induction | Q47941369 | ||
| P433 | issue | 5 | |
| P304 | page(s) | 197-200 | |
| P577 | publication date | 2002-05-01 | |
| P1433 | published in | Trends in Molecular Medicine | Q15265842 |
| P1476 | title | Healing a natural knockout of epithelial organogenesis. | |
| P478 | volume | 8 |
| Q48199379 | Ectodysplasin, Edar and TNFRSF19 are expressed in complementary and overlapping patterns during mouse embryogenesis. |
| Q55276985 | Generation of Cashmere Goats Carrying an EDAR Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing. |
| Q52103983 | Stimulation of ectodermal organ development by Ectodysplasin-A1. |
| Q37205410 | Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families |
| Q30463364 | The role of tumor necrosis factor receptor superfamily members in mammalian brain development, function and homeostasis |
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