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Research 30 of 59
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- An inductive signalling network regulates mammalian tooth morphogenesis with implications for tooth regeneration
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Pannexin 3 regulates skin development via Epiprofin
- Congenital atrichia and hypotrichosis
- Morpho-Regulation of Ectodermal Organs
- Dental derived stem cell conditioned media for hair growth stimulation
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Can UK undergraduate dental programmes provide training in non-surgical facial aesthetics?
- Application of Platelet-Rich Plasma as a Stem Cell Treatment - anAttempt to Clarify a Common Public Misconception
- The in vitro plasticity of hair follicle dermal and mesenchymal stem cells
- A Chemically Defined Culture for Tooth Reconstitution
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Sostdc1 defines the size and number of skin appendage placodes
- Molecular mechanism for transcriptional regulation of the parathyroid hormone gene by Epiprofin
- Epidermal patterning and induction of different hair types during mouse embryonic development
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- TONGUE, RED
- Periaortic venous necklace and renal right double arteries; Case report
- Mesenchymal Stem Cell-Derived Extracellular Vesicles for Therapeutic Use and in Bioengineering Applications
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome