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- Characterization of a mouse Scube3 reporter line
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Developmental Plasticity of Patterned and Regenerating Oral Organs
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- NFIC promotes the vitality and osteogenic differentiation of rat dental follicle cells
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Parry Romberg Syndrome: When the Diagnosis of a Rare Disease Is Made in the Primary Care Setting
- Roles for Msx and Dlx homeoproteins in vertebrate development
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Feather arrays are patterned by interacting signalling and cell density waves
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- <i>WNT10A</i> , dermatology and dentistry
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- A Holistic Approach to Antiaging as an Adjunct to Antiaging Procedures: A Review of the Literature
- Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
- 7 Aesthetic Facial Proportions
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Cutaneous manifestations of systemic infection in children
- Recent advances in oxasteroids chemistry
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A WWP2–PTEN–KLF5 signaling axis regulates odontoblast differentiation and dentinogenesis in mice
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation