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- <i>WNT10A</i> , dermatology and dentistry
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Long-term complications of Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN): the spectrum of chronic problems in patients who survive an episode of SJS/TEN necessitates multidisciplinary follow-up
- Congenital atrichia and hypotrichosis
- Severe cutaneous adverse reactions to drugs
- Dermatologic manifestations of endocrine disorders
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Converging physiological roles of the anthrax toxin receptors
- The role of WNT10B in physiology and disease: A 10-year update
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- TONGUE, RED
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- WNT Signaling in Disease
- E-Poster
- Skin Development and Disease: A Molecular Perspective
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate