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- <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
- Dental manifestations in Vitamin D dependent rickets Type II with Alopecia: a short pictorial case report
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Over-expression of thymosin beta4 promotes abnormal tooth development and stimulation of hair growth
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- An animal study on the effectiveness of platelet-rich plasma as a direct pulp capping agent
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- AMINOPTERIN IN TREATMENT OF LEUKEMIA IN CHILDREN
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Edar Signaling in the Control of Hair Follicle Development
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*