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Research 31–60 of 241
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- Ectodysplasin research—Where to next?
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Inherited Disorders of the Hair
- The Roles of EDA2R in Ageing and Disease
- Current Genetics in Hair Diseases
- Molecular Basis of Hereditary Hair Diseases
- Clouston syndrome associated with eccrine syringofibroadenoma
- Research Snippets
- sQuiz your knowledge: Polycyclic annular plaques on the trunk following dutasteride treatment
- Skin Development and Disease: A Molecular Perspective
- Hair shaft structures in EDAR induced ectodermal dysplasia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- KID Syndrome: Report of a Case and Support for Its Reclassification as an Ectodermal Dysplasia
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Trichoscopy in Hair Shaft Disorders
- Hair and Nail Relationship
- Dermatopathology and molecular genetics
- <i>WNT10A</i> , dermatology and dentistry