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Research 181–210 of 206
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Clinical Snippets
- In That Issue: Proceedings From the Third Intercontinental Meeting of Hair Research Societies
- The Role of Pannexin 3 in Bone Biology
- Clinical Snippets
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- Adenosine Promotes Human Hair Growth and Inhibits Catagen Transition In Vitro: Role of the Outer Root Sheath Keratinocytes
- 916 Gynecologic and hormonal comorbidities of scarring alopecia: A retrospective review
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- Building a Better Scar: Re-engineering Extracellular Matrix Structure in Dermal Scars
- Mutant Cx43 in Skin Differentiation and Disease
- Zinc Content of Hair from the Head of Carcinoma Patients
- Analysis of Cytokines and ATP in Plucked Hair Follicles
- Editors’ Picks
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Integrating zinc/silicon dual ions with 3D-printed GelMA hydrogel promotes in situ hair follicle regeneration
- Cell Movement in the Hair Follicle Dermis – More Than a Two-Way Street?
- Congenital atrichia with papular lesions
- Congenital atrichia associated with situs inversus and mesocardia
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Beyond the usual: a case of acrodermatitis enteropathica clinically resembling erythrokeratoderma variabilis
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Electroosmotic pore transport in human skin.
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Effects of Testosterone on the Expression of Connexin 26 and Connexin 43 in the Uterus of Rats During Early Pregnancy