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Research 91–120 of 1000+
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Polarized microscopy in genetic hair disorders: case series
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Westwood Carolina Conference on Clinical Dermatology
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Hair loss among a group of Egyptian children
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- Keratin disorders: from gene to therapy
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- Ankyloblepharon-ectodermal dysplasia-clefting syndrome: Surgical and medical management in an infant with bilateral corneal perforations
- Biology and Genetics of Hair
- Stem cells and aberrant signaling of molecular systems in skin aging
- Trichodystrophies: A hair-raising differential diagnosis
- Hair Loss in Children
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Defective trophoblast function in mice with a targeted mutation of Ets2
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Feasibility of repairing skin defects by VEGF<sub>165</sub> gene‐modified iPS‐HFSCs seeded on a 3D printed scaffold containing astragalus polysaccharide
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- Applications of Engineered Skin Tissue for Cosmetic Component and Toxicology Detection
- Small molecules facilitate single factor-mediated sweat gland cell reprogramming
- Characterization of an autoimmune condition associated with AEC syndrome
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS