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Research 211–240 of 1000+
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Acquired curved hair is caused by fusion of multiple hair matrix cells
- Hair & Cutaneous Development
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- Diseases of Hair
- Diseases of Hair
- Skin Pigmentation Types, Causes and Treatment—A Review
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- AcD : A Novel Bioactive Polymer Scaffold of Adipose‐Derived Stem Cells Combining With Decellularized Extracellular Matrix in Tissue Engineering
- Concerted gene duplications in the two keratin gene families
- TMT-based quantitative proteomics reveals the genetic mechanisms of secondary hair follicle development in fine-wool sheep
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Early inductive events in ectodermal appendage morphogenesis
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Ectoderm-Targeted Overexpression of the Glucocorticoid Receptor Induces Hypohidrotic Ectodermal Dysplasia
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Salivary gland function in persons with ectodermal dysplasias
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Scaffold-based developmental tissue engineering strategies for ectodermal organ regeneration
- Alopecia in congenital hidrotic ectodermal dysplasia responding to treatment with a combination of topical minoxidil and tretinoin
- FGF-9 accelerates epithelial invagination for ectodermal organogenesis in real time bioengineered organ manipulation
- Loss of a homologous group of proteins in a dominantly inherited ectodermal malformation