Search
for
Sort by
Research 121–150 of 1000+
- Concise Review: Translating Regenerative Biology into Clinically Relevant Therapies: Are We on the Right Path?
- Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Top applications of dermatologic ultrasonography that can modify management
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Cutaneous manifestations of endocrine diseases in children
- Human Scalp Hair Follicles Are Both a Target and a Source of Prolactin, which Serves as an Autocrine and/or Paracrine Promoter of Apoptosis-Driven Hair Follicle Regression
- Morpho-Regulation of Ectodermal Organs
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- BH03: Systemic sclerosis and frontal fibrosing alopecia: a novel combination of scarring alopecia
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- 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
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Skin manifestations of endocrine diseases
- Chancres in Syphilis-Reply
- Smad1 and 5 but Not Smad8 Establish Stem Cell Quiescence Which Is Critical to Transform the Premature Hair Follicle During Morphogenesis Toward the Postnatal State
- Role of the Wnt signaling pathway in keratoacanthoma
- Serum IL-21 Level and Its Relation to Activity and Severity of Alopecia Areata
- Fibroblast heterogeneity: implications for human disease
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Alopecia areata: a review on diagnosis, immunological etiopathogenesis and treatment options
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Hair Disorders
- Non-Neoplastic Disorders of Hair
- Congenital atrichia and hypotrichosis
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Wound Healing and the Use of Medicinal Plants
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis