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Research 871–900 of 1000+
- Historical and Current Adenosine Receptor Agonists in Preclinical and Clinical Development
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- ANTIANDROGEN THERAPY IN DERMATOLOGY
- Increased 25(OH)D3 level in redheaded people: Could redheadedness be an adaptation to temperate climate?
- Induction of synapse associated protein 102 expression in cyclosporin A-stimulated hair growth
- Skin Diseases (Noncancerous)
- Dermatologia e Procedimentos Estéticos Ed. XVIII
- Techniques d'épargne cutanée dans la chirurgie de la gynécomastie
- Photothermal hydrogels for infection control and tissue regeneration
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Astragalus membranaceus and Cinnamomum cassia Stimulate the Hair Follicle Differentiation-Related Growth Factor by the Wnt/β-Catenin Signaling Pathway
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- A Systemic Review on Topical Marketed Formulations, Natural Products, and Oral Supplements to Prevent Androgenic Alopecia: A Review
- Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Mesenchymal Stem Cell Exosomes Therapy for Acquired Trichorrhexis Nodosa: A Case Series
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Disorders of Keratinization
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Regional Variation in Androgen Receptor Expression and Biomechanical Properties May Contribute to Cryptorchidism Susceptibility in the LE/orl Rat
- Zebrafish Model of Hereditary Pigmentary Disorders
- Reliability of the Estimation of the Take of Split Thickness Graft by the Observation Method