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Research 421–450 of 1000+
- Oral Presentations
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Potential of the Nano-Encapsulation of Antioxidant Molecules in Wound Healing Applications: An Innovative Strategy to Enhance the Bio-Profile
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Secondary Amenorrhea and Clinical Hyperandrogenism in a 34-Year-Old Female: Polycystic Ovary Syndrome or Not?
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Genetic Hair Disorders: A Review
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Primary Hypothyroidism and Thyroid Goiter in an Adult Cat
- Linear alopecia in pediatrics: RCM and dermoscopy reveal diagnostic cues
- Skin Development and Disease: A Molecular Perspective
- Wnt/β-Catenin Signaling Stabilizes Hemidesmosomes in Keratinocytes
- A folliculocentric perspective of dandruff pathogenesis: Could a troublesome condition be caused by changes to a natural secretory mechanism?
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Skin Sceneries of Thyroid Disorders and Impact of Thyroid on Different Skin Diseases: A Scoping Review Focused on Pediatric Patients
- The Opportunities and Challenges regarding Induced Platelets from Human Pluripotent Stem Cells
- Identification of Drug-Disease Associations Using Information of Molecular Structures and Clinical Symptoms via Deep Convolutional Neural Network
- Role of 5 alpha-reductase inhibitors in the management of prostate cancer
- Green and Emerging Microextraction Strategies for Bioanalytical Determination of Hormones: Trends, Challenges, and Applications
- Efficacy of platelet-rich plasma in the treatment of thin endometrium: a meta-analysis of randomized controlled trials
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- Dermatologic care of patients with differences of sex development
- A guide to diagnosis and management of hypertrichosis
- A Clinical Review of Trichorrhexis Nodosa
- Ichthyosis
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- The distribution of melanocytes and the degradation of melanosomes in fetal hair follicles