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Research 661–690 of 673
- HA Filler Injection and Skin Quality–Literature Minireview and Injection Techniques
- Roles of steroid receptors in the lung and COVID-19
- Ovine placental steroid synthesis and metabolism in late gestation†
- Genetic variants in AR and SHBG and resistance to hormonal castration in prostate cancer
- Mandibular Ligament and the Prejowl Sulcus Explained
- Lymphatic vessel: origin, heterogeneity, biological functions, and therapeutic targets
- Non-surgical Modalities of Facial Rejuvenation and Aesthetics
- Hair transplantation in patients with hair loss or scar deformity in the side hairline after midfacelifting surgery
- Transtemporal Endoscopic Subcutaneous Face-and-Neck Lift with SMAS Plication
- The Economic Burden of Alopecia Areata: Evidence from a Survey in Norway and Sweden
- A Multimodal Approach to Facial Rejuvenation—Integrating HA Fillers, Collagen Stimulators, Botulinum Toxin and Energy-Based Devices for Optimal Patient Outcomes
- Retinoic-Acid-Related Orphan Receptor Alpha Is Involved in the Regulation of the Cytoskeleton of Hair Follicle Stem Cells
- JOLT: A Noninvasive Solution for the Correction of the Jowl
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Disorders of Keratinization
- Care of the newborn with ichthyosis
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Ichthyoses
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Androgenetic Alopecia