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Research 421–450 of 435
- What to Look for in Red Light Therapy: A Product Guide Backed by Science
- Towards cell-based therapy of alopecia areata: Autologous human Vδ2+ Foxp3+ γδTreg cells restore hair-follicle immune privilege and promote hair regrowth in human alopecia areata models ex vivo and in vivo
- Therapeutic potential of Ishophloroglucin a from Ishige okamurae in androgenic alopecia: inhibition of 5α-reductase activity and activation of the Wnt/β-catenin signaling pathway in human dermal papilla cells
- Peptide-Based Approaches for Pain Relief and Healing in Wounds
- Microneedle-Based Technologies for Long-Acting Transdermal Drug Delivery in Wearable Devices
- Dexmedetomidine-Loaded Hydrogel Microneedles Alleviate Acute Inflammatory Visceral Pain in Mice
- Hypothesis: platelet-rich plasma as an adjunct therapy for eczema targeting inflammation, skin barrier repair, and chronic recurrence
- Do Syrian conflict survivors show novel chronic cutaneous sequelae from chlorine gas exposure: A case report and literature review
- Introductory Chapter: Learning and Recognizing the Post-COVID Syndromes
- Functional regeneration strategies of hair follicles: advances and challenges
- Calcium channel inhibitor and extracellular calcium improve aminoglycoside-induced hair cell loss in zebrafish
- Virtual Insights into Natural Compounds as Potential 5α-Reductase Type II Inhibitors: A Structure-Based Screening and Molecular Dynamics Simulation Study
- Table_1_Bioinformatics and Network Pharmacology Identify the Therapeutic Role and Potential Mechanism of Melatonin in AD and Rosacea.xlsx
- Isolation, Structural Elucidation and Therapeutic Potentials of Root of Cucurbita pepo
- The use of NDYAG laser combined with pulsed light in the treatment of rosacea
- Influence of TRPV3 mutation on hair growth cycle in mice
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Hypotrichosis in a child with olmsted syndrome
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- News in brief
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- TRPV3 Ion Channel: From Gene to Pharmacology
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine