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Research 451–480 of 1000+
- Induction of synapse associated protein 102 expression in cyclosporin A-stimulated hair growth
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- The urine as a diagnostic key for a homozygous EGFR mutation
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Trichodystrophies: A hair-raising differential diagnosis
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Real-world pharmacovigilance insights into drug-induced risk of alopecia
- Uso actual de la vitamina D en dermatología
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- Molecular pathology of skin adnexal tumours
- JAK kinase pathway inhibitor drugs in patients with moderate-to-severe alopecia: a real-world experience
- Neuroendocrine Controls of Keratin Expression in Human Skin
- 507 Trial to investigate the role of ATP-sensitive potassium channels (KATPc) in dermal papilla cells (DPCs)
- Treatment of Alopecia in Children
- Aged Skin Cells Nurture Stem Cells toward Regeneration
- Gerontobiology of the Hair Follicle
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Cosmetic Outcomes and Safety of Hair Transplantation and Topical Minoxidil for Temporal Triangular Alopecia: A Systematic Review
- Diffuse Hair Loss
- An analytical study of serum ferritin, vitamin D, and thyroid function in females with diffuse hair loss
- An Approach to Detect Alopecia Areata Hair Disease Using Deep Learning
- Expert consensus on the management of telogen effluvium in India
- Scarring Alopecia in Pediatric Patients: A Narrative Review of Etiologies, Diagnosis, and Management Strategies
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- Tackling Adverse Effects
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia