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Research 211–240 of 1000+
- A randomized study of eflornithine cream combined with intense pulsed light versus intense pulsed light treatment alone for hirsutism in women
- Trichoscopy and Trichogram
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Successful treatment of ulcerated infantile hemangioma associated with PELVIS syndrome using oral propanolol
- Standards of Care for the Health of Transsexual, Transgender, and Gender-Nonconforming People, Version 7
- Scratching the surface of skin development
- Is dehydroepiandrosterone a hormone?
- Regulatory T-Cells: Potential Regulator of Tissue Repair and Regeneration
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- ATP-dependent chromatin remodeling during mammalian development
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Morpho-Regulation of Ectodermal Organs
- Comorbidities in alopecia areata: A systematic review and meta-analysis
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Dermatologic manifestations of endocrine disorders
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Brg1 Governs a Positive Feedback Circuit in the Hair Follicle for Tissue Regeneration and Repair
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Female type of adult acne: Physiological and psychological considerations and management
- Differences in Expression of Specific Biomarkers Distinguish Human Beard from Scalp Dermal Papilla Cells
- Different Trichoscopic Features of Tinea Capitis and Alopecia Areata in Pediatric Patients
- Hair Restoration Surgery: The State of the Art
- Diagnostic approach to low‐renin hypertension
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- A missing piece: the spiny mouse and the puzzle of menstruating species
- Expression of AKT1 along with AKT2 in granulosa-lutein cells of hyperandrogenic PCOS patients
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost