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Research 301–330 of 1000+
- Idiopathic Hirsutism*
- Use of chemotherapy during human pregnancy
- Somatization in the dermatology patient: Some sociocultural perspectives
- Scratching the surface of skin development
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Olfactory receptor OR2AT4 regulates human hair growth
- Identifying novel strategies for treating human hair loss disorders: Cyclosporine A suppresses the Wnt inhibitor, SFRP1, in the dermal papilla of human scalp hair follicles
- Mechanical forces in skin disorders
- Anagen effluvium
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Label Retaining Cells (LRCs) with Myoepithelial Characteristic from the Proximal Acinar Region Define Stem Cells in the Sweat Gland
- Comparative Transcriptome Analysis Reveals that a Ubiquitin-Mediated Proteolysis Pathway Is Important for Primary and Secondary Hair Follicle Development in Cashmere Goats
- Unruly hair
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Eyebrow restoration: the approach, considerations, and technique in follicular unit transplantation
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Trichodystrophies: A hair-raising differential diagnosis
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Inherited Epidermolysis Bullosa: A Clinical Case
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Abstracts