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Research 631–660 of 1000+
- Study on the expression patterns of inner root sheath-specific genes in Tan sheep hair follicle during different developmental stages
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Comparison between topical cetirizine with minoxidil versus topical placebo with minoxidil in female androgenetic alopecia: a randomized, double-blind, placebo-controlled study
- Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- New clinico‐genetic classification of trichothiodystrophy
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Lysophospholipid Mediators in Health and Disease
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Pregnancy and Skin
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Hair shaft disorders in children – An update
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Analogs of human genetic skin disease in domesticated animals
- The Roles of WNT Signaling Pathways in Skin Development and Mechanical-Stretch-Induced Skin Regeneration
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- First Symposium of Ichthyosis Experts
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Impact of Reporter Type on Signal Detection of Cancer Therapy–Induced Alopecia: A Hypothesis-Generating Study Using the FDA Adverse Event Reporting System