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Research 631–660 of 1000+
- Do Hair Bulb Melanocytes Undergo Apotosis During Hair Follicle Regression (Catagen)?
- Human hair keratin and its-based biomaterials for biomedical applications
- Male Pattern Alopecia A Histopathologic and Histochemical Study
- Aging of the hair follicle pigmentation system
- Trichoscopy in genetic hair shaft abnormalities
- Stress and the Hair Growth Cycle: Cortisol-Induced Hair Growth Disruption.
- Oestrogen functions in skin and skin appendages
- From hair to heart: nestin-expressing hair-follicle-associated pluripotent (HAP) stem cells differentiate to beating cardiac muscle cells
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Alopecia areata update
- Chemotherapy-induced alopecia
- Generation and characterization of hair-bearing skin organoids from human pluripotent stem cells
- A study of etretinate alopecia
- Telogen Effluvium
- Chemotherapy-Induced Anagen Effluvium: Diffuse or Patterned?
- Genetic Hair Disorders: A Review
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Alopecia in Epidermolysis Bullosa
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Development of Autoimmune Hair Loss Disease Alopecia Areata Is Associated with Cardiac Dysfunction in C3H/HeJ Mice
- Spectrum of mucocutaneous manifestations in human immunodeficiency virus-infected patients and its correlation with CD4 lymphocyte count
- Analysing the dynamics of a model for alopecia areata as an autoimmune disorder of hair follicle cycling
- Molecular Genetics of Alopecias
- Low-Intensity Ultrasound as a Potential Intervention Strategy to Protect Human Scalp Hair Follicles from Taxane-Induced Toxicity
- A Hairy Cituation – PADIs in Regeneration and Alopecia
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Psoriatic Alopecia in a Patient with Systemic Lupus Erythematosus
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Bitemporal Scalp Hair Loss: Differential Diagnosis of Nonscarring and Scarring Conditions.