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Research 331–360 of 1000+
- PAK4 signaling in health and disease: defining the PAK4–CREB axis
- The Effect of Plasma Rich in Growth Factors on Pattern Hair Loss: A Pilot Study
- Tumour regression predicts higher risk of sentinel node involvement in thin cutaneous melanomas
- β-Catenin Signaling Increases in Proliferating NG2+ Progenitors and Astrocytes during Post-Traumatic Gliogenesis in the Adult Brain
- Stem cell quiescence acts as a tumour suppressor in squamous tumours
- CXCR3 Blockade Inhibits T Cell Migration into the Skin and Prevents Development of Alopecia Areata
- Module-based complexity formation: periodic patterning in feathers and hairs
- Plasmacytoid dendritic cells in alopecia areata: missing link?
- Activin B Promotes BMSC-Mediated Cutaneous Wound Healing by Regulating Cell Migration via the JNK—ERK Signaling Pathway
- Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease
- Factors affecting the severity of central centrifugal cicatricial alopecia
- Microneedles mediated bioinspired lipid nanocarriers for targeted treatment of alopecia
- Monilethrix Treated with Minoxidil
- Yellow and orange in cutaneous lesions: clinical and dermoscopic data
- Polycystic Ovary Syndrome: A Common Reproductive and Metabolic Disorder Necessitating Early Recognition and Treatment
- Female Adolescent Hair Disorders
- Efficacy of Platelet-rich Plasma for Treating Androgenic Alopecia of Varying Grades
- miR-195-5p Regulates Hair Follicle Inductivity of Dermal Papilla Cells by Suppressing Wnt/<i>β</i>-Catenin Activation
- Keratin‐based particles for protection and restoration of hair properties
- Transgenic Flash Mice for In Vivo Quantitative Monitoring of Canonical Wnt Signaling to Track Hair Follicle Cycle Dynamics
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Metabolic dysfunction in female mice with disruption of 5α-reductase 1
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- Dermatologic manifestations of endocrine disorders
- Congenital atrichia and hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Male androgenetic alopecia (Part II)
- Dickkopf-1 Expression in Androgenetic Alopecia and Alopecia Areata in Male Patients
- Chest Hair Used as Donor Material in Hair Restoration Surgery