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Research 91–120 of 1000+
- Spreading of Isolated Ptch Mutant Basal Cell Carcinoma Precursors Is Physiologically Suppressed and Counteracts Tumor Formation in Mice
- Loss of Vascular Endothelial Growth Factor in Human Alopecia Hair Follicles
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- 905 Dysfunction of hair follicle mesenchymal progenitors is associated with age-related hair loss
- Regulatory T cells in inflammatory skin disease: from mice to humans
- <i>Hoxc13</i> mutant mice lack external hair
- Learning from nudity: lessons from the nude phenotype
- Signaling pathways in hair aging
- Rapid Genetic Analysis of Epithelial-Mesenchymal Signaling During Hair Regeneration
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- The Yin and Yang of Integrin Function in Re-Epithelialization During Wound Healing
- 9. Immunology and Genetics
- Mediator1: An Important Intermediary of Vitamin D Receptor–Regulated Epidermal Function and Hair Follicle Biology
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- The Impact of the 5α-Reductase Inhibitors (5α-RIs) on Male Sexual Function and Psychological Well-Being
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- The Roles of Smad2 and Smad3 in Mouse Skin Development
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Functional analysis of vitamin D receptor (VDR) using adenovirus vector
- TRP Channels in Skin Biology and Pathophysiology
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- Animal and in vitro Models for the Study of Hair Follicles
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- TRPV3 Ion Channel: From Gene to Pharmacology
- A kindred with mutant IKAROS and autoimmunity
- The amazing miniorgan: Hair follicle
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- 1314 Advanced age impairs self-renewal and biases fate choice of hair follicle dermal stem cells
- Insertional mutation of the hairless locus on mouse Chromosome 14