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Research 841–870 of 1000+
- TGFβ family mimetic peptide promotes proliferation of human hair follicle dermal papilla cells and hair growth in C57BL/6 mice
- Cronkhite-Canada syndrome associated with colon cancer metastatic to liver
- Diagnosis and management of hair loss in children
- SOX2 in the Skin
- Epidermal Wnt/beta-catenin signalling promotes dermal adipocyte differentiation during hair follicle morphogenesis and regeneration
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- From neural crest cells to melanocytes: cellular plasticity during development and beyond
- The Role of Stem Cells in Cutaneous Wound Healing: What Do We Really Know?
- Congenital hypotrichosis due to short anagen
- The Role of Extracellular Vesicles in Cutaneous Remodeling and Hair Follicle Dynamics
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- Whole-genome bisulfite sequencing of goat skins identifies signatures associated with hair cycling
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Hair Loss in Children
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Hair Shaft Dysplasias
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- The River of Stem Cells
- Gsdma3 regulates hair follicle differentiation via Wnt5a-mediated non-canonical Wnt signaling pathway
- Growth and viability of Liaoning Cashmere goat hair follicles during the annual hair follicle cycle
- Hair loss
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Disease causing homozygous variants in the human hairless gene
- Hair loss in children.
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Cronkhite-Canada Syndrome: A Case Report
- Knockout of p16INK4a promotes aggregative growth of dermal papilla cells
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family