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Research 481–510 of 658
- 1380 PPAR-γ modulation as a novel therapeutic strategy for scarring alopecia
- 1377 Decoding frontal fibrosing alopecia and lichen planopilaris: Macrophages hold the key?
- 1376 Dermal white adipose tissue enhances proliferation, pigmentation and hair shaft elongation in human hair follicles ex vivo
- 1379 Cell of origin contributes to the melanoma diversity
- Distancia promedio de la línea de implantación pilosa frontal y sus estructuras en una población de mujeres colombianas
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- Delayed Puberty
- LITERATURE REVIEW
- Adverse Reactions to Oral Retinoids An Update
- Acne
- Woolly hair generalizado: caso clínico e revisão da literatura
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- Evaluation and treatment of facial feminization surgery: part I. forehead, orbits, eyebrows, eyes, and nose
- Correction of the Cornrow Hair Transplant and Other Common Problems in Surgical Hair Restoration
- Correction of the Cornrow Transplant and Other Common Problems in Surgical Hair Restoration by James E. Vogel, M.D.
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Correction of the Cornrow Transplant and Other Common Problems in Surgical Hair Restoration by James E. Vogel, M.D.
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Skin regional specification and higher-order <i>HoxC</i> regulation
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Persistent Gynecomastia due to Short-term Low-dose Finasteride for Androgenetic Alopecia
- Mesenchymal cell specific deletion of Tsc2 regulates hair follicle development and patterning
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes