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Research 151–180 of 600
- Sonic Hedgehog signalling in the regulation of barrier tissue homeostasis and inflammation
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Clinical and dermatoscopic features of temporal triangular alopecia in infants
- Fibrosing alopecia in a pattern distribution after hair transplantation: A case report and literature review
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- TGF‐β<sub>2</sub> is specifically expressed in human dermal papilla cells and modulates hair folliculogenesis
- Androgen Treatment in Adolescent Males With Hypogonadism
- Ligand‐Independent Actions of the Vitamin D Receptor: More Questions Than Answers
- Mining and analysis of adverse event signals of isotretinoin based on the real-world data of FAERS database
- Effect of Fibroblast Growth Factor 10 and an Interacting Non-Coding RNA on Secondary Hair Follicle Dermal Papilla Cells in Cashmere Goats’ Follicle Development Assessed by Whole-Transcriptome Sequencing Technology
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- LHX2: a transcription factor in development, homeostasis, repair, and disease
- Madarosis: A marker of many Maladies
- Subject Index
- Single-Cell Transcriptomics of Traced Epidermal and Hair Follicle Stem Cells Reveals Rapid Adaptations during Wound Healing
- Conditional epidermal expression of TGFβ1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia
- Hair loss in children.
- Atypical Congenital Triangular Alopecia (Brauer Nevus): Case Report and Review of Literature in Occipital and Mid-Frontal Localizations
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- The Spectrum of Skin Disease Among Indian Children
- Hair Loss in Children
- Disorders of hair in children
- Inactivation of the Vitamin D Receptor Enhances Susceptibility of Murine Skin to UV-Induced Tumorigenesis
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The role of platelet-rich plasma in biomedicine: A comprehensive overview
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome”