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Research 301–330 of 1000+
- Growth factor mimetics for skin regeneration: In vitro profiling of primary human fibroblasts and keratinocytes
- The genetically programmed hair growth cycle and alopecia: what is there to know?
- Clinical use of 5α-reductase inhibitors
- Single-cell chromatin landscapes of mouse skin development
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Androgen Receptor Ligands: Agonists and Antagonists
- Spatial variation and associated genes of total hair follicle density in goats
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Industry update: the latest developments in the field of therapeutic delivery, July 2018
- Melanocytes and Vitiligo (and Hair Graying)
- Research progress on mechanisms of skin aging and anti-aging strategies
- Establishing a robust preclinical model to investigate early and late radiation-induced skin reactions
- From basic biology to engineered therapies: the keratinocyte stem cell playbook
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- The senescence-like activity of BMS-470539 is associated with anti-fibrotic actions in models of dermal fibrosis
- Nucleic acid-induced chemokine expression in keratinocytes: Implications for skin inflammation
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Exossomos na Dermatologia: revisão de sua ação em doenças cutâneas e rejuvenescimento
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Molecular and Pathological Studies on Sarcoptes scabiei in Sheep in Ismailia Province, Egypt.
- Effect of decellularisation methods on methacryloyl-substituted placental ECM hydrogels
- Inherited Epidermolysis Bullosa: A Clinical Case
- WNT10B (wingless-type MMTV integration site family)
- Genetic Defects of Female Sexual Differentiation
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Australasian Society for Dermatology Research Meeting, May 2006
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- The Rotterdam Study: 2018 update on objectives, design and main results