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Research 241–270 of 1000+
- Oil body bound oleosin-rhFGF9 fusion protein expressed in safflower (Carthamus tinctorius L.) stimulates hair growth and wound healing in mice
- Piecing together the pigment-type switching puzzle
- CD44 signaling in skin wound healing and regeneration
- Ectopic expression of FGF5s induces wool growth in Chinese merino sheep
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- No difference in the proteome of racially and geometrically classified scalp hair sample from a South African cohort: Preliminary findings
- Co-expression of PADI isoforms during progenitor differentiation enables functional diversity
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Canonical prolactin signaling and global mRNA expression in the skin of Holstein heifers carrying the SLICK1 allele of the prolactin receptor gene
- Recombinant Goat VEGF164 Increases Hair Growth by Painting Process on the Skin of Shaved Mouse
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Isoginkgetin, a natural biflavonoid from Ginkgo biloba, inhibits inflammatory response in endothelial cells via suppressing NF-κB activation
- The role of VEGF and thrombospondins in skin angiogenesis
- Advances in 3D printing for the repair of tympanic membrane perforation: a comprehensive review
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Transcriptome Profile at Different Physiological Stages Reveals Potential Mode for Curly Fleece in Chinese Tan Sheep
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- RAGE and Its Ligands in Melanoma
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Premature aging syndromes: From patients to mechanism
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Sensory Reinnervation of Human Skin by Human Neural Stem Cell‒Derived Peripheral Neurons Ex Vivo
- Phosphatase Regulator NIPP1 Restrains Chemokine-Driven Skin Inflammation
- 3D Printing—A “Touch-Button” Approach to Manufacture Microneedles for Transdermal Drug Delivery
- Magnetically driven formation of 3D freestanding soft bioscaffolds