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Research 301–330 of 1000+
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Epidermal growth factor, innovation and safety
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling
- Studies of the availability of soil phosphorus (P) and potassium (K) in organic farming systems, and of plant adaptations to low P- and K-availability
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Promotion of mouse ameloblast proliferation by Lgr5 mediated integrin signaling
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- The Charnoly body as a universal biomarker of cell injury
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Animal fibre: connecting science and production
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Inherited Disorders of the Hair
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- The G1/S transition in mammalian stem cells in vivo is autonomously regulated by cell size
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Generalised Glucocorticoid Resistance
- Dicer- and BSC-dependent miRNAs during murine anagen development
- Rac-dependent signaling from keratinocytes promotes differentiation of intradermal white adipocytes
- SOX2 in the Skin