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Research 721–750 of 833
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Developmental genetics of color pattern establishment in cats
- Is it getting in the hair? – Cortisol concentrations in native, regrown and segmented hairs of cattle and pigs after repeated ACTH administrations
- JAK inhibition decreases the autoimmune burden in Down syndrome
- The role of metabolism in cellular quiescence
- Wnt Signaling Influences the Development of Murine Epidermal Langerhans Cells
- The anti-inflammatory and analgesic activities of 2Br-Crebanine and Stephanine from Stephania yunnanenses H. S.Lo
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Skin Development and Disease: A Molecular Perspective
- Emerging roles of Sox6 in the renal and cardiovascular system
- TRPV Channels in Osteoarthritis: A Comprehensive Review
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Recent advances in the role of neuroregulation in skin wound healing
- Biofunctionalization of hydrogel-based scaffolds for vascular tissue regeneration
- The mechanical forces that shape our senses
- Injectable Biomimetic Gels for Biomedical Applications
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Small Molecule Treatments Improve Differentiation Potential of Human Amniotic Fluid Stem Cells
- Control of myeloid cell density in barrier tissues
- Hair and cord blood element levels and their relationship with air pollution, dietary intake, gestational diabetes mellitus, and infant neurodevelopment
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- The effect of melatonin implants administered from December until April, on plasma prolactin, triiodothyronine and thyroxine concentrations and on the timing of the spring moult in cashmere goats
- RNA-Seq Reveals the Roles of Long Non-Coding RNAs (lncRNAs) in Cashmere Fiber Production Performance of Cashmere Goats in China
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions