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Research 421–450 of 1000+
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Identification of differentially expressed genes affecting hair and cashmere growth in the Laiwu black goat by microarray
- Topological Distribution of Wound Stiffness Modulates Wound-Induced Hair Follicle Neogenesis
- Retinoic Acid-Induced Epidermal Transdifferentiation in Skin
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- Epidermal retinol dehydrogenases cyclically regulate stem cell markers and clock genes and influence hair composition
- Twist2 contributes to skin regeneration and hair follicle formation in mouse fetuses
- Effect of Coffee Berry Extract on Anti-Aging for Skin and Hair—In Vitro Approach
- Inhibition of prolactin promotes secondary skin follicle activation in cashmere goats
- Dermal lymphatic dilation in a mouse model of alopecia areata
- Meloside A Protects Dermal Papilla Cells from DHT-Induced Damage via Androgen Receptor Modulation
- Keratinocyte Growth Factor Modified Messenger RNA Accelerating Cell Proliferation and Migration of Keratinocytes
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- Mesenchymal Meis2 controls whisker development independently from trigeminal sensory innervation
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- 236 Wnt/planar cell polarity impairment and the genetics of yellow nail syndrome
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Weight Changes Are Linked to Adipose Tissue Genes in Overweight Women with Polycystic Ovary Syndrome
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- 741 Identification of a specific subset of monocytes/macrophages that coordinates skin wound healing
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- The activin binding proteins follistatin and follistatin-related protein are differentially regulated in vitro and during cutaneous wound repair