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Research 631–660 of 1000+
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Concise Review: Wnt Signaling Pathways in Skin Development and Epidermal Stem Cells
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Phospholipase C 1 is required for skin stem cell lineage commitment
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Polycystic Ovarian Syndrome
- Syndecan-1 Is Required to Maintain Intradermal Fat and Prevent Cold Stress
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- FOXO1, TGF-β Regulation and Wound Healing
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Vitamin D and calcium regulation of epidermal wound healing
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Dermal Blimp1 Acts Downstream of Epidermal TGFβ and Wnt/β-Catenin to Regulate Hair Follicle Formation and Growth
- Myocardial NF-κB activation is essential for zebrafish heart regeneration
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases
- PRC 2 preserves intestinal progenitors and restricts secretory lineage commitment
- Aging of the hair follicle pigmentation system
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- Zinc Deficiency in Rhesus and Bonnet Monkeys, Including Effects on Reproduction
- The role of nuclear hormone receptors in cutaneous wound repair
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- Different effects of phospholipase Dζ2 and non‐specific phospholipase C4 on lipid remodeling and root hair growth in Arabidopsis response to phosphate deficiency
- The role of macrophages in skin homeostasis
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Divergent roles of HDAC1 and HDAC2 in the regulation of epidermal development and tumorigenesis
- Lamins in development, tissue maintenance and stress