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Research 421–450 of 720
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Genome-wide Maps of Histone Modifications Unwind In Vivo Chromatin States of the Hair Follicle Lineage
- Very-long-chain Acyl-CoA Synthetases
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- The malignant capacity of skin tumours induced by expression of a mutant H-ras transgene depends on the cell type targeted
- Pathophysiological mechanisms implicated in postpartum depression
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- FGF5 is a crucial regulator of hair length in humans
- Agouti and Agouti-related Protein: Analogies and Contrasts
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- MicroRNA-302 Increases Reprogramming Efficiency via Repression of NR2F2
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Frizzled Receptors in Development and Disease
- Conditional epidermal expression of TGFβ1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Visualising Androgen Receptor Activity in Male and Female Mice
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- <i>Arabidopsis</i> VILLIN4 is involved in root hair growth through regulating actin organization in a Ca<sup>2+</sup>‐dependent manner
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- White Lupin Cluster Root Acclimation to Phosphorus Deficiency and Root Hair Development Involve Unique Glycerophosphodiester Phosphodiesterases