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Research 661–690 of 1000+
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Genetic Disorders and Defects in Vitamin D Action
- Estrogen and androgen signaling in the pathogenesis of BPH
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Regulation of Involucrin Gene Expression
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- FGF5 is a crucial regulator of hair length in humans
- Hyaluronate Fragments Reverse Skin Atrophy by a CD44-Dependent Mechanism
- Agouti and Agouti-related Protein: Analogies and Contrasts
- Zeb2 recruits HDAC–NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
- 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
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- Activation of Polyamine Catabolism Profoundly Alters Tissue Polyamine Pools and Affects Hair Growth and Female Fertility in Transgenic Mice Overexpressing Spermidine/SpermineN 1-Acetyltransferase
- Androgen sensitivity gateway to COVID‐19 disease severity
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Frizzled Receptors in Development and Disease
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- The structure and organization of lanceolate mechanosensory complexes at mouse hair follicles
- A slow-cycling LGR5 tumour population mediates basal cell carcinoma relapse after therapy
- Identification of a link between Wnt/β-catenin signalling and the cell fusion pathway
- 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
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2