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Research 841–870 of 1000+
- Spermidine/spermine-<i>N</i><sup>1</sup>-acetyltransferase: a key metabolic regulator
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- Challenges, Progress, and Prospects of Developing Therapies to Treat Autoimmune Diseases
- Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- Hyaluronate Fragments Reverse Skin Atrophy by a CD44-Dependent Mechanism
- Zeb2 recruits HDAC–NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
- 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
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Age-Related Loss of Innate Immune Antimicrobial Function of Dermal Fat Is Mediated by Transforming Growth Factor Beta
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Visualising Androgen Receptor Activity in Male and Female Mice
- Inhibition of β-catenin signalling in dermal fibroblasts enhances hair follicle regeneration during wound healing
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Two Hydroxyproline Galactosyltransferases, GALT5 and GALT2, Function in Arabinogalactan-Protein Glycosylation, Growth and Development in Arabidopsis
- Integrated analysis of long non-coding RNA and mRNA expression in different colored skin of koi carp