Search
for
Sort by
Research 481–510 of 763
- K6/ODC transgenic mice as a sensitive model for carcinogen identification
- Multiple cyclic nucleotide‐gated channels coordinate calcium oscillations and polar growth of root hairs
- DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration
- The Vitamin D Receptor as Tumor Suppressor in Skin
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- p63: a crucial player in epithelial stemness regulation
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Ornithine Decarboxylase Expression Leads to Translocation and Activation of Protein Kinase CK2 in Vivo
- BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Cell surface receptor kinase FERONIA linked to nutrient sensor TORC signaling controls root hair growth at low temperature linked to low nitrate in <i>Arabidopsis thaliana</i>
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Ornithine decarboxylase is upregulated by the androgen receptor in skeletal muscle and regulates myoblast proliferation
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Host-Directed FDA-Approved Drugs with Antiviral Activity against SARS-CoV-2 Identified by Hierarchical In Silico/In Vitro Screening Methods
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Inhibition of Wnt/β‐catenin pathway promotes regenerative repair of cutaneous and cartilage injury
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- The nude gene and the skin
- Against the Rules: Human Keratin K80
- CD34 <sup>+</sup> cell–derived fibroblast-macrophage cross-talk drives limb ischemia recovery through the OSM-ANGPTL signaling axis
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Targeting Wnt Signaling for Gastrointestinal Cancer Therapy: Present and Evolving Views
- SIRT 7 activates quiescent hair follicle stem cells to ensure hair growth in mice
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth