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Research 901–930 of 1000+
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Ornithine decarboxylase is a target for chemoprevention of basal and squamous cell carcinomas in Ptch1+/– mice
- Regulation of stem cell function by protein ubiquitylation
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Dissecting the genetic variations associated with response to first-line chemotherapy in patients with small cell lung cancer: a retrospective cohort study
- Overexpression of mIGF-1 in Keratinocytes Improves Wound Healing and Accelerates Hair Follicle Formation and Cycling in Mice
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Bioinformatics analysis of evolutionary characteristics and biochemical structure of FGF5 Gene in sheep
- Hydrogen Sulfide Disturbs Actin Polymerization via <i>S</i>-Sulfhydration Resulting in Stunted Root Hair Growth
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Actin-depolymerizing factors 8 and 11 promote root hair elongation at high pH
- CRISPR/Cas9-mediated<i>VDR</i>knockout plays an essential role in the growth of dermal papilla cells through enhanced relative genes
- Lack of the Vitamin D Receptor is Associated with Reduced Epidermal Differentiation and Hair Follicle Growth
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin
- The molecular basis of human keratin disorders
- Role of the Notch Ligand Delta1 in Embryonic and Adult Mouse Epidermis
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Morphogenesis and maintenance of the 3D thymic medulla and prevention of nude skin phenotype require FoxN1 in pre- and post-natal K14 epithelium
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- β-Catenin Signaling Evokes Hair Follicle Senescence by Accelerating the Differentiation of Hair Follicle Mesenchymal Progenitors