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Research 541–570 of 1000+
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- Dynamic expression of Runx1 in skin affects hair structure
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Betacellulin Regulates Hair Follicle Development and Hair Cycle Induction and Enhances Angiogenesis in Wounded Skin
- Evidence for 1,25-Dihydroxyvitamin D3-independent Transactivation by the Vitamin D Receptor
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- ERULUS Is a Plasma Membrane-Localized Receptor-Like Kinase That Specifies Root Hair Growth by Maintaining Tip-Focused Cytoplasmic Calcium Oscillations
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Hair Growth Cycle Is Arrested in SCD1 Deficiency by Impaired Wnt3a-Palmitoleoylation and Retrieved by the Artificial Lipid Barrier
- Study of seed hair growth in Populus tomentosa, an important character of female floral bud development
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Tissue Regeneration: Hair Follicle as a Model
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Essential Role for Integrin-Linked Kinase in Melanoblast Colonization of the Skin
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Single‐cell transcriptomics reveals a senescence‐associated IL ‐6/ CCR6 axis driving radiodermatitis
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Intramembrane Proteolysis of Astrotactins
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- An update of polycystic ovary syndrome: causes and therapeutics options