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Research 91–120 of 1000+
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Arabidopsis ZINC FINGER PROTEIN1 Acts Downstream of GL2 to Repress Root Hair Initiation and Elongation by Directly Suppressing bHLH Genes
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse
- Co-operation between follicular ornithine decarboxylase and v-Ha-ras induces spontaneous papillomas and malignant conversion in transgenic skin
- Defective control of growth rate and cell diameter in tip-growing root hairs of the<i>rhd4</i>mutant of<i>Arabidopsis thaliana</i>
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Genomic Organization, Transcriptomic Analysis, and Functional Characterization of Avian α- and β-Keratins in Diverse Feather Forms
- CD133-positive dermal papilla-derived Wnt ligands regulate postnatal hair growth
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- The role of Glucosylceramides in Keratinocyte Differentiation and Epidermal Barrier Function
- Arabidopsis retromer subunit AtVPS29 is involved in SLY1-mediated gibberellin signaling
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- Hox demarcates regional regeneration of adult hair follicle stem cells
- The role of functional variants in the aetiology of polycystic ovary syndrome
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- The role of Pygo2 during intestinal tumor initiation and progression in vivo
- Hairless: A nuclear receptor corepressor essential for skin function
- MTHFR C677T Polymorphism and Serum Homocysteine Level as Risk Factors of Coronary Heart Disease in Patients with Androgenetic Alopecia: A Case Control Study
- Human Derived Immortalized Dermal Papilla Cells With a Constant Expression of Testosterone Receptor
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Hairless is a nuclear receptor corepressor essential for skin function
- Scraggly, a new hair loss mutation on mouse Chromosome 19
- Decoding the role of <i>OsPRX83</i> in enhancing osmotic stress tolerance in rice through ABA-dependent pathways and ROS scavenging
- Hair & Cutaneous Development
- Stem Cell Heterogeneity and Plasticity in Epithelia
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- 1229 Melanocyte cell states defined and visualized in developing mouse skin