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Research 271–300 of 1000+
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
- Dynamics of Merkel Cell Patterns in Developing Hair Follicles in the Dorsal Skin of Mice, Demonstrated by a Monoclonal Antibody to Mouse Keratin 8
- Targeted Expression of Human Vitamin D Receptor in the Skin Promotes the Initiation of the Postnatal Hair Follicle Cycle and Rescues the Alopecia in Vitamin D Receptor Null Mice
- Overexpression of mIGF-1 in Keratinocytes Improves Wound Healing and Accelerates Hair Follicle Formation and Cycling in Mice
- Prolactin delays hair regrowth in mice
- Targeted Disruption of Stat3 Reveals a Major Role for Follicular Stem Cells in Skin Tumor Initiation
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- Ectoderm-Targeted Overexpression of the Glucocorticoid Receptor Induces Hypohidrotic Ectodermal Dysplasia
- Structural insights into SARS-CoV-2 spike protein and its natural mutants found in Mexican population
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- RANKL Induces Organized Lymph Node Growth by Stromal Cell Proliferation
- Expression of Cyclooxygenase Isozymes During Morphogenesis and Cycling of Pelage Hair Follicles in Mouse Skin: Precocious Onset of the First Catagen Phase and Alopecia upon Cyclooxygenase-2 Overexpression
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Body composition changes and inhibition of fat development in vivo implicates androgen in regulation of stem cell lineage allocation
- Targeted disruption of Bcl‐x<sub>L</sub> in mouse keratinocytes inhibits both UVB‐ and chemically induced skin carcinogenesis
- ERULUS Is a Plasma Membrane-Localized Receptor-Like Kinase That Specifies Root Hair Growth by Maintaining Tip-Focused Cytoplasmic Calcium Oscillations
- Meis1 Regulates Epidermal Stem Cells and Is Required for Skin Tumorigenesis
- Genetic Fate Mapping Using Site-Specific Recombinases
- Dermal papilla cells induce keratinocyte tubulogenesis in culture
- Allopregnanolone mediates the exacerbation of Tourette-like responses by acute stress in mouse models
- Leptin controls hair follicle cycling
- THY1-mediated mechanisms converge to drive YAP activation in skin homeostasis and repair
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Expression of the human Cathepsin L inhibitor hurpin in mice: skin alterations and increased carcinogenesis
- DPP-4 inhibition with linagliptin ameliorates the progression of premature aging in klotho−/− mice
- Matrix Metalloproteinase-9 Is Involved in the Regulation of Hair Canal Formation
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro