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Research 121–150 of 1000+
- Supplementary Methods, Tables 1-2 and Figures from Tumor Stroma–Derived Wnt5a Induces Differentiation of Basal Cell Carcinoma of <i>Ptch</i>-Mutant Mice via CaMKII
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- EdnrB Governs Regenerative Response of Melanocyte Stem Cells by Crosstalk with Wnt Signaling
- Overexpression of mIGF-1 in Keratinocytes Improves Wound Healing and Accelerates Hair Follicle Formation and Cycling in Mice
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Oncogenic senescence: a multi-functional perspective
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Genetic basis of polycystic ovary syndrome
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- High incidence of severe hand–foot syndrome during capecitabine–docetaxel combination chemotherapy
- COVID-19 Severity and Androgen Receptor Polymorphism
- Genetic variants in AR and SHBG and resistance to hormonal castration in prostate cancer
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Vitamin D Receptor gene polymorphisms taq-1 and cdx-1 in female pattern hair loss
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Commensal microbiome promotes hair follicle regeneration by inducing keratinocyte HIF-1α signaling and glutamine metabolism
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- GLP-1 Receptor Agonists: Beyond Their Pancreatic Effects
- The chemokine SDF-1/CXCL12 regulates the migration of melanocyte progenitors in mouse hair follicles