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- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Human FOXN1-Deficiency Is Associated with αβ Double-Negative and FoxP3+ T-Cell Expansions That Are Distinctly Modulated upon Thymic Transplantation
- Cyclosporin A-induced hair growth in mice is associated with inhibition of calcineurin-dependent activation of NFAT in follicular keratinocytes
- Inherited Disorders of the Hair
- FOXN1 deficient nude severe combined immunodeficiency
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
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