Search
for
Sort by
Research 181–210 of 1000+
- Spiny Keratoderma
- Embryonic keratinization in vertebrates in relation to land colonization
- Structure and expression of the ovine Hoxc-13 gene
- KRT17 promotes endometrial cancer cell migration as well as angiogenesis by regulating HIF-1α/VEGF pathway
- 840 Early and late matrix progenitors form the terminally differentiated cell layers of the hair follicle
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- The biology and genetics of curly hair
- Characterization of sciellin, a precursor to the cornified envelope of human keratinocytes
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- The cellular basis of mechanosensory Merkel-cell innervation during development
- Mechanical stress and the development of pseudo‐comedones and tunnels in Hidradenitis suppurativa/Acne inversa
- Studies of androgen metabolism and action in cultured hair and skin cells
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Tretinoin Treatment of Fox-Fordyce Disease
- <i>Hoxc13</i> and the development of hair follicle
- Alarm reaction of pilosebaceous apparatus
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- [Studies on monilethrix].
- Development and optimization of biotinoyl tripeptide-1 loaded solid lipid nanoparticles for protection against heat induced hair damage
- The Utility of De-epithelialization in Subcutaneous Skin Flap Transposition.
- Nestin as a marker of unipotent epithelial progenitor cells differentiate into outer root sheath keratinocytes in embryonic and adult hair follicles
- 성장기 모낭에서 큐티클층의 각질화 과정
- UV-A조사에 의한 반영구염색모발의 형태학적 변화
- Retinoids and Keratinization
- Histology, lectin histochemistry and ultrastructure of interdigital gland in crossbred sheep
- 321 Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- George Ernest Rogers 1927–2021
- Hair growth at a solid-liquid interface as a protein crystal without cell division
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- [Nevus comedonicus. A rare skin disease of the hair follicles].