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Research 331–360 of 613
- Female Adolescent Hair Disorders
- Systemic Absorption and Pharmacokinetics of Five Novel Topical Dermatologic Agents: A Review
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Matrix Metalloproteinase-9 Is Involved in the Regulation of Hair Canal Formation
- Human Hair Keratin‐Associated Proteins (KAPs)
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Analysis of Bimatoprost-Induced changes on Rabbits eyelash Follicle: Clinical and Electron microscopic study
- Keratins of the Human Hair Follicle
- Bazi Bushen capsule alleviates skin photoaging by targeting the KEAP1–NRF2 pathway
- The HOXC13-controlled expression of early hair keratin genes in the human hair follicle does not involve TALE proteins MEIS and PREP as cofactors
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Development of Hair Fibres
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Expression patterns of keratin intermediate filament and keratin associated protein genes in wool follicles
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- The biology and genetics of curly hair
- Expression of mineralized tissue associated proteins: Dentin sialoprotein and phosphophoryn in rodent hair follicles
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Gsdma3 is required for hair follicle differentiation in mice
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Against the Rules: Human Keratin K80
- Analysis of Bimatoprost-Induced changes on Rabbits eyelash Follicle: Clinical and Electron microscopic study
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene