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Research 31–60 of 1000+
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Activin Controls Skin Morphogenesis and Wound Repair Predominantly via Stromal Cells and in a Concentration-Dependent Manner via Keratinocytes
- A new path in defining light parameters for hair growth: Discovery and modulation of photoreceptors in human hair follicle
- The Notch Intracellular Domain Has an RBPj-Independent Role during Mouse Hair Follicular Development
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- The Emerging Structural Pharmacology of ATP-Sensitive Potassium Channels
- Identification of the Novel Membrane-Associated Protein AgK114 on Hamster Keratinocytes Recognized by a Monoclonal Antibody K114
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Minireview: vitamin D receptor: new assignments for an already busy receptor. - eScholarship
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Ruxolitinib for the treatment of severe alopecia areata
- An intergenerational androgenic mechanism of female intrasexual competition in the cooperatively breeding meerkat
- Tetrahydroxystilbene Glucoside Effectively Prevents Apoptosis Induced Hair Loss
- Effects of Selenium and Other Micronutrient Intake on Human Health
- Hair Loss Profiles and Ritlecitinib Efficacy in Patients with Alopecia Areata: Post Hoc Analysis of the ALLEGRO Phase 2b/3 Study
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Improvement in Patient‐Reported Emotional Symptoms and Activity Limitations due to Hair Loss in Patients With Alopecia Areata Treated With Ritlecitinib: Additional Analyses From ALLEGRO ‐2b/3
- The brief overview, antivirus and anti-SARS-CoV-2 activity, quantitative methods, and pharmacokinetics of cepharanthine: a potential small-molecule drug against COVID-19
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Aconiti Lateralis Preparata Radix Activates the Proliferation of Mouse Bone Marrow Mesenchymal Stem Cells and Induces Osteogenic Lineage Differentiation through the Bone Morphogenetic Protein-2/Smad-Dependent Runx2 Pathway
- Pearly Pinna Papules in a Young Female
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Atrichia with papular lesions
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function