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Research 481–510 of 823
- Intracrine androgen biosynthesis, metabolism and action revisited
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- FGF Family: From Drug Development to Clinical Application
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Free Testosterone: Pumping up the Tires or Ending the Free Ride?
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Host-Directed FDA-Approved Drugs with Antiviral Activity against SARS-CoV-2 Identified by Hierarchical In Silico/In Vitro Screening Methods
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Madarosis: A marker of many Maladies
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- FOXN1 deficient nude severe combined immunodeficiency
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- The role of WNT10B in physiology and disease: A 10-year update
- Genetically separable determinants of hair keratin gene expression
- Developing stratified epithelia: lessons from the epidermis and thymus
- Genetic Hair Disorders: A Review
- Poster Presentations