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Research 901–930 of 1000+
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Eziopatogenesi e terapia dell'acne:studio epidemiologico delle caratteristiche cliniche di una popolazione di pazienti affetti da acne e analisi dei polimorfismi del gene codificante per il recettore degli androgeni e del gene codificante per il citocromo P-450 1A1
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Stem Cells behind the Barrier
- The targeted overexpression of a Claudin mutant in the epidermis of transgenic mice elicits striking epidermal and hair follicle abnormalities
- A Systemic Review on Topical Marketed Formulations, Natural Products, and Oral Supplements to Prevent Androgenic Alopecia: A Review
- Laminin-511, inducer of hair growth, is down-regulated and its suppressor in hair growth, laminin-332 up-regulated in chemotherapy-induced alopecia
- A Comprehensive Review of Acne Treatments: Unpacking the Chemical Structures and Effective Bioactive Compounds
- Pathogenesis of Alopecia Areata and Vitiligo: Commonalities and Differences
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Identification of Anabolic Selective Androgen Receptor Modulators with Reduced Activities in Reproductive Tissues and Sebaceous Glands
- Citrullinome of Porphyromonas gingivalis Outer Membrane Vesicles: Confident Identification of Citrullinated Peptides
- Progress in the Expression, Purification, and Characterization of Recombinant Collagen
- Metabolic pathways of eicosanoids—derivatives of arachidonic acid and their significance in skin
- Advancements in research on the immune-inflammatory mechanisms mediated by NLRP3 inflammasome in ischemic stroke and the regulatory role of natural plant products
- The Rho guanosine nucleotide exchange factors Vav2 and Vav3 modulate epidermal stem cell function
- The Intermediate Filament Architecture as Determined by X-Ray Diffraction Modeling of Hard α-Keratin
- A Review of Keratin-Based Biomaterials for Biomedical Applications
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Quantification of the Vitamin D Receptor−Coregulator Interaction
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- CXXC5: A novel regulator and coordinator of TGF-β, BMP and Wnt signaling
- Unravelling the molecular basis for symbiotic signal transduction in legumes
- S100A6 Protein—Expression and Function in Norm and Pathology
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- Different Ligands of the TRPV3 Cation Channel Cause Distinct Conformational Changes as Revealed by Intrinsic Tryptophan Fluorescence Quenching
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families