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Research 931–960 of 1000+
- Evaluation of Signs of Skin Aging in Patients with Metabolic Syndrome after Substitution Therapy with Antioxidants. Summary of the Doctoral Thesis
- Analyse de la régulation du gène Hairless et identification des voies de signalisation affectées chez les mutants «bald Mill Hill».
- Trichothiodystrophy
- Quiescent Tissue Stem Cells Evade Immune Surveillance
- Thymosin β4 promotes angiogenesis, wound healing, and hair follicle development
- A subpopulation of itch‐sensing neurons marked by Ret and somatostatin expression
- Exploring Differentially Expressed Genes by RNA-Seq in Cashmere Goat (Capra hircus) Skin during Hair Follicle Development and Cycling
- Effects of glucocorticoid on human dermal papilla cells in vitro
- PPAR‐γ signalling as a key mediator of human hair follicle physiology and pathology
- Structural Hierarchy of Trichocyte Keratin Intermediate Filaments
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Transglutaminase Activity Is Conserved in Stratified Epithelia and Skin Appendages of Mammals and Birds
- Kinetics and Equilibrium of Solute Diffusion into Human Hair
- The Complexities of Iron Deficiency in Patients After Bariatric Surgery
- Vibrational Raman and IR data on brown hair subjected to bleaching
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Allosteric interactions prime androgen receptor dimerization and activation
- Author response: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Ingredients of Trichological Shampoos with Alleged Beneficial Effects on Hair—What Is Really Known About Their Efficacy? A Scoping Review of an Area with More Unknowns than Knowns
- The Anti-Flyaway/Frizz Effect by Inducing the α-Helical Structure Transition of Hair
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Decision letter: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- 707 Chromatin remodeler Lymphoid-specific helicase (Lsh) is a critical determinant controlling postnatal epidermal growth, differentiation and response to injury
- [Endocrine constellation in androgenetic alopecia in the female].
- Fibroblasts: Origins, definitions, and functions in health and disease
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- The human skin as a hormone target and an endocrine gland
- Proteome Analysis of Human Hair Shaft
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair