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Research 481–510 of 1000+
- Identification of Distinct Immune Signatures and Chemokine Networks in Scalp Inflammatory Diseases
- Hair shaft disorders in children – An update
- Innovations in Stem Cell Therapy for Diabetic Wound Healing
- A Clinical Approach to Severe Insulin Resistance
- High-confidence cancer patient stratification through multiomics investigation of DNA repair disorders
- Stage‐specific regulation of Gremlin1 on the differentiation and expansion of human urinary induced pluripotent stem cells into endothelial progenitors
- Employee engagement: el reto de trabajar juntos
- FGF5 is a crucial regulator of hair length in humans
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- The TNFRSF1B Connection: Implications for Androgenetic Alopecia Pathogenesis and Treatment
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Removing all obstacles: A critical role for p53 in promoting tissue renewal
- Effective treatment of intractable diseases using nanoparticles to interfere with vascular supply and angiogenic process
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Animal models of human skin disease
- CRISPR/Cas9-Mediated Generation of <i>COL7A1</i>-Deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa.
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia.
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- <i>Sept4/</i> ARTS Regulates Stem Cell Apoptosis and Skin Regeneration
- Spiking dependence of SARS‐CoV‐2 pathogenicity on TMPRSS2
- Targeted inactivation of integrin-linked kinase in hair follicle stem cells reveals an important modulatory role in skin repair after injury
- Association between TLR1 polymorphisms and alopecia areata