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Research 211–240 of 1000+
- Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Approach to androgen excess in women: Clinical and biochemical insights
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- Biomedical applications of organoids in genetic diseases
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Progress in Research and Prospects for Application of Precision Gene-Editing Technology Based on CRISPR–Cas9 in the Genetic Improvement of Sheep and Goats
- Aqueous Dispersion of Unmodified Fullerene C60: Stimulation of Hair Growth and Study of a New Molecular Target for Interaction
- Cutaneous wound healing: recruiting developmental pathways for regeneration
- Biotin and biotinidase deficiency
- Fibroblast growth factors: key players in regeneration and tissue repair
- What’s Sex Got to Do With COVID-19? Gender-Based Differences in the Host Immune Response to Coronaviruses
- TRP Channels in Skin Biology and Pathophysiology
- Targeting of Smoothened for therapeutic gain
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Unmet Medical Needs in Chronic, Non-communicable Inflammatory Skin Diseases
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- S100A4/Nonmuscle Myosin IIA/p53 Axis Contributes to Aggressive Features in Ovarian High-Grade Serous Carcinoma
- SOCS1 and SOCS3 as key checkpoint molecules in the immune responses associated to skin inflammation and malignant transformation