Search
for
Sort by
Research 331–360 of 573
- The role of protein lactylation in skin diseases: from molecular mechanisms to potential therapeutics
- Development of a Novel Mouse Model for Hair Regeneration Using Glue-like Adhesive Materials
- Nanotechnological reprogramming of the pathological skin microenvironment in scar formation and atopic dermatitis
- Dermatological Manifestations of Celiac Disease: a Literature Review
- Impacto del desequilibrio del microbioma del cuero cabelludo en la severidad de la alopecia areata, marcadores inflamatorios y cambios post-tratamiento
- Androgenetic Alopecia
- 5-Alpha reductase deficiency
- JAK-inhibitors in the therapy of comorbid diseases – atopic dermatitis and alopecia areata: literature review and experience of clinical practice
- Sequence of a Cashmere goat type I hair keratin gene and its expression in skin
- Utilizing the hair follicle to dissect the regulation and autocrine/paracrine activities of prolactin in humans
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Altered Dermal Fibroblasts in Systemic Sclerosis Display Podoplanin and CD90
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor
- Skin Microbiome, Metabolome and Skin Phenome, from the Perspectives of Skin as an Ecosystem
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Regulation of Involucrin Gene Expression
- Short-Chain Fatty Acids from <i>Cutibacterium acnes</i> Activate Both a Canonical and Epigenetic Inflammatory Response in Human Sebocytes
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Autophagy Controls the Protein Composition of Hair Shafts
- Expression of caspase-14 and keratin-19 in the human epidermis and appendages during fetal skin development
- Role of DNA Methylation in the Pathogenesis of Skin Disorders: Mechanisms, Inhibitors of Methylation‐Related Enzyme, and Molecular Docking Studies
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- “Structural imprinting” of the cutaneous immune effector function
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- 078 The transmembrane protein LRIG1 regulates receptor tyrosine kinases in skin development and homeostasis
- Murine Cytomegalovirus is Not Associated With Alopecia Areata in C3H/HeJ Mice