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Research 31–60 of 48
- Prefrontal 5α-reductase 2 mediates male-specific acute stress response
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- ENZYMES
- Genetic Insights into Acne, Androgenetic Alopecia, and Alopecia Areata: Implications for Mechanisms and Precision Dermatology
- Wasabi leaf extract changes the expression levels of cytokine related genes in dermal papilla cells, which identified by the whole transcriptome
- Integrated analysis of lncRNAs and mRNAs by RNA-Seq in secondary hair follicle development and cycling (anagen, catagen and telogen) of Jiangnan cashmere goat (Capra hircus)
- Keratinocytes of the Upper Epidermis and Isthmus of Hair Follicles Express Hemoglobin mRNA and Protein
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- Identification of N6-Methyladenosine-Related Factors and the Prediction of the Regulatory Mechanism of Hair Follicle Development in Rex and Hycole Rabbits
- Enzymes
- The Role of Linoleic Acid in Skin and Hair Health: A Review
- The Association of Hispanic Ethnicity with Nonalcoholic Fatty Liver Disease in Polycystic Ovary Syndrome
- The role of PEDF in ageing and development: reduction of oxidative damage and support for stem cells
- Rebamipide Induces Hair Regeneration Through EP4-Driven Lipid Metabolism Remodeling
- Intermittent fasting triggers interorgan communication to suppress hair follicle regeneration
- Autosomal recessive congenital ichthyosis due to <i>PNPLA1</i> mutation in a golden retriever–poodle cross‐bred dog and the effect of topical therapy
- Кореляційний аналіз взаємозв’язку хронічних дерматозів із соматичною патологією та обґрунтування детоксикаційної терапії
- Systemic Therapies for Scarring and Non-scarring Alopecia
- Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- New developments in the molecular treatment of ichthyosis: review of the literature
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients