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Research 30 of 39
- Transcriptome analysis of frontal fibrosis alopecia revealed involvement of immune cells and ferroptosis
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Transcriptomic analysis of human skin wound healing and rejuvenation following ablative fractional laser treatment
- A preliminary study of differentially expressed genes in expanded skin and normal skin: implications for adult skin regeneration
- Role of skin enzymes in metabolism of topical drugs
- Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids
- The Rotterdam Study: 2012 objectives and design update
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation
- Sterol Intermediates of Cholesterol Biosynthesis Inhibit Hair Growth and Trigger an Innate Immune Response in Cicatricial Alopecia
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- A multi-omic single-cell landscape of perinatal mouse skin maps lineage specification and reveals shared dynamics in human fetal skin
- TYK2 Inhibition with Deucravacitinib Improves Clinical Outcomes and Resolves Interferon-Driven Inflammation in Lichen Planopilaris
- Gut–ovary axis and multiomic insights into PCOS in a DHEA-induced rat model
- Modelling androgen synthesis and action during human sexual differentiation
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- <i>In vivo</i> response of GsdmA3<sup>Dfl</sup>/+ mice to topically applied fish oil – effects on cellular markers and macrophages
- ENZYMES
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- 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
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis