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Research 121–150 of 227
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Genetically modified laboratory mice with sebaceous glands abnormalities
- New developments in the molecular treatment of ichthyosis: review of the literature
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Iron Metabolism of the Skin: Recycling versus Release
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Off-label uses of retinoids in dermatology
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Medical Dermatology
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- <i>In vivo</i> response of GsdmA3<sup>Dfl</sup>/+ mice to topically applied fish oil – effects on cellular markers and macrophages
- Current Genetics in Hair Diseases
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Keratosis Pilaris-like Eruption during Treatment of Chronic Myeloid Leukemia with Tyrosine Kinase Inhibitors: Literature Review and Report of a Case Related to Imatinib
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- The molecular basis of human keratin disorders
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Hair follicles modulate skin barrier function
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- First Symposium of Ichthyosis Experts
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Extensive Ichthyosiform Sarcoidosis in a Patient With Juvenile Rheumatoid Arthritis
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- [Black piedra in South Africa. 1st description in a child with bamboo hair, pili torti and congenital erythroderma ichthyosiforme].