Search
for
Sort by
Research 31–60 of 56
- Matriptase-2, A Novel Suppressor of Hepcidin.
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Distinct Developmental Functions of Prostasin (CAP1/PRSS8) Zymogen and Activated Prostasin
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Congenital hair loss disorders: Rare, but not too rare
- Telogen effluvium in daily practice: Patient characteristics, laboratory parameters, and treatment modalities of 3028 patients with telogen effluvium
- Human Fetal Scalp Dermal Papilla Enriched Genes and the Role of R-Spondin-1 in the Restoration of Hair Neogenesis in Adult Mouse Cells
- Epidermal differentiation: The role of proteases and their inhibitors
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hair follicles modulate skin barrier function
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Pica for Uncooked Basmati Rice in Two Women with Iron Deficiency and a Review of Ryzophagia
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Current Genetics in Hair Diseases
- Iron–Skin Axis: Exploring the Interplay between Iron Homeostasis and Skin Disorders
- Identification of SLC40A1, LCN2, CREB5, and SLC7A11 as ferroptosis-related biomarkers in alopecia areata through machine learning
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- New developments in the molecular treatment of ichthyosis: review of the literature
- The secret identities of TMPRSS2: Fertility factor, virus trafficker, inflammation moderator, prostate protector and tumor suppressor