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Research 631–660 of 690
- Skin manifestations associated with COVID-19
- 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
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Melatonin induces a stimulatory action on the scrotal skin components of Soay ram in the non-breeding season
- Hair shaft disorders in children – An update
- A rare case of woolly hair with unusual associations
- Skin tissue engineering
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Congenital atrichia with papular lesions
- EGFR inhibitor-induced folliculitis decalvans: a case series and management guidelines
- Cutaneous toxicities of new targeted cancer therapies: must know for diagnosis, management, and patient-proxy empowerment
- Ichthyosis hystrix
- The origins of skin diversity: lessons from dermal fibroblasts
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Autologous smashed follicular dermal graft with epidermal cell suspension in chronic nonhealing leg ulcers
- Forsythiasides: A review of the pharmacological effects
- Claves diagnósticas en displasias pilosas II
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Congenital atrichia associated with nevus flammeus: A rare association
- Hair follicle epithelial stem cells contribute to interfollicular epidermis during homeostasis