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Research 451–480 of 1000+
- Cutaneous manifestations of hypothyroidism: An observational study in a tertiary care center of Eastern India
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Root Hair Growth and Development in Response to Nutrients and Phytohormones
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Secondary Syphilis in Cali, Colombia: New Concepts in Disease Pathogenesis
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Lack of classic histology should not prevent diagnosis of necrolytic acral erythema
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Animals in Dermatology
- Cell death by cornification
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Genetic hair and nail disorders
- Two Mechanisms Regulate Keratin K15 Expression In Keratinocytes: Role of PKC/AP-1 and FOXM1 Mediated Signalling
- Immunofluorescent findings and clinical overlap in two cases of follicular lichen planus
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- Regionalisation of the skin
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- New developments in occupational dermatology
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Topical L‐thyroxine: The Cinderella among hormones waiting to dance on the floor of dermatological therapy?
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Congenital atrichia associated with situs inversus and mesocardia
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?