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Research 151–180 of 1000+
- Mutant Cx43 in Skin Differentiation and Disease
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Toxic and Metabolic Disorders of the Nervous System
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Dermatoses in overweight and obese children and their relationship with insulin and skin color
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Cutaneous disorders related to obesity
- The molecular basis of human keratin disorders
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- A systematic review and meta-analysis on the effects of the ultra-pulse CO2 fractional laser in the treatment of depressed acne scars
- Ectodermal Dysplasia: Variable Expressions
- Lack of classic histology should not prevent diagnosis of necrolytic acral erythema
- Folliculotropic CD8+ mycosis fungoides associated with diffuse mucosal involvement
- Digital Pseudopad Correction in a Dog Using a CO <sub>2</sub> Laser
- Cutaneous manifestations of endocrine diseases in children
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Secondary Syphilis in Cali, Colombia: New Concepts in Disease Pathogenesis
- Endogenous retinoids in the hair follicle and sebaceous gland
- Disorders of Keratinization
- Alopecia secondary to anti-tumor necrosis factor-alpha therapy
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism