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Research 31–60 of 1000+
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Keratosis follicularis spinulosa decalvans in a female
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Circle Hairs in a Patient with Multiple Myeloma
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Genetics of Inherited Ichthyoses and Related Diseases
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Oral Retinoids in Dermatology
- Skin changes in pediatric transplant patients
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Ectodermal Dysplasia: Variable Expressions
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Madarosis from mitochondriopathy
- Connexin mutations in human disease
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Surgical approach of ectropion in lamellar ichthyosis
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery