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Research 121–150 of 749
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- LITERATURE REVIEW
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- An overview of zinc and its importance in dermatology-Part II: The association of zinc with some dermatologic disorders
- Topical L‐thyroxine: The Cinderella among hormones waiting to dance on the floor of dermatological therapy?
- The spectrum of nephrocutaneous diseases and associations
- Hair and scalp disorders
- Posters Presented at the 19th Joint Meeting of the International Society of Dermatopathology, March 2–3, 2016, Hilton Crystal City at Washington Reagan National Airport, Arlington, Virginia, USA
- Clinical Management in Psychodermatology
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- The molecular basis of human keratin disorders
- Keratins: the hair shaft's backbone revealed
- First Symposium of Ichthyosis Experts
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- The epidermis: rising to the surface
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Ichthyosis
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- “Degeneration” in Dermatopathology