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Research 601–630 of 1000+
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Effects on Steroid 5-Alpha Reductase Gene Expression of Thai Rice Bran Extracts and Molecular Dynamics Study on SRD5A2
- Weight loss regimens that control for carbohydrate quality or quantity: a review
- Effects of a complex mixture prepared from agrimonia, houttuynia, licorice, peony, and phellodendron on human skin cells
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Untersuchungen der Fremdstoffbindung in permanenten Keratinozyten- und Melanozyten-Zelllinien sowie die Eignung von Primärkulturen aus humanen Haarfollikeln zur In-vitro-Messung der Fremdstoffaufnahme im Haar
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Predictive Metagenomic Profiling, Urine Metabolomics, and Human Marker Gene Expression as an Integrated Approach to Study Alopecia Areata
- Spironolactone and XPB: An Old Drug with a New Molecular Target
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- Therapies
- Effects of the Level and Composition of Concentrate Supplements before Breeding and in Early Gestation on Production of Different Hair Sheep Breeds
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Single-cell transcriptomics defines keratinocyte differentiation in avian scutate scales
- Transcriptomic regulation of seasonal coat color change in hares
- 14-3-3σ Is Required for Club Hair Retention
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Advances In Mesenchymal Cell Therapy In Dermatology And Aesthetic Medicine
- Barley disease susceptibility factor RACB acts in epidermal cell polarity and positioning of the nucleus
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- A new look into an old problem: keratins as tools to investigate determination, morphogenesis, and differentiation in skin.
- Frizzled Receptors in Development and Disease
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Conjoint analysis of methylation, transcriptomic, and proteomic profiles in pemphigus vulgaris