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Research 781–810 of 1000+
- Light-Emitting Hair Follicles: Studying Skin Regeneration With In Vivo Imaging
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- The Catalog of Human Hair Keratins
- Host-microbiome interactions and recent progress into understanding the biology of acne vulgaris
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- Independent genomewide screens identify the tumor suppressor VTRNA2-1 as a human epiallele responsive to periconceptional environment
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Dynamic interplay between IL-1 and WNT pathways in regulating dermal adipocyte lineage cells during skin development and wound regeneration
- Lymphatic vessels interact dynamically with the hair follicle stem cell niche during skin regeneration <i>in vivo</i>
- Control by a hair’s breadth: the role of microRNAs in the skin
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Regulatory T cells in dominant immunologic tolerance