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Research 331–360 of 1000+
- GCN5-mediated H3K27cr regulates hair follicle stem cell migration and hair follicle development through KRT80 activation
- Painful thickened skin on the soles of the feet
- Hypotrichosis and Hair Loss on the Occipital Scalp
- 591 Chromatin architectural protein CTCF regulates terminal keratinocyte differentiation in the developing epidermis and hair follicles
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- 839 Spatiotemporal antagonism in mesenchymal-epithelial Signaling in sweat versus hair fate decision
- 837 From genotoxic stresses to skin damage: Distinct, novel mechanisms of skin and hair damage in chemo/radiation therapy
- Clinical Snippets
- Progress on hair follicle stem cells
- Dynamic analysis of skin transcriptome in Xinjiang goats and functional verification of ELOVL3 in dermal papilla cell proliferation
- Whole transcriptome sequencing of different hair types in inner Mongolian cashmere goats
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals
- 260 Anti-OX40 monoclonal antibody IMG-007 exhibited clinical activity of hair regrowth, suppressed scalp inflammatory biomarkers in patients with severe alopecia areata in a Ph1b/2a study
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- Few Simple Sequence Repeats in Human Hair
- Hair Anomalies in a 6-Year-Old Girl
- The Naked (N) Mutation, Chromosome 15
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Epidermolysis bullosa in calves in the United Kingdom
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Steatocystoma Multiplex
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- <i>Hoxc13</i> and the development of hair follicle
- Atrichia with papular lesions
- Early Dengue Virus Infection in Human Skin: A Cycle of Inflammation and Infectivity