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Research 361–390 of 1000+
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Diseases of Hair
- Diseases of Hair
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Dynamic expression of Runx1 in skin affects hair structure
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- The Proteins of Normal and Aberrant Hair Keratins
- New developments in the molecular treatment of ichthyosis: review of the literature
- Whole blood transcriptome profiling identifies candidate genes associated with alopecia in male giant pandas (Ailuropoda melanoleuca)
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- E-Poster
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- A decade of neglecting sublingual mass: A case report of epidermoid cyst
- Aging in the sebaceous gland
- Dermatology Patient Support Groups
- The biology and genetics of curly hair
- Animal and in vitro Models for the Study of Hair Follicles
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Madarosis: A marker of many Maladies
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Eyebrow Loss
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology