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Research 211–240 of 1000+
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Small extracellular vesicles from mesenchymal stem cells: A potential Weapon for chronic non-healing wound treatment
- Regulation of Semaphorin3A in the process of cutaneous wound healing
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Bladder cancer survival in men using 5-alpha-reductase inhibitors
- Adrenal causes of endocrine hypertension in childhood or adolescence
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- 137 Loss of myeloid Mcpip1 suppresses hair growth and development of epidermal papilloma of the skin
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Multi-omics and AI-driven advances in miRNA-mediated hair follicle regulation in cashmere goats
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- A general mathematical model for the in vitro assembly dynamics of intermediate filament proteins
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Overexpression of hepatoma-derived growth factor in melanocytes does not lead to oncogenic transformation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Bone morphogenetic protein-2 (BMP-2) transactivates Dlx3 through Smad1 and Smad4: alternative mode for Dlx3 induction in mouse keratinocytes
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Time-course RNA-seq analysis reveals stage-specific and melatonin-triggered gene expression patterns during the hair follicle growth cycle in Capra hircus
- Stimuli-responsive nanoformulations for CRISPR-Cas9 genome editing
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- Current Genetics in Hair Diseases