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Research 391–420 of 1000+
- Clinical cases of Darier-White follicular dyskeratosis
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- TERMIS ‐ AMERICAS Toronto, Ontario, Canada July 10–13, 2022
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Highlights
- Two females with hair loss
- Hypotrichosis in a child with olmsted syndrome
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Research Snippets
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Pathways to inflammation: acne pathophysiology
- The nude gene and the skin
- Gain‐of‐function variants in the <i>ODC1</i> gene cause a syndromic neurodevelopmental disorder associated with macrocephaly, alopecia, dysmorphic features, and neuroimaging abnormalities
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- New treatments for rheumatoid arthritis
- Comparison of Saccharina japonica–Undaria pinnatifida Mixture and Minoxidil on Hair Growth Promoting Effect in Mice
- The clock gene brain and muscle Arnt-like protein-1 (BMAL1) is involved in hair growth
- Acne
- Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish
- Restoration of hair follicle inductive properties by depletion of senescent cells
- High-Throughput Screening for Discovering Small Molecules Capable of Increasing the Wnt/β-Catenin Signaling Pathway to Promote Hair and Nail Growth
- Androgenetic Alopecia in Men: An Update On Genetics
- Concept of tinea capitis
- Alopecia androgénica femenina: nuevos factores fisiopatológicos y futuras tendencias para un abordaje clínico más integral
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- A genetic test for androgenetic alopecia: polymorphisms in the androgen receptor gene provide a genetic screening test for androgenetic alopecia and earlier medical intervention
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene