Search
for
Sort by
Research 931–960 of 1000+
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Scalp whorls
- The Basic Science of Hair Biology
- Advanced therapies of skin injuries
- LSD1 is Required for Hair Cell Regeneration in Zebrafish
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Female pattern hair loss: Clinico-laboratory findings and trichoscopy depending on disease severity
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- Signalling by senescent melanocytes hyperactivates hair growth
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Platelet-Rich Plasma for Treating Androgenic Alopecia: A Systematic Review
- Central Centrifugal Cicatricial Alopecia: New Insights and a Call for Action
- Hidradenitis Suppurativa
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- Three Streams for the Mechanism of Hair Graying
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- The biology of hair shape
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- Stem cells and aberrant signaling of molecular systems in skin aging
- Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome
- Genome-wide association study of skin complex diseases
- Central Centrifugal Cicatricial Alopecia: Retrospective Chart Review
- In vivo reflectance confocal microscopy: usefulness for diagnosing hair diseases
- Safe Selection of Genetically Manipulated Human Primary Keratinocytes with Very High Growth Potential Using CD24
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- Distinct mechanisms underlie pattern formation in the skin and skin appendages