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Research 871–900 of 1000+
- Study of seed hair growth in Populus tomentosa, an important character of female floral bud development
- Characterization of metabolic changes in the phenotypes of women with polycystic ovary syndrome in a large Mediterranean population from Sicily
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Morpho‐regulation in diverse chicken feather formation: Integrating branching modules and sex hormone‐dependent morpho‐regulatory modules
- Update on Melasma—Part I: Pathogenesis
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Efficient Gene Editing for Heart Disease via ELIP-Based CRISPR Delivery System
- Current Perspectives on Less-known Aspects of Headache
- Retrospective Study about the Causes and the Effects of Korean Medicine Treatment on Alopecia - Focused on Acquired Febrile Alopecia -
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- Rare Gli1+ perivascular fibroblasts promote skin wound repair
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- Comparative Skin Transcriptomics Reveals Key Regulators of Cashmere Fiber Production in Inner Mongolian Goats
- Integrated multiomics analysis reveals the molecular features and crucial regulators of hair follicles in yak (Bos grunniens)
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Effects of biomaterials derived from germinated hemp seeds for stressed hair stem cells and immune cells
- Alopecia Universalis with Frequently Relapsing Nephrotic Syndrome of Infantile Onset: A Rare Presentation
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Protein-Losing Enteropathy, Anasarca and Dermatological Manifestations on People of Advanced Age: Don't Overlook the Diagnostic Hypothesis of a Cronkhite Canada Syndrome
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Myotonic dystrophy type 1
- Gene polymorphisms and serum levels of BDNF and CRH in vitiligo patients
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- The color of human hair
- Multiscale spatial mapping of cell populations across anatomical sites in healthy human skin and basal cell carcinoma
- Editorial Comment