Search
for
Sort by
Research 961–990 of 1000+
- A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- The Mask Mutation Identifies TMPRSS6 as an Essential Suppressor of Hepcidin Gene Expression, Required for Normal Uptake of Dietary Iron.
- 494 Epidermolysis bullosa pruriginosa, muscular dystrophy, and immune-mediated myasthenia gravis in a patient with homozygous nonsense PLEC mutation
- 1391 Immune cells may have a role in hair loss process caused by TRPV3 gain-of-function mutation
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- MENSTRUAL DISORDERS IN ADOLESCENTS
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Hair physiology and its disorders
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Genetic Variants and Protective Immunity against SARS-CoV-2
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Hair Graying: Mechanisms, Prevention, and Innovative Treatment Strategies – literature review
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Genetic Control/Involvement in Hair Fiber Traits
- Research progress on mechanisms of skin aging and anti-aging strategies
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Modulating the stem cell niche for tissue regeneration
- The Rotterdam Study: 2018 update on objectives, design and main results
- The Rotterdam Study: 2016 objectives and design update
- Stem Cells and the Niche: A Dynamic Duo
- Alopecia areata
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth