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Research 571–600 of 1000+
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study
- Conditional epidermal expression of TGFβ1 blocks neonatal lethality but causes a reversible hyperplasia and alopecia
- Polycystic Ovary Syndrome (PCOS) and Fertility
- A simple method using ex vivo culture of hair follicle tissue to investigate intrinsic circadian characteristics in humans
- Witnessed trauma exposure induces fear in mice through a reduction in endogenous neurosteroid synthesis
- Association between male pattern baldness and testicular germ cell tumor: a meta-analysis
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- The citrullinating enzyme PADI4 governs progenitor cell proliferation and translation in developing hair follicles
- Patched1 Functions as a Gatekeeper by Promoting Cell Cycle Progression
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Keratins and skin disease
- Role of FGFR2-signaling in the pathogenesis of acne
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Genetic Hair Disorders: A Review
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Skin Development and Disease: A Molecular Perspective
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Hair shaft disorders in children – An update
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: Oral Presentations
- Update on polycystic ovary syndrome
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- First Symposium of Ichthyosis Experts