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Research 181–210 of 1000+
- Local and Systemic Reduction by Topical Finasteride or Flutamide of Hamster Flank Organ Size and Enzyme Activity
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- JAK kinase pathway inhibitor drugs in patients with moderate-to-severe alopecia: a real-world experience
- Epidermal Notch1 recruits innate lymphoid cells to orchestrate normal skin repair
- Interventions for nail psoriasis
- Main Plenary Sessions: Summaries of Papers
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- Genetic and molecular aspects of androgenetic alopecia
- Insight into the pathogensis of polycystic ovarian syndrome
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Hox genes in development and beyond
- Predicting Physical Appearance from Low Template: State of the Art and Future Perspectives
- A State-of-the-Art Overview on (Epi)Genomics and Personalized Skin Rejuvenating Strategies
- DNA Damage-Inducible Transcript 4 Is an Innate Surveillant of Hair Follicular Stress in Vitamin D Receptor Knockout Mice and a Regulator of Wound Re-Epithelialization
- The Role of Probiotics and Synbiotics on Hirsutism
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Novel Insights into TSC22D Family Genes in Metabolic Diseases and Cancer
- FOXN1 deficient nude severe combined immunodeficiency
- Polycystic ovary syndrome
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- The Distribution of Estrogen Receptor β Is Distinct to That of Estrogen Receptor α and the Androgen Receptor in Human Skin and the Pilosebaceous Unit
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.