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Research 451–480 of 1000+
- Cyclin‐dependent kinase 4 expression alters the number of keratinocyte stem cells in the mouse hair follicle
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Black Ginseng Concentrate Restores Hair Loss-Associated Dysfunction in Human Follicle Dermal Papilla Cells
- Epigenetic and transcriptional profiling of secondary hair follicle stem cells during cashmere growth
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Paxbp1 is Indispensable for the Maintenance of Hair Follicle Homeostasis
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Effects of Biomaterials Derived from Germinated Hemp Seeds on Stressed Hair Stem Cells and Immune Cells
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Utilising SNP Association Analysis as a Prospective Approach for Personalising Androgenetic Alopecia Treatment
- Insights into Alopecia Areata: A Systematic Review of Prevalence, Pathogenesis, and Psychological Consequences
- Männlicher Haarausfall – was uns unsere Gene verraten
- Mendelian randomization study highlights hypothyroidism as a causal determinant of alopecia areata
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Review on Alopecia Areata in the Middle East and Africa: Landscape and Unmet Needs
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- Monilethrix – Case report of a rare disease
- Hair Sciences: The hair cycle discussed with Dr. Gilliam Westgate
- Pathological Skin Scarring: From Mechanism to Targeted Local Therapy
- 5α-Reductase Isoenzymes: From Neurosteroid Biosynthesis to Neuropsychiatric Outcomes
- Androgenetic Alopecia and Risks of Overall and Aggressive Prostate Cancer: An Updated Systematic Review and Meta-Analysis
- 26-SNP Panel Aids Guiding Androgenetic Alopecia Therapy and Provides Insight into Mechanisms of Action
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome