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Research 181–210 of 1000+
- Genetic Markers of Male and Female Pattern Hair Loss
- Primary scarring alopecias. A literature review
- Skin wound healing in humans and mice: Challenges in translational research
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- The Genetic Architecture of Alopecia Areata
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- Lipedematous Alopecia: Clinical, Histopathological, and Trichoscopic Findings of a Single Case and Review of the Literature
- Debatable Topics in PCOS Patients
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Hair Graying: Mechanisms, Prevention, and Innovative Treatment Strategies – literature review
- Hormonal and Genetic Controls of Hirsutism: Link Between hyperprolactinemia, Polycystic ovary syndrome and Hirsutism
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities
- People’s experiences of eyebrow transplantation: A qualitative study
- Advances in the Molecular Pathogenesis and Targeted Therapy of Psoriasis
- The Specific Dermatoses of Pregnancy
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- Diagnosis and treatment of alopecia areata
- Two females with hair loss
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia
- Single-cell chromatin landscapes of mouse skin development
- Proceedings of the 7thworld congress of hair research