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Research 721–750 of 1000+
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- What′s new in cicatricial alopecia?
- Congenital adrenal hyperplasia
- ROR2 regulates self-renewal and maintenance of hair follicle stem cells
- Alopecia Areata of the Beard: A Review of the Literature
- Permanent diffuse alopecia after haematopoietic stem cell transplantation in childhood
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- CD133-positive dermal papilla-derived Wnt ligands regulate postnatal hair growth
- Indian Hedgehog Controls Proliferation and Differentiation in Skin Tumorigenesis and Protects against Malignant Progression
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Spontaneous cutaneous adverse drug reaction reports—An analysis of a 10‐year dataset in Singapore
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Hirsutism in the Adolescent Female
- Stem Cell Competition for Niche Occupancy: Emerging Themes and Mechanisms
- Biology of Human Hair: Know Your Hair to Control It
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Alcohol Exposure During Late Adolescence Increases Drinking in Adult Wistar Rats, an Effect that is not Reduced by Finasteride
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Drug eruptions in dermatology
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- The Biology of Hair Growth
- Molecular functional analyses revealed essential roles of HSP90 and lamin A/C in growth, migration, and self-aggregation of dermal papilla cells
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling