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Research 121–150 of 1000+
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Androgens and hair loss
- UTX (KDM6A) promotes differentiation noncatalytically in somatic self-renewing epithelia
- El papel de los inhibidores de JAK en la alopecia areata: revisión de la literatura
- Chapter 6. Darwinian Health and Other Contradictions
- Androgen receptors and their biology
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Winding the clock back on female androgenetic alopecia
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- How a Bird Gets Its Feathers: Insights from Chromatin Looping
- Cutaneous signals of immune system disease
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Ritlecitinib: First Approval
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Regulation of masculinization: androgen signalling for external genitalia development
- PBX homeobox 1 enhances hair follicle mesenchymal stem cell proliferation and reprogramming through activation of the AKT/glycogen synthase kinase signaling pathway and suppression of apoptosis
- Characterization of the Human Hair Shaft Cuticle–Specific Keratin-Associated Protein 10 Family
- The pioneer factor SOX9 competes for epigenetic factors to switch stem cell fates
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Dermatologic care of patients with differences of sex development
- Genetics of Diabetes in Childhood