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Research 31–60 of 1000+
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Acne
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Pathways to inflammation: acne pathophysiology
- The endocrinology of baldness
- COVID‐19, androgens, and androgenic alopecia
- The Molecular Basis of Androgen Insensitivity
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- SNP variation in male pattern hair loss in Russians with different dihydrotestosterone levels
- Molecular genetics of androgen insensitivity
- Androgens and androgen receptor action in skin and hair follicles
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Idiopathic Hirsutism*
- UPDATE ON IDIOPATHIC HIRSUTISM: DIAGNOSIS AND TREATMENT
- Methotrexate in dermatology
- In situ labeling of DNA reveals interindividual variation in nuclear DNA breakdown in hair and may be useful to predict success of forensic genotyping of hair
- Dermatological manifestations associated with pregnancy
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- Social selection favours offspring prone to the development of androgenetic alopecia.
- Genetics of Diabetes in Childhood
- Androgen receptor genetic variant predicts COVID‐19 disease severity: a prospective longitudinal study of hospitalized COVID‐19 male patients