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Research 511–540 of 1000+
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Hair loss in children.
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Human Hair Follicle and Epidermal Melanocytes Exhibit Striking Differences in Their Aging Profile which Involves Catalase
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Chronic overlapping pain conditions and nociplastic pain
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Regulation of masculinization: androgen signalling for external genitalia development
- FOXN1 deficient nude severe combined immunodeficiency
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- The molecular pathogenesis of Trichilemmal carcinoma
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- Predicting Human Appearance from DNA for Forensic Investigations
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Insight into the pathogensis of polycystic ovarian syndrome