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Research 91–120 of 1000+
- Registrars’ Symposium: Summaries of Papers
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Understanding autoimmunity of vitiligo and alopecia areata
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Alopecia Areata: A tissue specific autoimmune disease of the hair follicle
- Finding bald spots on chromosome 20p11
- 268 Male-pattern baldness and its association with coronary heart disease
- Associations between single-nucleotide polymorphisms of RFC-1, GGH, MTHFR , TYMS, and TCII genes and the efficacy and toxicity of methotrexate treatment in patients with rheumatoid arthritis
- Sacituzumab Govitecan-Hziy (Trodelvy™)
- Polycystic ovary syndrome is linked with the fat mass obesity (FTO) gene variants rs17817449 and rs1421085 in western Saudi Arabia
- WNT10B (wingless-type MMTV integration site family)
- 9. Immunology and Genetics
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- MC4R variants rs12970134 and rs17782313 are associated with obese polycystic ovary syndrome patients in the Western region of Saudi Arabia
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- Research Snippets
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- In response to the letter to the editor by Soha Ghanian et al. re our publication “Shorter androgen receptor polyQ alleles protect against life-threatening COVID-19 disease in European males”
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Central hair loss in African American women: Incidence and potential risk factors
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*