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Research 601–630 of 1000+
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- Associations between type 1 diabetes and autoimmune skin diseases: Mendelian randomization analysis
- Association between genetically predicted leukocyte telomere length and non-scarring alopecia: A two-sample Mendelian randomization study
- RETRACTED: Genetic association between asthma and alopecia areata: A two‐sample Mendelian randomization study
- Serum interleukin-37 and its gene polymorphism (rs3811047) in Egyptian patients with alopecia areata
- Hair Growth Regulation by Fibroblast Growth Factor 12 (FGF12)
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Causal Link of Distinct Mental Disorders with Androgenetic Alopecia and Alopecia Areata: A Bidirectional Two-Sample Mendelian Randomization Study
- Genetic variants in androgenetic alopecia: insights from scalp RNA sequencing data
- Exploring the Relationship Between Immune Cells and Non-Scarring Hair Loss: A Mendelian Randomization Study
- Elucidating causal relationships of diet-derived circulating antioxidants and the risk of non-scarring alopecia: A Mendelian randomization study
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Relationship between the level of vitamin D in bloof flow and skin dermatosis
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- The biology and genetics of curly hair
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Disentangling the Coronavirus Disease 2019 Health Disparities in African Americans: Biological, Environmental, and Social Factors
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Genetic and molecular aspects of androgenetic alopecia
- The Genetic Architecture of Alopecia Areata
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study
- Transcriptome meta-analysis reveals the hair genetic rules in six animal breeds and genes associated with wool fineness