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Research 121–150 of 1000+
- Genetic Variants and Lifestyle Factors in Androgenetic Alopecia Patients: A Case–Control Study of Single Nucleotide Polymorphisms and Their Contribution to Baldness Risk
- Commentary
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Woolly hair generalizado: caso clínico e revisão da literatura
- The Rotterdam Study: 2016 objectives and design update
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Distinct stem cells contribute to mammary gland development and maintenance
- Alopecia Areata
- The Rotterdam Study: 2018 update on objectives, design and main results
- Alopecia areata
- The Rotterdam Study: 2012 objectives and design update
- Genetic Disorders and Defects in Vitamin D Action
- The Pathogenesis of Primary Cicatricial Alopecias
- Disruption of FGF5 in Cashmere Goats Using CRISPR/Cas9 Results in More Secondary Hair Follicles and Longer Fibers
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- THE PATHOGENESIS OF ALOPECIA AREATA
- Hair Loss in Women
- Ferreting out stem cells from their niches
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Perspectives of Kennedy's disease
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Congenital hair loss disorders: Rare, but not too rare
- Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis