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Research 181–210 of 1000+
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Chronic overlapping pain conditions and nociplastic pain
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Predicting Human Appearance from DNA for Forensic Investigations
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- This month in JAAD Case Reports: October 2023—Central centrifugal cicatricial alopecia in Black men
- Insight into the pathogensis of polycystic ovarian syndrome
- Keratin disorders: from gene to therapy
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- FOXN1 deficient nude severe combined immunodeficiency
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- Update on Melasma—Part I: Pathogenesis
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses