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Research 16
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Increased Expression of TSPEAR in Colorectal Cancer Predicts Poor Prognosis
- Increased Expression of TSPEAR in Colorectal Cancer Predicts Poor Prognosis
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Notch Signaling in Hair Follicle Development
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- Genomic Characterization of Quality Wool Traits in Spanish Merino Sheep
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Comprehensive analysis of the expression profiles of mRNA, lncRNA, circRNA, and miRNA in primary hair follicles of coarse sheep fetal skin
- Are hair follicle stem cells promising candidates for wound healing?