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Research 181–210 of 329
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- E-Poster
- Decay of Skin-Specific Gene Modules in Pangolins
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Oral Presentations
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Trichoscopy in Hair Shaft Disorders
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Hair cycle control by leptin as a new anagen inducer
- Morpho-Regulation of Ectodermal Organs
- Proteome Analysis of Human Sebaceous Follicle Infundibula Extracted from Healthy and Acne-Affected Skin
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- 5α-Reduced glucocorticoids: a story of natural selection
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Long-term dutasteride therapy in men with benign prostatic hyperplasia alters glucose and lipid profiles and increases severity of erectile dysfunction
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Follikelhormone
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Function and underlying mechanisms of seasonal colour moulting in mammals and birds: what keeps them changing in a warming world?
- A curated catalog of canine and equine keratin genes
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development