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Research 61–90 of 495
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Acne-Associated Syndromes
- Abstracts
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Acne: Hormonal concepts and therapy
- Function and underlying mechanisms of seasonal colour moulting in mammals and birds: what keeps them changing in a warming world?
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Recent advances in oxasteroids chemistry
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Stereocontrolled synthesis of all eight stereoisomers of the putative anti-androgen cyoctol
- Association of Gly972Arg variant of insulin receptor subtrate-1 and Gly1057Asp variant of insulin receptor subtrate-2 with polycystic ovary syndrome in the Chinese population
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- Monocyclic Aromatic Compounds
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Alopecia Areata: Current Review
- Chronic graft-versus-host disease – the role of dermatological treatment
- Miscellaneous Steroids
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- In vitro hair growth-promoting effects of araliadiol via the p38/PPAR-γ signaling pathway in human hair follicle stem cells and dermal papilla cells
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Poster Presentations
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- β-Catenin Signaling Evokes Hair Follicle Senescence by Accelerating the Differentiation of Hair Follicle Mesenchymal Progenitors