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Research 691–720 of 1000+
- Systemic lupus erythematosus presenting with homonymous hemianopia
- Rare and misdiagnosed entity fibrosing alopecia in a pattern distribution: A case report
- Does D matter? The role of vitamin D in hair disorders and hair follicle cycling
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Ptosis in childhood
- Insights from Tandem Mass Tag (TMT) Proteomic Analysis on Protein Network Modification in Control of Yak Hair Follicle Cycle
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- The JAK/STAT signaling pathway: from bench to clinic
- Challenges and Strategies for Improving the Regenerative Effects of Mesenchymal Stromal Cell-Based Therapies
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Dermoscopy in General Dermatology: A Practical Overview
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Hair follicle immune privilege and its collapse in alopecia areata
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Frizzled Receptors in Development and Disease
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Aging of the hair follicle pigmentation system
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin