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Research 181–210 of 1000+
- Inflammatory priming enhances mesenchymal stromal cell secretome potential as a clinical product for regenerative medicine approaches through secreted factors and EV-miRNAs: the example of joint disease
- Natural killer cells in atopic and autoimmune diseases of the skin
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Insulin Resistance and Skin Diseases
- Human Hair and the Impact of Cosmetic Procedures: A Review on Cleansing and Shape-Modulating Cosmetics
- Leveraging nature’s nanocarriers: Translating insights from extracellular vesicles to biomimetic synthetic vesicles for biomedical applications
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Alopecias in lupus erythematosus
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Ovarian SAHA syndrome is associated with a more insulin-resistant profile and represents an independent risk factor for glucose abnormalities in women with polycystic ovary syndrome: A prospective controlled study
- Through the lens of hair follicle neogenesis, a new focus on mechanisms of skin regeneration after wounding
- Hedgehog signaling reprograms hair follicle niche fibroblasts to a hyper-activated state
- The Genetics of Human Skin Disease
- Expression Profiles of Reproduction- and Thyroid Hormone-Related Transcripts in the Brains of Chemically-Induced Intersex Frogs
- British Association of Dermatologists guidelines for the management of people with cutaneous lupus erythematosus 2021
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Celsr1 and Celsr2 exhibit distinct adhesive interactions and contributions to planar cell polarity
- Utility of GLI1 RNA Chromogenic in Situ Hybridization in Distinguishing Basal Cell Carcinoma From Histopathologic Mimics
- Identifying barriers and disparities in the healthcare of patients with alopecia areata: a mixed-methods analysis using claims data and qualitative interview data
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Sexual Dysfunction in Polycystic Ovary Syndrome (PCOS): A Biopsychosocial Approach to Assessment and Management
- Overlapping features of atopic dermatitis and alopecia areata: from pathogenesis to treatment
- UTX (KDM6A) promotes differentiation noncatalytically in somatic self-renewing epithelia
- eLife assessment: CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Store-operated calcium channels in skin
- Author response: Plant Trans-Golgi Network/Early Endosome pH regulation requires Cation Chloride Cotransporter (CCC1)