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Research 931–960 of 1000+
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Progenitor Cell Dysfunctions Underlie Some Diabetic Complications
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- B-Raf and C-Raf Are Required for Melanocyte Stem Cell Self-Maintenance
- Endoplasmic reticulum stress at the crossroads of progeria and atherosclerosis
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Molecular Regulatory Mechanisms in Chicken Feather Follicle Morphogenesis
- Advancements and Applications of Injectable Hydrogel Composites in Biomedical Research and Therapy
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Dermatologic care of patients with differences of sex development
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- A Clinical Review of Trichorrhexis Nodosa
- A volatile producing Bacillus subtilis strain from the rhizosphere of Haloxylon ammodendron promotes plant root development
- Delayed Puberty
- Hair & Cutaneous Development
- Resurgent Clinical Science (and it's all about Health)
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- 14-3-3σ Is Required for Club Hair Retention
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- Congenital atrichia associated with situs inversus and mesocardia
- Rare clinical features of the Ellis van Creveld syndrome: A case report and literature review
- Connexin mutations in human disease
- Hypomorphic mutation in the hairless gene accelerates pruritic atopic skin caused by feeding a special diet to mice
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Hereditary Chorea Associated With and Aggravated by Systemic Lupus Erythematosus
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Ehlers-Danlos syndrome: From bedside to bench
- 1497 Type 2-mediated oxidative reprogramming promotes the transition of macrophages into repair mode and is required for wound healing