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Research 721–750 of 1000+
- Progeroide Syndrome
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- The urine as a diagnostic key for a homozygous EGFR mutation
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Causality of Aging Hallmarks
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Metabolomic analysis of SMP30/GNL knockout mice treated with fermented vegetable and fruit extract (OM-X®)
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Rac-dependent signaling from keratinocytes promotes differentiation of intradermal white adipocytes
- SOX2 in the Skin
- Melanocytes and Vitiligo (and Hair Graying)
- The Skin and Subcutaneous Tissues
- Stem Cells and their Niches
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Evidence for murine cutaneous immune surveillance localized to hair follicle epithelium
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Editorial: Exploring innovative therapies for rare inflammatory skin diseases
- A regenerative stem cell-derived matrix accelerates functional dermal wound repair in a preclinical diabetic model
- Ca <sup>2+</sup> -mediated protein citrullination regulates proliferation in the regenerating and malignant CNS
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Concomitant acute alopecia and profound bone marrow suppression: An unusual manifestation of azathioprine toxicity
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerism
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan