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Research 901–930 of 1000+
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Comparative Anatomy of Mouse and Human Nail Units
- Sculpting the future: A narrative review of 3D printing in plastic surgery and prosthetic devices
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- The Use of Stem Cells in Plastic and Reconstructive Surgery
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Overview of Urethral Reconstruction by Tissue Engineering: Current Strategies, Clinical Status and Future Direction
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Rejuvenation: an integrated approach to regenerative medicine
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- AAPS and PSRC 2016 Abstract Supplement
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Prevention of Frey syndrome with superficial temporal fascia interpositioning: a retrospective study
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Serum brain‐derived neurotrophic factor and vitamin D: Two concordant players controlling depression among alopecia areata and vitiligo patients: A case–control study
- Establishment of Tsc2-deficient rat embryonic stem cells
- Molecular Genetics of Human Hair Diseases
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- The molecular basis of human keratin disorders
- Lipid-Based Drug Delivery Systems in Regenerative Medicine
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- RETRACTED: Tanshinone IIA Pretreatment Renders Free Flaps against Hypoxic Injury through Activating Wnt Signaling and Upregulating Stem Cell-Related Biomarkers
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Trichothiodystrophy without associated neuroectodermal features in two siblings