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Research 481–510 of 1000+
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Whole-Cell Bioprocessing of Human Fetal Cells for Tissue Engineering of Skin
- Prevalence, Phenotypes, and Comorbidities of Polycystic Ovary Syndrome Among Indian Women
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- A review of the cosmetic use and potentially therapeutic importance of hyaluronic acid
- Common Variants in the Sex Hormone-Binding Globulin (SHBG) Gene Influence SHBG Levels in Women with Polycystic Ovary Syndrome
- Chronic Treatment with Minoxidil Induces Elastic Fiber Neosynthesis and Functional Improvement in the Aorta of Aged Mice
- Current Status of PRP Manufacturing Requirements & European Regulatory Frameworks: Practical Tools for the Appropriate Implementation of PRP Therapies in Musculoskeletal Regenerative Medicine
- Pharmacological Efficacy of Tamarix aphylla: A Comprehensive Review
- Permeation of topically applied Magnesium ions through human skin is facilitated by hair follicles
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Chronic administration of minoxidil protects elastic fibers and stimulates their neosynthesis with improvement of the aorta mechanics in mice
- Molecular basis of congenital atrichia in humans and mice.
- Medicalized Aesthetic Uses of Exosomes and Cell Culture-Conditioned Media: Opening an Advanced Care Era for Biologically Inspired Cutaneous Prejuvenation and Rejuvenation
- Process Optimization and Efficacy Assessment of Standardized PRP for Tendinopathies in Sports Medicine: Retrospective Study of Clinical Files and GMP Manufacturing Records in a Swiss University Hospital
- A Unique Expression of Keratin 14 in a Subset of Trophoblast Cells
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- A comprehensive guide to upper lip aesthetic rejuvenation
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Fractional ablative CO<sub>2</sub> laser and oral isotretinoin—A prospective randomized controlled split‐face trial comparing concurrent versus delayed laser treatment for acne scars
- Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
- Associations between clinical data, vaccination status, antibody responses, and post-COVID-19 symptoms in Thais infected with SARS-CoV-2 Delta and Omicron variants: a 1-year follow-up study
- Eyes open on stem cells
- CD34 and BerEP4 Are Helpful to Distinguish Basaloid Tricholemmoma From Basal Cell Carcinoma