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Research 361–390 of 1000+
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Acute COVID-19 Syndrome Predicts Severe Long COVID-19: An Observational Study
- Hormonal and Genetic Etiology of Male Androgenetic Alopecia
- Molecular Targets in Modern Cosmetic Science
- Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects
- Stem Cell Secretome for Skincare: Of Cell Types, Exosomes, Extracellular Vesicles, and Soluble Fractions
- Emerging biomedical engineering strategies for hair follicle regeneration
- Molecular Morbidity Score–Can MicroRNAs Assess the Burden of Disease?
- Progress in Research and Prospects for Application of Precision Gene-Editing Technology Based on CRISPR–Cas9 in the Genetic Improvement of Sheep and Goats
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Bioactive Compound-Loaded Nanocarriers for Hair Growth Promotion: Current Status and Future Perspectives
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Topical minoxidil therapy in hereditary androgenetic alopecia
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Zinc‐responsive dermatosis in goats suggestive of hereditary malabsorption: two field cases
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- A Comparative Study of a New Food Supplement, ViviScal®, with Fish Extract for the Treatment of Hereditary Androgenic Alopecia in Young Males
- Topical minoxidil therapy for hereditary male pattern alopecia.
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature