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Research 391–420 of 1000+
- Jojoba (Simmondsia chinensis (Link) Schneider): An important Medicinal Plant- The Gold of the Desert
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Needle mesotherapy in adjunctive treatment of Androgenic Alopecia
- Therapeutic Efficacy and Safety of Platelet-Rich Plasma (PRP) for Hair Restoration: A Narrative Review
- Pharmacology of Induced Artificial Platelets in Regenerative Medicine: Beyond Transfusion
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Biology of Human Hair: Know Your Hair to Control It
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Trypanocidal Effect of Isotretinoin through the Inhibition of Polyamine and Amino Acid Transporters in Trypanosoma cruzi
- Induction of dermal fibroblasts into dermal papilla cell-like cells in hydrogel microcapsules for enhanced hair follicle regeneration
- Novel type 1 5a-reductase Inhibitors with Antiproliferative Potential on LNCaP cells
- Estudio de factibilidad para la creación de una clínica de implante capilar en Bogotá: Modelo de accesibilidad y calidad
- The Gut-Scalp Axis: A Systematic Review of Dietary Interventions on Microbiome Dysbiosis in Scalp Disorders
- Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Characterisation of Four New Genes in the Ovine KAP19 Family
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- In situ labeling of DNA reveals interindividual variation in nuclear DNA breakdown in hair and may be useful to predict success of forensic genotyping of hair
- Chronic overlapping pain conditions and nociplastic pain
- Adult Male Hypogonadism: A Laboratory Medicine Perspective on Its Diagnosis and Management
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Comparative biology of tissue repair, regeneration and aging
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits