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Research 631–660 of 1000+
- Green and Emerging Microextraction Strategies for Bioanalytical Determination of Hormones: Trends, Challenges, and Applications
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
- Genetically separable determinants of hair keratin gene expression
- Differential Expression of MITF, WNT3A, SLC7A11, and EDN3 in the Shoulder ‘Bider Marking’ of Dun Mongolian Horses
- Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere goats
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Disorders of Keratinization
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Multi-Walled Carbon Nanotubes Can Promote Brassica napus L. and Arabidopsis thaliana L. Root Hair Development through Nitric Oxide and Ethylene Pathways
- Restoration of Hair Luster via Novel Biomarker COL7A1 by Minoxidil, Caffeine, and Biotin
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Identification of Genes Related to Hair Follicle Cycle Development in Inner Mongolia Cashmere Goat by WGCNA
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- A newborn presenting with congenital blistering
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Functional Interpretation of Genome-Wide Association Study Evidence in Alopecia Areata
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Lung Cancer Awareness Symposium Highlights Necessary Focus Areas for Research
- Wounding induces dedifferentiation of epidermal Gata6+ cells and acquisition of stem cell properties
- Drug Repurposing for Rare Diseases
- Quantitation of human mitochondrial DNA and whole mtGenomes sequencing of fingernail/hair shaft samples
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Genomic and phenotypic characterization of Investigator Global Assessment (IGA) scale-based endotypes in atopic dermatitis
- Re‐Innovation in Clinical Trial Designs Based on Precision Therapy
- Adverse effects of the 5-alpha-reductase inhibitor finasteride on Daphnia magna: Endocrine system and lipid metabolism disruption
- Synaptic processes and immune-related pathways implicated in Tourette Syndrome
- A new type of pachyonychia congenita.