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Research 721–750 of 1000+
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Antiandrogenic activity of Riboflavin 5′-phosphate (FMN) in 22Rv1 and LNCaP human prostate cancer cell lines
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Whole-transcriptome analysis reveals the profiles and roles of coding and non-coding RNAs during hair follicle cycling in Rex rabbits
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Androgenetic Alopecia in Men: An Update On Genetics
- An <i>mTurq2-Col4a1</i> mouse model allows for live visualization of mammalian basement membrane development
- Involvement of DKK1 secreted from adipose‐derived stem cells in alopecia areata
- Keratinocytes of the Upper Epidermis and Isthmus of Hair Follicles Express Hemoglobin mRNA and Protein
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Topical Finasteride: A Comprehensive Review of Androgenetic Alopecia Management for Men and Women
- Endocrinology
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Cedrol restricts the growth of colorectal cancer <i>in vitro</i> and<i> in vivo</i> by inducing cell cycle arrest and caspase-dependent apoptotic cell death
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- Aberrant Activation of the Hedgehog Pathway in Cutaneous Melanoma: Therapeutic Potential of Pharmacological Inhibitors
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Pyruvate Kinase M2 Role in Cardiovascular Repair
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Foxn1 in Skin Development, Homeostasis and Wound Healing
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Game Changers: Blockbuster Small-Molecule Drugs Approved by the FDA in 2024
- The Role of Probiotics and Synbiotics on Hirsutism
- Spatiotemporal Labeling of Melanocytes in Mice
- Molecular Engineering of Recombinant Protein Hydrogels: Programmable Design and Biomedical Applications